▲ 7 r/hipdysplasia
What do people with hip dysplasia in the UK actually do with that info?!
I would love to know what people do. I can’t really think how to word this better, but for me I’ve known I have hip dysplasia for at least 20 years, now age 43. Having said that I’ve never really done anything about it, and just kind of lived with having sore hips, and being that stiff (yet also hypermobile) person who moans on the girls trip, night out etc.
Is it just that my case is mild? Although I think it is starting to now worsen… Do people have treatment plans, referrals from their gps? Have I just been accepting pain when they are options I should be considering? I feel like it’s always been delivered as “just the way I am” so live with it…!
u/No-Government1627 — 7 days ago