ICE Alliance’s Professional Advisory Board is a group of leading intractable childhood epilepsy, genetics, and drug development researchers from both academia and industry, clinicians who work with patients with intractable epilepsy, and experts from related fields. These members live all over the world and review grant proposals, and attend relevant meetings to help determine which research programs will get us closer to improving intractable childhood epilepsy and curing the disease
ICE is a voluntary non-profit with no paid employees. The contents of this website have been written by Harriet Davies, PharmD or Doctor of Pharmacy students under her direction through an ICE Drug Information rotation with accredited pharmacy schools in North Carolina. Additionally, other interns or professional volunteers contribute to the website from time to time.
All donations made to ICE Alliance go to support education or research initiatives.