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Discussions (294)
Comments (5,539)
Comment
Interesting to read about the tapering. I too have had a relapse at 8, and had...
https://connect.mayoclinic.org/comment/245736/
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Discussion:
PMR and the new Shingles vaccine
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Sep 25, 2020
Comment
Hi, your description of your experience with the vaccine s then the symptoms could have been...
https://connect.mayoclinic.org/comment/245735/
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Discussion:
PMR and the new Shingles vaccine
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Sep 25, 2020
Comment
No, I haven't done anything differently. I just hoped it wouldn't come back. I eat pretty...
https://connect.mayoclinic.org/comment/286670/
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Discussion:
Polymyalgia Rheumatica (PMR): Meet others & Share Your Story
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Aug 28, 2020
Comment
@desertsooner I can only have empathy because we have some similarities. I retired from nursing at...
https://connect.mayoclinic.org/comment/286663/
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Discussion:
Polymyalgia Rheumatica (PMR): Meet others & Share Your Story
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Aug 17, 2020
Comment
What biologic was tried?? The only biologic that I'm aware of and the only one that...
https://connect.mayoclinic.org/comment/319117/
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Discussion:
PMR coming back?
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Aug 13, 2020
Comment
I don't really know how long I will remain on Actemra. I have had a total...
https://connect.mayoclinic.org/comment/286648/
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Discussion:
Polymyalgia Rheumatica (PMR): Meet others & Share Your Story
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Aug 1, 2020
Comment
I know the feeling about tapering too quickly. I was accustomed to fast tapers before PMR...
https://connect.mayoclinic.org/comment/286645/
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Discussion:
Polymyalgia Rheumatica (PMR): Meet others & Share Your Story
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Aug 1, 2020
Comment
@calicojoy, from what I've read, some people report a change in taste while on prednisone. For...
https://connect.mayoclinic.org/comment/311285/
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Discussion:
Loss of smell and taste
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: May 17, 2020
Comment
Hi Charann, I have had GCA since 2016. I had no symptoms but it was discovered...
https://connect.mayoclinic.org/comment/197353/
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Discussion:
Medications for Temporal Arteritis/Giant Cell Arteritis (GCA)
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: May 10, 2020
Comment
I was diagnosed with GCA in January 2020 - my sed rate was 117 - and...
https://connect.mayoclinic.org/comment/303749/
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Discussion:
What's your experience with Actemra for GCA?
Support Group:
Polymyalgia Rheumatica (PMR)
Posted: Mar 30, 2020
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