"NASS is a beam of knowledge and connection with other people" - Jamie’s story

Your donation today to the NASS Winter Appeal can help give someone like Jamie the chance to say, "What can I do?" instead of "My life's over."
Click the link to make your donation today: nass-winter-ap...
More people than ever are feeling isolated living with axial SpA. Last year, the NASS Helpline alone supported 5,000 people. This year, we expect to help an extra 500 people. Nearly a fifth of people like Jamie receive no support at all when they're diagnosed. Your donation can help ensure no one like Jamie has to face living alone with axial SpA this winter. Thank you.
With thanks to Tom Aldous for recording the film.
Did any of Jamie’s experiences resonate with you? Let us know in the comments 👇
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We are the National Axial Spondyloarthritis Society (NASS) and we are here to transform the diagnosis and care of people living with axial SpA. Axial SpA works silently. We don’t.
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