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chronic myofascial pain syndrome
For the ones I saw here today with condition, I just had painful Lidocaine injections into the trigger points for relief. I take pain med daily, now the injections which are temporary but hopefully some relief. Try not to get down, it seems to make it worse for me.
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Hey, thanks jsssmith. Yes, the CMP gets me the most...more than the fibro...although there have been times when they only thing that got me through an FM flare was percodan.
No one every suggested the injections to me. I'll have to talk about that with my massage therapist and see what she thinks. I hope it helps you. |
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