Rally Foundation : Meet the Rally Kids

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 Abby B

Abby has always been a child that required a lot of sleep. Since the day she was born, she was a twelve hour sleeper plus naps. Her family was told that she would grow out of it, however, in December 2010, at the age of 7, she started needing even more sleep. Originally, her family thought she was just going through a growth spurt and was overtired from the long days at school. It continued throughout the month of January and she started withdrawing from her activities because she was too tired. She lost interest in her favorite activity, gymnastics, and did not want to participate after about twenty minutes of practice saying she was tired and her legs hurt.

When her birthday rolled around in February, she planned a slumber party at her house on a Friday night. However, on the day of her party, Abby fell fast asleep after getting home from school and was groggy and grouchy when being awoken shortly before her party and really was not interested in having her friends come over. This was not normal for Abby who was normally a bubbly, friendly, social little girl. The following week, Abby’s eight-year-old check-up was scheduled and her mother insisted on a blood test. Her counts came back low, so Abby’s pediatrician called the oncologist. After further testing, Abby was diagnosed with leukemia on March 11, 2011 and began treatment shortly after.

Meet Adaric

Adaric was born with a genetic disorder called "Noonas Syndrome." This predisposes him to JMML Leukemia since the mutation occurs in the same gene.

Meet Addison

Addison was diagnosed with Acute Lympocytic Leukemia at age 3, and he was treated with chemotherapy until age 6. He was a rapid responder and has been free of cancer for 11 years. Addison is an active young man who plays varsity soccer and is a member of an acapella group. He enjoys playing guitar and writing music.

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 breathe 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 is the youngest of three and was diagnosed on Feb. 4, 2009 with ALL Leukemia, right before her 3rd birthday. She had exhibited leg pain, fatigue, and had fought a respiratory infection for several weeks prior to her diagnosis. Her desire to play and be with friends ceased and the need for her mom and dad increased dramatically.

Through the course of Allison’s treatment, she went through weekly chemotherapy appointments along with nine visits to the Emergency Room and ten hospitalizations. She has endured bone marrow aspirations, numerous spinal taps, blood transfusions, platelet transfusions and intense chemotherapy in combination with steroids.

Allison completed her treatment on May 20, 2011. She was able to start kindergarten cancer-free and has been loving this new phase of life. Allison’s mom writes, “When a child is faced with cancer, it brings new meaning to life and family. Our Allison has taught us many things and is our hero for all that she has been through with extreme grace, dignity and patience.”

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.

When Amelia, was 3 ½, it was suspected Amelia had pink eye, and, after a trip to the pediatrician, it was dismissed as allergies. Two weeks later, her eye looked much worse, her retina spontaneously detached, and her pupil became fixed and dilated. From that point, she was quickly diagnosed with sporadic retinoblastoma, and less than 4 days later, she had surgery to remove her right eye.

Thankfully it had not yet traveled to her other eye or moved through her blood supply to her brain or surrounding bone where it often becomes fatal. She was also spared chemotherapy and her family thanks God regularly for her health. On June 8, 2011 Amelia and her family celebrated six years of being cancer free!

Amelia loves life and is a happy, healthy fourth grader who plays violin, swims like a fish, and is active in girl scouting and church. When she grows up she wants to be a pilot (she was named after Amelia Earhart) and a veterinarian. However, she will refuse to work with snakes because they bite with poisonous venom.

Meet Andrew V.

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 checkup. 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. I have started having problems with my teeth, and I recently had to have emergency dental surgery. I believe that the damage to my teeth is due to the chemo I received several decades ago. And so with lots of help, love, encouragement, prayers, and support from family and friends, my life, though very different now, still goes on one day at a time!

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 Angelina

Angelina is a happy and outgoing eight-year-old girl. She was diagnosed with Acute Lymphoblastic Leukemia on February 17, 2010. She just finished seven months of intense chemotherapy and spent most of her summer in the hospital. She has now started her two years of maintenance chemo and has started back at school for half days. She is doing really well and has come a long way in the last eight months.

