SPAZZIKA

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  Moment of Peace

  From jonah1 November 12

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  Hug

  From jonah1 November 11

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  Thanks

  From angela56 November 8

  I think you will find the people on this site to be nice, and helpful. Take care,
  Angela

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  Hug

  From angela56 November 8

  I have cervical dystonia and multiple sclerosis, I have had those for over 18 years, now have spasmodic dysphonia, affects the speech basically destroys it. I know it is difficult to deal with my cervical dystonia, started out very badly. It has gotten better over the years, still jerks occasionally, and the tremors are still there. I know how important it is to have support. I am 56, and all this started when I was 38. I honestly did not know what was going on, I was told it was just my imagination many times. Botox helps some people not so good with me. It is nasty disease and I think everyone that has it hates it. I remember in the beginning I slept a lot, that was the only way to get relief, as the years have passed, I have accepted it to a certain extent, there are days when I want to take it out of my brain, and destroy it, doesn't work though. I hope you have a good doctor, and family to support you and make sure you get the help you need. If you ever want to talk, just write me any time. Take care. Angela

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  From rita24 November 8

  hi,i also have cervical dystonia,are u on facebook,its easier to chat on there

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