Rally Foundation for Childhood Cancer Research

Meet Abby

In 2001, at the age of six, Abby was diagnosed with an aggressive brain tumor called anaplastic ependymoma. After surgery which completely removed the tumor, she had six weeks of radiation treatments. Everything was just fine when a routine MRI revealed a recurrent tumor in 2003. Additional surgery and brachytherapy radiation followed. Later that same year, Abby had more surgery to remove extensive radiation necrosis after which she completed two years of oral chemotherapy. In May 2007, a routine MRI revealed a "suspicious" area which required more surgery. Thankfully, the mass turned out to be non-malignant and Abby has recovered well. Abby is an independent girl who loves animals, especially the family pets, Charlie, a black and tan standard dachshund, and Snickers, a fluffy cat. She enjoys listening to music, playing games with her sister, and has participated in soccer and gymnastics. Abby's determination and strong spirit have helped her through the difficult times. At present, she is healthy and enjoying life.

Meet Aiden

Aiden was a charismatic and loving toddler. He loved to "wash dishes" and get his own snacks. Aiden was a healthy and robust child until he was diagnosed with ATRT, Atypical Teratoid Rhabdoid Tumor, which is a rare and highly aggressive pediatric brain tumor. Aiden, like his childhood cancer counterparts, never complained and valiantly fought cancer until he went to heaven in his mother's arms four months after diagnosis.

Aiden's mom shares, "Research is the key to a cure for our children. Aiden didn't just touch people's lives; he touched them deeply, and we are thankful to everyone who helps in the fight against this disease."

Meet AJ

AJ was born during a blizzard in March 1993, and didn't cry or breathe right away. But after he took that first breath, boy did he breath deeply for the rest of his life. He lived his short life to the fullest and did the right thing, always giving 110%. He loved sports and played football, hockey, track and soccer at a championship level. He was always smiling. He expressed his love of music by playing the guitar. He loved people, animals, movies and good books. He was a thinker, but he had fun. AJ always made people laugh and was simply just a joy to be around.

His sister Katelyn said, "AJ, you would say something to make me laugh or cry or think and I would just stare at you thinking, "How did you even think of that?'" His best buddy Pablo said, "AJ's character was like the sun-brilliant, golden, and able to light up the whole world".

AJ was diagnosed with Burkitt's Lymphoma and was admitted to the hospital on Fathers Day 2007. He fought bravely, elegantly and continually until January 5, 2008, when God decided that AJ was the only person on Earth who could do what needed to be done for Him. We miss him more than words can ever describe and will forever hold him in our hearts. He will always be Dad's "favorite son", Mom's "pistol" and Katelyn's "guitar hero."

We have decided to try to do something so that no other boys or girls or parents have to endure this pain and suffering. Please visit the following website to help with our fight. People Against Childhood Cancer: http://curechildhoodcancer.ning.com

Meet Alexa

Just days after her first birthday, Alexa was diagnosed with stage 4 Neuroblastoma, an aggressive form of cancer. She was given a 20% chance for survival. Fortunately, Alexa was enrolled in a clinical trial and for the next three years underwent surgery, chemotherapy, and radiation. After a few years of healthy childhood, she began to have several medical issues which were a result of all the cancer treatment she had as a young child. Alexa's spine began to curve sideways and inward towards her organs. The inward curve began pushing against her lungs and along with the scarred lungs from chemotherapy she ended up with only a 20% lung capacity.

In January 2008, Alexa flew to St. Louis to have scoliosis and lordosis surgery in order to straighten her spine and give her room to breathe. The results were amazing and she returned to Atlanta for physical and occupational therapy and to get back to being just a normal kid.

Although Alexa was far from being normal, she was a beautiful girl with a big, bright smile and an amazing attitude. She loved school, math and reading, helping others, playing the piano, and having fun with all of her friends. At age 11, she was so full of life but passed away on Thanksgiving Day with her family by her side.

Meet Allison

Allison was diagnosed on February 4, 2009 at the age of 2 ½ with ALL Leukemia. She complained of leg pain and fought a respiratory infection for several weeks before being diagnosed. She lost her energy, became pale in color and was very clingy to her mom and dad. After numerous trips to the doctor for different illnesses, blood tests were done which eventually led to her diagnosis with leukemia.

When Allison is not busy fighting cancer, she loves to play with her two older sisters. She likes to color, play games, play house, do arts and crafts, and any type of imaginative play. Since being diagnosed with leukemia, Allison has celebrated her third birthday. She should be finished with chemotherapy in the summer of 2011, and will start kindergarten off-treatment and cancer free!

Meet Amelia L.

On the December 23rd of 2005, Amelia was diagnosed with Acute Lymphoblastic Leukemia (ALL). She continued attending school throughout the initial phases of her treatment and is currently in remission.

Amelia turned 8 in May and looks forward to starting the third grade in August. Her attitude and spirit continue to be an inspiration to all who know her.

Meet Amelia M.

Amelia was born on October 31st, 2001 and was always a curious and happy child. At three and half years old, she was taken to the pediatrician because it was suspected she had pink eye, which was ruled out. Two weeks later the retina in her right eye detached and she was quickly diagnosed with retinoblastoma, a childhood cancer that begins in the eye.

Two days later her right eye was removed, and we were overjoyed to find that the cancer had not spread and she would not need chemotherapy. Her remaining eye is healthy with perfect vision, but she will always wear glasses to protect it. After she healed from surgery she was fitted with her "princess" eye.

Amelia remains cancer free. She enjoys time with her friends and her dog Sophie, playing violin, airplanes, and catching bugs in the yard. When she grows up she wants to be a police officer.

Meet Andrew

After weeks of painful headaches, constant nausea and loss of appetite, six-year-old Andrew was taken to his pediatrician once again. One day he was being treated for a sinus infection. The next day, he was diagnosed with a rare, inoperable brain tumor, known as a hypothalamic juvenile pilocytic astrocytoma.

Andrew participated in an experimental radiation protocol receiving daily brain radiation for eight weeks. After some shrinking, his tumor has remained stable for five years. Andrew has officially been off treatment for six years. Although he battles long-term side effects from treatment including many hormone issues, he feels fortunate to be able to enjoy the life that he does.

Andrew is now an active 13 year old. He enjoys school, and he loves to play baseball, basketball, and run cross country. He is an inspiration to his family and friends. He proudly raises funds to fight childhood cancer and doesn't want any child to suffer from cancer or the terrible side effects from treatment.

Meet Andy

Andy was diagnosed with stage IV Neuroblastoma shortly after his first birthday. The cancer had spread to his skull and his hips in addition to a large tumor in his abdomen. He went through nine rounds of chemotherapy followed by six months of Accutane treatment.

Andy was very brave during his treatment. He is now in 3rd grade and doing well. The side effects of his intense treatment continue to manifest themselves. His mom writes, "Much research needs to be done to increase survival rates as well as decrease the late effects. Thank you for supporting childhood cancer research!"

Meet Angela

Angela writes: My life changed in the spring of 1973. I was just three years old when my mom took me to my pediatrician for a check up. While he was examining the area around my stomach, a very serious look came across his face. After his partner examined me and confirmed what he had found, they told my mom to take me to the children's hospital where I had x-rays and a CT scan. I was then diagnosed with stage III neuroblastoma. At the time when I was diagnosed, I had no symptoms. My dad, who is a family doctor, feared the worst but prayed for a miracle. I endured surgery and one year of chemotherapy. My surgeon discovered during surgery that my tumor was caught early and had not invaded any of my vital organs.

Due to the amount of chemo that I received, I started having problems with my short and long-term memory. I'm quietly struggling with this day by day, but I enjoy swimming, riding my bike, scrapbooking, reading, painting, and listening to music.

My picture is from 1981, when I was a healthy 11 year-old and 7 years cancer-free. Today, I love sharing my story of surviving childhood cancer over 30 years ago with people who are living with childhood cancer now. Please donate to Rally so that researchers can find treatments with fewer long-term side effects!

Meet Anna

Just after her second birthday, Anna was diagnosed with leukemia. Petechiae, a type of rash that can indicate a low platelet count, had just barely appeared on her neck. Her pediatrician sent us to the hospital for tests "just to be safe." She started chemotherapy that night. For the next three and a half years Anna experienced the ups and downs of therapy, blood counts, fevers and trips to the hospital. Anna never let that stop her from being herself.

Anna's enormous determination showed itself at every step, from struggling against the treatments and tests, to insisting on wearing her Tinkerbell costume to walk the halls at the hospital with her IV pole and parents following behind. Now at the age of 13, Anna is a full-fledged teenager who plays lacrosse, the piano, and enjoys just being with her friends.

Meet Annika

On February 7, 2009, Annika underwent a laparoscopic procedure for an intestinal problem called intussusception. During the operation, which took place on her dad's birthday, surgeons realized the problem was more complicated and moved to a more involved surgery. Here, they removed a tumor from her abdomen. The cancer was eventually diagnosed as Stage II Burkitt's Lymphoma, but the prognosis was good. She required a short protocol of just two courses of chemotherapy and was able to have a PICC line instead of a port. Since any little amount of chemo is hard on a body, Annika lost a lot of weight and all of her hair.

On May 20, 2009, Annika had her first clear scan! Her mom shares, "Currently seven months cancer free, Annika's hair is growing back, and she is closer to a healthy weight. We are now involved in raising awareness of the need for research specific to pediatric cancer. Thank you Rally Foundation for your dedication."

Meet Autumn

At just 14 months old Autumn started vomiting each morning. Her pediatrician diagnosed her with an ear infection and treated her with antibiotics. A few days later she fell but seemed to be fine. At a follow up appointment for her ear infection, her parents told the doctor about the small bruise she had under her left eye from the fall. The pediatrician ordered an x-ray of Autumn's abdomen and a CT Scan of her head just to be safe. The CT scan was then followed by an MRI. On October 18, 2007, which is also her dad's birthday, Autumn was diagnosed with a brain tumor. She has undergone 60 weeks of chemotherapy, only to recently find out that the tumor is growing. Autumn has faced many challenges along her road and luckily she has overcome all of them. She is now facing tumor resection surgery at 3 years old.

Autumn loves Dora, baby dolls, playing outside, and most of all, the color green. She has a beautiful smile and is so proud that her hair has grown back. Her favorite song is the ABC song and she loves to sing it to you. She is a very happy child despite what she's been through.

Her mom says, "We consider ourselves a lucky family, we still get to hug and kiss our little girl goodnight, every night. Other families, sadly, do not get to do this. This is where the Rally Foundation comes in - raising money for research so that one day every parent gets to hug and kiss their child goodnight without the fear that it could be the last time. A cure is out there somewhere; we just have to keep looking, supporting, and fighting!"

Meet Avery

Always smiling, athletic and enthusiastic Avery began complaining of back and leg pain in the spring of 2005. She was diagnosed with Acute Lymphoblastic Leukemia (ALL) the most common childhood cancer and just completed two years of chemotherapy treatment. All through treatment, Avery maintained her contagious smile and a great sense of humor.

Avery, like most teenagers, enjoys hanging out with her friends and going to the beach. She is a swimmer and an inspiration to all who know her.

Meet Bella and Maddie,

On July 4th, 2007, our family was blessed with the birth of beautiful identical twin girls, Isabella (Bella) and Madeline (Maddie). On August 30th we noticed that Madeline's abdomen was a little swollen and firm. However, her behavior was unchanged so the pediatrician suggested some gas drops, which we tried but did not change her abdomen.

On September 4th we went to the pediatrician for the girls' 2-month checkup. He took a look at Isabella and said she looks perfectly healthy. He took a look at Madeline and he immediately sent us for an x-ray. After the x-ray, we waited in the waiting room for the doctor to call us back with the results. He didn't like what he saw on the x-ray, so he told us to go to the hospital immediately.

A CAT scan that very night indicated Maddie had a large cancerous tumor called neuroblastoma. In the next few days, Bella began exhibiting symptoms and was soon diagnosed with neuroblastoma as well. The doctors feel that the tumor started in Madeline and spread to Isabella via the placenta. The girls are only the 9th reported case of monozygotic twins with neuroblastoma in the world.

The girls have a proud older brother, Isaiah, who is 2 years old. He likes to visit them at the hospital but is looking forward to spending time with them at home!

Meet Ben

Ben gave infinite joy to his parents from the moment of his birth on April 18, 1998. He was a child of keen understanding, curiosity, kindness, and spirit, with a mind sharp and perceptive beyond his years. In games, he often beat adults handily, applying bold strategy and relentless resolve. From Memory, to chess, Ben was a formidable adversary. At the same time, he had endless playful energy. He loved Kung Fu, soccer, snowboarding and playing, especially with his younger brother, Jacob. His friends admired him for his deep knowledge of Star Wars and Lord of the Rings and his skill with their associated video games. He built an extraordinary collection of Pokémon cards to which many generous friends contributed during his illness.

Ben was diagnosed with Burkitt's Lymphoma in January 3, 2005 at the end of his first grade winter break. From the moment of diagnosis, he was a self-proclaimed cancer survivor. Ben fought with courage, grace and humor, distinguishing him as a hero to many. On August 12, 2008 after eight rounds of weeklong chemotherapy treatments, two bone marrow transplants, 30 blood transfusions, 21 sessions of radiation therapy, he went home from the hospital. He smiled as he walked into his home and his room that day. Eight days later on August 20, 2008 he passed away in our arms surrounded by loved ones.

Meet Benjamin

At the age of four, Benjamin was diagnosed in 2004 with two types of Leukemia (ALL and AML) at the same time. After a relapse, he continues in treatment for his cancer. He has spent three years of his life on chemotherapy.

Ben enjoys playing soccer and recently earned an orange-striped white belt in karate! Ben loves Ninja turtles, climbing on the playground, and playing with his brother. He is looking forward to beginning kindergarten soon.

Meet Brady

Just before his fourth birthday, Brady was diagnosed with cancer. A malignant tumor in his right ear canal extended through his middle and inner ear. The tumor wrapped multiple times around the carotid artery, which rests on the brain. The day after his fourth birthday, Brady began an aggressive treatment of radiation (28 treatments stretched over six weeks) and chemotherapy for the next 43 weeks. None of this stopped Brady. He remained the fun-loving, spunky child everyone had always known. In fact, Brady played his first baseball game just one day after receiving a heavy dose of chemo!

Now at the age of eight, Brady is currently off treatment and doing great! He loves playing baseball, riding his bike, and playing with his brother and friends.

Meet Brian

Brian was diagnosed with an inoperable brain tumor called Glioblastoma Multiforme in August 2009. Located on the left side of his brain, the right side of his body is affected; specifically, it can affect his face, arm, and leg. Brian has completed radiation therapy and is currently undergoing chemotherapy treatments.

