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RE Rheumatolagist   Message List  
Reply | Forward Message #438 of 612 |
Re: RE Rheumatolagist


HI!
My GP is awesome. I take information and experiences into the office
with me, and we work together. I'm one of two SD patients that he's
had. I think he's gotten more familiar with the disease since I
started visiting him. :) I'm healthier than I have been in a long
time. (Thank God) Being informed and active in your treatment is
essential.
Peace and hugs to all..
Hope

--- In sclerodermafriendsandfamily@y..., dynamicdebz <no_reply@y...>
wrote:
> Getting info from the internet has helped me enormously. I saw my
GP
> today because of severe itching & bruising on my legs. He only had
a
> vague idea about SD & because i told him of other peoples
experiences
> that I have learned about on the net, he was able to treat me
> appropriately. He was greatful for the information I gave him &
says
> he will find out more info for his self.
> Debby
>
>
> --- In sclerodermafriendsandfamily@y..., "mycoloredcoat"
> <mycoloredcoat@y...> wrote:
> > --- In sclerodermafriendsandfamily@y..., "mlss24" <lancey@b...>
> wrote:
> > > Hello everyone,
> > > Well i have finally had the appointment with the Rheumatoligist,
> > > I dont know what i expected,and he did seem to ask lots of
> question
> > > and he did check my joints,but......he seemed to tell me
> everything
> > i
> > > already knew when i asked if certain complaints i had were
linked,
> > > he just said "probably yes".As i say Im not sure what I
expected
> > but
> > > i came out of their with a perscription for my aches and pains
> but
> > > not much more. And it does look like i have sjogens as well as
> > crest.
> > > Im not sure weather to go back or not,it seems like such a lot
of
> > > money,to be told stuff I know.
> > > Thanks for listerning to me,
> > > I needed to get that out,
> > > warm hugs to you all,
> > > Michelle
> >
> > Hi Michelle
> > My Rheumatologist was the same way. He even went as far as to
tell
> me
> > NOT to read literature or go onto the Internet for information.
He
> > said that some of the things that I might find would alarm me
> > uneccessarily. Yeah, right. Not knowing is far worse, right?
> > I can't advise you whether or not to go back, but I will tell you
> > that you have a RIGHT to information, and not just a brush off.
> > Corner him, and tell him what YOU want. Meanwhile, you can do as
I
> > did, and surf the internet, and get as much reading material as
> > possible. I read a book on SD and I'll look up the exact name,
and
> > author, and post it a.s.a.p. Also, if you need to talk, email me.
> > Take Care,
> > Hope




Thu Jun 20, 2002 4:02 am

mycoloredcoat
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Forward
Message #438 of 612 |
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Hello everyone, Well i have finally had the appointment with the Rheumatoligist, I dont know what i expected,and he did seem to ask lots of question and he did...
mlss24
Offline Send Email
Jun 16, 2002
5:35 am

... i ... but ... crest. ... Hi Michelle My Rheumatologist was the same way. He even went as far as to tell me NOT to read literature or go onto the Internet...
mycoloredcoat
Offline Send Email
Jun 17, 2002
3:15 am

Getting info from the internet has helped me enormously. I saw my GP today because of severe itching & bruising on my legs. He only had a vague idea about SD &...
dynamicdebz
Offline
Jun 17, 2002
8:36 pm

HI! My GP is awesome. I take information and experiences into the office with me, and we work together. I'm one of two SD patients that he's had. I think he's...
mycoloredcoat
Offline Send Email
Jun 20, 2002
4:02 am
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