Hope for HH was founded by parents, grandparents, and aunts of HH patients because although our HH journeys are unique, we are UNITED in our hope that no one with an HH diagnosis will have to go it alone.
A team of compassionate caregivers and volunteers are working hard to plan a weekend where HH families can not only get the most up-to-date information, but also spend critical time together. More information follows below. SIGN UP NOW for the 2015 HH Family Conference, July 10-12 in Houston, TX.
why one of HH's founders supports the Rare Epilepsy Network and why you should too!
Lisa, Erica, Wendi, Julie, Emma & Ilene
HH Board & Caregivers