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Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index
Pages: 1 Showing 1 - 20 of 26 for crps and cold weather. (0.006 seconds)


... I'm glad I was able to help,even if just a little. This site is wonderful when looking for support. I know when I was first diagnosed I was 22 and felt completely alone,like I was the only one who knew what I was thinking and feeling. ... (28 replies)
... need to be able to talk to someone so thank you for responding , so you have episodes I call them flare ups they really shut me down for about 3 to 4 hours a day and I try to stop them but nothing seams to work . ... (38 replies)
... foot. It stays at the same pain level. In fact I use a hot tub several times a day and the water must be at least 102 degrees. any lower and it increases my pain and my "episodes". I live in an area where we are seeing temperatures reaching 94 to 98 degrees and with the heat index we're over 100. ... (38 replies)

... I certainly can relate to the cold weather being such a factor in the amount of pain. It's so cold here... I like you, keep my electric blanket nearby. I have a hard time with clothing as well. .. unfortunately... in my area... ... (28 replies)
... Thanks for all the replies folks its great to see so much support for one another out there. I had a particulary bad weekend the pain was unmerciful and the weather was very wet and windy and cold is there any connection here......... ... (28 replies)
... I completely understand the excess of pain with cold weather. I have the same problem. I use heating pads to keep my leg feeling warm. If it doesn't warm up it sends me into flare ups. ... (28 replies)
Cold CRPS plus
Feb 4, 2009
... broke leg and foot at work in Aril 2007. and became the WC case that won't go away no matter how hard they try. Dx by two WC docs with RSD in left foot. Cold is my enemy even though I live in Florida. ... (21 replies)
... I have a horrible time with the weather. I'm very sensitive to the cold and air movement. I live in the Pacific Northwest and it gets very cold in the winter and we get TONS of snow. We got over 6 feet last year in a matter of a month. ... (28 replies)
... Hi, I just had to write you both and explain my situation. ... (22 replies)
RSD/crps flare ups
Jan 14, 2014
... Thank you ill take all the support I can I know it's going to be a good thing as my feet are so sore already that I have that lovely feeling of walking on broken bones lol!!! I live in Minnesota and its been snowing a lot and very cold like below zero since I can't remember and that really kills me I'm glad your holding together I need to eat and medicate talk soon (48 replies)
... Thanks guys for your help and support. I have had some sessions of hydrotherapy, phisiyo, and occupational threapy. My pain is still as bad as ever and weather conditions are starting to get cold in Ireland, i find i'm very sensitive to the cold. ... (28 replies)
... Thank you for replying to my post. I came from a board on i village but there were only a few people on there and it would take weeks to get anytime of reply.I don't think there is even 20 people on there. I was looking for something where the people were more active. ... (19 replies)
... that is suppose to see you through your problems. I have spent almost 3 years now researching EVERYTHING,talking with doctors,looking at countless medical trials and studies so that I don't have to have that "alone" feeling like I did have when my surgeon told me. ... (28 replies)
RSD/crps flare ups
Jan 14, 2014
... ve for a little normalcy in our life. Being able to put your feet on the floor with out pain is major. Keep your head up.... of course I will be here to listen and support you! Im hanging in there... getting a brief break in the extreme cold weather... ... (48 replies)
... can relate to work situation...had to sell mine.HAD a very lucrative pest control biz....on full boat SSI disability now,i'll survive.Boy this CRPS IS A REAL BIT...! ... (22 replies)
... Quite honestly, you've provided quite a few keywords describing RSD and some of the things I've personally experienced with RSD... ... (7 replies)
... did my functional assessment. She seems fine. No problems there. She wants to get all of my body moving, stretching, working. Okay, no prob. I really am stiff and have never felt this rough before. Knew to expect that. I think I will manage for the most part. ... (14 replies)
... I guess they think by not saying anything they're sparing a person's feelings but in this case I don't think that's right since all you have to do is go online and see there is no cure. Geez, more people newly diagnosed get the crap scared out of them by reading things than by having the doc gently explain it all. ... (38 replies)
... Yes you can google everything about RSD, and then one day this site pops up, and you've found your comfort zone. ... (6 replies)
... Cold or any weather changes do make the pain go up, as will stress and for some loud noise and vibrations. Alice is right with heat....trying to stay warm in anyway possible is the best thing. I often take hot baths and that's so relaxing. ... (19 replies)


Associated Tags: crps, flare ups, isolation, meds, pain, rsd, rsd in feet, suffering, weather

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