An avid sports fan, Brian loves football, soccer, basketball and wrestling. His favorite college football team is Ohio State, his favorite pro team is the Atlanta Falcons, and his favorite high school team is the South Forsyth War Eagles! Brian played football from 3rd grade until he was diagnosed in high school. He was on the wrestling team and also participated in the band as a percussionist. As a young and enthusiastic musician, Brian played the drums by ear for five years before becoming a student of music theory. Today he produces music with his own studio program and maintains a library of music. Brian attends NorthPoint Community Church where he enjoys connecting with his small group.

Meet Brittany

Vibrant, energetic, beautiful, athletic, courageous...that was Brittany from day one. At 19, she was the picture of health and on her way to the future of her dreams

A double lung transplant looked to be her only option, but the cancer was especially aggressive and she began declining very quickly. Soon, due to her decline and the unusual nature of this cancer, the transplant was no longer an option and she was to be treated with a new targeted chemotherapy drug that had shown some quick results in clinical trials. Tragically, the cancer didn't respond as quickly as we hoped, and she just didn't have the amount of time needed for the treatment to take effect. Three weeks after being diagnosed, Brittany lost her battle with lung cancer.

Brittany's mom writes, "This beautiful young lady, not quite 20, was a fighter right up until the end. A role model of grace and dignity, she's left a wonderful legacy for her siblings and friends to follow. Our prayers now are that her legacy lives on through us. Brittany's Battle is far from over...we are fighting on until the day NO ONE has to fight anymore."

Meet Bryson

Bryson was born on January 9, 2008, and his journey with childhood cancer began seven months later. After spending a long night in two different emergency rooms, a CT scan revealed that Bryson had a bleed on his brain caused by a tumor. He was immediately life-flighted to Children's Healthcare of Atlanta where a procedure was performed to relieve the pressure until the tumor could be removed.

On September 2, 2008, a successful brain surgery removed 85% of the tumor. A few days later, Bryson was diagnosed with Glioblastoma, a malignant brain tumor, and was placed on a two-year chemotherapy treatment plan. He has recovered from five surgeries that he endured over the course of one month and now attends therapy two times a week. He also receives chemo treatments once a month. Although Bryson has a long road ahead of him, he is a strong child and has already proven to be a fighter in so many ways.

Meet Caleb

Caleb began complaining of leg and arm pain in August 2007 when he was 3 years old. Although there was no visible fracture on the x-ray, Caleb was put in casts on his right arm and right leg. A few days later, his left leg began hurting and blood work revealed leukemia. Ten days after Caleb's diagnosis, he was diagnosed with a rare subtype of leukemia called Hypodiploid ALL. Caleb was immediately placed on a protocol that included a bone marrow transplant, which he received in November 2007 at Duke University. The transplant was best described as textbook. After four months at Duke, Caleb finally returned home to Florida, only to relapse four days later. There is no protocol for a patient who has relapsed so close to a bone marrow transplant, so we placed our 3-year-old son in hospice care and prayed for a miracle. One day, Caleb noticed that I had been crying. He simply said to me, "Don't worry about me, Daddy. I will be ok." On March 28, 2008, Caleb went to be with God, only 11 short days after his 4th birthday.

Caleb was a superhero to all who knew him. He loved Spiderman, and he actually thought he was Spiderman! His strength and faith carried him through his treatments until the end. Caleb wanted to be a doctor when he grew up.

Meet Cam

Mid-way through the summer before Cam was going to start seventh grade, he was diagnosed with Ewing's Sarcoma in his left leg. For the next year Cam underwent surgery, 14 rounds of chemotherapy, radiation treatments and physical therapy. Unfortunately, Cam relapsed in May 2009. He is currently undergoing an experimental antibody treatment called IGFR. He is a typical teenage boy who is hungry all the time, enjoys video games and playing "airsoft" with his friends. His favorite subject is math, and he just made Star rank in Boy Scouts. Cam writes, "I've just found out that I've had a recurrence of my Ewing's sarcoma cancer. Yuck! I thank you for raising money to help kids like me."

Meet Camden

Camden began having problems with his ears and balance at the beginning of 2007. After several weeks of appointments with many different doctors, a CT scan showed a tumor on Camden's brain in February 2007. Camden was flown to a hospital several hours away from home for brain surgery to remove the tumor. The pathology report showed that Camden had medulloblastoma, a type of brain tumor, which had also spread to his spinal cord. He underwent chemotherapy treatments until shortly before he passed away in September 2008.

Camden loved to watch movies, play with his puzzles and playdoh, read books, sword fight with his brother, and listen to music. He was a personable kid who loved to interact with others. His mom says, "He had the best spirit of anyone I know; and I, as his mother, looked up to him for strength and support. What he had to endure on a regular basis was something I don't know I would be able to do and with such a wonderful character."

Meet Carina

Carina was diagnosed with Non-Hodgkin Lymphoma (T-cell Lymphoblastic Lymphoma) on Feb 25, 2009 when she went to the emergency room because she was very tired and complaining of difficulty breathing. She hadn't been feeling well all week, and had gone to the doctor's office just two days before and was diagnosed with a virus. The emergency room doctor ordered an x-ray, which led her to order a CT scan. The CT scan showed a mass in Carina's chest and fluid in her lungs, and the results changed Carina and her family's lives forever. Carina is an amazing child full of life and joy. She has an incredible kind and caring spirit. She likes computers and music, and she wants to learn how to play the guitar, keyboard, violin, and base. She also wants to be an actress. She is a beautiful young lady and the joy of her family's lives.

Meet Carmel

Carmel was diagnosed with AML leukemia on January 1, 2004. After extensive chemotherapy and radiation, she underwent a bone marrow transplant in which her sister was a perfect match. Off treatment for over a year, Carmel is doing great.

Carmel's mom says, "Today we are grateful for a boring normal life." Carmel is currently a 4.0 student at Georgia Highlands College. She does volunteer work at her local library. She loves cooking, singing, reading, and small children. She has also adopted a rescued pit bull named Daisy. She is currently doing very well, and will celebrate being cancer free for five years in April 2009!

Meet Carsten

Carsten is a loving, intelligent, funny and fun boy who loves to learn. He was diagnosed with Acute Lymphoblastic Leukemia (ALL) in December 2005, and is undergoing chemotherapy treatment at Children's Hospital in Washington, DC. He continues to maintain a positive, upbeat attitude, and enjoys learning about how his body is working to defeat this disease.

Carsten is in third grade at Key Elementary School, where classes are instructed in English and in Spanish. It has been great fun for him learning another language. He loves to create. One of his favorite activities is to build flying machines out of Lego blocks. He also loves to draw, paint, and to glue things together. Carsten loves to read, and is a big fan of Star Wars, and other adventure stories.

Meet Carter

At the age of seven, Carter faced cancer with determination and a smile - not once did he complain. All who knew Carter adored him. Carter loved God, Georgia Tech, his dog Comet and his family and friends tremendously. He excelled in art, sports and academics. Carter thrived on competition, and he won almost every battle. When this young warrior met his match in cancer, he challenged the disease with his own piggy bank coins and asking his mom to give the money to find a cure.

Despite 14 cycles of chemotherapy and an experimental form of therapy, Carter's battle against cancer was lost. But this courageous young man, who knew cancer could take his life, told his mom, "Cancer can't take away love."

Meet Carter R

On May 9, 2008, 8-year-old Carter was taken to Scottish Rite Children's Hospital following a virus. We were expecting to get some blood work done, and find out why his blood counts were lower than they should be. The next eight hours were a blur as the doctors expressed "concern" over some "suspicious" cells. They admitted Carter to the hospital to await a bone marrow test on Monday, and on Tuesday, May 13, 2008, Carter was diagnosed with ALL (acute lymphoblastic leukemia).

Carter immediately started treatment, which consisted of implanting a port, checking his spinal fluid for leukemia cells, and starting chemotherapy. He is now in the maintenance phase of treatment and his estimated treatment end date is July 2011!

Although there is so much out of our hands, we know that with the continuous thoughts and prayers of our friends and family, we will ultimately help Carter reach his final goal of a full recovery!

Meet Catherine

Catherine was diagnosed with a brain tumor on her optic pathways when she was 27 months old. She underwent chemotherapy for 18 months and finished on March 17, 2009! Although Catherine is officially finished with chemo, she will continue to be busy with brain MRIs scheduled every three months for the next 2 years, weekly blood checks to monitor her platelet counts, and eventually, bladder repair surgery. So far, she has done well, with a few bumps along the way. Incredibly observant, she reminds her parents to put cream on her port before going to the doctor. She helps the nurses flush her tubes by pushing the syringes. Catherine gets the toys ready to play tug of war with the doctor to test her strength. If anyone ever forgets who she is, she shows them her hospital bracelet so they can check her identity.

Her journey with cancer has not slowed this busy toddler down. She loves going swimming and recently enjoyed a vacation trip to Disney World. We are praying that her vision will be fine, the tumor will never return, and the chemo will have no lasting side effects. We are blessed to have Catherine in our lives and blessed with the wonderful team of people who care for her. We are excited to see how she will gain strength, weight and energy throughout the next year. She is a delight and joy to everyone she meets

Meet Catie

Catie was an adorable toddler who had a twinkle in her eye and brought a smile to your face. She loved animals, princesses and her friends. She was also a very determined and courageous little girl. On her first birthday, she was diagnosed with a brain tumor. Catie has endured eight surgeries, 22 months of chemotherapy and 30 radiation treatments. Catie fought long and hard, but in the end, her body could not tolerate any more treatment.

Catie's mom, Jenny, says, "Children's days should be filled with playtime, laughter, and friends not chemotherapy, hospitals, and medicine. It is only through research like that funded by the Rally Foundation that doctors will find more and less toxic cures for our children. That's why we fully support the Rally Foundation and the work it does. Join us and rally with Catie to give all kids diagnosed with cancer a better chance at living the full life they deserve."

Meet Chelsie

Chelsie was diagnosed with stage III High Risk Neuroblastoma in August 2004 at the very young age of 4 months. By her first birthday she had endured multiple rounds of chemotherapy, 12 rounds of radiation, oral chemotherapy, surgery to remove the remaining tumor, and a very risky stem cell transplant. Through it all she remained a trooper. In February 2005, she was declared NED (no evidence of disease), which she remains today.

We were very fortunate to live in a community with a cancer center for children. We count our blessings daily that she is where she is today, especially since many of her friends are not so fortunate.

Chelsie loves school and cheering on her favorite team O-H-I-O. She is still followed very closely by her oncologist and is scanned every 3 - 6 months. She is such a joy to our family and we pray that a cure is found, so that others may live.

Meet Chris

At the age of five, Chris was learning Tae Kwon Do and getting ready for kindergarten when his parents were given the devastating news that he had cancer. For the next five years, Chris had three surgeries, 34 rounds of chemotherapy, radiation, a stem cell transplant and hundreds of blood and platelet transfusions. He was a Cub Scout, served on the school safety patrol, and had a first degree black belt and an incredible sense of humor.

At age 11, his body could not tolerate more treatment and he passed away with so much more life yet to live.

Meet Christopher

Christopher was diagnosed with Acute Lymphoblastic Leukemia (ALL) in May of 2000. He went through three years of daily chemotherapy. Throughout his treatment, Chris kept his positive attitude and sweet smile. He is now 14 years old and in the 8th grade, where he excels at Social Studies and hopes one day to go into politics. In his free time, he enjoys working in the barn with his horses, gathering the chicken eggs, and taking care of all of the other animals. He also likes to go skiing with his family, collecting old coins, and loves to go to garage sales. Chris is actively involved in various cancer awareness groups and hopes that one day all childhood cancers will be wiped out.

Meet Christi

Christi began experiencing back pain in the spring of 2002. Doctors found nothing wrong. One day, she woke up from a nap screaming in pain and unable to breathe. A CT scan found a tumor along her spine and around her heart. September 11, 2002 she was diagnosed with Neuroblastoma, a rare childhood cancer of the nervous system. It had spread throughout Christi's tiny body and into her bone marrow. She was Stage 4, the most advanced stage with the poorest chance of survival. Intense cancer treatments, two hours from home, put Christi in isolation for many months - no school, church, or friends.

Despite the harsh treatments, the cancer remained and it became medically necessary to transfer Christi's cancer care to New York City. Christi's parents left their youngest daughter at home (500 miles away) and moved into the Ronald McDonald House where they lived for 9 months during Christi's treatments. The treatment included surgeries, chemo, and other experimental trials. Still, her cancer remained.

Christi took many more experimental treatments some allowed her to live a relatively "normal" life at home. A profoundly gifted child, she loved school. She also took weekly: horse riding lessons, ballet, jazz, religion and piano lessons. She received the "Clara Barton Award" (the Red Cross's highest honor), for sponsoring blood drives. Christi knew first hand the importance of donating blood as her life has been saved over and over by loving blood donors.

Sadly, in January of 2006 Christi's cancer worsened and spread. Despite nine more months of experimental treatments, the cancer proved to be too much for Christi's body who had endured four continuous years of treatments. Christi gained her Angel wings on September 19, 2006 with her parents by her side.

Meet Claire

Claire was the kind of child that always seemed larger than life. As a baby, she cried more than any other baby; as a toddler, she was always busy learning about everything, and as a little girl, she could do anything. Claire was an excellent gymnast, contortionist and swimmer. Everything came easy to her, so much so, it made her brother and sister jealous. As a teenager, she was a cheerleader and member of the debate team. She was beautiful, and had a lot of friends.

Then, cancer reared its ugly head. Not just cancer, but the terminal kind with a challenging 14 months, at best, to live. Claire took on this new challenge with her usual pluck and strength. She was determined to beat it, and she fought for all she was worth.

Claire lost her battle to cancer, but not because she didn't fight. She lost it because we don't know how to stop her kind of cancer. We don't know how to stop a lot of childhood cancers. If Claire had been diagnosed with a brainstem glioma in 1974, her prognosis would have been the same then as it is today. This is unthinkable that we are allowing our children to die because we don't put our money into research for childhood cancers. Please join Claire, me, all of the children who have and are battling cancer, and their families in giving money for cancer research.

Meet Clark

Clark was diagnosed with Osteosarcoma in August 2006 at the age of 15. Clark loved all sports but was an avid baseball and football player. While training for football, Clark experienced a pain in his leg, which was later diagnosed as Osteosarcoma. He spent his first year of high school receiving chemotherapy treatments in Atlanta and New York City.

Clark's attitude and determination have,enabled him to overcome many obstacles and minor set-backs. He is currently preparing for his senior year of high school. He has redirected his love for sports to golf and fishing. He coaches middles school football and baseball. He stands by his motto of "adapt and overcome" as he continues to embrace all that life has to offer.

