Emma Nott, an HH parent and Hope For Hypothalamic Hamartomas (HH) board member provides an in-depth description of this complex syndrome, the importance of early diagnosis and having a multi-disciplinary team to treat the HH patient throughout their lifetime. She also outlines Hope For HH mission and services we provide internationally. We appreciate American Epilepsy Society (AES) for providing us this opportunity to raise awareness of HH to the attendees of the 2019 AES Annual Meeting in Baltimore, MD.
