PMR Flare with New Issues
I have had PMR for 5 years and GCA for 3
Years.GCA seems under control or gone now PMR flared when I hit 3 /4 mgs alternating.
Additional symptoms with Flare are burning in upper arms and itching like my nerve endings are on fire. My rheumatoid doesn’t see the connection to PMR.
Very very irritating
Anyone else experience this ?
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After a rheumatologist visit last week, I went from 15 mg daily to 12.5 one day and 15 the next. Unfortunately, my PMR has been flaring more and more each day, lots of body aches from shoulders to knees. Ran a fever all day yesterday, down a bit today. I'm going to stick with the new regime until my body gets used to less Prednisone. No burning, sounds like some type of neuropathy which you should consult with your rheumatolgist regarding. Best of luck, I hope you get your condition under control.
Thanks so much for your informative reply.
I dont have a diagnosis but electrical zaps just after Rheumy upped me to 10 mg from 3
Last night I was miserable,I didnt sleep all night
I took more Benadryl than normal 3 pills and also extra strength Tylenol . My pain has decreased by 90 per cent today. Go figure
Maybe worth a question to your doc - should we consider, etc.
Low-dose naltrexone fixed my neuropathy. You might want to check it out.
I have read in several sources that biceps tendonitis is often a symptom of PMR. When my PMR first started I would get shooting pains in the area of this tendon, on the front side of the upper arm below the shoulder. Burning would not be the first word I would choose to describe it, but many of the PMR pains I have around my shoulders have a burning quality to them. I just wanted to let you know that there is a "classic" PMR symptom that occurs in the upper arm.
Itching in sunlight, hot showers, exercising, and sex can be attributed to iron deficiency anemia.
It took 20 years as well as several endocrinologists later to finally check my iron levels even though I had high normal red blood cells.
After 2 iron infusions I am itch-free.
Thanks very much for your reply … food for thought for sure
PMR is hell on earth. The BEAST of a disease. The internet has a lot of information. Are you just curious, or think that you have it?
For sure I have it and had it for 5 years . For me it has been pretty easy until this flare because the has nerve endings in Arms were driving me crazy. Doc said not connected to PMR but don’t know where it comes from.
I have had issues with my bicep tendon throughout. Thanks for the confirmation that it is a part of this ongoing process.