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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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#1 | ||
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Junior Member
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My hand therapist, a close friend with RSD, and I are wanting to start a local RSD support group in our city. My therapist has several RSD clients and has contacted other therapists who have patients. Have any of you started a group or know of someone to contact to help? When we moved here I met my friend at church for the first time. Her first comment was "You have RSD!" I had just been diagnosed. She has been so much help. She routed me to my awesome therapist and has been a great sounding board and support. Our husbands work together at our church. Thanks for any suggestions you might have. (When we do start a group guess what web site will be on our list???) Susie
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#2 | ||
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Yappiest Elder Member
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susie,
what about asking your dr to hold an informal meeting at his/her office on a saturday? just a coffee tea type of thing. see how much interest just from that office. then contact any of your therapists "friends" to do the same thing. all it takes is a few to start. i'm sure more will chime in here. there maybe members here who live near you. ![]()
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#3 | ||
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Junior Member
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Good idea, I live in the the Wichita Falls area. ![]() |
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#4 | ||
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Yappiest Elder Member
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my daughter..lil'monkey..her good friend is there for the summer visiting her dad. lil'monkey is planning a weekend there.
i'm in the dfw area. ![]()
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#5 | |||
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Co-Administrator
Community Support Team
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Maybe make up some flyers or signs and ask if you can place them in Drs offices?? add a sign up sheet for those interested...
RSD/CRPS ?? We'd like to start a support group - if interested please call or email {phone number & email address} {make a free email account for this in case of spam or weirdos} {I wouldn't use your home phone number either - maybe get a tracfone something for this part and let messages go to voice mail??}
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#6 | ||
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Magnate
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Hi. I too have been trying to start a group not only for rsd but chronic pain. The one rsd support group in my area has been canceled for like 4 months cause the leader got really ill with her rsd. I made a post on craigslist under groups with little replies. I am also going to call a local hospital here that offers many groups but nothing for this type of thing. I too would ask your therapist if they have any suggestions. Where do you live if I may ask?
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