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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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Does anyone know if there is a support group for MID Michigan? If there isnt, would anyone be interested in getting one going?
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#2 | ||
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Magnate
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When you say mid Michigan where do you mean? Sorry to sound dumb but what county? I don't live in MI anymore but may know of one.
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#3 | |||
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Junior Member
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Not sure if this is near you or not but hope this helps
Grand Rapids, Michigan --RSDS Support Group Meetings are held the 2nd Monday of every month from 7PM - 9PM at the Kent Community Hospital 6th Floor Meeting Room Hosted by Sherry and Cliff Mulder RSDS Support Group of Grand Rapid, MI 1259 Diamond NE Grand Rapids, MI 49505 616-364-4014 cheers, Dee ![]()
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~ Refuses to use speller checker becasue Im not perfect and Im okay with that ~ . |
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#4 | |||
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Junior Member
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We are in Gratiot county, township of Wheeler
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#5 | |||
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Member
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Hi, I'm in Eaton County, Michigan. I too would be interested in a "support" group. Also, have you had any luck finding a good doctor in Mid-Michigan? I am starting to question my doctor's ability in treating my problems. I am either one of the unlucky ones where every surgery goes wrong or he just doesn't know what he is doing. It almost seems that it's a "guessing" game or trial and error. I feel that they aren't treating me as an individual, but treating me as following an outline in the text books.
It hard to talk to others that aren't suffering from this. I get their sympathy, but sometimes I think they don't fully understand or just get sick of hearing me "complain" that it's a "yes dear" response. I love my husband dearly, and I know there is no question about his love for me, but sometimes when he hugs me and if it hurts, I feel bad about the cringing, the screaming in pain. I see the hurt in his eyes, the pity in his eyes and it is just sad. I guess talking about this with others will help keep this disease from taking control of my life. Maybe if I "vent" or learn about this from people who are suffering like me, I can talk about other things with my family. ![]() |
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#6 | ||
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New Member
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Has anyone from Michigan had support or treatment from Children's Hospital of Philadelphia under Dr. Sherry care? If so I would be interested in your opinion.
Bill |
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#7 | ||
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Newly Joined
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#8 | ||
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Newly Joined
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"Thanks for this!" says: | RSD ME (12-29-2014) |
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#9 | ||
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Senior Member
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sorry i don't live in michigan so don't know of a group there but along with the other great suggestions posted here you may find some groups in that area listed online on rsd hop and rsdsa. hope you can find and/or get a group started soon. take care.
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RSD ME . |
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#10 | |||
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Administrator
Community Support Team
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Hi chick40 and welcome
I just wanted to be sure you know that this thread is on our RSD/CRPS forum and I see in your profile that you have Chiari Malformation, so not sure if you are actually also looking for an RSD support group or rather a Chiari one Here is the Chiari forum where you also posted asking about local groups http://neurotalk.psychcentral.com/sh...43#post1115243
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~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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