Category: HSC Research

HSC Research

Announcing the 2026 HSC Clinical Fellowship Recipients

The Huntington Society of Canada is pleased to announce the recipients of the 2026 Clinical Fellowships. These fellowships will fund a period of advanced training to allow this year’s recipients the opportunity to develop deeper expertise and specialized skills in Huntington disease and neurodegenerative disease care.
Thursday, July 2, 2026

HSC Research

Meet the next generation of HD researchers and clinicians

Together with our partner, Brain Canada, we are proud to announce the recipients of the 2026 HSC and Brain Canada Undergraduate Student Summer Fellowship. Supported in part by the Canada Brain Research Fund, these fellowships offer undergraduate students across Canada the opportunity to work alongside senior HD scientists and contribute to projects that help advance HD research.
Thursday, June 18, 2026

HSC Research

Researchers tackle major health challenges with $16 million in funding from CIHR.

We are excited to follow the research of Dr. O’Donoghue, our HSC Research Chair, as he and a fabulously talented team investigate personalized therapies for Huntington disease and other genetic disorders.
Wednesday, February 5, 2025

HSC Research

2025 Navigator Award Recipients

The Huntington Society of Canada (HSC), Brain Canada, and the River Philip Foundation are pleased to announce the recipients of the 2025 Navigator Awards. HSC’s Navigator Research Program is designed to provide funding for Canadian scientific research projects of direct and immediate relevance to Huntington disease.
Wednesday, November 12, 2025

HSC Research

Clinical Movement Disorders Fellowship

Canadian movement disorders organizations join together to train the next generation of specialists.
Tuesday, March 17, 2026

The Huntington Society of Canada is a proud partner of HDBuzz. 

Launched in early 2011, HDBuzz.net provides a readable, trusted, and up-to-date source for all the latest news on Huntington disease research and clinical trials, written by researchers and scientists specifically for families and individuals affected by HD.