Welcome to The Scottish Huntington’s Association Website
The Association provides expert care to families living primarily in their own homes. Just as importantly, support is offered by families for families via a network of local family support groups.
Help Us Tell The HD Story
SHA are looking to tell the story of the devastating impact that Huntington's disease (HD) has on families.
We're looking to fund a 15-minute film about one family's journey coping with HD, how it affects their lives and the role SHA plays in helping them cope.
Click here to view a short trailer and find out how you can help.
SHA Christmas Cards On Sale!
Rudolph's back! - designed by last years' Christmas Card Competition winner Keira Amy Russell, aged 11.
We have a total of 8 designs this year, as well as a variety pack, so we're sure you'll find something that appeals.
To view the range and purchase (remember, you'll need a PayPal account), simply click here.
Living with Huntington's disease?
Need support, but it's past 6 o'clock?
Scottish Huntington's Association is partnering with Breathing Space Scotland to provide an
out-of-hours telephone support service for families living with Huntington's disease.
Click here for more information.
Get the latest news, read Sarah Winckless' blog and check out our Events CalendarVisit Community
Find out more about the different ways you can get involved and help us raise much-needed funds.Fundraising
Whether you are finding out about HD for the first time or are a professional looking for more information about HD, visit here.Resource Centre
Find location and contact details for our HD Specialist and Youth services.Full SHA Services
Got a Question? Please Ask!
Use the dropdown menu to find answers to the most frequently asked questions we recieve from users of our website. Alternatively if you have a specific question then click here. We will endevour to answer you back within five days. This service is available from Monday to Friday.