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| Dannie - Aug 6th, 2006 9:06 AM | |
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I have that too! It's awful. I was diagnosed with MP 4-5 years ago. If it helps to hear it & did lessen up for me over time. I aslo get Tp injections. the doc gives me morphine, says it's the scariest place to get the pain....YUP! no one really understands who doesn't have it. tennis balls or massage really helps sometimes & heating the area w/ moist heat too. my masuese found Tp's in my pectorals the size of silver dollars... stress hey? it's CRAZY. | |
| Tim - Aug 10th, 2006 9:54 AM | |
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I was diagnosed feb2005 with cmps, and am now off of work because I developed chronic asthmatic reactions to the dust there. I was a supervisor for 10 years and my entire lifes work is in the wood products industy, now my life is on hold my Dr. doesnot believe that there is a connection to the cmps and the allergies. I dissagree .I have carefully followed the reactions with written diary and am desperatley seeking some type of relief have found a specific type of treatment that I intend to pursue.. Look for Dr. Gunn on the net and read about his treatment for cmps. Looks promising to me. Luck to you all. | |
| R.S.Hagen - Sep 6th, 2006 12:42 AM | |
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I have thought for a couple of year that I have CMP, I have only known it as Myofacial Pain Syndrome, what tests did you have, and did you see a rhumetologist?, My Dr is not doing too much at this point we are just treating my Flare ups, I have been diagnosed with fibro... but I have way more problems and pain for just that, I was also resently in a secon auto accident, Don't have chest pain so much as heart palpitations and shortness of breath, | |
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