Good too read your typing. so sorry that anyone has to go thru any of
this. I know is hard on us and just as hard for them around us as well.
My dear,, the reactions n side affects of these meds are really hard.
Stupid Govt that we have sure wants to be God,,,, wish that they had to
go thru what we do. Then n only then will things change. Darn it,,
dear,,, meds are suppose to be there for us not have to go off of or
without meds. No let laspse in the time frame given to take meds. Pain
is hard enuf to get under control n that time frame is important too
stay in as meds are suppose too keep going thru too keep it all in
check. Noone should have to go thru that kind of reaction to meds. Tho
meds are going too react too each person soo differently is amazing what
n how does affect. Drs n FDA noone can tell what or how a person is
going too react too any of these chemicals. They were designed too
help,,, thankful for them,,,,, our bodies were not designed for these
chemicals in first place. Hope that pain issues are now better under
control. I really do. We just keep hammering away. There are ways n
answers out there for us.. We keep searching is all that we can do..
Let me know how n what U r doing. Hugzzzzzzzz
--- In rsdsupport1@yahoogroups.com, jeanette polk
<turkeylips_sammon@...> wrote:
>
> Brook I haven't talked to you yet but I am on the methadone treatment
which is regulated to the extreme. I couldn't function for at least a
month but now I am doing OK I do take other meds but anytime we add one
I have to deal with reactions for a week and then see if the new meds
work. I couldn't deal with the Morphine however, I seriously wanted to
hurt people, made me mean. I know everybody is different but my biggest
fear is when the doses wear off completely then what?
>
>
>
> ----- Original Message ----
> From: brook_s2001 brook_s2001@...
> To: rsdsupport1@yahoogroups.com
> Sent: Monday, July 28, 2008 9:41:58 PM
> Subject: [RSDSupport1] Re: CRSD
>
>
> Hi ther Vannessa ,,,, so sorry that is happened to you. There are not
> many people that I know that can function on meth. Let alone the other
> meds. Sad that we all haveto go thru this. I would talk to dr about
> another route. Or seeing if there is a pain dr management around close
> to you. It is hard one with rsd for real. We all have had a nitemares
> with drs that is for real. Hope that there is a pain management dr
> around. Really do.
> --- In rsdsupport1@ yahoogroups. com, "Vannessa" nessa4631@ ..> wrote:
> >
> > Hi,
> >
> > My Name is Vannessa Hicks,I was diagnosed with RSD,in 2006.I have
> > been to so many doctors.I have a spinal cord stimulator that
controls
> > my right leg,were it first started,now it has traveled to my left
leg
> > and in my back.
> >
> > I am so scared I have been released to a primary doctor,for two
> > years now for medication control.All he will give me is
> >
> > 1)Lyrica 150 mg 3 x day
> >
> > 2)Loratab 10 mg 2 x day
> >
> > 3)xanax 1 mg 2 x day
> >
> > 4)metoprolol 100 mg 1 x a day
> >
> > 5)lexapro 20mg 1 x a day
> >
> > 6)ipratropium bromide every 6 hours(for copd)
> >
> > Now he is so scared of the DEA that he is wanting to reduce my
> > medications and put me on methadone. I have taken it before and
> > wasn't able to function. I am at the end of my rope and just don't
> > know what to do anymore. Any help that you can give me would be most
> > appreciated.
> >
> >
> >
> >
> > Sincerely,
> >
> >
> > Vanessa Hicks
> >
>
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>
>
>
>
>
>
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>



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