The more info I get the more I believe I’ve had ra for many years: just no one diagnosed it until I got referred to a rheumatologist.
I’ve had surgeries, pain clinic, spine clinic, Psych’s, disbelief and uncertainty.
The ra and the fibromyalgia are front and center now.
It’s so nice to find some support.
Welcome I have only been diagnosed about 5 months went to physio exercising then fingers started changing shape swollen now I have been on methotrexate for 12 weeks lot better than I was put me on steroids as well this week just got to find what’s right for you keep your sprits up it dos help talking as we’re all in the same boat tc 😎☀️
Welcome to the RA family where we bounce off each other and perk each other up when feeling down 👍
welcome
I'm sorry you're part of our group...RA is horrible. But welcome, you've found a great place where others can understand you.
Hopefully things will improve for you now.
It's lovely on here, welcome
I feel i’ve caught MRSA at my Infusion Clinic. Anyone else had this?
Bananas- and I don’t just mean RA
How do you get moving?
Not sure if I have RA
How do I get a COVID jab sooner rather than later
