Pmr, Costochondritis
Posted , 5 users are following.
Are PMR and Costochondritis related?
0 likes, 10 replies
Posted , 5 users are following.
Are PMR and Costochondritis related?
0 likes, 10 replies
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EileenH kathy67492
Posted
In PMR tendons and ligaments can be inflamed but I don't know if it can cause inflammation in cartilage which is what happens in costochondritis.
bob73443 kathy67492
Posted
I am one of the people who have rather severe costochondritis along with my PMR. I see stars when I sneeze. I think a lot of my shortness of breath comes from the discomfort involved in my rib cage.
Eileen mentioned myofascia pain sydrome, which I think I have. When I lie down on a hard floor, I have a lof of pain just to the right of my spine, just under shoulder-blade level. I sense that this pain somehow is causing, or contributing to the costochondritis.
I'm not sure what happened first -- the PMR or the costochondritis. They are definitely different (affect different parts of the body), but for me they happened right around the same time.
EileenH bob73443
Posted
https://patient.info/doctor/Relapsing-Polychondritis.htm
Now this is a very rare illness that is widespread in the body so I doubt any of us have it - but obviously cartilage damge can also be autoimmune and I wonder if there is a bit in PMR...
bob73443 EileenH
Posted
Thanks for this. In revewing it, I don't have enough of the symptoms (especially the ear pain which they say is always present), but thanks for this anyway.
My more general question is "how in the world did you find this?"
EileenH bob73443
Posted
Google is a brilliant instrument for finding medical stuff - though you do need the right search words and I've come to the conclusion it is quite clever since whenever I am looking it is "proper" medical references that come up for me! Other people keep saying "I can't find..." and it takes me only a few minutes to find what they need
pat73046 bob73443
Posted
pat73046 EileenH
Posted
EileenH pat73046
Posted
The back muscles are very forgiving and take a lot of abuse - and that includes having to balance out the strains of a scoliosis to keep you upright. I had a mild scoliosis identified when I was in my 20s - I'd had back pain for years - and a couple of years of treatment by a orthopaeic specialist who was also a chiropractor and massage for the very hard muscles including real knots of muscle fibres in a few places actually dealt with the scoliosis as well. It had mostly been due to posture because of the spasmed muscles making me adopt the most comfortable position.
I keep saying - in the early years of my PMR the back pain was awful and Bowen therapy was the only thing that kept me upright and mobile. It too works on such tight muscles and encourages them to go back to the position they should be. Being put on pred made it much less painful - but the really dodgy bits still pop their heads above the parapet every so often.
bob73443 EileenH
Posted
I've looked into this Bowen therapy that you keep talking about and the closest to where I live ia 4 hours. Gees. If they were closer, I'd try it.
bob73443 pat73046
Posted
Thanks for sharing this.
I'm glad your pain does not occur often. Mine is there all the time, worse in the AM and then deceasing throughout the day, just as the PMR symptoms.
Hey, I'm not complaining! I still do yardwork, walk 2 miles a day (rapidly), travel for business, etc. The prednisone has been a life-saver for me, even for the back pain.