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“While I waited for answers, I was in so much pain. For weeks at a time, I could get no relief at all. I felt claustrophobic in my own body.”
“For years, I was told that my chronic pain was all in my head. I was so frightened.”
What NASS has done for me over the years has been immeasurable, so it’s lovely to be able to give something back!
“I’m ‘Stepping Forward for AS’ in memory of my father, who lived with axial SpA for 55 years, and who touched the lives of so many people living with the condition”
“When I’m swimming, it’s the only time I feel truly pain free”
“My goal is to continue doing a job that I love for as long as possible.”
“By the time I was diagnosed with axial SpA, permanent damage to my spine had occurred. I’m now walking to make a difference to others”
NASS launches campaign to achieve Gold Standard Time to Diagnosis for Axial SpA