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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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I was wondering if anyone else has ever been prescribed Nortriptyline HLC?
My neurologist prescribed it after I mentioned my headaches feeling like they were in the middle of my brain. (I also have the cerebral shrinking going on.) After a month of taking it I noticed not only my headaches decreasing but I'm starting to have dreams again. I was just wondering if anyone else experienced this.... ![]()
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Hope for better days..... Russ okska'sssini ómahkapi'si . |
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"Thanks for this!" says: | gabbycakes (10-28-2011) |
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Hey Jimbo,
I am still trying to figure out how to use this site. Thaks so much for requesting the friendship. It will be so nice to know someone going through the sam e thing as my daughter. She has been referred to Mtn Neurology here in Asheville, Dr. Jones. Do you mind sharing who your neurologist is? I really want to provide the best care for my daughter. She is a senior this year, has always been at the top of her class but I worry with the RSD.... |
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#3 | ||
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Quote:
I don''t dream anymore either, I wonder what the connection between RSD and not dreaming is. Prior to my injury I was a great sleeper and had dreams all the time, and up to a year ago I still was dreaming. My sleep is terrible since the RSD, but actually that is getting better recently. If you have any information on the subject I would love to hear it. gabbycakes |
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Quote:
Now that I'm noticing the change with this new med I'm beginning to reach out for some answers. Sad to say that my interest out weighs my information at this point but my curiosity is sure sparked...
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Hope for better days..... Russ okska'sssini ómahkapi'si . |
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"Thanks for this!" says: | gabbycakes (10-28-2011) |
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I think I can remember dreaming about two times since I was injured last December. I used to dream all the time. I was finally put on Silenor recently (my two dreams
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