Caroline's story
“Walk your AS Off is a great initiative, as I can tailor my steps to whatever I’m able to manage each day whilst still fulfilling the brief of keeping active and I’ll be fundraising at the same time!”
Read Caroline's storyWalk Your AS Off (WYASO) is an annual virtual step challenge every May. It's all about getting active for health, raising awareness about axial SpA and raising vital funds for NASS.
It’s organised by Walk AS One, an all-volunteer organisation that mobilises and motivates a global community to raise awareness and address the challenges of those affected by axial spondyloarthritis and its family of related diseases.
NASS supports this event, alongside other organisations worldwide, to help raise awareness of axial SpA and raise funds to support our vital work.
33 amazing fundraisers joined #TeamOrangeApples, #TeamNASSPAWs and #TeamASBuzzers, led by Gillian Eames, NASS Trustee, and Kathy Miller, lifetime NASS supporter steppers, and raised over £8,500 for NASS, took thousands of steps and raised awareness of axial SpA by sharing their stories, walks and journeys. Thank you.
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Read the stories of some of those who took part in Walk Your AS Off 2023
“Walk your AS Off is a great initiative, as I can tailor my steps to whatever I’m able to manage each day whilst still fulfilling the brief of keeping active and I’ll be fundraising at the same time!”
Read Caroline's story“When I saw Walk Your AS Off, I immediately signed up.”
Read Victoria's story“This is my first year helping to raise funds for NASS and I am delighted with the support of my friends and family during such a difficult time. I’m so lucky to be so supported.”
Read Kevin's story“If you are like me and have never been ‘into’ exercise and you struggle with pain, can I encourage you to just take one step at a time, even if that means just hobbling down the road, keep going, it will help in the end.”
Read Abi's story“I have decided to take part in Walk Your AS Off to raise awareness but also to make sure I’m active every day and walking more.”
Read Carol's story“I feel I’ve been given a new lease on life and am physically able!”
Read Amy's story“Walk Your AS Off has given me a target and encouraged me to keep positive.”
Read Fiona's storyYour 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 Walk Your AS Off, please email fundraising@nass.co.uk or call 020 8741 1515 and press option 2.
1 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.