Support Davian Navarro's Lifesaving Treatment

Our son Davian is 7 years old and is the happiest little boy who always has a smile on his face. He loves cars, skateboarding, and all things Halloween. He has recently been diagnosed with a rare genetic brain disease called Adrenoleukodystrophy. It is a terminal illness and early treatment is necessary to improve his quality of life. Without treatment, our son will lose his life within a few short years. The only available medications for this disease are in Paris, France. My son and I would need to fly to Paris every year in order to receive the medication he desperately needs to fight this disease and give our son his life back. Davian will continue to go back and forth to Primary Children's Hospital for appointments, tests, scans, and treatment throughout his entire life to monitor his disease. We are asking people to please donate towards our son's medical bills and travel expenses to get his medical treatment. Any help would be greatly appreciated; even the smallest donation will make a difference. If you can't donate, please just share. Thank you all so very much.