> Thanks for sharing that site. However, the news about Femara will not
> help people like myself who already have bone/joint pain and can't take
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>
> Bea
had to join this link Bea and Alex,I too am ER neg,what new things are
happening for us ?
kathleen
> Bea I can understand how you feel since I am ER neg and this doesn't respone
> to hormones. Alex
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> >
> > Bea
bartalo@webtv.net - 21 Jan 2004 14:51 GMT
>had to join this link Bea and Alex,I too am ER
> neg,what new things are happening for us ?
>kathleen
Sorry for the misunderstanding, Kathleen but I am not ER neg. I am ER+
and Her2+. What I posted about my problem with the Femara was because
although they are finding certain drugs which can help ER+ people, my
concern is that my system may not be able to cope with taking the drugs.
But at least they are searching for ways to help us and I am thankful
for that. I do hope that in the near future research will find some
good drugs to help you ER neg folks too.
Bea
Kaye301 - 21 Jan 2004 17:46 GMT
Bea wrote << hey are finding certain drugs which can help ER+ people, my
concern is that my system may not be able to cope with taking the drugs.
But at least they are searching for ways to help us and I am thankful
for that. >>
Just wondering would there be anything you might be able to take for your
stomach that would alow you to take the Femara? Have you seen a
gastroenterologist. I am only suggesting because about 10 years ago my
stomach got messed up after taking 6 mos. of antibiotics to try and clear up a
very stubborn sinus inf infection. I was finally given steroid inhalers which
along with the basics seemed to do the trick but my stomach had been left a
mess from all that. Not having any meds orally for awhile helped. Then I
started interferon beta for M.S. and am not sure that helped but problem went
away. Now, if a medication bothers my stomach I take oral aloe vera gel and it
it makes such a difference. The problem area seems to heal quickly and I am
able to tolerate whatever drug it might be. I don't know if that would work
for you but thought I should at least mention.
Pat from Apple Valley, CA - 21 Jan 2004 18:26 GMT
I listened to the conference, Very interesting, by the way, and there is
nothing new for us neg's...You should listen to the conference,. Makes
you wnan to go to Sloane Kettering to be taken care of by the principal
speaker...Pat from Apple Valley...
>had to join this link Bea and Alex,I too am ER neg,what new things are
>happening for us ?
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>
>
Alexandra Koffman - 21 Jan 2004 22:42 GMT
I got a bit depressed after I listened to it. But in confirms what I have been told here in Boston is accurate. Alex
I listened to the conference, Very interesting, by the way, and there is nothing new for us neg's...You should listen to the conference,. Makes you wnan to go to Sloane Kettering to be taken care of by the principal speaker...Pat from Apple Valley...
Alexandra Koffman - 21 Jan 2004 22:40 GMT
Nothing...they are "thinking" of doing some research... how exciting for. I
have heard this swan song for the past 7 years since my diagnosis.
ALex
> had to join this link Bea and Alex,I too am ER neg,what new things are
> happening for us ?
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> > >
> > > Bea