Meet CJ

In April 2008, Christopher, better known as CJ, was diagnosed with cancer at the age of 18. He was diagnosed with Osteosarcoma with Ewing's Translocation, which CJ called a hybrid tumor. CJ had a very rare form of cancer, and there is very little if any research on his cancer type, but CJ had a very positive attitude about the journey that he was on. When he was diagnosed, CJ had a large tumor in his left humerus bone and shoulder along with small tumors throughout his lungs. After 7 months of intense inpatient chemo, CJ had surgery in August 2008 to remove the tumor and his bone. Unfortunately the tumor was wrapped around his radial nerve, which had to be cut, and this left him with limited use of his arm, hand, and fingers. CJ was to continue on the same chemo​ for another seven months then radiation, but a CT in October 2008 showed new tumors in his lungs, and CJ started a new chemo. In December 2008, the tumor in his left arm returned. Scans in February 2009 showed that the chemo was not effective, and the tumors were growing in size and number. In March 2009, the tumor on his arm was removed, but it quickly returned in April. CJ soon began having trouble breathing, and a CT showed rapid growth of the tumors in his lungs. The tumors continued to grow in spite of chemo and radiation, and CJ made the decision to stop treatment and focus on quality of life. CJ took his side by God on May 16, 2009 at the age of 19.

Meet Cole

In November 2006, Cole was diagnosed with cancer just before turning six years old. Doctors discovered several large masses in his abdomen, later to be diagnosed as Desmoplastic Small Round Cell Tumors. He endured nine rounds of high-dose chemo, a MIRACULOUS surgery in NYC that successfully resected 100% of the tumors, and full abdominal/pelvic radiation therapy. Cole ended treatment in August 2007, and has been in remission since. While relapse is a possibility for Cole's disease and many others, Cole is determined to stay strong and healthy to be ready to fight if it returns. Cole is a charmer who makes friends wherever he goes and loves sports, especially baseball. He has an undefeatable positive spirit - and remembers more about all the fun opportunities he's had during treatment than the cancer itself. While he is one of the lucky ones to beat this awful disease, there are currently no treatments to prevent recurrence. Cole's mom says, "More research on immunology and genetic therapy is much needed to help kids like Cole who beat cancer stay cancer free!" divider

Meet Coleman

Coleman's journey began September 21, 2006 when he and his twin brother Caden were 2 1/2 years old. Coleman had begun displaying signs of dizziness and complaining of head and neck pain. Our pediatrician was concerned and ordered an MRI. The news was devastating, the word tumor cut like a knife right through our hearts. Coleman had surgery to remove the tangerine sized tumor that was embedded in his cerebellum, and he was diagnosed with medulloblastoma.

He had completed one year of chemo when a routine MRI revealed that two tumors were growing in the same spot as his original tumor, and his spinal fluid also contained cancer cells. Chemo was stopped and Coleman did 7 weeks of radiation. Caden was there every day to talk to him over the loud speaker during his treatments, and Coleman was able to complete radiation without sedation! The tumors responded but had not disappeared, so Coleman underwent a stem cell transplant. In August 2008, Coleman relapsed 4 months after stem cell transplant with 7 small tumors found in his spine and cancer cells in his spinal fluid. In November 2008, Coleman was undergoing a clinical trial when an MRI revealed that the tumors had grown.

Coleman used to say, "some day I won't need NO more meds or pokes, wight mommy? THEN I tan be NO-MAL!" His journey didn't end the way his family had hoped, but he was freed from the life of meds and pokes when he passed away on January 5, 2009 with his family by his side.

Meet Colin

Colin was born in Edinburgh, Scotland, where he hitched a ride around most of Europe with Mom and Dad before his first birthday. After returning to Chattanooga, TN, a workup for failure to thrive revealed severe gastroesophageal reflux which was treated with some success medically. However, during one of the upper GI scope procedures, an abdominal mass was noted incidentally which was eventually diagnosed as stage 2a Neuroblastoma, N-myc amplified. This is an aggressive tumor which is usually stage 4 at diagnosis. After major abdominal surgery, over 7 smaller surgeries, 6 rounds of chemotherapy, a stem cell transplant, and 12 radiation treatments, Colin is currently undergoing antibody treatment before finishing with 6 months of Accutane therapy.

Since his diagnosis, Colin touched hundreds of lives around the world through his courage and resilience. Colin enjoys showing off original dance moves for his nurses and parents, throwing balls, watching Thomas the Train (A.K.A. Car-Car), and attacking daddy's chin. He is also learning to share with his new baby brother, Ryan. With no current evidence of disease, Colin is ready to rally as a warrior against cancer. Rally on, Weeman!

Meet Cooper

During a routine check up at six months of age, Cooper was diagnosed with Stage IV Neuroblastoma. He had a softball-sized tumor in his abdomen and cancer that had spread to his liver. Since that time, Cooper has been through surgery, 6 rounds of chemotherapy, a stem cell transplant, radiation, and a retinoic acid and antibody study. He just had his first off-treatment scans which showed that he is cancer free! Despite the ordeal, Cooper is the happiest kid one could imagine. He is now four years old.

Meet Corey

Corey was born on June 4, 2004. At the age of 2 1/2, he was diagnosed with Stage IV Neuroblastoma. He underwent chemotherapy, stem cell harvest, surgery, and a stem cell transplant. He had complications including septic shock and kidney failure, which required dialysis treatments. After recovering he had 12 rounds of radiation, antibody treatment and Accutane therapy. He enjoyed 11 months of being cancer-free and six months off treatment before relapsing in October 2008. He then had more radiation and chemotherapy until March, when his scans were clear again. Unfortunately, his cancer returned only one month later. Corey started chemotherapy again but immediately began suffering severe side effects. His medical team tried to treat his low blood pressure and respiratory failure, but the cancer was taking over his body. On May 8, 2009, Corey's journey with cancer ended peacefully, and he is now free from cancer and enjoying heaven.

Corey was a loving and energetic boy who loved firefighters, trucks, trains, and fishing. He was the youngest member of his community's fire department. He is deeply missed by his family.

Meet Corey Z.

Corey was born on 1/1/05 and was diagnosed with Wilms' Tumor, a pediatric kidney cancer, on 1/1/06. At diagnosis, he had Stage 1 Wilms' Tumor with favorable histology, which had a 95% cure rate. A two pound tumor was removed, along with his right kidney and some lymph nodes. Unfortunately, just three months after finishing chemotherapy treatments, Corey's cancer relapsed to his lungs and lower spine area. He was paralyzed for a few weeks until the new chemotherapy and radiation treatments started working. After finishing an intensive twenty-four week protocol that kept Corey in the hospital most of the time, Corey enjoyed ten months of being cancer-free and relearned how to walk.

During follow-up scans in December of 2007, a small tumor was found in Corey's left lung. Since this was his second recurrence, there was no protocol to follow. After considering many opinions from different doctors, Corey was treated at Children's Hospital of Los Angeles. He received chemo for four months to kill the tumor and then had lung surgery to remove the dead tumor. Once he recovered from surgery, Corey was hospitalized to undergo high dose chemotherapy with a rescue of his own stem cells. Corey spent thirty-four days in the hospital, but the process has put Corey in remission.

After a long and trying battle, Corey has been cancer-free for over sixteen months! He checks in with his doctors once a month now, has scans every six months, and he and his family are hoping to live life "happily ever after."

Meet Coulter

Not only was Coulter deaf and blind in one eye, but at 18 months old he started showing signs of a cancer called Aplastic Anemia. He was a child who was full of life and loved to play outside. He loved Woody and Buzz Lightyear from the movie Toy Story, and liked to dress up as different characters. He loved his brother and sister dearly and enjoyed going to school when he was well enough to do so.

After fighting for six and a half years, he lost his battle and died March 29, 2005. He was 8 years old and had so many more plans for his life.

Meet Daniel

At age 12 and 13, Daniel underwent surgery to correct a leg length discrepancy. Sixteen months later, as a high school freshman, Daniel's dad noticed a walnut-sized lump near the previous incision.Daniel underwent surgery for this soft tissue tumor, but it was misdiagnosed by pathology. Daniel felt the recurrence six months later at the end of football season of his sophomore year, now a six-inch tumor completely internal and wrapped around a nerve at the side and back of his knee. He was subsequently rediagnosed with a Desmoid Tumor, also known as Aggressive Fibromatosis, an often misdiagnosed, highly recurring, fast growing type of tumor that strikes often in adolescence.

Daniel received 30 radiation treatments during high school soccer season, but he still played every minute of every game. Seven weeks after major surgery to remove the tumor and previous scar tissue, Daniel contracted a staph infection in his incision, requiring another surgery and seven weeks of wearing a portable wound vacuum. Daniel kicked for the football team while his skin was still healing, even using his one hour unhooked from the wound vacuum to attend football practice. Daniel has not let cancer slow him down ñ he was named Special Team's MVP by both the freshmen and J.V. football teams.

Daniel has incredible inner strength and has always been determined that his medical treatments would not interfere with his life. He also insisted that his tumor tissue be donated for research to help other children fighting this disease. He has already started preparing for his career as a doctor by shadowing his orthopedic oncologist/surgeon in the operating room and in the office. His doctor even taught him how to read an MRI while reading Daniel's first six-month post-surgery clear MRI.

Meet Delaney

Delaney was diagnosed on June 26, 2002 at the age of six with localized Ewing's Sarcoma/PNET. Her symptoms began as early as January of 2001 when she was only four years old. The tumor started in her left maxillary sinus, but was initially overlooked as "congestion". When she was finally diagnosed 18 months later, the tumor had spread further into her maxillary sinus, destroying the ethmoid bone and invading those sinus passages as well and began to distort her facial features. At that point, surgery was not an option due to the proximity of the central nervous system and her eyes. Delaney was treated with 14 rounds of chemo and 28 days of radiation to the face and frontal lobe.

She is now thirteen years old and remains cancer-free. Sadly, the late effects continue to cause damage to both the structure of the area as well as to the frontal lobe region of her brain. She will need special education assistance for emotional developmental issues, many reconstructive facial surgeries as her face continues to grow, and it appears that her pituitary gland is not functioning properly. The name "Delaney Renée" means "The Challenger Reborn", and Delaney certainly lives up to her name!

Meet Donnie

At the early age of 17 months, Donovan was diagnosed with Stage IV Neuroblastoma with metastases to his bone marrow, pelvis, spine, chin and right eye. To fight this disease, Donovan underwent 7 rounds of chemotherapy, a surgery to reset the tumor on his adrenal gland, a stem cell transplant, radiation, and Accutane treatment. We are happy to say that after 18 months of treatment he has now been in remission for 18 months and is finally grown to a normal size for his age.

Donnie lives his cancer free life as a fun 3 year-old that has a lot of energy and loves to spend his days going to church, playing monster trucks and flirt with nurses. We are blessed that he is still here with us, and are excited to get involved in making a difference in the lives of others.

Meet Elise

Elise has Down's syndrome and was diagnosed with Leukemia in February of 2004. She went through regular chemotherapy infusions and has been off of treatment now for over 13 months.

While she was in the hospital, she was famous for her many expressive, funny faces. Some of her favorite things to do are looking at books, listening to music, and playing outside. Elise is an adorable three year old who loves her brother and is doing just great!

Meet Elizabeth

Elizabeth was born on April 21, 2004. On December 23, 2006, her parents took her to the doctor for a cough, and what they thought was a routine visit, changed her life forever. After tests were run it was determined that Elizabeth had Neuroblastoma, but because tests did not indicate that it had spread, she had the 11cm tumor removed on January 11, 2007. The biopsy revealed that she had high-risk Neuroblastoma and needed the most intensive treatment possible. Elizabeth completed six rounds of chemotherapy, a stem cell transplant, ten rounds of radiation, and CIS retinoic acid treatment. After completing those treatments, her parents decided to enroll her in a clinical trial involving monoclonal antibodies. When the tests were run to determine her eligibility for this clinical trial, they found Neuroblastoma in her marrow, which destroyed her chances for entry into the clinical trial. However, doctors were able to gain access for her to the monoclonal antibodies through compassionate release. She then began the first of five antibody treatments, and by April 21, 2008 she was able to celebrate her 4th birthday with no evidence of disease!

Her mom writes, "We are so lucky that she had access to experimental treatments; for without them we do not think she would have been with us for her 5th birthday. The work that Rally does makes 5th birthdays possible!"

Meet Emily

Emily is seven years old and has been fighting Anaplastic Medulloblastoma since August 2006. She has endured several surgeries, extensive chemotherapy, radiation and in mid summer '07, a research protocol chemotherapy regimen. Thus far she has survived much longer than most children diagnosed with this form of medulloblastoma. Emily has brought great awareness to childhood cancer in her community, and she continues to amaze and inspire anyone that meets her.

Emily used to enjoy riding her bike, boating, going to the beach, dancing and going down waterslides. While unable to walk and do her previous activities, she still likes having her picture taken, dolls, princess stuff, jewelry, coloring & drawing, Dora, and Scooby Doo. Emily also loves to cuddle with her new puppy, Oreo! Emily recently enjoyed her wish being fulfilled by visiting Walt Disney World in Florida with her family.

Meet Ethan

Ethan was a smart and active child until shortly after his 4th birthday when he developed bruises that would not go away and began complaining of leg and stomach pain. A few hours after being diagnosed with Acute Lymphoblastic Leukemia (ALL), a port was placed in Ethan's chest and chemo began.

Ethan underwent a 3.2 year regimen of chemotherapy - the long duration of the chemo is to hopefully keep him from ever relapsing. He completed his treatment in January 2009. Ethan is still very smart, but too much activity tires him out. He suffers from some cognitive functioning issues with ADHD- symptoms that are most likely a side-effect of the intrathecal chemo. At age 8, he still can't tie his shoes or ride a bike and has problems with organization and staying on task.

Ethan loves playing with NFL football helmets and knows all the teams and divisions. He loves playing with his little sister - anything from stuffed animals to drawing. He likes Scooby Doo and is an animal lover, especially otters. He has recently started playing video games!

Ethan's mom shares, "My hope is that research will help us identify a gene that causes this disease, or a direct environmental link so we can stop exposing children to whatever it is. I also hope that chemotherapy will get more and more personalized so that each child gets enough but to permanently kill the cancer. Too much chemo is also bad, as the side effects are several pages long and include other cancers later in life."

Meet Evan

Evan was hardly ever sick until last year when he started having a fever that would not go away. After seventeen days of tests, he was finally diagnosed with Acute Lymphoblastic Leukemia (ALL). He has a rare kind of ALL, and he has been undergoing chemotherapy since April 2009 in preparation for a bone marrow transplant in the fall.

Evan is a high school junior and honors student. He loves all kinds of sports and has played soccer, baseball, tennis, and lacrosse. He is looking forward to conquering cancer so that he can get back to playing on the varsity lacrosse team!

