Hope for Luca

Luca was born 2 months premature. Upon normal testing, doctors found that his red blood cell count was low, which can be common at times in premature babies. After spending a month in the NICU, Luca had 2 blood transfusions to elevate his red blood cell count. After 3 months, it was discovered that his red blood count had dropped to a dangerously low level requiring hospitalization and 3 additional transfusions. Luca underwent extensive testing to find out that he was diagnosed with a rare genetic  mitochondrial disease known as Pearson’s Syndrome.  Pearson's Syndrome is a multi-system disease caused by a deletion in mitochondrial DNA characterized by sideroblastic anemia and exocrine pancreas dysfunction. There are less than 100 reported cases worldwide. Currently, there is no cure for this rare disease.

For more information and awareness about Pearson’s Syndrome go to https://thechampfoundation.org

All funds raised will help the Rosales Family in their difficult journey ahead.  Luca will be traveling to medical facilities in the US, as well as internationally, to see doctors who specialize in rare mitochondrial disease. Luca will have a team of doctors ranging from cardiologists, hematologists, gastroenterologists  to endocrinologists and neurologists. 

These funds will provide ongoing assistance for Luca toward future travel expenses, medical expenses, clinical trials and alternative and experimental therapies.  Luca has proven to be an amazingly strong fighter.  We hold great hope for him and hope to raise awareness, funds and will continue fighting for a cure!