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RSD · This is a list for people that have Reflex Sympathetic Dystrophy,(RSD). This is a list to share information, and gain support
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this and that with RSD   Message List  
Reply | Forward Message #14793 of 15000 |
this and that with RSD

Hi,
Ah...very interesting mine is a he, and I haven't seen him yet..waiting for
aproval..have a friend seeing him..says he is good. I have been to
UCSF....already told me stuff already knew and probably charged workers comp
a billion dollars. (I dont really recommend them...but I may go see them
again just to get an update if they have anything cutting edge going on)
Have had RSD left foot since 1999...and tried every drug on the market,
chemical sensitive so its taken a long time to figure out that valium and
wellbutrin combined help...with remron once a week to defuse me when I start
having a nervous breakdown which happens more then I want to be conscious
of. I now take valium as soon as I wake up, so I am not a nasty to everyone.

I use a Dynatron machine which helps, like a tens unit with electrodes...its
a computer programmed generated electical stimulation machine of 1 hour a
day in my own home. Right now I am really into magnets. I have a magnetic
blanket, magnetic massager, necklace, bracelet..and more. As good as going
to accupuncture in moving energy to a better place out of pain.
Bought a dishwasher today..as I cant stand to long to wash my jack lalaine
juicer...so I can quickly juice and throw it in the dishwasher...this is my
biggest new RSD therapy. I experiment all the time with my RSD. I am one big
RSD experiment !
Also Ionic Fizz helps allot with the pain to...drink that every night, helps
with allot of stuff. I couldn't survive RSD without it.

http://www.pureessencelabs.com/ionic_magnesium_fizz.php

Hugs

Jefree


>
> Hi there....glad you decided to stop just lurking and join in! I am really
> curious if you are going to see my pain doc....mine is Dr. Schuchard and
> is a
> she. Her and her hubby are both pain management docs - I actually see each
> of
> them, depending on their schedule. I go to their Fremont clinic, which is
> only open 3 afternoons a week, but maybe they have one in Santa Rosa too.
> Never
> really asked! I have been seeing them now since August 1999 after going
> through all the other area pain mgt. programs, Stanford, UCSF, Pacific
> Pain, you
> name it. If this is the same doctor, I think you will like her...let me
> know.
> It would be kind of a strange coincidence to have two pain docs in the
> area
> with a name like that. The way you spelled it is exactly how it is
> pronounced.
> Let me know, ok? You can email me off the loop too if you feel more
> comfortable about that...it's _carolnjo@..._ (mailto:carolnjo@...)
> .
>
> Love and soft hugs, Carolyn
>
> When I took the leap,
> I had faith I would find a net;
> Instead I learned I could fly.
> - John Calvi, 1994
>
>
>


[Non-text portions of this message have been removed]




Mon Aug 22, 2005 10:32 am

whalerocker
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Forward
Message #14793 of 15000 |
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Hi everyone, Been lurking for awhile ...six years later still in shock that I have RSD. Life has swung around 180 degrees. They just put me on social...
beefree@...
whalerocker
Offline Send Email
Aug 20, 2005
9:23 am

Hi, Ah...very interesting mine is a he, and I haven't seen him yet..waiting for aproval..have a friend seeing him..says he is good. I have been to ...
beefree@...
whalerocker
Offline Send Email
Aug 22, 2005
10:32 am
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