Your gift ensures our Specialist Youth Advisors can support young people impacted by Huntington’s disease.
Support today, gift hope for tomorrow
For those without support, the challenges of living with Huntington’s disease can devastate the wellbeing of everyone in their family, for generations.
Every penny donated by you will go towards ensuring families are supported by our specialists.
A guide to fundraising
Raising funds for the Scottish Huntington’s Association is a fantastic way to support individuals and families affected by Huntington’s disease. Whether you’re planning a sponsored challenge, a community event, or a workplace fundraiser, this guide will provide you with tips, inspiration, and resources to make your efforts a success. Every penny raised helps provide essential care, advice, and research to improve lives. Let’s make a difference together!
Guide to Fundraising – full size version
Your gift can provide Huntington’s disease specialist care for families throughout Scotland.
Your gift can lower household poverty through the work of the charity’s Financial Wellbeing Service.
Ways to donate
There are many ways to make a difference! Every contribution helps us continue our work. Explore the options below to find the best way for you to give.
Online:
Phone:
0141 848 0308 (Monday to Friday between 9.30am & 3.00pm)
Bank transfer:
Scottish Huntington’s Association
Bank of Scotland
Sort code: 80-16-53
Account number: 10056968
Please use the reference Winter Appeal if you choose BACS transfer
Cheque:
Please make your cheque payable to:
Scottish Huntington’s Association
and send to:
Scottish Huntington’s Association
Business First
Burnbrae Road
Paisley
PA1 2FB
“Scottish Huntington’s Association has been in my life since I was 12 years old. My Specialist Youth Advisor helped me through the testing process, before and after, and I’m still in touch with Pete who works with young people in Fife and Lothian. He’s been my rock over the years and supported me a few years ago when I was struggling with my Dad’s death. I went to camps, family gatherings and days out, and have shared my experiences one-on-one with people about the HD testing process. The charity has been a constant in our lives and I hope for it to continue that way.”
