There was no treatment for their child’s rare condition. Now they’re trying to create one. November 10, 2019 Tags:a:national, ahc, alternating hemiplegia of childhood, genetic disease, hope for annabel foundation, neurologists, News, nih, nina frost, s:National, simon frost, t:Original, The Washington Post, WaPo Video, Washington Post Video, Washington Post YouTube Related Posts Boris Traces His Secret German History | Who Do You Think You Are The way we think about biological sex is wrong | Emily Quinn Fire Emblem 4: Genealogy of the Holy War [Ep.2] – Horrifying Half-naked Hooligans About The Author John Henderson 5 Comments Jim Bakes This is the difference between USA and the EU. September 10, 2019 Reply Jim Bakes That's awesome 👍 September 10, 2019 Reply vishnu vardhan Salute. September 11, 2019 Reply Hung Vu Great job September 14, 2019 Reply Dorothy Lanasa Go through foods and plants at NIH's Pub Med NCBI of 28 million citations. Look for nutraceuticals that treat epilepsy. You will probably find help or even a cure. October 20, 2019 Reply Add a Comment Cancel reply Your email address will not be published. Required fields are marked *Comment Save my name, email, and website in this browser for the next time I comment.