Tipping Points for PsA Diagnosis?

The NHS is stretched, for sure. But there is also a worldwide shortage of rheumatologists which makes things even worse.

The London waiting times are pretty much the same elsewhere I think. Meanwhile, it often helps to shell out for at least one private appointment if at all possible. And then clamber, push, nag, cajole and argue for the promptest service and treatment possible.

Yup! For years I had a diagnosis of undifferentiated spondyloarthropy. Which basically means you have something but you don’t have severe enough symptoms for any other diagnosis. See also sero negative rheumatoid arthritis. Then I developed a sausage finger and my toenails started to separate and voila…PsA! It only took about 12 years. :blush:

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