Before her diagnosis, she was just like any other eight-year-old. She loves riding her bike, going swimming, playing with her friends and her little sister, Alexia. She loves all animals, but cats are her favorite. She has a kitty named Tiggy. Since being diagnosed with leukemia, Angelina has showed much strength and inspires those around her everyday. Her mom says, “She has endured so much and just to see her smile through it all is just amazing! I am so proud of her and any child that has to go through this.”

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 Ansley

Ansley was diagnosed on February 10, 2009 with Optic Pathway Glioma. She was just five months old at the time. Since then, she has completed 64 weeks of Carboplatin and Vincristine Chemotherapy. She completed treatment on April 21, 2010. A recent scan showed that the bilateral tumors are now showing new growth, and starting in May 2011, she will be undergoing 52 weekly treatments of Vinblastine Chemotherapy.

Due to the tumors, Ansley is now blind in her left eye with decrease vision in her right eye. She loves Disney princesses and music and singing. Ansley also loves to dance, especially tap and ballet.

Meet Anthony

When Anthony was 4 ½ months old, he was diagnosed with a brain tumor called Choroid Plexus Papilloma. He underwent four years of chemotherapy and surgeries. He then started going to school, playing ball and doing everything else that active little boys do. When he was 8 ½ years old, he hurt his shoulder while playing football with his cousins and his mom took him to an orthopedist who found that he had a tumor in his arm that had caused his arm to break. He was diagnosed with Osteosarcoma and went through more chemotherapy treatments and surgeries to treat the cancer. Almost two years after he finished treatment, his family found out that the Osteosarcoma had returned and spread to his chest wall. He tried many types of treatments, but nothing worked. He died on October 30, 2008, just one month before his twelfth birthday. Anthony was a miracle. According to statistics, he should have died when he was 10 months old.

Anthony's life was filled with doctors, nurses, medications, hospitals and isolation, but it was also full of laughter, love, friendship, sports and fun. He and his family made the most of every day, and even though cancer treatments took up a lot of their time, it never slowed them down. Anthony never once complained about anything, and he even helped other children that were newly diagnosed deal with what was happening to them. He lived everyday with purpose and meaning and was always in search of as much fun as he could find.

Meet Ashlyn

Ashlyn’s parents were blessed with her birth on September 13, 2009. Nine months later, on Mothers Day, Ashlyn became ill with persistent fevers that were misdiagnosed. After multiple visits to three different pediatricians, her family was finally sent to the children’s hospital. Ashlyn's bone marrow was so packed with dead cancer cells that it took eight days and three bone marrow aspirations, a few bone biopsies and a CT Scan to finally be diagnosed. Ashlyn was diagnosed with an M7 variant of Acute Mylogenous Leukemia. She began her first round of chemotherapy on July 1 and went into remission after the first round was completed. She completed her fifth and final round of chemo on December 12, 2010, and stayed in the hospital until January 8, 2011 when her blood counts were high enough to be discharged.

Her mom shares, “We feel so blessed from the generous donations given to us through the holidays, and the great volunteer system that supported us. Ashlyn was blessed to have minimal side effects. Her biggest challenge was mucositis, sores that caused her pain and discomfort. She has grown and learned a lot through these six months of treatment, and so have we. Much love goes out to all the other children and their families that struggle with similar challenges.”"

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 Ava

Ava was a brave 4 ½ year-old who was only two weeks away from starting pre-kindergarten when she was diagnosed with stage 4 cancer. She had developed a large bump on her head that persisted for nearly two weeks, and a precautionary CT scan showed that she had several bleeds on her brain. From there on out, each day brought on more devastating news as her family learned that she had tumors in her heart, liver, both kidneys, spleen and adrenal gland. Within three days of her first scan, she began her first round of chemo, and her family was suddenly tossed into the world of childhood cancer. All of the pathology tests were inconclusive, so her cancer was called Undifferentiated Sarcoma. Though early indications showed that the cancer was responding to treatment, she passed away unexpectedly shortly before her 5th birthday.

