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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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11-14-2009, 12:41 PM
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New Member
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hey all!!!
I was just wonderin does anyone know of any support groups or people with RSD in Ireland that can help me? Erica |
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| "Thanks for this!" says: | loretta (11-14-2009) |
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11-14-2009, 01:54 PM
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I don't know, but if you go to RSDSA (our national organization) and there is a space for your zipcode. Put that in and if there is a support group close to you, it will give you a name and phone number of the closest one to you. Hope there is!! You are always welcome to PM (Private message) me and ask anything. I've had RSD 15 years and full body. RSDSA has a lot of good information and so does rsdrx.com Dr. Hooshmand is retired but has his website up. Under puzzles List there are 146 questions and his answers.= very infrormative. Hope the best- your friend, loretta tell us about yourself and concerns, and this is a wonderful group of supportive,caring friends. soft hugs 
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| "Thanks for this!" says: | ewizabeth (11-14-2009) |
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11-14-2009, 06:13 PM
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I'm not from Ireland but live in England and have had RSD for 2 and a half years since I was 12 years old (am now 14). There doesn't seem to be many people near where I live that have RSD.
Just wanted to let you know i'm here if you ever want to talk! 
__________________
To the World you may be one person, but to one person, you may be the World. |
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11-16-2009, 02:18 PM
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Junior Member
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Hi Erica,
I live in Scotland, and I can't find any support groups near me. I've had RSD for 5 years in my left arm/hand. Please get in touch if you need anything. Take care.
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| "Thanks for this!" says: | loretta (11-18-2009) |
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12-04-2009, 05:15 PM
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New Member
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thanx all for ur help at least u to are closer to ireland than other people in america.
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06-10-2010, 02:35 PM
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Hi, I am in Ireland, my husband has Rsd, I have also been looking for support groups and information on it as it seems nearly impossible to get!
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06-10-2010, 02:46 PM
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Hi, i am in Ireland and my husband has been diagnosed with rsd. we are also having trouble finding support sites. Did you ever find any
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06-10-2010, 02:51 PM
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Grand Magnate
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Name "Chiron" that posted in the SCS forum. I recall chiron mentioning a chronic pain site (CPI) Chronic Pain Ireland, I believe.....
Not sure if they discuss RSD, but am curious to find out. |
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| "Thanks for this!" says: | chiron (09-29-2010) |
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09-29-2010, 01:00 PM
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Member
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Yes, Rrae you are right. Is called Chroniic Pain Ireland [C.P.I] and is based in Dublin, but has support groups in many areas.Just google the above and you will get the site and details. Thanks for highlighting this. regards
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Any support groups or people in Ireland?
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