Treating PMR with Prednisone and Hydroxychloroquine
My doctor just added Hydroxychloroquine to my PMR treatment. He said it helps Prednisone do it's job. Seems like there are more side effects associated with it then there are with the Prednisone. Does anyone know if the Hydroxychloroquine helps. Also heard Hydroxychloroquine can take up to three months to build up enough in your system to be therapeutic.
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yes..... working from 5mg again to 4 mg.... seems to going well.... First time in 3 years with no pain!!
I have taken both from the beginning of my diagnoses (sept 2023) and my doctor told me that when I finally come off prednisone that hydrochloriquinne would be the drug I will stay on. I feel that it had done a very good job and I didn’t have any side effects from the hydro. For me diet is critical, there is certain foods that when you stay away from them there are no flare ups. When I cheat a little my hands will ache and I get slight pain in both shoulders. My last blood test, which my doctor had done every 3 months, my CRP and SED RATE have been very good, and I contribute that to both the two meds and watching my diet.
PMR seems like it is very hard to diagnose. I'm not sure where you are located, but have you tried getting an appointment with a well known hospital, like Mayo Clinic, University of Pennsylvania Hospital (UPenn - Perelman Center), etc.? I just had my appointment at UPenn. It did take 6 1/2 months to get one at the time, however, it seems other people have gotten an appointment within 2 weeks. The doctor I had was wonderful, and very open minded. He is exploring every possibility with my symptoms and sending me to different departments within the hospital, further extensive testing, recommended aqua therapy, etc. He was probably one of the best doctors I have been to and also has access to explore various options.
Unfortunately I cannot take prednisone due to blood sure issues my rheumatologist didn’t suggest hydroqluriquine she is either stubborn or clueless
I was dx with PMR at the University of Michigan about 30 years ago. I have seen 4 rheumatologists since that time. 3 at UM and one in Palm Springs, CA. The third one I saw in Palm Springs, CA, did a very complete physical and lab exam and in the end he said he didn't think I have PMR, but didn't know what I did have. The last rheumatologist at UM doesn't think I have PMR. He thinks it is some form of spondylitis or spondylosis. I doubt if this clarifies anything. Yes, PMR is difficult to dx and treat.
@johnbishop and all...John, have you ever taken Hydroxychloroquine with Prednisone for the PMR? Taken Hydroxychloroquine for anything? I wanted to take it for Covid but my primary doctor wasn't willing to give it to me due to his hospital's attitude re using it for Covid and the politics involved. I wanted to take it 3 years ago!
How is it supposed to help with PMR? Is it like using it for Lupus? Autoimmune disease...I see my Mayo rheumatologist on Tuesday and will discuss this with him. I don't want to stay on Prednisone any longer than necessary but so far haven't been able to reduce it without increasing my PMR symptoms. Add to that I'm dealing with my 2nd Covid infection in 6 months and I'm ready to get this thing started if it'll help...and I do believe it will!!! I think it would have helped with Covid !!!! I'm going to ask a lot of questions and I'll let you know what he says...
Feel well my friend and be blessed...Elizabeth
Hi Elizabeth, I don’t have any experience with it but I did post a reference earlier in the discussion that you may want to share with your doctor to see if they might consider it for your treatment - https://connect.mayoclinic.org/comment/738585/
I started 3 1/2 yrs ago on prednisone…after several years of no success reducing pain and getting off it Sulfasalazine and hydroxychloroquine were added …after 18 months of no consistent improvement..Actemra has been added …I think now thing are actually getting better …I’ve only been on the Actemra for a month and I’m able to sleep much better as I have less pain in joints and can almost walk normally …also feel much less like I have flu all the time …hope to drop prednisone very soon as down to 1 mg daily now…
I forgot to add in the above that Methotrexate tablets were added with sulfasalazine and Hydroxychloroquine…after 6 months …the Methotrexate was changed to injections weekly…and now the Actemra injections every two weeks …
I convinced my rheumatologist to prescribe HQC to go with my Pred after reading it could help. This was during Covid. I don’t think it helped with my PMR but am convinced it did help protecting against Covid. Just my two cents.