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She is partially homeschooled, but she’ll be spending a lot of time with her brand new “Celebrities.” She will be an honorary member of the Cedar Park High School drill team.
Eva’s favorite quote is “Never give up,” and her hobbies include basketball, cheerleading, dance and gymnastics. He has been diagnosed with primary hyperoxaluria, a disease that causes repeated kidney stones, enteric hyperoxluria, celiac disease, failure-to-thrive, anorexia, gastroparesis, gastrointestinal motility disorder, asthma, REM sleep behavior disorder, a weekened immune system, gastroesphogeal reflux disease, executive function disorder, secondary ADHD, significant short-term memory impairment, adjustment disorder with anxiety and fibromyalgia. He is on several medications, infusions and a gluten-free, low oxalate, low sodium and high potassium diet.
Ty is home-schooled, but this fall he will spend his Friday nights cheering on his new honorary teammates, the Hays High School football team. Dia underwent several surgeries over the next four months and doctors felt hopeful that her vision would return. Her official diagnosis, craniopharyngioma, a type of brain tumor derived from the pituitary gland, is rare amongst young children.
When she’s not commuting to the Children’s Medical Center of Dallas for treatment or in school, she’ll be with her brand new teammates on the Anderson High School Drill Team. For the past four years, Chase has been under the care of the Infectious Department at Dell Children’s Medical Center. After his eyes became shaky at three months old, Jeremy’s eyes stopped tracking movement one month later. Doctors in Dallas, at the National Institutes of Health and Duke University guess that Jeremy has an endocrine disease because of the involvement of both bone and muscle. The Regents School of Austin football team is excited to have Jeremy hop on board this season as their newest honorary teammate. Job syndrome is a rare, inherited disease that is known to trigger problems with the skin, sinuses, lungs, bones, and teeth. For the first three years of her life, Caroline visited Texas Children’s Hospital, Mayo Clinic and an Immune Deficiency Foundation Conference hoping to obtain insight into immune disorders. Caroline’s favorite quote is “No fear.” At school, she plays the violin, and she loves to cook and bake when she’s at home.
This year, she is a proud, new honorary member of the Georgetown High School Girls Lacrosse team… Eagle Fight Never Dies! His favorite quote is “When you get knocked down, get back up.” The Hutto High School Football team is excited to welcome Drew as their new honorary teammate this season. By age three, Evelyn was having increasing issues with her gastrointestinal health, respiratory and immune system health.
Pierce was diagnosed with Anaplastic Astrocytoma, a grade three tumor, on his right thalamus when he was 10 years old.

His treatment included proton radiation, chemotherapy, multiple surgeries and a ketogenic (a high-fat, adequate-protein, low-carbohydrate) diet. Four months after his diagnosis, the tumor was upgraded to a Glioblastoma, a grade four tumor. Pierce’s favorite quote was “Keep the faith, bro!” The Vandergrift High School lacrosse team was wonderful in bringing Pierce in as their honorary teammate earlier this season. Sending huge thanks to Cho Sushi Japanese Restaurant for hosting our annual volunteer appreciation luncheon! She had repeat sinus and respiratory infections, and when she was four years old, she had sinus surgery. This disease occurs when the body doesn’t have enough immunoglobins to fight off infections. This particular type of arthritis is a joint problem that often occurs in conjunction with psoriasis. The Lake Travis Cavalettes are excited to welcome her into their family as an honorary Cavelette this year. Over the course of time, he has been given 20 different diagnoses with no treatment or explanation. Dia’s next step is to undergo radiation to remove the tumor, but doctors are prolonging this treatment in hopes that she will start to regain her vision first. He had been playing football in the yard and within moments, had fallen into unconsciousness. Doctors believe his disease is more specific and continue to work toward a more specific diagnosis. His favorite quote is “Be strong… Live life!” This basketball season you’ll find him cheering on his new teammates at Bowie High School. Doctors in Houston and at the Cleveland Clinic weren’t successful in finding any type of diagnosis but warned his parents that he was quickly deteriorating and most likely would not live past one year. His condition causes his muscles to be so weak that he cannot walk, talk, sit or lift his head for long periods of time. He works extremely hard at daily exercises to strengthen his muscles and is working hard to find an easier way to communicate with everyone around him. Nineteen months after the diagnosis, a series of illnesses led him to two more diagnoses—Lyme disease and occipital neuralgia. Occipital neuralgia is chronic pain in the upper neck, back of the head and behind the eyes.
Evelyn’s new doctors also added autism, eating and sleeping disorders, epilepsy and asthma to her diagnoses.

Maddie remained relatively healthy for a few years after that, but then she developed a sinus infection that wouldn’t clear after 10 days on an antibiotic.
It affects the body anywhere there are mucous membranes present, both internally and externally, and causes a blistering rash inside and out. They are supposed to last three years, but her body continually rejects them after roughly one year.
Following the surgery, she went blind and the doctors concluded that there was no way to remove the tumor.
With a three percent chance of survival, Chase stayed in a coma and on life support for 10 days with little to no brain activity. Each infusion is a mixture of 20,000 different donor’s antibodies, giving him the best chance of being able to fight the many germs he comes in contact with.
This is a birth defect that causes all of the skull plates to fuse together, preventing the skull from expanding to accommodate brain growth. It is caused by damage to the greater occipital nerve, a spinal nerve that affects blood supply to the occipital artery. She was diagnosed with obesity, immunoglobulin G deficiency, gastroesophageal reflux disease and behavioral issues.
Because of the tumor’s diffused nature and location, surgery was deemed not plausible, and it presented too many risks of complications at the time of diagnosis. She has seen three different types of ophthalmologists and is currently under the care of a neurologist. Through trial and error, the staff at Dell has done an amazing job matching him with a donor pool that has little rejection on his part.
Jeremy underwent surgery to relieve the cranial pressure at 13 months old, and his vision returned but his muscles remained extremely weak. Jeremy has had more than 40 surgeries, including five major skull surgeries, two heart surgeries and eight on his eyes. Slowly, his doctors began to realize after repeated illnesses and infections that his body’s ability to make his own antibodies had been destroyed by meningitis.

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  1. Koshka, 06.09.2013
    That he is prepared to train issues such as anger or depression.
  2. Almila, 06.09.2013
    Truly can be much more about so what we did is just.