Bethany's story of the wait for an axial SpA diagnosis. (Act on axial SpA)

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Bethany lost her teenage years waiting for a diagnosis of axial SpA. Meet her as she talks to comedian Jess Fostekew about her experience (and their love of the Spice Girls). #ActOnAxialSpA.

1 in 200 people live with axial SpA.

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.

FOLLOW US ↓

JOIN OUR COMMUNITY ↓

USEFUL RESOURCES ↓

#ActOnAxialSpA #ankylosingspondylitis
Campaign funded by UCB
  1. National Axial Spondyloarthritis Society
  2. axialspa
  3. axialspondyloarthritis
  4. back pain
  5. back ache
  6. spice girls
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Комментарии
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Thanks for sharing you story Bethany, can I ask how the final diagnoses was actually made? What were the deciding factors?

happydays
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Literally what my family said when I the doctors diagnosed me with arthritis, “you’re too young for arthritis, everyone gets it anyway and the doctors just want your money”

bluaurora
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Spondylithis ankilozant affect spine with inflamation and fusion....this is not the case....

danplugaru