Ava always told her family that she loves everybody, even people she does not know. Ava's strength and resolve were amazing during her fight with cancer.

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 Bart

Bart writes, "It was a few days before my 15th birthday when I found out I had AML. All my life, I had been on a baseball field, and this was the first thing that had happened to me that a bat and ball could not fix. However, after months of chemo, a bone morrow transplant and, most importantly, a lot of prayers, I was back on the ball field. I played 2 years at Central Alabama Community College and two years at Shorter College."

Meet Bella and Maddie

At just 2 months of age, Isabella and Madeline were both diagnosed with stage 4S neuroblastoma. Through testing, their family learned that Madeline had developed a tumor in utero and the cancer cells had metastasized to Isabella via the placenta they shared. As a result, Isabella and Madeline became the 9th known case of monozygotic twins to have neuroblastoma. Bella and Maddie were both admitted to the neonatal ICU at the children’s hospital where they would spend the next 44 days battling this cancer. They both had cancer cells all through their abdomen, liver, and bone marrow.

Both twins went through 4 rounds of chemotherapy treatment and as of December 2011, they are 4 years clear of cancer! Their family thanks God everyday for their continued health and they blessing that they are to their family. Today, the twins are 4 1/2 years old and are normal, active and energetic little girls that love playing with their older brother, Isaiah, and fawning over their younger brother, Liam. They still make regular trips to the children’s hospital for check-ups but continue to do well!

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 Ben

Ben was diagnosed with a large tumor occupying and enlarging his entire right kidney during the spring of his junior year of high school. After doctors removed it, he was diagnosed with a stage-3 malignancy, which usually results in four types of cancer cells found in other organs. However, he was fortunate to be diagnosed and treated before it managed to spread to other organs. He was able to play on his school's hockey team his senior year and ran in the Music City Half Marathon exactly one year later. For the race, he wore a jersey proudly displaying the words "Cancer Survivor" and encouraged many others who were running in honor of cancer patients.

He is now a freshman at Auburn University and plans to major in Building Sciences. He is excited to become a Rally Kid and help raise funds to stop childhood cancer. He knows that research is the way a cure will be discovered.

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 Blayne

Blayne is now almost 7 years old and is the toughest little boy his family knows! He goes to the hospital every four months for scans and a check-up with his oncologist. He is very active in sports and loves to play football and basketball.

Meet Bo

Bo was diagnosed with Medulloblastoma, a highly malignant brain tumor, on August 21, 2009. On August 25, 2009, the surgeon was able to remove 99 percent of the tumor. Bo had weakness in his right side, and partial facial paralysis. Furthermore, he lost the ability to walk due to the location of the tumor. He went through three rounds of regular chemo and three stem cell transplants. He was a tough little man and his mama and daddy's pride and joy.

Bo fought bravely, but his battle with cancer ended at a young age. He inspired lots of people, including his parents.

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 Brayden

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 loved football, soccer, basketball and wrestling. His favorite college football team was Ohio State, his favorite pro team was the Atlanta Falcons, and his favorite high school team was 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. He even produced music with his own studio program.Brian attended NorthPoint Community Church where he enjoyed connecting with his small group. Brian'Today he produces music with his own studio program and maintains a library of music.

Brian fought bravely, but passed away at the age of 20. He will be forever missed.

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 Brittney W.

Brittney is a 14-year-old high school freshman. She was diagnosed with Stage 2 Hodgkins Lymphoma in May 2010. Since then, she has undergone surgery, chemotherapy and radiation. Brittney says, "Nevertheless, by faith and God's love, I am remaining strong through it all." She is a member of the National Honor Junior Society. She wants to become a Pediatric Nurse Practitioner and work in the pediatric oncology clinic where she is treated.

