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
- When the hope for a cure causes unexpected doubts
- The importance of a support system in Huntington’s disease
- HDSA 2026: Huntington’s gene therapy may move to clinical trials
- HDSA 2026: Reframing can help caregivers navigate challenges
- HDSA 2026: Oral therapies take center stage in ongoing Huntington’s studies