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New Message on Pituitary Chat

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From: APorpoise
Message 16 in Discussion

Williard1H I was diagnosed with my prolactinoma in 1983, before there were 
computer support groups  and a few years after they came up with the 
Transphonnoidal surgery, prior to that they cut you ear to ear.  I went to one 
of the first meetings of the Pituitary Network Assn (formerly the Pituitary 
Tumor Network Assn) meetings in No California, which was just forming. They are 
one of the largest networks of information regarding Pituitary tumors and can 
be found at http://www.pituitary.org  But I too checked out the National Brain 
Tumor Foundation, which is huge, but doesn't do a lot of networking on 
Pituitary Tumors. Also, one of your comments was that you didn't have chemo.  I 
would think it is rare if ever used on a Pituitary tumor unless it was 
cancerous, which happens, but is rare. As far as the benefit of Support Groups 
such as this one.  It is here 24/7, and there is no requirement that you be 
too.  Its just like everything, moderation.  I have had a lot of years dealing 
with this and another cancer, and I will tell you that I find this MSN Pit Chat 
to be a very excellent Support Group.   I posted the link for the article on 
Apathy probably a year ago, so you can find it here too.  And I also listed the 
book ManMade by Ken Baker, which you may find very interesting and helpful.   I 
will continue to read the stories here on occassion.  And sometimes I'm blown 
away at how many MRIs people have for these slow growing tumors...........but 
there is a lot to be learned here.  When I had my surgery there was only one 
drug Parlodel's Bromocriptine, so I read a lot of people's experiences and have 
learned tons here. 

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