Meet Gregory

On February 25, 2009, at the tender age of three, Gregory was diagnosed with Juvenile Myelomonocytic Leukemia (JMML). Gregory's only option for treatment was a Hematopoietic Stem Cell Transplant (HSCT), which is more commonly referred to as a Bone Marrow Transplant (BMT). Gregory lives in Spokane, WA with his parents and two older siblings. Gregory traveled to Seattle with his mom for his treatment while his dad and siblings stayed in Spokane. Gregory faced several challenges through transplant and has not been home in eight months. He is currently facing Chronic Graft Versus Host Disease, which is a result of Gregory having another set of DNA for his bone marrow. We take it moment to moment, rejoicing when times are good. As of January 2010, he has no evidence of disease.

Gregory likes riding his tricycle around the oncology unit of the hospital. He enjoys spending time with his siblings, Curtis and AnnMarie, because any time they can spend together is precious. He loves blowing bubbles, and he loves to read and re-read If You Give A Mouse a Cookie.

Meet Harrison

Harrison was diagnosed with high-risk acute lymphoblastic leukemia (ALL T-cell) on February 29, 2004. During the phases of his aggressive chemotherapy, radiation treatments and healing, his family and friends followed the ups and downs of his grueling tour through the Tour de Harrison narratives.

Inspired by real life hero Lance Armstrong, Harrison mounted a courageous race against cancer. He went through two and one half years of treatment (20 red blood infusions, 9 platelet infusions, chemotherapy, cranial radiation, spinal taps, implantable port surgeries and a gazillion needle sticks), climbing every mountain that he encountered. His legs were sometimes weary, but his spirit was always strong, and he wore the maillot jaune (yellow jersey) all the way to his victorious finish in June 2006 when he completed treatments!

Meet Hailey

Hailey's story began at a check up when she was seven months old. She had been very healthy up until that point - hitting all milestones, eating, sleeping well, smiling, laughing, playing, etc. Everything looked great at her visit except that her head was constantly cocked to her right side with her chin rotated towards her left shoulder. The pediatrician diagnosed her with torticollis, a tightening of the neck muscles, so we began physical therapy at the hospital and at home. Hailey also began to vomit every morning after breakfast and began refusing solid foods. She was then sent for an upper GI and blood work, and all came back normal. A new pediatrician ordered an MRI, which revealed that Hailey had two masses in her brain and a build up of cerebrospinal fluid.

Hailey immediately had surgery to place a shunt that would drain the excess fluid, and she was taken to surgery again the following day to have the large, golf ball size tumor removed from the base of her skull. She was then diagnosed with atypical teratoid rhabdoid, an aggressive form of cancer that attacks the brain and central nervous system.

Hailey's three older siblings are eager to be able to play with their baby sister at home again. Hailey's mom writes, "Join me as we pray and encourage her to fight this disease so she can get on with her life and be the little girl she is supposed to be."

Meet Hayley

Hayley captured the hearts of all who knew her. She loved circles, chasing cats and horses. Hayley was diagnosed with an aggressive form of leukemia shortly after her first birthday. For months, Hayley was a model patient. She took hospital life in stride, and celebrated many of her firsts there,including walking and talking. After a few months of treatment, Hayley's leukemia went into remission. A few months later every one was surprised when Hayley relapsed in the skin and bone marrow two weeks short of completing her therapy.

She was never to reach a solid remission again despite numerous chemotherapy and experimental protocols. Her relapses were fast and furious, and included cancer hiding in her spinal fluid and stomach. Knowing time was of the essence, Hayley's treatment was quickly moved forward with a cord blood transplant. She received intense chemo and total body irradiation prior to the actual transplant, but it wasn't enough. She relapsed 14 days later, with 23 percent cancer in her blood.

Less than year after her cancer was discovered and a courageous and exhausting battle, Hayley received her much deserved rest and went home to be with her Heavenly Father, cancer-free at last.

Meet Heidi

Heidi was diagnosed with with a high-grade astrocytoma in May 2004, the end of her junior year in high school. Three years later, the tumor became a glioblastoma, one of the deadliest kinds of brain cancer. Over the course of five years, Heidi underwent three brain surgeries, radiation therapy, numerous rounds of different chemotherapy treatments, and a stem cell transplant. During that time, she attended college, working towards a degree in nursing, after being inspired by those who cared for her at Children's Hospital. She loved telling her story in hopes that it helped others dealing with cancer and treatments. Heidi eventually lost her battle with brain cancer on April 17th, 2009. Heidi was an inspiration to anyone who has ever met her or heard her story. Her infectious personality, beautiful smile, positive attitude and determination made Heidi an inspiration to everyone young and old.

Meet Jack

Jack is a seven year-old who was diagnosed with a form of childhood cancer called Neuroblastoma. He underwent chemotherapy, surgery, radiation and tandem stem-cell transplants.

Currently off therapy and doing well, Jack loves music of all kinds. He is known for singing and dancing to silly songs. If he does not grow up to be a rock star, he is likely to become a scientist, having a love of experiments, puzzles and gadgets. Jack's first love is his herd of stuffed "moo moos," which travel everywhere with him.

Meet Jack S.

Jack was diagnosed with leukemia at the age of four and spent most of his life undergoing chemotherapy and radiation. Everyone at the hospital enjoyed his wry sense of humor, and he was well known for keeping the nurses on their toes during his hospital stays. Although Jack loved animals of all kinds, he was fondest of snakes, lizards and turtles, earning him the title of "Reptile Man." Jack also loved traveling and went to places as diverse as Africa and Alaska during his fourteen short years.

After many years of chemotherapy and radiation for numerous relapses of ALL, Jack's long battle with cancer ended suddenly at the age of thirteen. Jack's zest for life will be remembered by all who knew him.

Meet Jackson.

Jackson was the picture of health for the first fifteen months of his life, but that all changed on September 6th , 2005 when his parents found blood in his diaper. Within five hours of this discovery he was diagnosed with cancer. Two days later he underwent surgery to remove the tumor and kidney. The official diagnosis of Rhabdoid Tumor of the Kidney came a week later, and he immediately started an aggressive treatment plan of chemotherapy and radiation. The next six months were filled with an intensive battle involving long hospital stays, several adjustments to chemotherapy dosing, and many, many blood transfusions.

The battle was worth it! Jackson is now five years old and cancer free. Aside from regular visits to the oncologist, cardiologist (heart doctor), and nephrologist (kidney doctor), Jackson leads an almost "normal" life: he enjoys playing baseball, doing puzzles, going to school and riding his scooter.

Meet Jacob

Jacob is a happy, funny, little clown. He is always trying to make someone laugh. He loves his family, pirates, Spiderman, and his dog Rosie. He was an unusually healthy child, with no colds, flu, or ear aches. Then he started having strange symptoms and illnesses at two and a half years old. After finally having a bone marrow biopsy done, he was diagnosed with Pre-B Acute Lymphoblastic Leukemia on September 11, 2003.

He has been so tough through it all. Jacob has endured numerous spinal taps with injections of drugs into his spinal fluid without having to be put to sleep; he took a handful of pills at one time; he has had many blood transfusions, random viral illnesses with weeks of hospital stays, and daily toxic painful chemotherapy, more than any child should ever have to endure. But he keeps in mind the ultimate goal---growing up and living a long full life. He is doing so well and is in remission. He took his last chemo pill on November 13, 2006 and five years from now Jacob will be considered cured.

Meet Jake

Jake has been battling neuroblastoma since October 2001. Jake underwent five rounds of high dose chemo, surgery to remove his primary tumor, two more rounds of chemo, and a stem cell transplant. After relapsing almost 15 months later, he underwent more chemo and antibody treatment before his scans showed no evidence of disease. When the cancer returned 15 months later, Jake received more chemo, radiation, and accutane therapy. Jake then had a wonderful summer free of cancer and the pain of chemo treatments before the cancer returned once again, and Jake has been undergoing chemo and radiation since then.

Jake's cancer treatments often take him far from home, but he enjoys spending time at home with his older sister and twin brother in between treatments. He also enjoys the internet and spends a lot of time surfing the web and playing games online. Jake loves baseball, and he attends his twin brother's baseball games whenever he can. Jake likes to play with his white lab dog, and his dog even retrieves all of the baseballs that Jake hits!

Meet James

One night after having sharp pains in his lower back, James was taken to the hospital and an ultrasound was performed on his kidney. It showed a grapefruit-sized tumor. James was taken to surgery where the tumor was deemed malignant and his left kidney was removed. He was diagnosed with Ewings Sarcoma of the kidney in February 2005 at the age of 11. This aggressive cancer is commonly found in the bone. There are fewer than 30 cases in medical history where it originates in the kidney. After surgery, he had five surgeries, 14 rounds of five types of chemotherapy, and 28 radiation treatments.

James, his sister, and his parents celebrate the miracle of life each day. James is now a high school sophomore. He plays football and baseball while wearing a protective guard over his right kidney.

James writes, "I live partly because of supporters in the last century who stepped up with gifts. Each generation literally rides on the shoulders of those patients and generous donors of past generations. In the United States, more than 12,000 children are diagnosed with cancer every year. About 3,000 children will not survive. You will make a difference for the next generation. You will make a difference for your kids and your children's kids. I am living proof. I am honored with your presence and generosity."

Meet Jamie

In July 2005, Jamie began complaining that her left leg hurt and was swollen. After going to her pediatrician and urgent care, she was sent to the children's hospital for an MRI. The MRI showed a mass, and a biopsy diagnosed the mass as a Stage IV Rhabdoid Tumor. On August 1st, Jamie had surgery to place her port and began chemo. An MRI at the end of August showed that the chemo wasn't working and the tumor was still growing. After visiting Dora the Explorer in Disney Land and celebrating her 4th birthday, Jamie had surgery to amputate her leg above the tumor. Jamie's cancer continued to spread, and she began an experimental chemo, which did not slow her cancer down.

Jamie's family celebrated the holidays early with her and she passed away in her sleep on Christmas Eve morning. She was a precious girl who loved her family, and she is deeply missed by her parents, sister, and three brothers. Her family is passionate about raising money for childhood cancer research so that other children will not have to go through what Jamie went through.

Meet Jamison

Jamison is 5 years old. He was diagnosed on December 19, 2008 at the age of 4 with high risk ALL leukemia. His family was devastated, but Jamison holds everyone up with his beautiful spirit, fight, and sense of humor. His little body has been through so much with chemo and treatments, but he's holding on. He has 2 more intense phases of chemotherapy and we hope to get to the maintenance phase by the first of next year - then he will be taking chemo at home everyday and we will only go to the clinic once a month.

He keeps all of the doctors and nurses laughing with his jokes. He is really into X-Men right now and pretends that he and his mom are the X-Men characters. His mom says, "He is just the most amazing son - strong, sweet, and smart. We absolutely see the power in prayer ever day we look into our son's eyes."

Meet Jarrett

Jarrett was a son, a brother, a friend, a gifted student, and an athlete who had a smile that could brighten up any room. He was a role model to all who knew him displaying a calm maturity in the face of impossible odds. Jarrett was diagnosed with one of the most deadly forms of cancer, malignant melanoma in 2002. When asked how he was doing, his standard answer was "I'm good", accompanied by a brilliant smile, even when he was not.

Jarrett was fiercely competitive both on and off the field. On the field, Jarrett played the "big three" sports: football, basketball, and baseball. Quarterback, point guard, and left fielder are the three positions that Jarrett held with pride and at the time of his death, Jarrett was ranked in the top five percent of his class.

Jarrett's battle began when he was just 13 years old. A flat freckle mole suddenly turned black and ugly. No one was more shocked than the dermatologist who removed it, when the pathology report came back: "malignant melanoma." Jarrett underwent surgery and a sentinel node biopsy. The lymph nodes that were removed were declared "cancer free". Jarrett was Stage 1 with a ninety-five percent survival rate. But in 2004 an enlarged lymph node was discovered directly under the original scar line. It was removed and found to contain a melanoma tumor that was channeling out of the lymph node. Jarrett was now Stage 3 and his chance of survival was at fifty-nine percent, with treatment. In October of 2005, Jarrett's CT scan showed two masses in his right lung. Melanoma again! His survival rate was slashed to a mere two percent. Jarrett and his family rallied the troops and raged a fierce battle but nothing could stop the cancer. Finally, on February 22, 2006 melanoma claimed 17 year old Jarrett's life but not his spirit.

Jarrett's quick wit, his loyalty, his very presence will forever be missed and mourned for. Please remember Jarrett Boston--a short life, well lived & well loved.

Meet Jaxon

Jaxon was two and half years old in July, 2007 when we went to a surgeon to schedule hernia surgery for a lump we had found on his tummy. The doctor quickly started testing and after bloodwork and a biopsy, Jaxon was diagnosed with metastatic stage 4 hepatoblastoma, a rare liver cancer that had spread to both his lungs. Hepatoblastoma affects .09 in one million children. After months of chemotherapy, Jaxon received a liver transplant on February 5, 2008. The first liver was not a good match for Jaxon, and he received the gift of life again on February 22, 2008! He had a long recovery after chemo and transplant, but he is currently enjoying life at home, cancer free! Jaxon lives in Missouri with his mom, dad and older sister, Abby. He likes motorcycles, tractors and football. The Kansas City Chiefs are his favorite team!

Meet Joe

On December 9th, 2005, seven weeks after his second birthday, Joe was diagnosed with acute lymphocytic leukemia and has been undergoing treatment since that time. While his first couple months of treatment were difficult due to a virus and staph infection, Joe was actually in remission after eight days of treatment! In mid-June, Joe started the "maintenance" phase of his treatment which will continue into early 2009.

Aside from the rough start, you would have a hard time believing Joe is being treated for such a serious disease. He is a rough and tumble kid who just wants to play with his construction trucks, friends, and swim. Aside from Mom and Dad, Joe's brothers Andrew and Nate, as well as a sister Emma, have been instrumental in helping him get through these tough months. A day does not go by without them making him laugh or him making them laugh. Thankfully, his infectious personality is still intact,he is a nut! Joe's mom shares, "Joe is our hero and anything we can do to help support Rally is a priority for our family."

Meet Johnathon

Johnathon's mom shares, "Well, when it comes to talking about Johnathon, it isn't hard. He was the light of my life, my sweet little angel. And although his time here was short, he touched so many people and changed lives as well. He was a beautiful baby boy with the biggest blue eyes that would just melt your heart! He had such a great laugh and a personality that just shined, and he spread so much warmth and love to everyone he touched. He was my special "little man"."

Johnathon was 17 months old when he was diagnosed with stage 4 neuroblastoma in November 1997. His mom continues, "I didn't know until then that kids got cancer, but I quickly had a rude awakening to the fact that children really do get cancer. Most of the options that we were given were "trial and research" options, but we chose to fight!"

