Myofascial pain syndrome
I am trying to cope with chronic pain and am not getting any compassion from my medical profession community. I was hoping to find some support online to share my story and not feel so alone.
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This isn't meant to be a commercial for this specific therapeutic approach - just a suggestion made with the thought that it may be helpful to some.
I have had "tight muscles" as long as I can remember. Soon after 9/11, a massage therapist / body worker volunteered to come do chair massages for those of us working at Red Cross since in the early days we were all under stress which we initially expected to continue indefinitely. She found so many tiny spots that hurt when she touched them that I thought I needed to find out more. I've been seeing her for regular massage sessions since then, and find that her work has helped me feel better. She has modified her approach based on lessons learned through her more than 30 years in practice, but her initial training was in the approach pioneered by Paul St John.
https://www.stjohn-clarkptc.com/paul-st-john-1
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2 ReactionsDry needling in addition to myofascial release has helped me a lot. The trick is finding really good practitioners. On the fourth try I got a great PT that does dry needling. The 3rd myofascial release Expert level was the trick for me. Unfortunately sometimes the best ones aren't covered by insurance but myofascial release practitioners train you to do a lot on your own. Just suggestions. Doesn't get rid of all the pain but 30-40% reduction for months at a time can help.
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1 ReactionThanks for sharing your experience.
I have visited a myofascial release practitioner for a series of treatments in the first half of 2022, and sadly, did not notice great relief.
Perhaps coincidentally, one of her treatments preceded by a very short interval a GI bleed.
In retrospect, this may have been the earliest signal that my pancreas was starting to malfunction. So was this a good result?
I'm not sure, although I do know that I never enjoy being hospitalized; this admission followed the development of hematochezia with a very high white count which the doctor who saw me in the emergency room felt could be a serious infection at risk of becoming septicemia.
How is everyone diagnosed with Myofascial pain syndrome. Right now I have been diagnosed with everything else from Bursitis, Facet joint arthrosis, Gluteal Tendinopathy, SI Joint dysfunction, Piriformis syndrome etc. I do feel like sometimes when I get the debilitating sharp pain around upper glutes that spreads all along lower back and buttocks that maybe I do have knots that I caused by repetitive motion when doing some yardwork, pulling weeds, vacuuming etc. It always seems to be when I am in a bent over position too long working on something and when I pull backwards from it, just causes severe spasms. I don't know. I have been to 3 different orthopedic doctors and they just give a new diagnosis and area. Nobody brings up myofascial syndrome. I do have inflammation throughout my body that I can't seem to stop which also contributes to many issues.