Crps

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Support group for people who have Crps, created by eHealthMe (http://www.eHealthMe.com). To join the group, do any of these: create a post to introduce yourself, ask a question, or simply follow the group.

  • I have CRPS and had a painful wound biopsy done an...

    I have CRPS and had a painful wound biopsy done and pathology said it is "Lichen sclerosus". Im looking for related research.

    Post created 1 month 3 days ago

  • I've had RSD for 25 years Full body and organs ...

    I've had RSD for 25 years
    Full body and organs

    I just starting on valproic acid and would love advise from your support group!
    Thank you!

    Post created 1 month 2 weeks ago

  • I have had RSD for 3 years and 2 years ago started...

    I have had RSD for 3 years and 2 years ago started showing signs of early menopause. Last month my gyn confirmed early menopause. can the 2 be linked?

    Post created 2 months 2 weeks ago

  • I have had CRPS since 2009 and first time WBC elev...

    I have had CRPS since 2009 and first time WBC elevated 2012. At first GP thought I had chronic lymphocytic leukemia but now labeled it leukocytosis

    Post created 2 months 4 weeks ago

  • Has anyone with RDD experienced hypotension while ...

    Has anyone with RDD experienced hypotension while taking nortriptyline and gabapentin?

    Post created 3 months 2 weeks ago

  • I have had crps for 8 months today an ecg showed I...

    I have had crps for 8 months today an ecg showed I have marked sinus bradycardia. I am wondering if it CRPS connected? Could it be caused by gabapentin?

    Post created 3 months 2 weeks ago

  • I'm new to this just wanted to say Hello and tell ...

    I'm new to this just wanted to say Hello and tell you a little about myself.
    I'm a 38 yr old who was diagnosed with CRPS / RSD in April 2011. About 2 years ago I had my D3 tested and It was 18, right now is the highest it has been since it was tested which it is at a 22.

    Post created 3 months 2 weeks ago

  • My name is Cindy, 54, and I am taking several med...

    My name is Cindy, 54, and I am taking several medications to prevent afib and help blood pressure stay within normal limits. My recent round of afib was this past February, and I was given the blood thinner xarelto. This week, I am having an increased number of bloody noses along with blood in the urine. My cardiologist thinks it must be something else causing the blood in urine, but I have read it is a symptom of xarelto. Does anyone else have this problem, and is it something that I should be very concerned about?
    Thank you

    Post created 4 months 1 day ago

  • I have recently finally been diagnosed with RSD/CR...

    I have recently finally been diagnosed with RSD/CRPS. For a while other doctors thought I might be developing it, however my injury to my spinal cord and shoulder was at work. Doctors didn't want to diagnose me because they are doctors picked and paid for by workers comp. Is there any clinic in the Southwest who specializes in the treatment of CRPS? Im having a lot of challenges to deal with and pain to cope with, I have many questions and get few answers. Now I'm getting painful varicose veins. Thanks, kk

    Post created 4 months 3 weeks ago

  • My name is Amber I am 32 years old. I was diagnos...

    My name is Amber I am 32 years old. I was diagnosed with CRPS in 2014 after a doctor shot me in the shoulder with a Cortizone shot and then I had a response of burning pain down my right arm to my fingers and been like this ever since. I am depressed and anxious and have difficulty and many areas of life and functioning since getting the stupid crps. I found some relief or with blocks, I received for 4 stallion ganglion blocks in the past year. They were effective in improving blood flow and some pain relief. But I'm in a workmans Comp system and it's incredibly slow, so much red tape. So I feel hopeless when the pain never stops. Normal pain is supposed to go away. And this just doesn't. I need to survive this. I have a 6 year old daughter who looks up to me. I was the breadwinner and that's over now because of this stupid constant burning pain. Any advice on what to do from people who are actually experiencing what I am. I would appreciate advice on what you are doing to help you cope with this incredibly difficult ailment. Thank you for your time in advance.

    Post created 5 months 21 hours ago