Diagnosed with RA at 23
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I was diagnosed with RA a couple months ago I've been having the hardest time dealing with it . Idk if my rheumy just sucks or what right now I'm taking 6 methotrexate pills once a week vitamin & Celebrex 200 mg I think the Celebrex stop working because I've been stuck in bed for the past 3 days . I get up and move around a little but it hurts so bad especially my hands & shoulders.
0 likes, 8 replies
RAyogi angel30729
Posted
I'm also 23 with RA. I understand where you are coming from. I'm having a hard time trying to figure out what my new "normal" is going to be, so I think that might be a good question for your rheumatologist. If your medications don't seem to be doing enough, I would call the doctor. I know it can sometimes feel like we are always talking to doctors or always feeling bad, but you'd hate to not call, and the doctor has an easy solution for you.
Hope this helps!
Buckeyes angel30729
Posted
Good luck and keep us posted!
Rowbirdie angel30729
Posted
i hope you can contact your rheumy to say how bad things are as it s all a bit trial and error for each individual in the first 6 months or so to see what works.
For example they could try a higher dose of mxt as a very normal next step or offer a corticosteroid shot for short term relief while waiting to see if the mxt is working. It can take 3 months to see if mxt works but if it doesn't sufficiently they should reconsider how they are managing as it s so important to hold back progression of the disease in the early stages.
in the meantime the waiting to see what works is tough, but there will be light at the end of the tunnel. I guess you are trying hands in hot water and shoulders in hot shower? - also do gentle open and closing of fingers and arm movements as you are able .( one I was told to do by physio when shoulders were so bad is to lean forward and just let arm swing a little )
Don't know if any of that will help but wishing you all the best as you find your way through this.
lyn1951 angel30729
Posted
I was up to 35mg once a week, and the tablets were making no inroads at all on my inflamtion levels, rheumo arranged a blood test the day after my tablets if I remeber correctly, I do remeber her saying you are not taking up the medication, there is very little in your bloodstream, and you are going to now start injecting yourself, we will teach you.
Local GP was wonderful and walked me through the whole process a couple of times in his office, and then has left me too it, commented a couple of times since that you are very needle skilled, and can give me an injection anytime you want, I do not bruise now, have also been told by a nurse, better than most.
shirlee86000 angel30729
Posted
I do seem to be in remission or since I had half my thyroid removed 7 weeks ago funny enough as it had nodules on it, my doc seemed to think it could be that pressing on a nerve, I was really hoping but no I have had a couple of small things nothing like before on my hands but I took it that it must be something else, so yes very recently diagnosed.
I just hope I get no harrendous side effects off this methotrexate as I have read so much about it and some people are absolutely fine on it and others had to come off it as were ill, it's a waiting game so we will see
Light angel30729
Posted
I haven't read the others here, but I've just this to say...
It's hellish painful, but you will get it under control, and life will get more or less back to normal. It just takes time and patience.
One piece of advice: Try not to stay in bed when you're in pain.... your joints will benefit from movement even though it's painful. The day will always start bad but get better as you walk your way through it.
So without actually straining yourself so you damage your joints, use them to the border of what you can bear and you'll find your evenings are good to you...
meg83590 angel30729
Posted
ann19155 angel30729
Posted