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10,154 total results
Comments (9,593)
My husband was diagnosed with PMR in May 2023 and Giant Cell Arteritis (GCA) in February...
https://connect.mayoclinic.org/comment/1043812/
My husband was diagnosed with PMR in
Hello all, Several folks asked me to report on my Kevzara experience when I could, so...
https://connect.mayoclinic.org/comment/1044434/
PMR began for me overnight in November
I would like to know what the latest science says. If the recommendations only say to...
https://connect.mayoclinic.org/comment/1117976/
I didn't think it was a PMR problem ... things happened but I didn't have a PMR
My pleasure. Live to share and help others. Hep B is transmitted by another infected person,...
https://connect.mayoclinic.org/comment/1122152/
PMR & Rheumatoid Arthritis are pretty ... If the PMR is not treated it could lead
I'm a 52 year old male, and just got diagnosed with PMR about 10 days ago,...
https://connect.mayoclinic.org/comment/862798/
male, and just got diagnosed with PMR ... I had never heard of PMR before then
Hi@suemck, I was diagnosed in July 2018 and have been trying to taper down for the...
https://connect.mayoclinic.org/comment/138092/
as there is so little known about PMR
I am new to the group also. So happy to have this forum! In early July,...
https://connect.mayoclinic.org/comment/211451/
He said I have PMR.
I had multiple triggers, extreme stress in the years leading up to dx due to helping...
https://connect.mayoclinic.org/comment/871588/
When I did, that is when the pmr hit
Hi, So sorry to hear about your early onset of these autoimmune diseases. I know, life...
https://connect.mayoclinic.org/comment/925274/
One week ago I was diagnosed with PMR
Hello, I live in the UK and have pmr. You may find these tapers a little...
https://connect.mayoclinic.org/comment/1062007/
Hello, I live in the UK and have pmr
"None of these drugs work on helping to restart your cortisol." I mostly agree with this....
https://connect.mayoclinic.org/comment/1116415/
PMR was thought to be my primary problem ... have worked for uveitis except my PMR
Ihave Churg Strauss disease aka, Polyarteritis nodosa Eosinophilic granulomatosis w/polyangitis I never linked the PMR with...
https://connect.mayoclinic.org/comment/806662/
/polyangitis
I never linked the PMR
Hello Barbararene’ (@barbararene), I'm sorry you are in pain and feeling a little down. I'm having...
https://connect.mayoclinic.org/comment/155474/
prednisone for my polymyalgia rheumatica (PMR
Hello @kgoodwin9, thank you for sharing your story. For a lot of us prednisone is the...
https://connect.mayoclinic.org/comment/56477/
occurrence of polymyalgia rheumatica (PMR
I have found that tapering even 5 mg at a time is too fast and I...
https://connect.mayoclinic.org/comment/144985/
enough experience and I think this PMR
Hi. I'll defer to the support leaders and others for verification/opinions, but my sense is that...
https://connect.mayoclinic.org/comment/668562/
are well aware that about 20% of all PMR
I find your post interesting. I am 63 and have been having symptoms that seem to...
https://connect.mayoclinic.org/comment/102136/
others who have been diagnosed with pmr
So sorry to hear about your struggles and they long road to a diagnosis. My PMR...
https://connect.mayoclinic.org/comment/930999/
My PMR was triggered by my 4th covid
I'm not aware of real-time medical information or specific details about current appointment availability at The...
https://connect.mayoclinic.org/comment/979217/
primary specialist for conditions like PMR
@johnbishop, and all...John, I had bloodwork and tests Monday, and very high urine protein, other kidney...
https://connect.mayoclinic.org/comment/1002840/
#39;m taking 10mg Prednisone now for PMR
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