Meet Brooks

Brooks was diagnosed with Ewing's Sarcoma, a rare bone cancer, in June of 2011. This was a complete and total shock to his entire family. He had no symptoms other than some swelling that increased during a short three week amount of time. He has begun chemotherapy and is adjusting well with his "new normal". He will be assessed again soon to see if chemotherapy shrunk his tumor enough to do surgery to remove it. He will continue therapy for almost a year. Brooks is a very energetic six year old that loves baseball! His smile and good attitude are contagious to all.

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 Multiforme (GBM), a malignant brain tumor, and was placed on a two-year chemotherapy treatment plan. Since then, Bryson has endured 9 surgeries related to his diagnosis and has completed 24 chemo treatments. He continues to go to therapy several times each week and gets regular MRI’s and follow-ups with all his specialists.

Bryson is now 3 years old and enjoys going to pre-school and being with other children his age. He continues to beat the odds and thoroughly enjoys living life!

Meet Caitlyn

Caitlyn is in seventh grade and has been battling Metastic Solid Pseudo Papillary Pancreatic Cancer since she was 7 years old. Caitlyn has undergone four major surgeries, including the one to have her portacath placed for chemotherapy. Unfortunately, they have found that Caitlyn's surgeries have caused the cancer to speed up in growth rate and spread much faster. At this time, they are not seeing the positive effects from the only known treatment, surgery.

Fortunately, the surgeries have temporarily stopped the cancer from growing, but it is not destroying it. Since her cancer is extremely rare, there is no funding for research, and her battle continues. She has been on chemotherapy for about five months now and still has another three months to go. She is currently facing the decision of whether to have radiation or not and is taking great consideration of the side effects and how it will change her life.

Caitlyn is a very strong girl who has also been diagnosed with bipolar disorder, which creates even more hurdles for her. She is such a fighter and refuses to give up, even when it feels like the world is against her, and the cancer has won. She loves to play with her younger sister Kenzie and her dog Copper for fun and relaxation. Her mom writes, "We are a strong family, but this is a journey I would not wish upon anyone."

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

In July 2006, 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 January 2008. Cam wrote, "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." In spite of several different treatments and experimental chemo, Cam's cancer continued to grow. Cam passed away on November 28, 2009 at the age of 15.

Cam was a typical teenage boy who was hungry all the time and enjoyed playing video games "airsoft" with his friends. His favorite subject was math. He achieved the Eagle Scout award just a few weeks before he passed away.

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

On February 25, 2009 Carina was diagnosed with T-Cell Lymphoblastic Lymphoma. She was in remission after the first cycle of treatment and stayed in remission for 10 months. Unfortunately, after Christmas 2009, she relapsed, and the options for her was a bone marrow transplant. We started her in a clinical trial right after the new year. Carina became very weak as the weeks went by, and on February 7, 2010, she earned her angel wings. Carina, a beautiful 12-year-old girl, with a maturity beyond her years. Through it all, Carina never complained, never asked why me, never said it's not fair. She fought a good fight, and she became an inspiration of strength and courage to her family, friends and church. We miss her dearly, and she will be forever in our hearts!

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 Caroline

Caroline was adopted from Central America at seven months old. On Christmas day, at two years of age, she had a seizure and our brain tumor journey began. Caroline was diagnosed almost nine years ago with a low-grade glioma brain tumor. Her specific diagnosis was a Oligodendroglioma. She had many surgeries and two years of chemotherapy but is currently doing amazingly well despite having a residual tumor. Her family thanks god for her and her health every day.

Caroline was recently matched with a seizure service dog. Her family has waited more than 5 years for this great news and the dog has been a wonderful addition to Caroline's family thusfar.

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 M.

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).

After over 3 years of treatment which included spinal taps, infusions, hospitalizations, countless ER visits, and daily and monthly chemotherapy, Carter took his last chemo pills on July 11th, 2011. He is looking forward to starting 4th grade cancer-free. Two weeks after finishing chemo, Carter fulfilled one of his dreams by grabbing a helmet and pads to begin playing football. Carter’s family feels proud, thankful, and blessed.

