Helping Huntington's Disease Families Find Resources


HDSCN Support Groups are co-facilitated by LCSW or MSW from caregiver agencies to ensure confidential and professional oversight.


Help in Finding the best Care
We focus on helping you find the appropriate clinic or facility for the care of your HD loved ones.


 Networking Resources
Many resources are necessary to manage HD. Referrals will help you make the best possible choices for your situation.

HD often affects the whole family, for generations.

Caregiver Support Groups
To help HD families find the best possible support services, care professionals and community services for their HD loved ones. In some cases children are affected with Juvenile Huntington's disease. Our beloved JHD children require much more attention to support and care. HD Support & Care Network is here to help.
HD Support & Care Network, is a free service provided to HD families in the US. We take pride in our mission is to help HD families find the best possible support and care resources, and community services for their HD loved ones.
According to the Hereditary Disease Foundation, Huntington’s disease (HD) is a dominantly inherited, neurodegenerative disease causing involuntary movements, severe emotional disturbance and progressive cognitive loss over ten to twenty years. There is currently no cure. Each child of an affected parent has a 50% risk of inheriting the same lethal affliction. HD usually strikes between the ages of 30 to 40, in an individual’s prime productive years, though children as young as two years old and adults in their eighties may also develop symptoms. Most individuals in the late stages of illness require enormous assistance; they lose the ability to walk, talk, and feed themselves, but are still conscious, aware and know themselves and their families.

Our mission at HD Support & Care Network

Thank you sponsors and partners!