Hi all, I posted for the 1st time last week, just in so much pain all time! And the s/f from the tablets are starting to bad, getting sick of it all, and to think I have to put up with this for the rest of my life, had a flareup in my hands Friday and have only just started using them now! My wife god love her keeps asking how I am, I got to the point where I just say yea I'm ok! I know she is only looking out for me, but unless you have RA you not going to under stand how it feel,
Ok rant over
Thanks x
Hi Marcus well this is exactly what the site is for for people to rant away when they need to LoL! I really feel for you, I felt exactly the same when I was first diagnosed withRA. I like you would tell my husband how I felt that at the end of the day eventually became like you and just said oh yes I'm fine. But I wasn't fine i was in pain, very very tired, and didn't know where to turn.
I eventually realised with a lot of discussion with my doctors and my specialist nurse that once the drugs got into my system I would start to feel a lot better. They also thought a STeroid injection would help me and they gave me this which within a couple of days make me feel so much better, the pain and swelling went down quite quickly.
If I were in your shoes I would telephone your rheumatology helpline and ask them for help with your Flare. Also I would make sure I had enough painkillers to help, I was told by my rheumatologist that Panadol as prescribed is one of the best painkillers, also I was giving non-Steroidal anti inflammatory drugs such as brufen. I also found that for me hot packs where very very calming on my hands but some people find cold much better to ease their pain.
I bet you are sick fed up of all this but when the drugs kick into your flares tend to become much less . There is light at the end of the tunnel, honestly.
I found their NRaShelpline very helpful and the listens to me when I felt that I didn't really want to talk to the family any more about my on this as I just thought at the time they were getting fed up of it. But they weren't, I found out later, they didn't want to ask me about it because I appeared to to them to be coming very defensive.
I hope you get some rest today and get some more information on the illness from the Nras website and I am thinking of you and any time you want to chat come and talk to us all here, lots of love A xx