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 Celah

Celah was born with her twin brother Jacob in August of 2010. She was diagnosed with Acute Lymphoblastic Leukemia (ALL) when she was just three months old. She is currently going through treatment. She loves music and going on walks in the double jogger with her brother!

Meet Charlotte

In May of 2008, Charlotte turned 4 years old. A month later, her parents noticed her skin tone was yellowish, so her pediatrician tested her blood and found that all her blood counts were really low. He sent Charlotte and her family to the children's hospital where she was diagnosed that night with Acute Lymphoblastic Leukemia (ALL). The next day, she had surgery to install a port, had a bone marrow biopsy, and began chemotherapy.

After 26 months of difficult chemotherapy treatments that took her hair and her energy but never her spirit, Charlotte is off-treatment and ready to be a regular kid again. She loves kindergarten and ballet. Her family writes, “We are looking forward to five years from now when she will be declared cured! Thank you, Rally, for all you do to stop children’s cancer!”

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 Chip

Chip writes, “My name is Chip. Without much previous drama, on August 17th, 2010, my pediatrician ordered an MRI for what I thought was a concussion. My Mom and Dad picked me up from school, took me to the appointment, and our lives went from zero to sixty in about 2.2 seconds that day. We were immediately sent to the children’s hospital, where in 72 hours, I had two brain surgeries, a MRI, and CT scans, followed by 14 days in PICU, and several more months inpatient. I was diagnosed with Metastatic (spreading) Anaplastic (aggressive) Medulloblastoma (brain cancer). Go ahead, read between the lines. I was in school that morning. Suddenly, words I had never heard defined our lives and people I had never met were the most important people on earth.

As a side effect of the main tumor resection brain surgery, I also suffer from a rare complication called Posterior Fossa Syndrome. This syndrome has left me completely debilitated. I have spent the last year attempting to relearn everything – from holding up my head, talking, swallowing, eating, sitting, walking, using my hands – everything. I have some hearing loss and significant vision loss. Currently, I work through about 14 home therapy sessions a week to regain my function. I am making progress, but the road is still a very long one. I am still completely dependent on my parents for everything. I have just started a rehab program where I plan to regain my life.

On the cancer front, I underwent six weeks of cranial and spinal radiation and chemotherapy with 38 round trip ambulance rides. Next, came six months of intense Chemotherapy with multiple admissions for infections, including another stay in the PICU. I have had several surgeries to place G-J feeding tubes, two shunts and two shunt revisions, and crumbling teeth. Over nine months, I spent over 130 nights at the hospital.

With all of this being said, our family considers ourselves extremely blessed. From the first hour of our crisis, our community has completely surrounded us. Immediately, schedules were in place to handle everything peripheral in our lives so that my parents could focus on me. My two brothers were driven to school each day, helped with homework, sports uniforms cleaned. My pantry was stocked, meals delivered, laundry folded, toilets scrubbed, grass mowed, and even beds made so tight my brother Bret found it hard to climb in at night! The Heavens were stormed with prayers of all types. I will be forever grateful.

The people surrounding and supporting my family have been our lifeline. The term “lifeline” is not one I use loosely. This support has saved all of our lives. My brothers have not missed a baseball game or a birthday party. Dad’s friends supply the running seasonal hunting or fishing reports. My Mom’s friends run my errands and visit frequently to chat. Both of our families are of course helpful as well, they have to be. It’s the friends who could have easily moved on with their own busy lives, but instead have chosen to stick around that I am so thankful for.

Before I got sick, I was a normal 13 Year old kid. I played on my school’s baseball team, goofed off with friends, and loved anything to do with the outdoors. My main passion revolves around anything to do with hunting and fishing…..any kind of hunting and any kind of fishing! My favorite color is Camouflage!!! I am determined to get walking again soon so I can get back in the woods. My Dad and I have always been partners in this passion.

