Myofacial Pain Syndrome

Posted , 8 users are following.

I think EllenH stated she also had myofacial pain syndrome.  My question is anyone else have this and did your doc diagnose this?  What do you do to help it?  Is it also an autoimmune disease?  If so, shouldn't pred help?  These are things I am going to talk to my doc about.  BUT get the best information here so thought I would ask you all first. Thanks.

 

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    Yes, I have just posted a heartfelt Thank you to Eileen, who also suggested that my severe back problems were due to MPS and suggested Bowen Therapy. Not even my Physio got it!

    Bowen Therapy has turned me arround and I am now feeling much better.

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