Guest guest Posted April 29, 2010 Report Share Posted April 29, 2010 That's always so frustrating when something you have hopes for doesn't work well.I hope they support you through this. Carolyn Eddy " Sweet Goat Mama " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2010 Report Share Posted May 1, 2010 Jade the details are different and i don't have ACM but the same problems constantly occur with me. You try something to fix one thing and the side effects are worse than the original disease. That is why I have been so leery about changing any of my medications. I take amytriptiline for pain from Fibromyalgia, TMJ, Vulvodynia, and as a migraine preventive. I have been told maybe i should switch to Lyrica or Cymbalta but they aren't drugs used for the other purposes I take the Amytriptiline for. Besides the druggist refused to even fill a prescription for me when I had one for Cymbalta due to the high risk of seizures and bad interaction with my Migraine meds. I haven't had seizures from the amytritiline I have taken for 7 years now. I also take verapamil which gives me low blood pressure and I take 3-4 asthma medications when I need to for asthma. They give me heart palpitations along with the amytriptiline so I try and limit taking them unless i absolutely have to and cant breathe. When I had Botox I had a similar problem too as the muscles in my neck were also injected and then I couldn't even lift my arms up above my head and had so much weakness that it caused pain in other areas of my back. a >Jade wrote: Now that the botox has the trapezius muscle paralyzed, I can feel the full weight of my arm because I have no muscle to hold it up. Then I My point, I guess is that I think some things are novel and useful, like the botox for example. While it did nothing for the original nerve pain that I had, it did work on the original trapezius muscle spasm that it was intended to fix. On the other hand, I would warn anyone with ACM to watch out before paralyzing any muscles near the neck. Looking back I have to wonder what I was thinking. At the time of the injection my mind was soaring at the idea that maybe one day I would be off pain medication for my nerve pain. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 5, 2010 Report Share Posted May 5, 2010 , jade tadaima wrote: > > My point, I guess is that I think some things are novel and useful, like the botox for example. While it did nothing for the original nerve pain that I had, it did work on the original trapezius muscle spasm that it was intended to fix. On the other hand, I would warn anyone with ACM to watch out before paralyzing any muscles near the neck. Looking back I have to wonder what I was thinking. At the time of the injection my mind was soaring at the idea that maybe one day I would be off pain medication for my nerve pain. > > Oh well, live and learn. I'm living my mistake now. The doctor I saw today said that I can expect to have this pulling, pressure, headache, neck, cramping, pain and all the low blood pressure an shakiness to continue for 6 months or at least until the botox wears off. One member of this c_p list said 3 months. I am hoping for 3 months. Jade, Most of us have more than one thing that comes with our pain, and when one thing gets better, we feel the other thing that has something wrong. For me, it is my back, then the SI joint, then the hip. One depends on the other and I get muscle shearing when I walk that hurts my hip. I am so sorry this happened to you and the doctor I saw said that this Botox was a last option for me and I will now take the information you gave me so I will be sure to mention this and thank you for sharing. Bennie Quote Link to comment Share on other sites More sharing options...
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