On November 30, 2011, I officially completed my chemotherapy and am considered “off-treatment” and my December 1, 2011 MRI scans are clear. As for now, I work hard every day at the spinal rehab center and at home at gaining back my strength, coordination, walking, balance, speech, vision, and eating. Everything has to be relearned. I want to go back to school someday soon as well. I try not to get discouraged. This is where I am thankful for my brothers, Mom and Dad, and friends.”

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 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 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 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.

CJ had a smile that you would never forget, and when he walked in the room you could sense his calm presence. He was an avid soccer player and a very talented tennis player. He loved listening to all kinds of music, writing songs, "rapping" with his friends, and drawing. He accepted his journey with grace and is truly missed.

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 has redirected his love for sports to golf and fishing. He stands by his motto of "adapt and overcome" as he continues to embrace all that life has to offer.

Currently, Clark is a sophomore at Georgia Tech studying Management. He is a member of the SAE fraternity and manager for the GT baseball team. Go Jackets!

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!"

Meet Coleman

Coleman's journey began September 21, 2006 when he and his twin brother Caden were 2 ½ 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 Colvin

Colvin is 17-years old and was diagnosed with carcinoma in August of 2010. He had six tumors in six different places, and is currently going through treatment. Colvin is very grateful for everyone that has been there to support him and writes, "In some ways, I have to say, it has been a journey and an adventure." He has faith that God will continue to smile down on him as he undergoes treatment.

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 ½, 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 Courtney

Courtney was diagnosed with Medulloblastoma, a childhood brain tumor, on May 14, 2009. She had brain surgery to remove the tumor on May 18, and she then developed posterior fossa syndrome. She has had 30 rounds of radiation and nine cycles of chemotherapy over the past year. She completed chemotherapy in July 2010. She still goes to physical, occupational and speech therapy, and she is growing stronger each day. She is determined and strong-willed, and she is learning how to walk and become independent again.

Courtney loves arts and crafts projects, and she loves participating in her Girl Scout troop. Before she was diagnosed, she enjoyed soccer and dance.

Meet Courtney C.

On August 1, 2011, Courtney showed her mom some bruising on her legs. Initially, her mother was not too concerned as she had just returned back from the beach where she had done a lot of playing in the ocean, but decided to show their doctor at their well check-up that week just to be sure. The doctor did not seem too concerned, but did say to call her if any bruising occurred on her stomach or back.

That week, Courtney helped move her older sister into a new apartment at Auburn. She seemed unusually fatigued, but her iron had been a little low at her appointment so it was thought it could be that. Courtney spent that Friday night with her older sister, Ashley, and the next morning she woke up with a large bruise on her stomach. When her mother saw the bruise, she knew it was not normal, and made a note to call the doctor after the weekend.

On Sunday of that week, Courtney moved into her dorm room at Auburn University. She met her roommate and began rush week the following Monday. On Monday morning before recruitment, Courtney called her mother and told her that she could not walk very well due to being very sore. She continued with the first day of rush, and her mother called her doctor to talk about the additional symptoms Courtney was having. On Tuesday of that week, her doctor ordered more labs for her and Courtney and her mother went to the hospital at Auburn to get them drawn.

The next day, Courtney’s doctor called saying the results were in and that it looked like Courtney might have leukemia and that they needed to get her to the hospital as soon as possible. Her mother writes, “After getting off the phone with the doctor, I then had to make the hardest call I have ever had to make in my life. I called Courtney and told her that I had to come get her and take her home because her labs did not look good and we needed to see what was wrong. Courtney had to leave Auburn to go back home to Atlanta.”

After making it to the hospital, Courtney and her family got confirmation that she had Acute Lymphoblastic Leukemia. Courtney and her family were very upset and scared, but knew that they had to prepare for the fight. After the first phase of treatment, Courtney’s bone marrow showed that she was already in remission with no cancer cells left in her body.

In high school, Courtney was heavily involved in cheerleading and cheered competitively for six years. She was planning on trying out for Auburn’s cheerleading squad this year, but will have to postpone that for after she is finished with treatment. Courtney is a huge Auburn fan and even had the opportunity to go the national championship game this past January to cheer Auburn on to their national championship win.

