Join in, it’s simple!
It is now easier than ever to participate in Walk Your AS Off! Simply register on the SAA website and you will find a step counter waiting for you. Log your steps daily, weekly, or monthly!
Walk Your AS Off (WYASO) is an annual, global and virtual step challenge every May run by The Spondylitis Association of America (SAA). We are partnering up again this year with SAA for World AS Month to generate global momentum and raise awareness of axial SpA! WYASO is all about bringing people together from all over the world, challenging yourself to stay active and raising awareness. Together, we can do this!
It is now easier than ever to participate in Walk Your AS Off! Simply register on the SAA website and you will find a step counter waiting for you. Log your steps daily, weekly, or monthly!
Many of our supporters take the opportunity to fundraise whilst challenging themselves to take more steps during the month of May. This year, we are encouraging our supporters to all sign up to the Walk Your AS Off 2025 JustGiving campaign page in order to raise funds for NASS.
That means that every penny that our fundraisers raise goes into the same pot! Wether you raise £20 or £200, every little bit counts and helps us to provide much needed support and information to people living with axial SpA. You can join a team, such as our long-standing yearly participants NASS Orange Apples, AS Buzzers and NASS PAWs, or get your friends and family together and create your very own walking team! Or you can simply share the link with your friends and family while posting your step updates and as them to support you.
This is about being a part of something together, taking on a step challenge, tackling World AS Month and raising as much awareness as possible. Create your fundraising page here: https://www.justgiving.com/campaign/walkyourasoff2025
Here’s how you can help raise awareness of axial SpA during Walk Your AS Off:
How can I get a NASS t-shirt during my walks?
Once you raise £20, get in touch to get your orange NASS t-shirt! Call us on 020 8741 1515 or email fundraising@nass.co.uk to order your t-shirt. We stock small, medium, large, XL or XXL sizes for men and women – just ask! Sizes are subject to availability.
Do I have to do a certain number of steps every day?
You can do as little or as many steps as you like at any time during May. It’s just about getting active. Whether you walk 50 steps or run 5,000, it all adds up to our collective team step total.
I’m a wheelchair user – can I still join in?
Absolutely! You can convert time spent in your wheelchair, or doing other activities like housework, swimming, cycling or Pilates, into steps too. It can be all converted with our step conversion chart.
I’ve been recently diagnosed with axial SpA. Do you have any advice for walking with axial SpA?
Yes, we’re here to help. Here are our top tips:
Does NASS organise Walk Your AS Off?
No. Since last year, Walk Your AS Off has been organised by the Spondylitis Association of America. Thank you to Walk As One for all the amazing work they have done since 2015 to mobilise and motivate a global community to raise awareness and address the challenges of those affected by axial Spondyloarthritis and its family of related conditions.
A huge thank you to Gillian Eames and Kathy Miller for leading 3 amazing NASS teams to walk an incredible total of 32,399,847 steps to raise awareness of axial SpA.
Thank you to our amazing team of fundraisers for raising over £4,500 for NASS – enough to support another 450 people with axial SpA to live better with their condition.
Sign up here and join a community of people axial SpA on Facebook by joining either NASS Orange Apples, AS Buzzers or NASS PAWs.
We can’t wait for you to join us for Walk Your AS Off 2025!
By joining Walk Your AS Off (or WYASO, for short), you:
If you have any questions about Walk Your AS Off, please email fundraising@nass.co.uk or call 020 8741 1515 and press option 2.
“I went on a search for support groups and came across NASS. I had so many unanswered questions, so I was so relieved to find a hub that could give me answers and assistance.”
Read Michelle's storyGet inspired by reading more stories of others affected by axial SpA who have chosen to fundraise to support people with axial SpA.
Read more storiesFind out why your support really does matter, the impact your support can have, and why your support has never been more urgent.
Find out more1 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 26.
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.