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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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UnderArmour tube socks
T-shirts & fleece jackets ThermaCare heat wraps understanding hubby hot chocolate |
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"Thanks for this!" says: |
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#2 | |||
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Magnate
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Atheletic Works pants. They are from Wal-Mart. They not only feel good, they look good.
I agree on hot chocolate, lidocaine patches, heating pads, electric blankets, warm decaf green tea at night. My right hand and foot is always cold. I shook hands with someone the other day and thought about how cold my hand was compared to his. It's been warm here also so it hasn't been from cold. Also, warm wind blowing. Yesterday was the worst day I have had in a long time. The wind was blowing pretty hard, even inside I felt it. I'm still looking for those sheets that you don't feel every thread in. Also the floor. I had tile put in my hallway last summer and when I step on it at night, it wakes up the sensitivity in my feet. I think I can feel every line in it. Carpet for me is better. Ada |
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"Thanks for this!" says: |
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#3 | |||
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Administrator
Community Support Team
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this seems a very helpful thread with great information
![]() would members like this to be a "sticky" thread at the top of the forum so it can always be easily found?
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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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"Thanks for this!" says: | bassman (03-02-2009), DejaVu (09-09-2015), mcfly (10-03-2012), MominPainRSD (03-11-2009), Pauliana (02-28-2009) |
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#5 | ||
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New Member
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hi there,
I was able to find this thread while searching for specific symptoms I have....I have sat here shocked, reading every post. I have felt like a freak of nature for 2 years, with symptoms that even my mother and fiance cannot help but question. I cannot believe what I have read; everyone has the same issues I have- this is the most helpful and validating thing I have found since my injury and diagnosis. thank you for making this "sticky"- i think it helped Google put it high in my search results. I cannot express how much this thread has helped me. I have never spoken to one person who truly understood, let alone so many. thank you to everyone. |
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"Thanks for this!" says: | RSDcandice (10-18-2012), stillsmiling (08-28-2015) |
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#6 | ||
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"Thanks for this!" says: | DejaVu (11-09-2015) |
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"Thanks for this!" says: | DejaVu (11-09-2015), stillsmiling (09-07-2015) |
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#8 | ||
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Junior Member
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Hmm my survival bag looks like this:
Back of the wheelchair: Bag full of medications, cellphone, wallet, it is basically my purse. I never go out without my wife, she keeps an eye on the bag for me. Oh and my water bottle full of ice water. Footware: I'm fiddling around with it, I bought some REALLY nice Nike shoes before my foot started hurting for working out, and my feet are like 'nope' to the max. But I have found my Uggs are pretty okay, except when my ankles and feet are swollen, then its mind over matter really. As for socks, the wife has big thick wool socks from being in the military, I was going around in just one sock, but now have upgraded to two. Also those fuzzy socks? Its like heaven. Blankets: Just none, my feet remain uncovered even at night, as is I can only sleep on my front right now, and even that is painful. I can't sleep on my side or back because of positioning. Still working on it, as Im up for hours at night randomly. Clothing: As its mostly in my feet/ankles (though I get random spikes up into my calves), I wear things that are nice and comfy and easy to put on. Usually yoga pants, a nice light shirt, with a hoodie. I don't even care how far up my wool socks are. Stare at my fashion faux pas! Mobility: I have canes, crutches, and a wheelchair. Right now the only solution is my wheelchair. I don't use the foot support on it, because it juts out at an awkward angle and leaves me vulnerable for bonking into things. I have found I can lightly cross my ankles and my feet just dangle. When I get my wheelchair (this is a rental) I'm getting the foot support that don't jut out. Other: Warm cat cuddles, just not on the feet, don't look at the feet, don't touch the feet. But having snuggles from kitties always cheers me up. My wife when we go out, she fends off the glares and rude people, also helps me up steep hills, we live on an island, an island that is made out of mountains....Hills suck. Video games/distractions, the more it distracts me the better. Tissues, eyes water from pain, tissues are godsend. Haven't figured out the car, for a while putting my foot on the dash worked, but its now cold out and the sun has gone away, meaning no more comfort (feet are usually ice cold). The vibrations and bumps from the car make me want to scream. Any other type of warmth usually is horrible. Epsom salts SOMETIMES help, other times don't. Maybe its a mind over matter thing? Hope this helps someone =) |
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