Meet Creed

Creed was born at 29 weeks and spent the first five years of his life in and out of the hospital. He was born with an adrenal insufficiency and at the age of 2 was diagnosed with a primary immune deficiency. At age 5, Creed was diagnosed with myelodysplasia /monosomy 7. He underwent a bone marrow transplant as the only treatment for his disease. It has been 10 months since his transplant, and as of now, he is disease free and starting to get back into the full swing of things.

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 at all. 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 Daniel G.

When Daniel was only eight months old, a CT scan revealed a large brain tumor that took up nearly the whole left hemisphere of his head. The doctors immediately admitted him to the hospital and operated the next day to remove as much of the tumor as possible. The operation seemed to be a success; however, complications followed, and Daniel underwent another brain surgery and stayed in the hospital for an additional week. He suffers from seizures, some vision loss, and developmental delays. However, he has done very well and enjoys playing with his sisters. He even began to walk at the age of 16 months.

At the age of 17 months, a follow up MRI revealed 3 more tumors. Two weeks later, he was back in surgery, which we believe was successful. The doctors have also found a spot on his spine and are unsure if it is tumor or scar tissue. Thankfully, it has not grown dramatically, so they are just monitoring the spot. He is recovering well and getting back to his old self. His family is very grateful.

Meet David

David, a.k.a. Bubba, is a 16 year-old with the mind of a 3-5 year-old. He has both Cerebral Palsy and Epilepsy due to a head injury. In September of 2009, he was diagnosed with two different types of Lymphoma (Burkett's non hodgkins and aggressive large B cell stage 4). His hero is Buzz Lightyear, and he loves his family, all Disney movies, and books.

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 3 years.

Donnie lives his cancer free life as a fun-loving little boy that has a lot of energy and loves to spend his days playing soccer, dancing, and modeling. He is currently attending kindergarten. 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 Dorian

Dorian was diagnosed in May 2007 at the age of 4 with a stage-3 brain tumor called Anaplastic Ependymoma. Since diagnosis, Dorian had five brain surgeries, a total of 66 rounds of radiation, and was on a two separate chemo regimen. He and his family traveled to three different children's hospitals for treatments, but his tumor was relentless. In July 2010, doctors discovered that Dorian's tumor had grown back in two places and had spread to the spine. All of the tumors were inoperable, and his family was told to get hospice involved. Dorian had six tumors in the brain and one on the spine, but if you looked at him from the outside, you could not even imagine what was going on inside. Dorian continued to amaze everyone by attending school part-time and continuing to walk, talk and even run on his own.

Dorian's long battle with cancer ended when he was just 8 years old. He loved Spiderman, funnel cakes and playing on the Wii. When he was able to go to school, everyone wanted to sit next to him in his first grade classroom and he charmed everyone that he met.

Meet Dylan

Dylan loved to play football, basketball, soccer and play outside all the time. He had no signs or symptoms of a brain tumor until he was playing and was spun in a computer chair in June of 2010. Dylan started screaming in pain, could not get out of the chair, and the left side of his face looked like he was having a stroke. Since then, he was diagnosed with a very rare brain tumor. There are only 42 known cases in the U.S., and so far, no doctors have known how to treat the cancerous tumor. Since last June, his family has had to travel to different hospitals far away from his home to see how to treat the brain tumor. Dylan has had two brain surgeries and eight weeks of radiation. With his last brain surgery, the tumor was 100% removed, however, he still requires treatments. Because the tumor is often recurrent, Dylan will have to be in treatment for the rest of his life and must also be monitored for secondary problems from the radiation. Dylan is not currently able to play contact sports, but he plays outside with his friends, plays basketball at home, and plays video games.

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 was diagnosed with Anaplastic Medulloblastoma in August 2006. She endured several surgeries, extensive chemotherapy, radiation and a research protocol chemotherapy regimen. Emily brought great awareness to childhood cancer in her community, and she amazed and inspired anyone she met.

