Danny was so excited to receive his cape! He told me he is now a real super hero! This couldn't have come at a better time as Danny is having surgery next month. Danny was born with a rare syndrome, Femoral Hypoplasia Unusual Facies Syndrome (only about 100 cases worldwide) and Proximal Femoral Focal Deficiency. Visit his Facebook page.
Elaina Rose Owens has Methylmalonic Acidemia. Elaina’s sister, Adalynn, is also so brave and courageous for being so strong for her little sister and trying to help whenever she can. Visit her Facebook page.
Emma is an almost 8 year old social butterfly whose smile can light up a room. Emma has a rare condition called Cerebellar Facial Dental Syndrome caused by a mutation of her BRF1 gene. So far there have been 6 other patients identified in the World with Emma being the only one in the US. Although we understand that we may not be able to “fix” her, we have an answer, a reason. We have learned to take each day one at a time and enjoy each day we have with her and try to be just as happy as she is.
Naomi was born 3/22/2016 with HLHS and other heart issues. She received a heart transplant on 8/15/2016. Visit her Facebook Page.
On March 16, 2017, he was diagnosed with Acute Lymphoblastic Leukemia. The first few months were very hard for him. Every week he has chemotherapy. Now he is 5 years old. Day by day he is fighting with this terrible disease. He is a very happy child and enjoys every second of his life.
Ryder absolutely loves it and will wear it while delivering his smile packages. Ryder is a 10-year-old brain tumor survivor. Visit his Facebook Page.
Meet superhero Kaitlynn. She suffers from Common Variable Immune Deficiency! Kaitlynn is a superhero because she battles every week of three sets of infusions. Kaitlynn is sure sporting all her superhero powers in these pictures!
The cape made Nora’s whole day. She loves her new cape!
Little girl Chloe underwent 5 brain surgeries in 8 weeks this summer due to a stroke/Cavernoma tumor!
Mia was diagnosed with a brain tumor on her pituitary gland just days before her 2nd birthday in November 2011.
Shes a super hero because she had surgery before she was even born. Her mom, Stephanie, decided to have fetal surgery once they learned that Miah had Spina Bifida. Nothing keeps this little lady down and she's so proud to show off her cape!
He's a 6 year old who loves music and is working hard at being a drummer. He's very inquisitive and loves traveling to different places. Christian also has an extensive list of medical complications, but he has the best smile! Although he cannot speak, he knows how to show you what he wants! ..... which includes showing off his superhero cape!
Emma Routh is spunky, fun loving 7-year-old girl that like so many other girls her age - have an affinity for Hello Kitty and Justin Bieber. However, unlike her peers Emma is battling fanconi anemia – a rare blood disorder that leads to bone marrow failure.
Caden was diagnosed with Leukemia when he was 28 months old, he was previously a typical healthy little boy, that all changed overnight-literally.
Meet Superhero Brody! "Brody celebrated a huge milestone last month. He celebrated one year of being cancer free. We had some professional photos taken with his adorable cape. Visit his Facebook Page.
Introducing Superhero Brantley! What a sweetheart! Brantley was born with Congenital Heart Disease called Tetralogy of Fallot/PA. He has had one open heart surgery, and two catheter procedures so far. He is a superhero because "he does it all with a smile". Please drop by his Facebook page at to learn more about Superhero Brantley and CHD.
This is 1 1/2 year old Ava diagnosed with Down Syndrome and AVSD heart defect. She defies everything that people think of when they think of Down Syndrome. While she has some delays, she reaches her milestones with great pride at her own pace. She brings light into the lives of everyone she meets! Visit her Facebook Page.
My name is Andy Velazquez and on July , 2014 I was diagnosed with a GI Disorder, and others medical conditions, please pray! Visit his Facebook Page.
Noah Loves his cape. He has autism, epilepsy and dysphagia. Our little guy has never ate real food because his sensory issues (he eats only thin pureed, same food everyday) and he wears his cape when trying something new cause that's just what superheros do. He has had many medical testing and surgeries. he is our little hero. Thank you so much
Sweet princess Bristol….showing her strength in more ways than one. Bristol had fetal surgery for Spina Bifida in December 2013. Follow her Facebook page.
Jacob Goeders, also known as the Leukemia Slayer, was diagnosed with Leukemia at age 9.
Introducing Super Braedyn!! This amazing 7 year old was born with BA aka Biliary Atresia. By the time she was 3 1/2 months old, she had already had a liver that was failing. Within 4 months of diagnosis and many MANY test being run, she was transplanted with a whole baby liver at 7 1/2 months old. She is a fighter and is MY hero everyday. She is now 7 and loves to sing and dance. Thank you to her awesome sponsor Nadia Durant for helping bring her a smile.
Sweet Layla wearing the cape she received tonight. This superhero is recovering from a heart transplant and is doing phenomenal. It's been 23 days and from what we've heard she has been recovering extremely well!
After fighting 4 viruses that caused cardiac/respiratory failure, Deklan has been diagnosed with Severe Combined Immunodeficiency (SCID). Monitor his progress via his Facebook Page.