Turns out I do not have RA. I have hypermotility which can give symptoms of arthritis but there are absolutely no signs of any form of arthritis in my joints. I will be going to a pain clinic for treatment for several different things involving the hypermotility
Just got out of doctors. : Turns out I do not have RA... - NRAS
Just got out of doctors.


Yay!! I think...
Yay!! At last you have an answer. It's been a long painful road for you & hopefully from now on, you'll be able to get whatever help is needed.
Keep us informed though. I'm sure many of us would love to know how your getting on.
Ruth x
That's better news! Except with it being your joints it will be a diagnosis of hypermobility you've received, hypermotility is something different. It could explain your IBS type symptoms though. Very pleased it wasn't RD at your young age.
Well, upwards & onwards now, I hope you're able to start exercises soon & strengthen your muscles to help ease things. I wonder if the folks over at the HU Ehlers-Danlos Syndrome site would be able to help at all, or maybe point you in the direction of another forum who could? healthunlocked.com/edsuk
All the very best & Happy Christmas. x
Good news
Happy to hear you finally have a diagnosis, being stuck in limbo is the pits! Keep us informed, and be safe!
Merry Christmas!
That's great to have a diagnosis. FIrst step in working out how to live with it as easily as possible. Still painful tho' but at least you have a name for it and your parents should understand better and help you more.
Wondering if the two go hand in hand or if it means you will develop RA further down the line? I say this because my mother and I have RA and my youngest daughter and 9 yeAr old granddaughter have hypermobility although they don't seem in pain with it , need special insoles for their shoes etc but not much else....
They said some people can go their whole lives without ever feeling pain but I️ don’t think it can cause RA. If it is in her dna she might have it later on in her life but until then if she has pain I’d tell the doctor about her hypermotility. I’ll be having to get insoles too to arch my feet better and then see a physical therapist, a Psychologist, a social worker, all in one day to get a treatment plan.
It can be associated with OA (osteoarthritis) though. This from Arthritis Research UK may be useful reading, tap on the Read more for more info on each section arthritisresearchuk.org/art...
Great to get diagnosis so you know what you are dealing. Take care and Happy Christmas. X
Great news and the first step towards effective treatment. Wishing you all the very best for a happy Christmas and healthy new year. Hugs
J
Hi Ccrowlu - I don't know much about hypermobility, but I'm glad it is not RA. Best of luck with the pain clinic
That's great. It's still not great that you have an issue causing you pain and will need to work to reduce that, but it must be a relief to know it isn't arthritic.
Congratulations an Merry Christmas! Good luck with the pain clinic.
I have a friend who has hypermotility, turns out she was diagnosed with Ehlers Danlos Syndrome.activebeat.co/your-health/w...
Hypermobility can cause pain and symptoms very similar to arthritis, so you may still have to follow the same advice around joint protection, pacing etc that you will have read up on when you first thought it was RA. This link may be helpful.
I was diagnosed with Hypermobility at 16 and now I've been told I have RA, 10 years later!
Hope this diagnosis is helpful to you and you start feeling better soon.
Hello - I just looked up hypermobile and EDS here and found your post. How are you getting on I wonder? My niece was diagnosed with hypermobility at 15 and is 18 now. She seems fine but I think it was pain that took her to the doctor at first.
I’m looking into it for myself at 55! I think my family may have a rare type that has caused connective tissue problems with stretchy skin and organ slippage, constipation/ IBS.
I have had odd symptoms all my life - was diagnosed as hypothyroid and then RA and now Sjögren’s. They think I’ve had Sjögren’s since I was a child - I am definitely a lifelong autoimmuner whichever came first! I think an earlier diagnosis for my double jointed hands, elbows and knees, thin stretchy skin, overcrowded teeth, IBS and allergies etc would have helped me a lot. So I hope it’s helping you🙂

I am getting along just fine now. My doctor prescribed me a new medication and I haven’t felt any pain since I started taking it a couple days ago! Usually you go to a rheumatologist to Get diagnosed but I’m sure your primary doctor could test you for it if you ask her too. She’ll test the flexibility of your joints. For example she’ll gently push your thumb back into your wrist and your fingers as well. Good luck and I wish you good fortune and happiness. Please do keep me updated on your results.
Oh this is great news to learn that your diagnosis has brought you help and relief from pain - I’m so pleased!
My rheumatologist phoned me yesterday to discuss my new symptoms and change my meds. I couldn’t bring myself to ask her about it though as encountering new more scary health problems (asthma and possible pulmonary hypertension) so we had to focus on these.
But one of my otherwise pristine fingers (with only very mild ageing wear and tear) keeps dislocating and is very sore and unstable and this has baffled me as I’ve asked here and on arthritis community and they all just say my hands look in an excellent state!
I attend pilates class and the instructor is physio trained / identified that I have a rheumatic disease from my description of poor balance and then assumed I also knew I was hypermobile. I’d never realised that my knees and elbows fit the criteria at all despite often being told by fitness people that I’m “over flexible”! I looked it up for my niece ages ago but she’s tall and thin so she fitted the profile whereas I’m short and plump! X

Any size and shape can have it. And my guess would be that you are indeed hyper mobile due to your hypertension and you should definitely bring it up to your rheumatologist when you go.