
Georgie's story
“Geoff and Jamie have axial SpA themselves, so they are able to understand what it’s like for you.”
Read Georgie's story
In September 2025, NASS and Yoga for AS introduced Strength-tember – a way for people living with axial SpA to exercise safely whilst raising awareness and vital funds for all those who are affected by the condition.
Every September for the past few years, we have joined forces and run Stretch-tember, reaching hundreds of people across the globe and encouraging them to stretch, move more for their axial SpA and fundraise. This year, we shifted the focus onto building strength, not only to feel stronger physically, but to demonstrate the inner-strength of each person living with the condition.
Watch the video below to find out more about Strength-tember, how you can take part next year, what you will be receiving if you take part, and how you can help us raise funds to reduce the time to diagnosis and provide support to everyone affected by axial SpA:
Everyone who fundraised, supported and shared the page helped us raised £4,300 including gift aid. We are truly grateful to everyone who took part and cannot wait for next year!
Georgina has been taking classes with Yoga for AS for the past 4 years to help manage her symptoms. Here is she took part in Strength-tember this year:
Affected by axial SpA, it took years for Victoria to find a way to exercise in a comfortable and safe way for her condition. Many can relate to Victoria’s journey.
If you have any questions about signing up to Yoga for AS, please email Jamie at admin@yogaforas.com.

“Geoff and Jamie have axial SpA themselves, so they are able to understand what it’s like for you.”
Read Georgie's story
“I started yoga in lockdown and now practice it as much as I can. I find that yoga is everything I need to help manage my condition. Stretching, a little cardio, strength and very importantly, balance.”
Read Nicola's story
“When I saw the Stretch-tember programme I thought that this would be a great opportunity for me to try a new gentle activity – something that I can add to my AS management tool kit!”
Read Clare's story1 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.