Emily enjoyed riding her bike, boating, going to the beach, dancing and going down waterslides. When she became unable to walk and do her previous activities, she liked having her picture taken, dolls, princess stuff, jewelry, coloring & drawing, Dora, and Scooby Doo. Emily loved to cuddle with her puppy, Oreo! Emily enjoyed having her wish being fulfilled by visiting Walt Disney World in Florida with her family.

Emily was healed of cancer forever on April 18, 2008 at the age of 6.

Meet Emilyn

Emilyn was a healthy little girl until she woke up one morning and could not stand up straight without holding on to the walls. Just days after her 7th birthday, she was diagnosed with a brain stem tumor. She, like all children with pediatric cancers, endured the chemotherapy, radiation, pokes, scans and therapies that her family hoped would make her better. She died six months later in her parents' arms.

Emilyn loved dancing, the colors green and purple, her black lab Bear, her American Girl Doll kit, the Bumblebee ride at the beach and pineapples, but she loved her siblings most of all. When given the opportunity to have a wish granted, she replied that she just wanted to stay home and be with Meghan, John, and Brian, nothing more. She was a great sister. She was friendly and funny. She was naughty sometimes. She was happy go lucky and full of spirit. She was our daughter. She was more than cancer. She was, and still is, loved.

Meet Emma

Meet Emma C

Emma is a smart, beautiful four-year old who relapsed from a Wilm’s tumor in June of 2011. She was first diagnosed at the age of three-years old and underwent her first surgery to have her kidney removed followed by chemotherapy for six months.

On her three month scan, it was discovered that the tumors were back and had spread to her lungs. Upon relapsing, it was found that she had six additional tumors on her lungs. Emma had the tumors biopsied and is starting back on chemotherapy. She just finished her third surgery to remove the rest of the tumors from her lung. Her parents call her their “little honey badger” that never gives up and is always in a good mood. She has a big sister, Sam, who she loves and adores, and loves being a big sister to her brand-new little brother that she cannot put-down.

Emma is obsessed with Justin Bieber, or just music in general, and loves games and learning. Her family feels very thankful for all of the support they have received from friends, family, neighbors, their church, and absolute strangers.

Meet Esther

Esther (Persian for "Star") Grace was born on August 3, 1994. She was the bridge between two older sisters, Abby and Angie, and two younger brothers, Graham and Abraham. In November 2006, Esther was diagnosed with metastasized papillary thyroid cancer in Marseille, France, with extensive tumors already in her lungs. Following a thyroidectomy and seven months of treatment, her family moved back to New England for her continued treatment. Esther patiently endured radioiodine treatments, X-rays, CT scans, a bi-pap machine, extensive medications, occasional stays in the hospital, and eventually experimental chemotherapy. As Esther's need for supplemental oxygen increased, her mobility decreased. Yet she found new avenues for meaning, investing herself in growing online friendships through Nerdfighteria and the Harry Potter Alliance, creating videos and a cyber presence. She thrilled in her mild escapades into virtual stardom, embracing her self-proclaimed nerdiness as she dispensed advice, all-night talk fests, and free hugs. On August 25, 2010, much too soon, cancer silenced Esther and stilled her slender fingers. In 16 years she packed a lot of living and loving into her life, and those who surrounded her. Esther didn't let her light stop shining. Rest in Awesome, Esther!

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 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 had a rare kind of ALL, and went through chemotherapy treatment beginning in April 2009. Evan also received a bone marrow transplant in the fall of 2009.

Evan recently started classes at the University of Georgia and loves being in college so far. He is majoring in biomedical engineering and is considering going to medical school later on. He will have his first appointment in the Survivorship Clinic since finishing treatment in September of 2011. The two year anniversary of his bone marrow transplant will take place on September 29, 2011. Evan and his family are excited to celebrate this great milestone and are happy that there has been no evidence of recurrence of his cancer.