
Kayden’s Dream
Born with an omphalocele and pentalogy of the heart, Kayden is a true superhero. He has over come so many challenges already in his young
Born with an omphalocele and pentalogy of the heart, Kayden is a true superhero. He has over come so many challenges already in his young
Emery-Jordin lives with epilepsy, her seizures began at 6 months old and for her this disease will forever be a part of her life. She
Life changed instantly for Toby and his family in May 2020 when the then 9 year old Toby collapsed and was non-responsive. He was rushed
Born at just 25 weeks, weighing 550 grams, Luke spent the first 3 months in the NICU. Dealing with the life long complications of chronic
13 year old Keagan was born at just 27 weeks gestation. Though he spent 82 days in the NICU when he was born, and as
Quin was diagnosed with chronic kidney disease at just 6 years of age. She loves tackle football and since there was no girls league for
Living with Clathrin Light Factor Disorder I, gross motor, speech and cognitive delays can make life challenging at times but when you have new BFF
The past year has been challenging for this lovely family of 4. Ellie has struggled to get her seizure disorder under control. With multiple surgeries
Diagnosed with GRIN 2B, 10 year old Brooklynne relies on a wheelchair for mobility so being active, playing baseball, and getting down to the beach
Thyana may be quiet and a bit shy but she is a dedicated LEGO engineer who through sheer determination and a passion for building, assembled
Saul is a bubbly, boisterous, and thoroughly delightful little boy with a rare condition called transverse myelitis. He loves all things Paw Patrol, monster trucks,
Reeghan was born with Cerebral Palsy, she is legally blind and deaf, and has a paralyzed vocal cord. Despite her physical challenges, she is an