My name is Tanita Allen, and in 2012, I received life-changing news: I was diagnosed with Huntington’s disease (HD), a rare, neurodegenerative condition. Huntington’s is rare enough as it is, but the belief that it doesn’t affect people of African descent made getting a proper diagnosis even…
HD in Color - a Column by Tanita Allen
Recent Posts
- Giving thanks for the brave volunteers who participate in HD clinical trials
- The challenges of navigating dating while living with Huntington’s disease
- Guest Voice: I hate Huntington’s disease, but I love my husband
- New Zealand OKs Phase 1 trial of Huntington’s therapy SRP-1005
- Nothing compares to a punny Valentine’s Day play