Hope for HH
ope for Hypothalamic Hamartomas (Hope for HH) is a volunteer-based nonprofit organization founded by parents of children with hypothalamic hamartomas (HH).
Our goal is to create a single, credible source for information about the diagnosis, treatment, and support of individuals with HH. Every family touched by this rare disorder has a unique and often heart-breaking story of how they attained a correct diagnosis. Obtaining a correct diagnosis can take months and even years and often involves incorrect diagnoses. Once a diagnosis is confirmed, many families struggle with choosing an appropriate course of treatment, if one is even available. Regardless of treatment, managing the daily lives of HH patients and dealing with the long term and frequently devastating effects of HH requires ongoing information and support.
About Us
Contact Information
- Phone:
- Email: info@hopeforhh.org
- Website: https://www.hopeforhh.org/
Our Location
Hope for Hypothalamic Hamartomas PO Box 941 Eagle, ID 83616Social Media
- Twitter/X: @https://twitter.com/HopeforHH
- Facebook: https://www.facebook.com/HopeForHH
Have you been diagnosed with one of these conditions?
- Other Rare Disease
- Central Nervous System
If you have been diagnosed with any of the above, get in touch with us.
Or email Hope for HH
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