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DiscussionPMR in cold or inclement weather
Polymyalgia Rheumatica (PMR) | Last Active: Dec 4 7:30am | Replies (32)Comment receiving replies
Replies to "I am on West Coast of Canada - wet and cold most all winter with very..."
So glad I found your post! I had started using a near-infrared light system years ago before being diagnosed when I just couldn't figure out what was happening to me. I was so stressed out that I couldn't see it made a difference so stopped. After 7 years on the PMR roller coaster I developed GCA and started from scratch on high dose pred. As I started my weaning I decided to revisit the red light therapy before any pain has started to kick in to see if it would help. I try to use it twice a day.
Thank you!
I too am going on 7 years of the PMR journey.
The weather changes really affect me, and even on Medrol, and injectable methotrexate, I still have flare ups.
It’s been a long journey of ups and downs for me.
Right now I’m feeling tired of it, and wish there were better options to help all of us.
Kathy