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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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05-11-2007, 08:14 PM | #1 | |||
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Hey Robin,
Just wanted to say I am from your side of the pond! I live in SE UK. My gosh, someone within 500 miles of me!! Sorry you have to be here!! Love frogga xxxxxxxx |
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05-13-2007, 03:27 AM | #2 | ||
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Hi frogga, nice to meet you! Maybe we'll be able to help each other out with UK-specific information from time to time. Not that I know much just now. And I'm sort of hoping I don't have to learn too much!
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05-14-2007, 07:13 AM | #3 | |||
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.... if I should move my intro post to this thread.
When I first joined, I posted my intro thread in the "new members" forum. It never dawned on me that each disease would have it's own intro thread, don't ask me why, lol.... it certainly makes more sense. As I seem to be spending a lot of my time in here, should I move it or rewrite it here? I have talked with a few people in the chat room who didn't know my story... nor could I find their intros either. I just wanted to know if it would be better or more helpful if my intro is in here.
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"Thanks for this!" says: | Theburasfam (05-01-2020) |
05-14-2007, 08:59 AM | #4 | ||
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Hi Rogue, I was advised I could just copy (Ctrl-C) and paste (Ctrl-V) my intro from there to here, and that's what I did.
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"Thanks for this!" says: | Theburasfam (05-01-2020) |
01-14-2008, 01:18 AM | #5 | ||
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Senior Member
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Hi JennyK38,
Hi Jennifer, So Sorry to hear about your injury at work and having RSD now. I had breast surgery, both tumors benign, but also got frozen shoulder following the surgery. My arm swelled up, followed by the frozen shoulder. It probably took 100 physical therapy treatments plus massage therapy to get full range of motion. Ortho Dr. wanted to operate, but said no. Shortly later, it moved to the oppposite shoulder and froze. Not so many treatments, got an earlier start. About 5 years from the surgery, was water skiing and pulled nerve in the left hand. Was misdiagnosed with arthritis and bad pain. Finally diagnosed with RSD and back to therapy. Left hand is permanent claw, Then right hand rsd then both feet and legs. full body plus trigeminal nerve pain and half my face. I have finally found a wonderful Dr. Have switched from neurotin (3200 mg to Lyrica 400 mg. The Lyrica is much better for me and lessens the nerve pain. Am on Ambien Cr for sleep. The Lorazepam helps with anxiety and two different blood pressure meds and two different anti-depressants that help with nerve pain. I used to have the electrical jolts bad and spasms. High blood pressure and then sudden drops. This disorder really affects so much of your life, memory, depression, sleep deprivation, energy level,the pain is unbearable . I had a tens unit too Jenny, Swimming is one of the best things that help me. I hate the weight gain from the meds, and the exhausation from the meds and depression. I'm afraid to try to scale down, because I had a bad drop in pressure and passed out for over an hour. B/P was 60/40 4 days in icu. I was able to drop down two vicodin a day because the Lyrica was more effective for me than neurotin. This forum and helped me too with the isolation and missing so much my old active life. It is a real adjustment in life and missing all the things we used to do. I try and be grateful for what things I have now, a husband that does so much-shopping, drug store, housework. etc. Our daughter is married-7 years now and just moved to Chicago. Life is full of change isn't it. I'm 59 and guess this has been with me for maybe 14 years. I have a good friend here in AZ with full body RSD from car accident. Jennifer, are you on SSDI, I read somewhere, it's easier to get now. If I every try, Ii'll use an attorney. Jennifer, hand in there, there is a lot of understanding and knowledge on this forum. Lots of encouragement, I'm trying to exercise more and loose weight. It's really hard emotionally to gain so much weight and not really have the energy to work out. I'm starting out slow and adding a minute or so a day.Please know we are all here for you. Sincerely, loretta jewell |
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