News
In memory of Dr Andrew Keat
When I was first diagnosed, I couldn’t touch my toes. Today, I’m proud to say that I’m fitter and stronger than I was in my 20’s!
I want to make sure no one else with axial SpA has to go through what I did
Axial SpA, My Dad and I
“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”
