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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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09-10-2009, 08:47 PM
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Hey Karen,
It's good to see your back on the boards. Your logic makes sense and I understand what you are saying. Cold RSD never can get warm Hot RSD can never get hot enough. For me I just keep burning and burning. Today for example I am on the 3rd day of a full body flare. Even the neves in my face and mouth are flared. At dinner I held my ice tea in my mouth for few seconds before swallowing it to help cool the burning nevers in my mouth to my throat it felt like hot tea. My entire body head to toe is on fire I have increased my meds like I normally do and it isn't helping (yet). To look at me I look like I laid on the beach all day and have a sever sunburn (it's almost 10PM). Be it hot or cold RSD neither is enjoyable. Take care, Sherrie Last edited by SBOWLING; 09-10-2009 at 09:03 PM. |
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09-11-2009, 02:14 AM
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Exactly! :-) Holy cow....sunburned without the sun touching your skin. You're right, it all sucks!
Hugs, Karen Quote:
__________________
Laugh until you cry, don't cry until you laugh. Living, loving and laughing with RSD for 14 years and counting. |
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09-12-2009, 02:42 PM
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I am so sorry you are in a full body flare. I know how miserable that is. Please know many of us are thinking of you and hope it doesn't last long. I just finished a long flu, making the body miserable. Even 10 days of super strong antibiocs didn't end it. Must have been pnemonia. I live in Arizona and it's been an extra hot summer. Still about 104. Looking forward to some cooler weather. We were formerly from Oregon. In my 14th year,now full body. Have a great Dr. Am going to try his new HBOT in his new clinics. Please take care, loretta soft hugs 
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