Johnathon had surgeries to remove the tumors, chemotherapy, radiation and stem cell rescue. He spent two months in the Pediatric Intensive Care Unit and fought to get home, even when the prognosis was ,poor. We walked out of that PICU with the entire staff clapping.

After a short time of being cancer-free, the cancer returned, and this time it was everywhere. In December 1998, the surgeons told us the tumors were inoperable, and I opted to stop treatments. I chose to let him spend his last few weeks surrounded by family, his stuffed animals, his pet dog and me. We sat around and watched his favorite movies, and I never left his side. Johnathon passed away quietly in my arms in January 1999, he was only two and a half years old.

Johnathon changed my life then, and he continues to change it today. He would want me to continue to share his love and his story, so that one day, other children will not have to face this fight. I pray that day comes soon.

Meet Jordan

Jordan was an extremely sweet, shy, and quiet teenage with the most beautiful smile ever that had the world in front of her. She loved her family, cheerleading, vacations and her friends. In February of 2004, while Jordan was in the 8th grade, she was diagnosed with Acute Lymphoblastic Leukemia. Her diagnosis was even more difficult because she was also considered hypo-diploid, which did not hold a promising survival rate. Jordan never gave up hope that she would overcome her leukemia, even though she went through an extremely aggressive treatment program for 20 months. Jordan was a model patient and loved all of her doctors and nurses at the Egleston campus of Children's Hospital of Atlanta. Sadly, Jordan relapsed in November 2005, and passed away two weeks later. Jordan was 15 years old when she went to her heavenly home.

Jordan endured her illness and treatments with amazing grace and bravery. Our family and friends were truly blessed to have such a hero and an inspiration in our lives. She will always be with us in our hearts and memories. Jordan is missed every day!

Meet Jordan W.

Jordan started feeling bad the weekend of the 2009 Super Bowl. At first his pediatrician thought he had either strep or mono, but both tests were negative. On Wednesday, February 4th, 2009 his pediatrician told his family that blood tests showed Jordan's white blood cells to be off the charts and that they suspected leukemia. Jordan was sent straight to the children's hospital where he was admitted. He was diagnosed with ALL T-cell leukemia. That night he had surgery to place a port-a-cath and his cancer journey began. Jordan spent 12 days in ICU while undergoing chemo and being treated for complications, which included being on a breathing machine and undergoing dialysis. He has since spent many nights in the hospital for other complications related to his sensitivity to chemo.

Fortunately, things have now calmed down and Jordan is enjoying the things he loves most as a teenage boy. He enjoys playing football and baseball, and loves hanging out with his friends. He has battled this disease with a great attitude and spirit with the help of friends and family.

Meet Joseph

In November of 2007, when Joseph (or Joe P., as he introduces himself) was just over 3 years old, his parents started noticing his head was tilted to one side and his left eye was not moving quite like his right one. They took him to the emergency room for an MRI, where they received the earth-shattering news that he had a brain tumor. He had surgery a few days later, where they removed about one-third of the tumor, and from the biopsy they found out it was a grade 3 astrocytoma. They later found out at St. Jude's that it was actually a grade 4 astrocytoma called Glioblastoma Multiforme in his cerebellum and brain stem.

Joseph underwent a second surgery where they were able to remove most of the rest of the tumor, and he slowly learned to walk again and regained his buoyant personality. He also went through 6 weeks of radiation and several clinical trials before he passed away on the day after his fourth birthday. Joseph was a boisterous little boy who loved to ride his bike, play with his sister, go swimming and of course, play cars!

Meet Josh

Josh is a 16 year old who has survived cancer and is now in the 10th grade. He was diagnosed with Neuroblastoma at the age of 8. He went through a long hard battle of dangerous chemotherapy, two surgeries, stem cell transplant, radiation, and experimental monoclonal antibody treatments in New York City. He also had doses of accutane, a drug which is supposed to help kill fast growing cells for acne but is used on some cancer patients because cancer can be a fast growing cell.

While going through his treatments, Josh would face his fear by writing poems about his treatments, his doctors and his nurses. He was an inspiration to all throughout his journey and gives others great hope. As painful as some of the therapies were, he wanted to continue to do all he could, in hopes the cancer would not return.

He has been in remission now for seven years. Josh realized he wanted to help others brave the storm he had gone through. So, he is very active in his own community in spreading awareness about childhood cancer and the need for others to help join in the Rally to raise funds for this cause. He knows there will not be a cure for childhood cancer unless more money is given for research.

Meet JR

JR has always been known to his family and friends as a fun-loving, caring, and sweet boy. In August 2007 when JR was eight years old he started suffering from severe headaches which his parents thought might be dehydration since he had just finished a fun summer of sailing and a day camp. A trip to the emergency room revealed a mass in his brain and he was transported by ambulance to NYC. He underwent emergency brain surgery and was diagnosed with a grade 4 glioblastoma multiform. He recovered beautifully and started radiation and oral chemo (Temodar). He never complained and made the most of our daily trips to New York from Connecticut. He rarely felt the side-effects of his treatments and returned to third grade in October, just after his ninth birthday. He spent time running around the neighborhood with his friends and enjoyed a fairly normal life.

In February 2008, a routine MRI showed the return of his tumor and a second craniotomy was done in March 2008. The tumor was removed successfully again and JR recovered well. He then started new chemo treatments, but as he was getting back to playing baseball and attending school, his cancer started spreading to more of his brain and spinal fluid. He was in and out of the hospital for the next several months and was home for his final days when he lost his courageous fight on July 16, 2008 at the age of nine and three quarters. His parents and his sister Addie miss him every minute of every day.

Meet Julian

Julian was a fun little guy. He had a lot of imaginary friends - mainly frogs, alligators and sharks. He is the third of four brothers and was the peacemaker, always getting upset when his brothers fought and argued. He had an awesome smile with beautiful dimples. Julian was not quite 4 when his parents took him to the doctor for awful headaches and nausea. A golf ball sized tumor was found in the back of his brain. It was successfully removed by surgery and was diagnosed 3 days later as a malignant childhood tumor called medulloblastoma. He spent less than 24 hours in the Pediatric ICU and only a week in the hospital after surgery before he got to go home.

After a few rounds of chemo, not even half way through the clinical trial, the cancer came back with a vengeance. His family went on his Make-A-Wish trip to Disney, where he had his first seizure, and it was all down hill from there. He beat cancer in Heaven on January 19, 2008, but not after fighting for every breath.

Julian liked to be called King Julian, and his kingdom was Julian's World. He touched a lot of people and gave several of them hope. His amazing spirit and his love for music, dancing and God made him who he was - a little dancing king!

Meet Kelsie

Kelsie was a beautiful young lady, inside and out. She was a loving, caring girl, always more concerned for others than herself. She loved playing sports - softball, volleyball, and basketball to name a few. She loved children and planned to have a job working with kids when she was older.

Kelsie was so excited to finish 8th grade and move on to high school, but unfortunately she never had that opportunity. She had been having back pain, bruising, fevers, a urinary tract infection, and had been very tired. After taking antibiotics for the infection Kelsie continued to feel ill, so blood work was done. Abnormal labs led to her diagnosis on June 23, 2007 with Burkitt's Lymphoma. Kelsie immediately began treatment and went into remission shortly after. Unfortunately, Kelsie relapsed a few months later and the disease continued to progress until she passed away exactly five months after diagnosis.

Her family writes, "So now we fight for Kelsie and all of the kids affected. We need to make a difference so some day we will have better treatments and more cures. We continue on, missing Kelsie and honoring her memory by helping others just as she would want us to do. Kelsie will not be forgotten....love you Kels!"

Meet Kennedy Grace

Fun-loving, determined and adorable three year old Kennedy Grace, also known as KG, began complaining that her legs hurt. Then she started running a fever. Her blood work revealed that she has Acute Lymphoblastic Leukemia (ALL) the most common childhood cancer on April 27, 2007. Three days later, she began chemotherapy treatment that will last for the next two years.

KG loves school, playing with her dolls and stuffed animals, swimming, and dancing.

Meet Khalid

At the beginning of March, 2008, Khalid stopped jumping, playing and smiling and began to just lie around. He was taken to the doctor and they immediately sent him to the ER. At first doctors thought that his system was just a little backed up, but a week later Khalid returned to the hospital. A CT scan on March 26 showed he had a very large mass in his abdomen accompanied with disease in his bone and around his orbital bone.

He was biopsied on the 27th and began chemotherapy on the 28th. He has had 5 rounds of chemotherapy, is in the process of seeing if the tumor can be ressected, has one more chemo treatment to go and will have a Stem Cell rescue later this year. Since starting treatment, Khalid has been back to his old self, if not more active than before. He has 8 brothers and sisters he loves to play with. He loves Dora the Explorer, the number four and riding his bike.

Meet Killian

On October 8, 2001, a week after his sixth birthday, Killian was diagnosed with Rhabdomyosarcoma. The tumor was located on his vas deferens and was slowly wrapping around his bladder. He was immediately signed up for a clinical trial and began a year long chemo treatment plan and six weeks of radiation. During treatment, Killian lost over 40 pounds and spent a lot of time in the hospital due to constant infections. He finished chemo in November of 2002.

Today, Killian is pretty much an average 14 year-old. He is into guitars (owns two electric and one bass), cars, and video games. He also enjoys hanging out with his friends playing football or basketball. He loves playing with his three month old baby brother, Carter.

Meet Kristen

Kristen was born in Georgia in June 2003, much to the excitement of her parents and 5 year old brother. In March of 2007, their lives suddenly changed when Kristen's parents noticed some bruising and red spots (petechiae) that sent them to the pediatrician. After blood work results, it was confirmed that she had pre B acute lymphoblastic leukemia. Aside from the few bruises, you would never have known anything was wrong with her. She was immediately admitted to the hospital, and after blood and platelet transfusions, a port was placed in her chest 2 days later for her chemo treatments. Kristen has been remarkably brave and strong through all of the chemo, steroids, shots, and oral medications. Her maintenance phase began in November of 2007 and she will continue on this path until June 2009.

Meet Krystle

Krystle has always truly loved life, others, and herself. She loves to sing and can always be found doing something funny or crazy. She has fun no matter what and never worrying about what others might think of her. As a child, this animal lover had many pets, some of which lived outside so that her parents wouldn't know about them! When she was six, she moved in with her grandparents. Life was going great, she was healthy and loved school.

Around the time that high school started, she slowly started to feel sick all the time, and her eye became severely swollen before she started tenth grade. Her doctor ran some tests and then sent her to the children's hospital because he could tell there was something behind her eye. On what was supposed to be the first day of tenth grade, Krystle had surgery to remove the large tumor behind her eye. A few days later, she and her family were told that the tumor was cancerous, and she was diagnosed with diffuse large B- cell lymphoma.

After a year of chemo and many infections, Krystle found out that her cancer had returned. She then underwent more chemo before having a bone marrow transplant. Soon after the transplant, a mass showed up in her right breast, which was another return of the lymphoma. Krystle remains on chemotherapy and is hopeful that she will soon beat this disease once and for all! After missing two years of high school, she has returned to the tenth grade, where she has made many friends and loves being back in the high school chorus.

Meet Kyle

Kyle was such a happy baby and little boy. His favorite things were Barney, Elmo and the color purple - there was no other color as far as he was concerned! He would notice anyone wearing purple in a crowd and would find purple in everything around us! But most of all, Kyle loved cuddling with Mommy and hugging and kissing his little brother Collin. He was an incredibly loving big brother and couldn't get enough of "his baby". His favorite things to do were blowing bubbles, feeding the ducks, taking a bus to the mall, riding his tricycle, watching sunsets and sunrises, and best of all, visiting with family. Kyle always wanted to be a fireman, along with his little brother, when he grew up.

In 1992, Kyle was diagnosed with Leukemia and fought cancer for 5 ½ months. He underwent chemotherapy, radiation and a bone marrow transplant. However, after a most courageous and incredible fight, Kyle lost his battle with battle. His mom writes, "Our hearts have been broken ever since. There was far more to his short life than just cancer."

Meet Kylie

After several months of extremely high fevers and stomach pain, Kylie was diagnosed with Stage III, N-Myc Amplified, High Risk Neuroblastoma on October 7, 2004 when she was only 16 months old. She received 7 rounds of intense chemotherapy, a major abdominal surgery, 14 rounds of radiation, a stem cell transplant, many blood and platelet transfusions, and 8 rounds of 3f8 antibodies in New York City.

After an unsuccessful tumor resection, the doctors felt that Kylie's chances of overcoming this horrible disease were slim. Kylie beat the odds and by the grace of God Kylie has been disease free since April of 2005. She continues to be monitored by doctors in Atlanta and in New York City and has graduated to the Survivor Clinic.

Kylie enjoys gymnastics, ballet and cheerleading and loves school. Like many other children who have suffered through cancer, Kylie hopes to one day be a pediatric oncologist to help other children beat this disease. Her back up plans include being a rock star, a model or actress.

Meet Lauren

Lauren was diagnosed at age 14 with Hypothalamic Hystiocytosis-X, which was found on the brain. She played basketball, softball and was involved in many academic clubs. While in 8th grade, Lauren underwent brain surgery followed by 15 months of chemotherapy. Lauren's last chemotherapy was May 14, 2002 during her freshman year of high school.

Currently, Lauren is attending Piedmont College, where she is pursuing a degree in education. Her plans are to become a hospital homebound teacher or to be the main school teachers in one of the children's hospital's cancer clinics. She loves to play golf and loves spending time with her family and friends. She loves to be an advocate for childhood cancer and looks forward to working with children in the future.

Meet Laura

As an atheletic and carefree 15 year-old, Laura was diagnosed with Osteosarcoma, a rapidly growing and aggressive form of pediatric bone cancer. Following summer cross country practive, Laura experienced throbbing pain in her right knee and thigh and was taken to an orthopedist. An x-ray discovered the tumor above her right knee. She was treated with chemotherapy and had limb salvage surgery for the remainder of her sophomore year. This past September, it was discovered in a regular post-treatment CT scan that Laura's cancer had returned to her lungs. She had a tumor resection surgery to remove the cancer, and is now ready to get back to "normal" after a month off from school. She plans to participate in many school activities and is ready to enjoy her senior year. As Laura puts it, when life gives you another set back, make it into a stepping stone. We count our blessings everyday that Laura is well, and we make sure to cherish the beauty life has to offer.

Laura used to run track and cross country. She also played basketball. She is now very limited on her participation in sports due to her leg surgery, so she is focusing on helping other kids who are going through similar challenges. She enjoys volunteering at the hospital where she was treated and with the Make-a-Wish Foundation. She enjoys being outdoors, making jewelry, going to the gym, and spending time with her friends.

