These are the x-rays of my joints from September 2024. The first time that the consultant has ever shared them. I have psoriatic arthritis. You can see the little nibbles out of the joints and the degeneration and the out of line bones! No wonder I'm in so much pain.
I still have some swelling and pain in my foot 8 weeks after my hip replacement - should I be concerned ?
I've got OA in various joints, including my feet which can be particularly painful at times. I'm looking for indoor shoes/slippers, but the ones I have tried all have very flat soles and really hurt my feet and legs. To add to the problem I have very small feet and only take a size 2.5 or 3 at a push (depending on the…
Morning lovely people. I am now 3.5 weeks post op and I have been blessed with a fast recovery. I am walking without any aids and have been pain free for half of that time. I am very grateful for this but……. there is always a but! I have gained 4cms/1.5” in height and I am looking for advice on what to do for the best for…
in a flare and off work and just feeling really down about everything. Usually very good at putting my positive pants on but struggling right now. What do people do to pull themselves out of a slump?
Does anyone take Methotrexate 20mg together with Leflunomide 10mg and tell me if it has any side effects and how you feel???
HI i have just been diagnosed with OA and been prescribed parcetamol with ibruphen gel for my left knee. I know its early days but I'm struggling to get around. I cant take ibruphen tablets because I have a heart problem. Can anyone suggest any other medication please
Hi everyone I've been here a while now, reading all of your lovely THR diaries and so very grateful you've all taken the time, they've helped me a lot. I'm at step 2 of my THR journey having just had my pre op appointment last week and I've still got so many questions, I'm hoping you'd be good enough to help. As an…
Hi Community - I have been on Imraldi for 2.5 years now (PSA) and it’s changed my life. Today I received a letter from the NHS stating they are moving everyone to a BioSimilar (Yuflyma) - assuming due to cost. I am going to contact my consultant but wondered if anyone has any experience of changing from one to another? I’m…
Hi, I'd like to hear other people's experience - I don't have a feeling about whether I'm doing ok or not and not seeing anyone 'till the end of the month. I'm doing all the exercises ok. I'm walking without crutches in the house, one crutch outside. Pain is manageable. I do feel I lack stamina. Just made some hummus and…
It looks like you're new here. Sign in or register to get started.
