← Return to PMR with hand/wrist pain and swollen veins?

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@ropnrose

I began taking Prednisone in July 2024 for PMR/GCA. 60 mg. for 6 weeks. My voice was affected. I don't know if it was the Prednisone or the disease. Once, I tapered down to lower dosages, the voice issue went away. During those 6 weeks, I also had chest pain and a dry cough. Those eventually went away, too. I really think it was the Prednisone. It's the drug that keeps giving (although you don't want what it gives you). At 60 mg. I had no body ache (other than an occasional headache). I'm down to 6 mg. now (thanks to monthly Actemra infusions). I had wrist, shoulder and knee aches prior to Actemra. The aches would usually subside by mid day. They weren't dibilitating. I still have very mild wrist aches, but it's barely noticeable

Good luck with your journey.

What doseage of Prednisone are you taking?

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Replies to "I began taking Prednisone in July 2024 for PMR/GCA. 60 mg. for 6 weeks. My voice..."

Thank you for your reply, much appreciated. They only started me on 15mg in October by January everyone noticed the change in my vocal cords. I thdn had to reduce down by 1mg per month. I am down to 8 mg at the moment which does not seem to be working have got terrible lower back pain affecting my walking . Last month I had phlebitis of the legs , treated in hospital followed by picking up the norovirus . So it has been a tough few weeks with more added drugs like blood thinners etc. I am coeliac , have osteoporosis and under active thyroid but until this was very fit , I do not drive but I walked everwhere and am only a small lady, but this has taken its toll on my body and also on my moods which are all over the place, which do not seem to settle in the same place. For having something I had never even heard off I am well aware now of not taking the life we have for granted .. a lesson learned there any way .