Meet Leigh

Leigh was diagnosed with cancer in her bones when she was 17. She was a varsity cross country runner for her high school, and ran six miles the morning she was diagnosed. She had her primary tumor removed from her leg bone and was unable to walk for seven months. Leigh received a total of 15 rounds of chemotherapy and many surgeries to remove all 36 tumors from her chest; nevertheless, she persevered and went into remission in May 2005. She astonished everyone when she ran the region cross country meet with all of her teammates just one month after she began to walk again.

Leigh currently attends Liberty University and plans to become a nurse because of the profound impact her oncology nurses made on her life. She knows the only way to help defeat cancer is to research it. She looks forward to the day when no one has to suffer from this disease.

Meet Lindsay

At 8 years old, Lindsay went from an energetic and happy child to a lethargic, sick, and pale little girl. She started out with a sinus infection, then after numerous antibiotics, it progressed to pneumonia. She started having intense pain in her hips and stopped walking. A new pediatrician ordered blood tests, which showed she was anemic, and a follow up CT scan, which showed a mass in her lung that did not shrink after a strong course of antibiotics. Her pediatrician sent her to the children's hospital, where she was finally diagnosed with Acute Lymphoblastic Leukemia on Aug 10th, 2007.

Lindsay has now been through more procedures than the average adult. More than two years' worth of spinal taps, blood draws, and chemo have her looking at the light at the end of a very long and dark tunnel. Despite some horrible side effects from the chemo such as AVN (bone death) in her knees and ankles, Lindsay is still the happy, bubbly child who is everybody's friend. She is looking forward to finishing chemo in a few weeks; however, knows that our journey with childhood cancer is not over for good, not until every child can be cured

Meet Lily

Lily is an outgoing and fun-loving 8-year-old girl. Last September, Lily was diagnosed with Stage 4 Neuroblastoma. Although she has been through several rounds of chemotherapy, two intense surgeries and several bone marrow tests, Lily continues to have the most positive attitude and contagious smile.

Lily loves singing, art and cheerleading. She believes "everything happens for a reason" and is opening the hearts of people all over the world. She is a living angel.

Meet Logan

Logan was diagnosed with a rare brain tumor, a Craniopharyngioma, on July 29, 2007. After four surgeries and 31 radiation treatments, the tumor is gone; however, Logan is now legally blind, left only with a small amount of tunnel vision in his right eye. The location of this tumor makes it a life-long condition because of the hormonal deficiencies, vision loss, obesity, and social and psychological issues.

He will be on several medications for the rest of his life, and while these medications are critical, they fix some problems and can cause others. The radiation he received can cause malignancies in his brain in the future. The growth hormones that he will need due to the side effects of his brain tumor treatments can cause the tumor to grow back. A return of the tumor could take the rest of his vision.

In spite of all this, Logan began middle school and loves all of the subjects and all of his teachers. He enjoys Taekwondo and Goalball, a sport for the visually impaired. He loves doing word puzzles and building Legos. Although he and his younger brother have rougher moments post-brain tumor, they love each other very much and are great supporters of one another. Logan is a hard worker, determined, and optimistic.

Meet Logan B.

Logan was diagnosed with a spinal cord tumor in September 2008. Since that time he has had two surgeries to remove tumors, one which caused nerve damage leaving him in a wheelchair. He is undergoing multiple treatments including radiation and chemotherapy, as well as physical therapy to help improve his overall condition.

Logan is 14 years old and has spent both his 13th and 14th birthdays in the hospital. Logan has spent all of Fall 2009 in the hospital with complications from treatment, including H1N1, respiratory failure, hemolytic anemia, and gall bladder problems. He is a witty, energetic child with an inspiring spirit who loves tigers, dragons, and music.

Meet Luke

When Luke was born on October 31, 2008, his parents were relieved at the birth of their healthy baby boy. It had been a difficult pregnancy. He was an identical twin, but his twin did not survive. His parents were eager to stop worrying and start protecting their new baby. At 10 months of age, their world was again shattered when Luke was diagnosed with a Wilm's tumor on his left kidney. He has since gone through surgery, radiation and chemo.

Luke is an incredibly happy baby who loves to play with his trucks, balloons and his pal Scout. He enjoys being outside and running around with his big sisters, Lily and Jenna. His family is looking forward to the summer when he can spend all day outside with his sisters.

Meet Lydia.

Lydia was four years old when she was diagnosed with ALL leukemia in 2006. After she was in remission, she went through two years of chemotherapy. For the following year she was off treatment but then she began having severe back pain. She was taken to the emergency room where she was diagnosed with a leukemia relapse. Currently she is in remission and will be enduring two more years of therapy.

Even through all the difficult times, Lydia has remained an incredible little patient, enjoying life as much as she can. In her moments of feeling good, she loves to do crafts and draw. She can't wait to go back to school. She is in the second grade.

Meet Madeline

On January 27, 2009, Madeline was diagnosed with CML, Chronic Myelogenous Leukemia. It all started at dance rehearsal one Saturday when her dance teacher, Beau, noticed large bruises on her legs. Her parents took her to the pediatrician the following Monday, and they drew blood. On Tuesday morning the doctor's office called to say that there were cancer cells and that Madeline needed to go to the hospital and begin immediate treatment. Her parents picked her up from school, and on Tuesday night, Madeline began chemotherapy.

Madeline is currently doing well and is back at dance class four nights a week!

Meet Madie

In March 2003, Madie was a very sick four- year-old girl. She could barely walk, had nightmares every night, and was covered from head to toe in black and blue bruises that seemed to appear out of nowhere. The fourth trip back to the doctor with high fevers over 104, lung congestion and back pain was not going well. The blood work that her pediatrician took was extremely abnormal, and we took the first of many trips up to our children's hospital.

That night, we got the terrible news that Madie had cancer along with an enlarged liver, pneumonia in both lungs and a raging ear infection. She had a blood cancer called Acute Lymphoblastic Leukemia, and because she had stopped making red blood cells and platelets a few days earlier, she most likely would have died that night at home in her sleep. Madie started chemo along with blood transfusions and twice-daily platelet transfusions, but she had to wait two days for any surgery for her port and bone marrow tests because of her low platelet counts and pneumonia. The second day at the hospital, the doctor told me that Madie was dying, but they were doing everything they could to stop that from happening.

After two years and three months of chemo, along with over three dozen blood/platelet transfusions and numerous spinal taps, hip pokes, bone scans, CT scans and five hospital stays with a few extremely "close calls", Madie is now cancer free! She quietly struggles each day with late-effects from the chemo, but that doesn"t stop her. When you look at Madie today, you will see a vibrant, animated 10-year-old girl who loves to collect Webkinz, swim, and play softball. Her happiness is contagious.

Meet Margaret

After being sick with what we thought was a virus, Margaret was diagnosed with Leukemia on October 9, 2007. Her only symptoms were fever, neck and back pain. We are blessed she has ALL, the type of Leukemia that is more easily treated and cured! So far, all of her test results are very encouraging, and she is responding to her treatments.

Meet Madison

Madison was diagnosed in August 2007 with medullablastoma, a malignant brain tumor. She has had 2 tumor resections, 30 treatments of brain and spine radiation, and 9 months of intense chemotherapy. Madison is currently off treatment and is now cancer free. Madison, a junior, attends high school full time and hopes to work someday at the hospital where she was treated as a child life specialist, helping other children with cancer.

Meet Martin

Martin was diagnosed with Medulloblastoma, a cancerous brain tumor, in July 1998. He went through the chemo and radiation protocol and was free of cancer until April of 2003. Recurrence in his spine resulted in surgery, more chemo, radiation, and a stem cell transplant that summer. He was recovering well, when the return of his brain tumor was found in October 2004. Spine tumors were found in early 2005. Martin tried a variety of chemo treatments in addition to alternative medicine options. In February 2008 he was diagnosed with AML leukemia - most likely a side effect of his chemo and radiation treatments.

Martin received an Achievement Award for being the top 10th grader in his school's Junior ROTC program. He also enjoyed building things in his engineering class and woodworking at home. When he was feeling well enough, Martin could be found riding his three-wheel bike around his neighborhood. He also liked spending time with his family and friends. At the age of eighteen, after fighting cancer for almost 10 years, Martin passed away at home surrounded by his family.

Meet Mary Grace

Mary Grace loves t-ball, gymnastics and EVERYTHING about camping! She is an energetic and fun loving child that was diagnosed with a stage IV germ cell tumor when she was 26 months old. (Aug 2004) The main tumor was located in her spine and extended to her liver and lungs. Due to the location of the tumor, she completed chemotherapy and 23 radiation treatments before she had surgery to remove the remaining tumor in her spine. She is now in remission and continues to have "checkups" every 6 months to monitor her health.

"Opening day of baseball season was extra special this year," says Mary Grace's mom, D.D. "According to the "statistics", Mary Grace should not be able to walk right now. When she did walk up to home plate, I thought my heart was going to overflow with excitement! However, when she RAN to first base with a giant smile on her face, well there just isn't enough money in the world to buy that feeling!" Thank you for supporting Rally Foundation!

Meet Matt

Matt loved football and played with the same team since the 5th grade. His sophomore year at Pope High School, Matt earned a Varsity Letter as Defensive End and was working hard to achieve his dream of playing collegiate football. When Matt was 16, he was diagnosed with a rare and aggressive bone cancer called Ewing's Sarcoma. After seven rounds of chemotherapy, a bone marrow transplant and 28 radiation treatments, Matt returned home cancer-free to join his football team for his senior year. He was back on the field for the early season scrimmages, and when he took the field the whole crowd chanted, "Go, Matt, Go!" Unfortunately, Matt's cancer returned, and he was unable to finish the season.

Matt enrolled in a clinical trial at the National Cancer Institute in Bethesda, MD where he underwent a donor stem cell transplant. Matt's dad was the perfect match. Matt applied the same toughness and determination from the field to his battle with cancer. His teammates came up with the motto "STAND TOUGH" which he did throughout his entire battle with cancer. Matt died on May 30, 2006 surrounded by his loving family.

Meet Matthew

Matthew was diagnosed with rhabdomyosarcoma, a solid tumor in his bladder, on January 17, 2007. He awoke from a nap one afternoon in pain and said he could not pee. An ultrasound revealed a possible sarcoma and a biopsy confirmed that it was rhabdomyosarcoma. He recently went to Mass General in Boston for proton radiation treatments and has now resumed his chemotherapy treatments at Vanderbilt Children's Hospital where he began his battle.

Matthew loves Star Wars Legos, splashing in the pool, and playing light sabers with his three older brothers David, Stephen and Jonathan. His favorite food is a plain McDonald's double cheeseburger (hold the cheese). His family loves to hear him sing "I Belong to Jesus" and see him enjoying life.

Meet Matthew T

Matthew was diagnosed with a Craniopharyngioma (brain tumor) in 2000 when he was 4 years old, and he had surgery and radiation to treat the tumor. For the next five years, he enjoyed a period of stability and no tumor growth, and he was able to lead a normal life for the most part. Beginning in early 2006, his tumor began to regrow, and he underwent 10 more surgeries over the next 3 years as the tumor continued to recur and regrow. Matthew lost all vision in his left eye in March 2008, likely due to radiation damage from 2007. He lost peripheral vision in his right eye in August 2008. By November, he began to have seizures, and he had a port placed and began chemotherapy in the hopes that his tumor might respond to chemo. Although the chemo seemed to slow the progression, it did not stop it. The seizures continued and worsened and in March 2009, he appeared to have suffered a minor stroke. Everyone agreed that it was time to stop the chemo and concentrate on alleviating Matthew's headaches and making him more comfortable. In mid April 2009, he began hospice care and his family tried to enjoy every moment they had left with Matthew, armed with the faith and determination that had carried them through the past 9 years. After a long and hard fight, Matthew passed away on Mother's Day 2009 at the age of 13. An inspiration to even those he had never met, he faced everything that came his way with extraordinary courage and determination. Matthew was quite an artist and loved to share his masterpieces with people. Music was very special to him and he became quite a musician, composing music on the computer as well as playing the upright string bass - an instrument taller than he was. He loved the beach, hot wings, Japanese steakhouse dinners, being a big brother to Cameron, and hanging out with his best friend Bryan.

Meet Merrill

Merrill was diagnosed with AML, a type of leukemia, in April of 2004. She had lots of chemotherapy and a bone marrow transplant. How fortunate that her own dad was her donor! She relapsed in June 2008 with tumors in her chest, which were eliminated with radiation. In May 2009, she relapsed again with additional AML/ALL tumors in her chest and is currently undergoing treatment.

Since her transplant in 2004, Merrill has been active in athletics, school activities, driving her brother and sister crazy, and busy being a normal teenager. Inspired by the amazing care of her nurses, Merrill hopes to one day become a pediatric oncology nurse.

Meet Mckinley

Mckinley is a fun loving and spunky child that was diagnosed with leukemia when she was 18 months old. Since then she has been a brave and strong little girl undergoing a year and a half of chemotherapy. She is now in remission but will not complete her cancer treatment until this summer. Mckinely loves to spend time playing with her little brother Woods, and her big sister Brooke. She also enjoys dancing like a ballerina, dressing up as Cinderella, and going to music class. Her favorite color is purple, and every night she likes to sleep with her purple unicorn.

Mckinley's mom, Shawn, asks, "Please help support Rally Foundation so children like Mckinley will continue to survive and the children to come will have a fighting chance. It's my prayer that in my life time we will see dramatic results and cures for all childhood cancer!"

Meet Mia

Mia was diagnosed with High Risk Acute Lymphocytic Leukemia on Friday, March 13 2009. After an immediate platelet transfusion, she was ready to begin chemotherapy Monday. Mia was hospitalized 70 miles away from her twin brother, Noah. She responded well to her initial treatment and has been in remission since April 13, 2009. After eight months of intense treatment, Mia is home and has begun her maintenance phase of chemotherapy, which will last until summer 2011. Maintenance includes oral chemotherapy five days week, one week a month of oral steroids, and a monthly hospital visit to get chemo injected directly into her spinal fluid.

Mia and Noah just celebrated their third birthday and their family is so thankful that they were able to wake up together and celebrate at home. Mia's mom shares, "It's unbelievable how strong a toddler can be and each day we are so proud of Mia for being brave throughout her treatment and so proud of Noah for being a loving and supportive twin brother. Nothing beats seeing them run to each other with open arms with big smiles." Mia loves riding her bike, dancing, listening to music, and playing her new purple guitar. She is a very energetic and imaginative three year old, she is a hero to her family, and she keeps them strong everyday.

Meet Mitchell

Mitchell was diagnosed with leukemia when he was three. He started chemotherapy immediately and all was going according to his protocol until he relapsed with leukemia cells in his central nervous system fluid. Mitchell's chemotherapy treatments increased significantly, including 20 hospitalizations in 13 months followed by cranial radiation and another year of chemotherapy.

