Winter Appeal
Steve shouldn't have had to choose between heating the house and putting food on the table for his family. You can help ensure no-one else has to.
Donate todayYour support will help transform the diagnosis, treatment and care of people axial SpA, an inflammatory condition of the spine and joints, live better with their pain, exhaustion and fatigue.
Your support will help transform the diagnosis, treatment and care of people axial SpA, an inflammatory condition of the spine and joints, live better with their pain, exhaustion and fatigue.
There are 4 ways to make a one off donation to NASS.
Send a cheque or CAF voucher made payable to NASS to:
NASS Fundraising, Ground Floor, Unit 6, Cambridge Court,
210 Shepherds Bush Road,
Hammersmith,
London,
W6 7NJ
Call 020 8741 1515 and press option 2.
Bank name: Barclays Bank Plc
Account name: National Axial Spondyloarthritis Society
Account number: 53976149
Sort code: 20-46-76.
IBAN: GB84 BUKB 2046 7653 9761 49
Please include your name in the reference and email fundraising@nass.co.uk to let us know to expect your donation.
Please note that we cannot accept cash donations at this time.
If you are a UK tax payer, please don’t forget to add Gift Aid to your donation which can add up to 25% more to NASS at no cost to you.
Whenever you donate to us, online or over the phone, you’ll be asked if you want to add Gift Aid to your donation.
Don’t worry if you’ve forgotten to add Gift Aid – you can sign up today by filling in this form and returning it by post: 2023 Gift Aid Declaration form updated
Your support for NASS and people with axial SpA is more critical than ever:
Axial SpA is an inflammatory condition of the spine and joints. Inflammation where muscles attach to the bones, causes extreme pain. It’s an invisible and often misdiagnosed condition. Often leaving people feeling powerless, in increasing pain and extreme exhaustion. If left untreated, it can permanently fuse bones together.
NASS is the only charity in the UK dedicated to supporting people with axial SpA. NASS doesn’t receive any statutory funding. We rely on your kindness and generosity, and other people like you, to help us transform the diagnosis, treatment and care of people with axial SpA and help more people live well with the condition sooner.
If you have any questions about making a gift to NASS, please email fundraising@nass.co.uk or call 020 8741 1515 and press option 2.
Steve shouldn't have had to choose between heating the house and putting food on the table for his family. You can help ensure no-one else has to.
Donate today1 in 200 of the adult population in the UK have axial SpA (AS). That's twice as many as multiple sclerosis and Parkinson's disease.
Axial SpA (AS) is a condition that affects young people. Symptoms start late teens to early twenties, with the average age of onset being 24.
The current average delay to diagnosis from when symptoms start is 8.5 years, by which irreversible damage to the spine may have occurred.
59% of people with axial SpA (AS) report experiencing mental health problems compared to 25% of those with musculoskeletal conditions overall.