Thread: New to RSD
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Old 06-23-2012, 12:48 PM
tos8 tos8 is offline
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Join Date: Sep 2009
Posts: 286
15 yr Member
tos8 tos8 is offline
Member
 
Join Date: Sep 2009
Posts: 286
15 yr Member
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Hi Finz. If i would have told my nueroligist that i had RSD 3yrs ago he would have known then. But its been easier for me to be in denial about it i guess and even though ive known ive just never told any of my doctors. The only reason i got an official dx was because I had to ask him why im having autonomic problems with controlling my body temp and he right away said its do to RSD, secondary to the tos surgery. So he knew immedetly what was wrong with me without me even having to tell him.

I do have a quistion, what is everyone doing with summer here and trying to keep your body temp regulated? Last night I got so hot and my pain shot threw the roof with the air conditioners on and the fans blowing that it made me very sick and i had to go to bed for awhile to try and lower my temp.

My nueroligist told me to watch my envioroment, but im in my own house and still have a ton of difficulty.


Thanks everyone!




Quote:
Originally Posted by finz View Post
Hi tos8,

I'm a TOS to RSD'er too.

I wouldn't rule out injections....a series of stellate ganglion blocks CAN be quite beneficial to people with our conditions. For me, the SGB's helped with my L arm symptoms, but the L arm stuff has never been my primary issue. They did nothing for the 'burning golf ball' just to the left of T1 that is my major complaint.

The nerve blocks don't do much for me long term (from the steroids), but I do get a few pain free hours from the lidocaine in them. I wish I could schedule one just before I go to a party or family occassion Even though there aren't lasting physical effects, I find it a positive experience just to 'remember' what a lack of severe pain feels like. Sometimes it gets me angry......if the right shot can make me feel better for a few hours, why won't docs who've blown me off and WC pay for tests or treatments to look for more lasting results. Mostly, it gets me hopeful that SOMETHING out there can help me. Maybe a radio frequency abblation ? Who knows.

I'm laughing a bit, in a sad way, about your comments about knowing you has RSD for years before getting the official dx. I had to play the same games to find docs who knew about TOS and then RSD. That frustration doesn't help pain levels !
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