After more than fours years of treatment, Mitchell completed the relapse protocol in February 2006 and is in remission! He still has to undergo monthly check ups but otherwise Mitchell can be found enjoying Cub Scouts, swimming, basketball, riding his scooter and, of course, video games!

Meet Miracle

Miracle Faith was born on March 7, 2005. Miracle has always been an energetic and vibrant toddler. After spending three days in the hospital and treating her for acid reflux, her pediatrician ordered a CT scan, which revealed several masses in her stomach. Miracle was immediately transported to Medical College of Georgia in Augusta, Ga. Just two weeks before her 3rd birthday, she was diagnosed with stage III Burkitt's Lymphoma, an aggressive form of cancer.

A six-hour successful surgery removed the cancerous mass from her abdomen and her right ovary. The cancer had also spread to her spine. Forty-eight hours later, another mass had grown, causing her intestines to collapse, and she then had another surgery. Miracle was immediately put on an aggressive chemotherapy treatment protocol. Miracle received treatments 24 hours a day for seven days at a time and numerous transfusions. Miracle was initially hospitalized for 45 days; after that she was hospitalized for 15 days each month.

Miracle is now in the maintenance phase of her treatments and still full of energy. Her battle with cancer has not slowed this busy energetic toddler down at all. Now she is looking forward to starting Pre-K this fall!

Meet Nicholas

Nicholas was diagnosed with Acute Lymphoblastic Leukemia on Valentine's Day 2008 at the age of three. His diagnosis was devastating to his family, but he has amazed everyone with how well he has done in his treatment so far. He loves Thomas the Train, Sponge Bob, and trucks. His new love is boxing!

Nicholas lives in Pennsylvania with his Mommy, Daddy, and dog Chase. His Mom shares, "He will finish treatment in April 2011, and we pray that the rest of his treatment goes as well as it has so far. He is the strongest and most courageous boy we know."

Meet Nicholas

Three-year-old Nicholas is full of life, and he has a big heart that brings joy and happiness to all those around him. His parents took him to the hospital on September 20, 2008, with a high fever and paleness. He was diagnosed with High Risk Acute Lymphoblastic Leukemia two days later. He spent a month in the hospital undergoing bone marrow biopsies, chemotherapy and surgery to remove an adrenal mass. He has been in remission since October 23, 2008, and receives chemotherapy at the clinic once a month in addition to taking oral chemo at home every night. Nicholas developed muscle weakness from his first spinal tap, and he is now undergoing physical, occupational and speech therapy to help him grow stronger. His chemotherapy treatments will last approximately three and a half years.

One rule at Nicholas's house is the "No Crying Rule". If anyone does start crying while visiting Nicholas, he will walk over and wipe their tears off with a smile. Nicholas knows all of his colors and is very clever - he has named all of his medications by color! He knows which colors are to be taken at which time of day. He loves Thomas the Train, Diego, Curious George, Mickey Mouse, and Dr. Seuss books.

Meet Nicholas L.

In 2000, at 15 months old, Nicholas was diagnosed with Acute Lymphoblastic Leukemia (ALL). He underwent two and a half years of chemo, even though he went into remission in the first month of treatment. On his last visit at the end of the 2 1/2 year period, the doctors discovered that he had relapsed, and this time it was in the spinal fluid. Another two years of chemo and 2 weeks of radiation were ordered to try to get rid of leukemia for good!

Nick is a sensitive, bright, and imaginative boy who enjoys art and music. He loves Pokemon, animals, playing with Legos, and making movies. Nick has a patient, kind, and caring spirit that touches the lives of all he meets. He is currently in 5th grade and enjoying a healthy life.

Meet Nolan.

Nolan was diagnosed with anaplastic medulloblastoma on October 8, 2009. He had a seven-hour surgery to remove the tumor on October 13th. The doctor was able to remove most of the tumor except some on the brain stem and two lesions on his spine. The surgery left him with left-sided weakness, and he is now relearning how to walk. Nolan has had 30 rounds of radiation treatments and has finished one round of inpatient chemotherapy, with five more to go. However, he was given a six-week break from treatment and was able to enjoy his Make-A-Wish trip to Disney World.

Thus far, the scans look good. The lesions in his spine are gone, and he is handling chemo really well! Nolan enjoys coloring and watching SpongeBob! His activities before surgery were riding bikes, skateboarding, climbing and playing basketball. He hopes to return to these activities after he has overcome his weakness from surgery.

Meet Olivia

Olivia started getting sick at the end of October 2008 and was taken to the children's hospital. At midnight her parents were told that she had a brain tumor, and the next day she surgery to place a temporary shunt in her brain to relieve the pressure of the fluid that had built up. On December 1, 2008, Olivia had brain surgery to remove the tumor, and the biopsy confirmed that she had medulloblastoma, a fast growing and highly malignant brain tumor. After surgery, Olivia was mute and incapable of sitting up on her own, and she learned to walk again two weeks after surgery. Eye patching was done to rebuild strength in her damaged right eye. Olivia started her first round of chemotherapy on December 23, 2008, and has completed seven rounds of chemo with three more to go. She traveled to Boston for 30 Proton Beam Radiation treatments. She visits a child psychologist weekly for post-traumatic stress related to the hospital stays. She also has hearing loss due to the chemotherapy.

Olivia loves to dance! She has been dancing since she was 18 months old, and she had already been in two recitals when she was diagnosed at age three. She also loves arts and crafts.

Meet Parker

Parker is a little boy filled with spunk, smiles, and a zest for life. In June of 2006, at the age of 4, Parker was diagnosed with Stage IV Neuroblastoma. He quickly went from sliding down a waterslide one day to spending the next day in the hospital being told to be ready for the fight of his life. Not only did he have a softball-sized tumor in his abdomen at the time of his diagnosis, he also had cancer in his bones and bone marrow. Parker underwent several rounds of chemotherapy, surgery to remove the tumor, radiation, and two stem cell transplants.

He took localized radiation to his belly, the original site of the tumor, and he endured accutane therapy. Parker was truly an angel sent from above to teach us all a lesson of wisdom, showing us the courage and strength to move on, fight and persevere through this trying time. One glance of his smile and the twinkle in his eye was enough to light up the room, and through it all, he remained such a bright shining star. In November 2007, the disease eventually took over his body, and his reward for the brave battle was angel wings in heaven. Parker touched so many lives in a short 6 years of life. Although he is not physically here with us today, he has left his amazing spirit within us

Meet Peyton

Peyton was a normal two and half year old until the day she was diagnosed with Acute Lymphoblastic Leukemia. July 13, 2006 was the day that changed our lives forever.

She has bravely battled this cancer with every fiber of her being, never losing her spirit, always inspiring us with her smile. Peyton was diagnosed as a high-risk case as she was positive for Leukemia in her spinal fluid, and her treatment has been long and harsh. She is a joyful child who has never lost her smile, her incredible zest for life and she would not be here today if not for research that enabled her to have a treatment plan. We are thankful for the many who gave her the tools with which she continues to wage war on cancer.

Meet Rachel

Rachel was born on April 21, 1995, the fifth of six children. Rachel was a wonderful baby and delightful child. She loved all things fit for a "Princess" and dressed for tea all the time. On December 6, 1998 she was diagnosed with Neuroblastoma. She bravely fought the battle with chemotherapy and radiation. She also endured two stem cell transplants. Rachel made friends where ever she went, especially during her cancer treatments in New York City and Northern Virginia.

Her wish was to be a Flower Girl. Since there were no weddings to be found, she asked her Mommy and Daddy to get married again so she could be their flower girl. Rachel ran the whole wedding program as her parents renewed their vows. There wasn"t a dry eye in the church as Rachel's wish came true by walking down the aisle in her beautiful dress. Rachel's mom, Meg shares "She continues to bless us here on earth with her Heavenly Presence. She was an incredible gift from God. Sadly for us, God needed her back and she left us on July 3, 2001."

Meet Rhema

Rhema is a 13-year-old blue-eyed doll fighting a rare, aggressive childhood cancer called a desmoplastic small round cell tumor. She underwent six rounds of chemo, surgery, two more rounds of chemo and six weeks of radiation. She has met each challenge with determination and a smile. Rhema recently had her central line removed and is looking forward to being able to go swimming again. She also just started back at school for part of the day and is building up her strength to go all day. Her family has not forgotten all of the friends they met at the hospital, and her mom says, "We rally in honor of her and all the children fighting this horrible disease."

Meet Russell

Russell was diagnosed with anaplastic ependymoma, a brain tumor, in April 2008. The first step in treatment was surgery to remove as much tumor as possible. He's currently going through four rounds of very aggressive chemotherapy. He will then start six weeks of daily radiation therapy.

Russell enjoys many activities including running, football and playing the drums, but one of his favorites has been cycling over the years. Back in 2006 Russell's cycling team, Frazier Cycling, helped Rally Across America raise money for childhood cancer research. Russell was the first kid to turn in a donation.

While Russell loves to ride and race on his bike, he and so many other kids are enduring a bigger and more challenging race that test the body and mind to the extreme, a race with cancer.

Meet Ryder

Mother's Day babies, Ryder and her twin sister were two peas in a pod until a tumor separated them. Just four months shy of her second birthday, Ryder was diagnosed with a brain tumor. Surgery and months of recovery in ICU would follow, keeping Ryder away from home. Ryder had lost everything following her surgery. She would have to start life all over again.

After more than a year of chemotherapy and numerous other therapies to help her relearn everything, Ryder is here today. Now eight years old, the peas are together again. Ryder and her sister can be seen flitting about mimicking ballet steps, or found plopped on their toy car mat lining up cars to face the traffic, or believe it or not, taking their "babies" of all places, to the doctor.

The road has been long, with a few bumps along the way that may never recede for Ryder. However, her contagious giggle and determination to catch up for lost time keep all who know her pushing forward. Ryder's mom, Joanna, states "Hope is in the future--the research, the prevention, and ultimately a cure. We should all ban together like peas in our own pod and rally this research on for children everywhere."

Meet Sam

When Sam was about 6 years old, he started getting sick a lot. The symptoms were much like a stomach virus, but the episodes became more frequent. By the summer of 2006, when Sam was 10, he began complaining of lower back pain. Since he was playing little league baseball, everyone assumed the pain was caused from a pulled muscle. In July of that year, Sam developed a low grade fever and dry cough. He began taking antibiotics, but after a week he was worse and could not get a deep breath. A CT scan was ordered and a large mass was discovered on the right side of Sam's chest, compressing his lung to half its capacity.

On August 8, 2006 he was diagnosed with neuroblastoma. Because of Sam's age (neuroblastoma has a better cure rate in younger children) and the fact that his disease had spread to several lymph nodes, he was classified as Stage IV, high risk. The good news was that the disease had not invaded Sam's bone marrow, and there were no metastases in his bones. Sam began chemotherapy immediately and three months later the tumor had shrunk enough that surgeons were able to remove about 95% of the mass. Sam continued taking chemotherapy for six more months, and then had 20 rounds of radiation. Although he has never had clear scans, he is considered stable and was able to return to school in August 2007. His disease progressed with new tumors in October 2008 and he is currently undergoing treatment. He loves being on the baseball field, playing his heart out. He may be the smallest player on the team, but his coach said if he could put Sam's determination and winning attitude in all his players, he would have an unbeatable team!

Meet Samuel

Samuel was diagnosed with Stage IV Neuroblastoma on September 5, 2007 at the age of 16 months. His diagnosis came as quite a shock to his family because he had shown no signs of symptoms until he suddenly became very ill. His first round of chemo made him extremely ill, so he was flown to another children's hospital much farther from home. Samuel slept through his very first plane ride! After recovering, he received radiation and then a second round of chemotherapy. This additional round of chemo made his kidneys shut down and he spent over a month in the hospital on dialysis. Samuel is a fighter though, and eventually recovered. Samuel had surgery to remove his tumor on December 31, 2007 and was able to begin 2008 cancer free!

Because of the toll that chemo took on Samuel's little body he was not able to have all of the treatments he should have had. No one knows what the future holds, but Samuel's family is trusting that God has healed him of neuroblastoma forever! Today Samuel loves playing with his seven brothers and sisters, going on wagon rides, singing, and going to church.

Meet Savannah

Savannah is an incredible girl who was diagnosed with a brain tumor called Medulloblastoma on February 10, 2005. She has had three brain surgeries, many months of chemotherapy, 31 radiation treatments and spent more than 150 nights in the hospital in 2005 alone!

Savannah's tumor was quite large and nasty but never destroyed her spirit or fierce determination. The aggressive surgery to remove the tumor left her with left-sided body weakness, left-sided facial weakness, and a condition called cerebellar mutism. The mutism originally left Savannah unable to swallow, speak, and caused her to have bouts of irritability that were not well controlled with any medications. She has since re-learned how to sit up, eat, crawl, stand, speak, and walk! Savannah loves swimming, painting, Dora, Spongebob, and princesses. She is our hero and an inspiration to all who meet her!

Meet Sean

Sean was diagnosed with Stage 3 Neuroblastoma in September of 2003 when he was 11-months-old. Just after his first birthday, he endured a 12 hour surgery to remove the cancer from his spine, which left only a residual tumor that appears to be regressing without further treatment.

Now a happy and playful eight year old, Sean enjoys the company of his brother, three sisters, and other friends, particularly at the beach of their hometown, Cape Cod. He continues to be monitored with scans and tests for his Neuroblastoma, and with each test, Sean is showing improvement.

Meet Sean Michael

Sean was diagnosed with osteosarcoma, a solid tumor in the bone above the growth plate in his left knee, on July 11, 2007. Sean first started complaining about his knee during lacrosse camp. After a few x-rays and a few more weeks of increased pain, a MRI revealed it was osteosarcoma.

Sean loves football, basketball and, especially lacrosse. His first passion, though, was any and all types of extreme sports. Thankfully, his older brother, Patrick, was involved in more conventional sports, so Sean followed him instead of Tony Hawk! To Sean, participating in any sport activity is like breathing - he must do it! Sean is also a loving, caring and compassionate young boy. He is totally unselfish whether on the basketball court or the playground. A perfect day for Sean would be playing a game or two, getting together with friends, playing with his dog Nala, eating a Philly cheesesteak, and ending the day with a big ice cream at Brewster's.

Meet Shelby

Shelby was all girl and loved everything pink and purple. She loved puppies, kittens, and her Barbie dolls. The one girly thing she never had was long, blonde, curly hair which she would have loved. The chemotherapy treatment caused her hair to fall out, but her eyes seemed to sparkle even more with her beautiful bald head.

Shelby was diagnosed with Neuroblastoma and died at home on October 22, 2004 at the age of five. Her amazing smile and spirit will never be forgotten.

