When I met my GP, they said I don’t think you have AS because you’re too old and you’re a woman.
At NASS, we always hear about difficult diagnosis stories
Join our community of over 4000 supportive Members so you can live well with your axial SpA.
Before they joined NASS only 13% of our Members knew where to get the support and advice they needed.
Like many of our Members, Fiona had a turbulent journey to diagnosis but with NASS Membership, she now has support of 4000 people who understand what it’s like to live with axial SpA.
As the UK’s largest organisation devoted to transforming the diagnosis and care of people with axial SpA, we know how difficult life can be with this condition. With NASS Membership you have access to our expert advice and information, as well as to our incredible community of like-minded people.
Join now to get a range of benefits and connect with thousands of people living with axial SpA. You will get access to our thriving members forum to support others and chat about the issues that matter to you, as well as an invitation to our annual Membership Day, where you can meet other people and get the latest advice on living well with the condition.
Your membership fee also helps to fund our vital helpline service, up-to-date resources including videos and guides, and supports our 94 local branches around the UK.
Join today. Axial SpA works silently. We don’t.