Your donation is essential to continue the ground-breaking research and international collaboration efforts at Children's National led by Dr. Adeline Vanderver, Elliott’s neuro-geneticist, expert in rare genetic disorders. Beside her clinical care, Dr. Vanderver’s remarkable research work focuses on enabling an early diagnosis and establishing a medical protocol for children diagnosed with SCN8A gene mutation.
Make a gift today.
Your contribution could enable progress unlocking the mysteries of Elliott’s rare genetic disorder and offer the only real hope for Elliott and far too many children like him struggling with its debilitating effects. Please donate at a level that works for you – no donation is too small.