Within a month of my diagnosis, my rheumatologist handed me a NASS brochure. I found the website full of easy-to-understand information, resources and NASS highlighted the fact that I was joining a membership community of over 3000 people. Being part of NASS almost gave me a sense that I had an inside scoop on anything that was new. I’ve had the chance to talk to some wonderful people who are living in exactly the same world as me.
Join us and never feel alone with the condition.
Take control of your axial SpA (AS) and make the most out of life.
Before they joined NASS, only 16% of our Members felt like they had someone to talk to about axial SpA, whilst only 13% knew where to get the support they needed.
As Paul tells us, we provide expert support to Members, but also help them connect with thousands of like-minded people who know what it’s like to live with the condition. Our Members are always at the forefront of all our work and have a direct impact on ensuring everyone with axial SpA can make the most out of life.
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.