Meet Shelby H

Shelby Hope was diagnosed with leukemia, ALL, in November 2006 when she was only 3 years old. She loved to dance, play dress up, and go to school. There were many bad days during her treatment including sleepless nights, horrific bone pain, side effects of her chemo, and the loss of her precious baby hair. Shelby always tried to do whatever her mind was set on even when she wasn't feeling well...running with her siblings, riding her bike, doing ballet. Thankfully, Shelby completed treatment in January 2009. She will continue to have her blood monitored, and she will be monitored for signs of side effects of the chemo she endured. However, we are ultimately grateful to have her here with us and for the many strides in medicine that got us here.

Today, Shelby loves to play softball, ride her bike, and run alongside her siblings. She is still small but is growing quickly. She loves life in every way. She holds an appreciation for life that only a child who has been through what she has can have. She knows every day is a gift and she knows that gift is from God.

Meet Simon

Simon was diagnosed with Stage IV Neuroblastoma in May 1998. After surgery, 7 high doses of chemotherapy, head and abdominal radiation, a targeted liquid radiation, 115 days of monoclonal antibodies and 6 months of accutane, Simon finally finished his treatment in August 2001. Simon remains in remission, and attends Packer Collegiate in Brooklyn, NY.

He plays tennis, is on his school soccer and baseball teams, and has performed in the school play. He is very active in pediatric cancer advocacy and fundraising, especially with the annual Kids Walk for Kids with Cancer in Central Park, which was founded in 2001 by his sister Sophie.

Meet Sophia

Sophia was diagnosed with Acute Mylogenous Leukemia on July 25, 2008. The news came as a shock since Sophia has always been a very active child, and she was into all kinds of sports and physical activities. She was considered very high risk and by July 29 her doctors had placed a central line for chemotherapy administration and Sophia began chemo. Further tests would later reveal the presence of a mutation in her blood cells, and she would require a bone marrow transplant to survive. Sophia, who is a twin, but she received a transplant from her younger sister in December 2008, and her family jokes that they are now triplets! Today Sophia is doing well and is cured of her cancer. But like all cancer survivors, there is always the risk of recurrence from the original disease, and also from the chemotherapy she has been given.

Sophia loves soccer and she's been playing since she was 3 years old. She has not regained her old stamina, and her doctors have cautioned us from allowing her to engage in team sports.  Right now she's running and she's planning on doing a 5K soon. She loves being on her bike, learned to knit during her time in the hospital, and also enjoys photography.

Meet Stephanie

Stephanie was an athlete and a competitor. She was an all-star fast pitch softball player who loved the color pink. Not only did she battle on the softball field, but she also battled cancer for six years, beating her cancer twice but losing her final battle at the age of 18 when there was no further treatment available for her. At Stephanie's Celebration of Life service, everyone wore pink, even her male cousin went out and bought a pink shirt!

"Stephanie was my baby and I miss her every minute of the day," shares her mom.

Meet Steven

Steven was five years old when his mother discovered a mass in his upper left arm. After several visits to specialists and surgery, Steven was diagnosed with a Neurogenic Sarcoma attached to the Schwann nerve. Doctors determined that another surgery was needed to remove a diseased nerve and they grafted in a new nerve using nerves from both of his legs. Steven then underwent several months of radiation therapy at Shands Hospital in Gainesville, Florida. For the next 10 years, Steven traveled from his hometown in Orlando, Florida to Gainesville for check-ups every three months.

Steven attended the University of Florida and graduated in December 2007 with a degree in history and religion. Steven realized that one of his passions is missions work. He has traveled to Kenya four times as a missionary intern working in the urban slums of Nairobi. On one of his trips to Kenya, he met his wife, Nicole, and they married in May 2008. Steven is currently the High School Youth Director at The Vine Community Church in Cumming, Georgia and is taking seminary courses at Reformed Theological Seminary in Atlanta, Georgia.

Meet Tasha

Tasha finished her freshman year of high school in May of 2009 and was looking forward to a summer full of family vacations and pre-season volleyball training. A week later, visiting family in Canada, her knee started hurting after going out running with her dad. Back in Atlanta, the next week, her knee was still hurting. Her mom took her in to have it checked, and a few days later she was at the children's hospital for a biopsy.

Tasha was diagnosed with periosteal osteosarcoma, and immediately started on chemotherapy. She was fitted with a central venous line, a tube inserted into a large vein in her chest to reduce the toxic effects of the chemo on her skin. After 5 rounds of chemo, she had a growth in her forehead partially removed and biopsied, which thankfully turned out to be benign. She then went on to have a major operation to remove the tumor from her leg, and the surgery went flawlessly.

Tasha is still walking with a slight limp, but nonetheless expects to make a full recovery, and is looking forward to playing volleyball again as soon as the doctors will let her. Thanks to an early diagnosis and a top-notch team of oncologists, surgeons and nurses, her prognosis is excellent. The fight isn't over yet, but Tasha's definitely in it to win it.

Meet Taylor

Before July, 2007, Taylor was a normal teenager, looking forward to starting as a freshman at high school where she would be taking all honors and gifted classes. She is a first degree black belt in Tang Soo Do and enjoyed playing soccer and taking guitar lessons.

Taylor's life changed radically in July of 2007 when her family noticed that her stomach was swollen. Her pediatrician sent her to the hospital where she was admitted and tests were begun. The doctors discovered there were tumors in her stomach and did a biopsy of her lymph nodes. On Friday, July 13, 2007, just before her 14th birthday, we got the news that every parent dreads hearing, Taylor had cancer. Specifically, she had Stage IV Desmoplastic Small Round Cell Tumor cancer, a very rare type of cancer usually found in boys.

Taylor began chemotherapy treatments the day that she was diagnosed. Because her cancer is rare and funding for children's cancer research is limited, her treatments were planned by the doctor searching for documented cases and trying these regimens to see if they delivered positive results. Taylor relapsed in early 2008, and she lost her battle with cancer and won a place in heaven just after 3AM on April 1, 2008 in the arms of her family.

Taylor went to school everyday she was not in treatment, and she acted as team manager for her high school girl's varsity soccer team. She also served in her community by volunteering at an International Karate Competition and being a poster child for a blood drive. Taylor also wanted to make a difference for the cancer patients at the hospital where she was treated. In addition to raising money for new technology, she also organized a holiday party for the patients and families.

Meet Tony

In 1990 Tony was diagnosed with Osteosarcoma, a type of bone cancer, at the age of 3. He was found to have a tumor just above his ankle in his left tibia. He endured a below the knee amputation about five months after the diagnosis, just after he turned 4. Tony underwent 1 1/2 years of chemotherapy. He quickly developed severe hearing loss and requires hearing aids. He has since been diagnosed with chemotherapy-induced cardiomyopathy, as well as chronic kidney disease. Both are being treated with daily medications.

Tony is very active at church playing his guitar. He attended Criswell Baptist College in Dallas, Texas, and is currently planning to enroll at Lamar University. He is working full-time for his prosthetic practitioner with plans to begin studies so that he can become one himself!

Meet Trey

Trey was diagnosed at the end of March 2007 just after his third birthday with Neuroblastoma, stage 4. There was a large tumor at the top of his adrenal gland that almost filled his abdominal cavity. There were other tumors along his spinal column reaching into his chest. His bone marrow has been compromised by the cancer as well.

Thus far, his treatments have reduced the largest tumor by about half, other tumors are no longer visible on the scans, and results of his bone marrow are forthcoming. Depending on the future effects of the chemotherapy on the remaining cancer, he should have two bone marrow transplants starting in the late summer and continuing through fall. Trey may need surgery or radiation, or both, to completely eradicate the largest tumor. This could be required prior to the bone marrow transplants and result in a push-out of the dates for those procedures.

Even though this is an extremely difficult time, Trey has an amazing attitude and keeps us smiling. He even started laughing when his hair started falling out because it fell into his cereal! He enjoys playing with his Thomas trains and is pretty good at Monopoly Jr. and Crazy Eights. Trey's latest accomplishment is becoming a junior Jedi Knight after getting a light saber!

Meet Tristan

Tristan's mom shares, "When I was 33 weeks pregnant, a routine sonogram revealed that Tristan had a huge mass in his abdomen. It was so large that the doctors couldn"t tell where it was coming from, and it was in contact with all of his organs and had pushed his heart to the wrong side of his chest. He was taken by emergency c-section a few days later, and was born weighing 3 pounds 12 ounces with 10% of the weight being his tumor. When he was three days old he had his first surgery to remove his primary tumor, which they discovered was originating from his right adrenal gland. While the doctors were making a diagnosis, more and more tumors were popping up in his right lung. When he was just over a month old we found out he had adrenocortical carcinoma (ACC), which is a very rare cancer.

ACC is an extremely aggressive and often fatal cancer and Tristan was Stage IV. He had his second surgery soon after to remove the pulmonary tumors and ended up losing 40% of his right lung. For the next year, he was treated with an extremely toxic neurological chemotherapy agent. Since he took it during the first year of his life when his brain was doing so much growing and developing, he had major delays and side effects.

Tristan lost his one adrenal gland during his first surgery and the chemo killed his remaining adrenal gland, giving him Addison's disease which is also a potentially fatal disease. We deal with the Addison's one day at a time with daily medications. We found out this summer that he is Autistic so we are once again in unfamiliar territory.

Tristan loves NASCAR, especially Tony Stewart. He spends just about every Sunday rooting for Tony! He loves all sports - baseball, basketball, football, you name it and he likes it! He has been in karate for two years now and is currently an advanced yellow belt. There isn"t much he doesn"t like besides fruits and vegetables!"

Meet Tyler

Tyler loved all kinds of sports and played baseball and basketball before he was diagnosed with cancer at age 12. On January 15, 2002, Tyler was diagnosed with Ewing's Sarcoma in the left tibia/fibula with metastasis in his lungs. He underwent almost a year of chemotherapy with six weeks of radiation to both areas and finished treatment November 8, 2002. A biopsy was performed at the end of June 2004 when Tyler began complaining of pain, but the biopsy was negative. After the pain worsened, a second biopsy on October 8, 2004 showed that Tyler had indeed relapsed with metastases to the lungs.

After three years of "quality of life" chemo, Tyler decided it was time to "go big or go home". He made a huge decision that was not influenced by any doctor. On July 31st, 2007, Tyler had his left leg amputated 7cm above the center of the kneecap. He quickly adjusted to life as an amputee and worked hard to get back into "normal life". Tyler began training to do multiple triathlons against able-bodied athletes, with the hopes of competing in endurance sports at international events. He continued to follow sports religiously, especially his Ohio State Buckeyes; beloved Red Sox; Green Bay Packers and the Atlanta Thrashers!

Sadly, on May 27, 2008 Tyler's lung CT showed many tumors growing in his lungs. Tyler chose to live his life to the fullest without any more treatments. He passed away in his sleep in the early morning hours of Aug 7, 2008. A couple of unfinished items on his bucket list included watching the 2008 Summer Olympics and voting for President in November.

Meet Welles

Welles was diagnosed with Acute Lymphoblastic Lymphoma (Pre B cell), a rare form of ALL in October 2008. It was discovered by Welles' pediatrician during his four year physical that his testicles were slightly enlarged and hard. No other symptoms were present at the time of his physical. After a series of diagnostic tests, it was determined that Welles' cancer had already spread to his testicles, both kidneys and the lymphnodes in his neck and arm. Since then, Welles has endured several spinal taps and over 15 months of daily and weekly medicines and chemotherapies.

Fortunately, he has not needed any radiation or surgeries outside of his original biopsy and port placement. Welles will complete his ALL treatment in November 2010 and will not be considered cured until five years post treatment. He has an 85 percent chance of being cured the first time around thanks to so much research that has been done over the last 10 years.

Welles loves to play on the Wii, watch SpongeBob, and play with Bakugan's. He loves dinosaurs, pirates and playdates! He is a special 5-year-old boy; even older boys in our neighborhood enjoying playing with him.

Meet Will

At age five, Will was diagnosed with cancer in his leg. Will received 14 rounds of chemotherapy and had limb salvage surgery. Today Will is cancer-free and is enjoying life to its fullest.

He loves all sports but especially baseball. His sister Clare calls him "The Walking Baseball Card!" In the fall and spring you can find Will playing on a local baseball team, and he's quite a hitter! Will has a huge heart and is always taking care of his friends when they get hurt. Although we never want kids to get cancer, if they do, we long for the day that they all come through treatment like Will.

Meet William

William was diagnosed with a malignant brain tumor at the age of 14. He had to have brain surgery, learn to walk again, and endure chemotherapy and radiation, all while going to middle and high school. His cancer returned two years later, and he had to do it all over again, this time with an aggressive stem cell transplant during his senior year of high school.

He graduated from high school and now attends Auburn University and is majoring in chemical engineering. He loved pitching for East Cobb baseball, but when he could no longer pitch, he turned to humor. He loves performing stand-up comedy on his college campus and in Atlanta comedy clubs. Yes, he has lots of side effects, but he also has hope, determination, and gratitude for the many friends and strangers who help fund childhood cancer research.

Meet Zachary

Zachary is a sweet and loving boy who was diagnosed with Acute Lymphoblastic Leukemia (ALL) on November 15, 2005. He has been in remission since early December 2005 and has taken chemotherapy daily for the past 3.5 years, in addition to enduring numerous bone marrow aspirations, lumbar punctures and blood transfusions. He never complains and is brave and wise beyond his years.

In July of 2006, his family had the distinct honor of hosting the Rally Across America team during their ride through NYC. Zachary started school in September 2006 and although he is frequently absent, he very much enjoys his time there when he is able to attend, Some of Zachary's favorite things are riding his ATV, Pokemon, Digimon, Dinosaurs and spending time with his brother Jonathan and sister Lauren.

Zachary and his family are confident that once Zachary's cancer is cured his leukemia journey will be just another snapshot in a miraculous life. The cure rate of Zachary's cancer jumped from 40% to75% in two decades due to the generosity of our predecessors who supported pediatric cancer research, but a 75% cure rate is not good enough. Please consider making a donation to help find a 100% cure!

Meet Zoe

At 6 months old, Zoe was diagnosed with ATRT, an aggressive and often fatal brain cancer. She endured brain surgery, 6 rounds of high dose chemo (including stem cell rescue), and 6 weeks of proton beam radiation. Treatment ended in Aug 2008, and she is currently showing no evidence of disease. Treatment brought many ups and downs, including many scary times, but thankfully she recovered each time. Treatment also created new problems. She stopped eating orally and is now fed through a tube in her belly. She has some gross motor delays, moderate to severe hearing loss and significant communication delays. But these are manageable problems, and we are delighted to support her in her continued growth and development.

Zoe is an independent, self-assured, strong willed and persistent 2 1/2 year old. She is an amazingly expert, and somewhat dangerous, climber. She brings such joy to our family! We hope and pray the cancer is gone forever, and that she will continue scaling great heights for a long time.