Chronic Myofascial Pain Myofascial Pain Syndrome Community Group
This group is for people who have Myofascial Pain Syndrome- anyone with a diagnosis of MPS is welcome to join. Our mandate is to provide support, information, and friendship to people with MPS.
I went to a Physiatrist (Physical Medicine specialist) last fall, and asked about TP injections, and she said NO WAY (she said I have too many TP's for it to work). Anyways, I just saw an Anesthiologist (Pain specialist) at a Pain Clinic last month, and he tried the TP injections and they worked great! I am hoping to have them done regularly to help me manage my pain.
One thing I've learnt is that NO ONE knows my body or how it will react to specific things, how if feels etc like I do. I am ultimately the person who has to live in my body full of chronic pain, and while Dr's may be experts in their field/ specialties, I am the expert on MY body.
However, I've also learnt that you can catch more flies with honey than vinegar... so I've had to learn how to advocate for myself and my needs in a way that is kind, sweet, and respectful (yet at the same us firm and resolute and stands up for myself).
JC