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New Message on Pituitary Chat

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From: hunus
Message 42 in Discussion

I will share my experience. Around ten years ago I had a migraine that lasted 
21 days in a row. I ended up in the hospital. After an MRI they found the pit 
tumor, also my prolactin was extremely elevated. They got me into surgery right 
away and I had the tumor removed. They put me on parlodel for my elevated 
prolactin, and I went home with diabetes insipidous. Within three months the 
tumor grew back. My endo put me on Dostinex, and it did shrink the tumor. I 
have had MRI's ever since and there is no visible sign of the tumor. However 
over the course of the last 8 yrs, alot of my pit functions were going away. It 
was happening so gradually that I never really noticed a difference until 2 yrs 
ago. I was having extreme joint and muscle pain, extreme fatigue, short term 
memory loss, felt like I was walking around in a fog. I was withdrawing from 
friends and family, and just felt lousy. I really didn't put it together that 
it was pit related. I was in so much pain, I
 figured the other symptoms I was having was pain related. I went to doctor 
after doctor, had many xrays, tried acupuncture. Nothing helped the pain. I 
have been on a steady stream of muscle relaxers and vicodine. I was let go from 
my job in January, I kept falling asleep at my desk, I was making mistakes. I 
just couldn't get it together. Finally, I saw my endo for my yearly check up 
and told him what had been happening. After lots of labwork, he told me I had 
no GH, No cortisol, and my thryroid was underactive. I was Hypopit. That was in 
November. I finally got on GH I have been on it a month, He put me on 
prednisone for the low cortisol. I'm also on levoxyl for my thyroid. So far I 
don't feel much different. I see him again in June, I'll have labs done again 
to make sure I'm even on the right doses. I'm still not working, I couldn't 
make through an 8 hr day. I have issues driving, I get panic attacks, usually 
only when I'm driving, so I try to limit my driving. It's been
 hell. I feel like crap most of the time. But I'm really hopeful the meds will 
help. I'm not giving up yet. My endo said all of this is a result of having the 
pit surgery. Quite a chunk of my pituitary was destroyed in surgery. That is 
why I say get a second opinion. Not all surgeries end badly. But do your 
homework and get as much info as possible. My pit tumor was so large it had to 
come out. I wont' do surgery again though. Hopefully the tumor will stay as 
tiny as it is. I don't know if my surgeon at the time could have avoided 
destroying most of my pit, I don't have alot of confidence in him, he first 
diagonsed me with a brain tumor and told me I'd be lucky to make it ten yrs. 
Scared the hell outta me and my family. He said I would lose all my faculties, 
and motor skills, Basically i'd be a vegetable.  When he realized his mistake, 
he didn't even apologize to me and my family. His name is Dr. Weiss out of 
Puyallup, Washington(just incase there are any
 washingtonians here)  Anyhoo I have rambled enough, if you have anymore 
questions feel free to ask. Keep your chin up, and stay positive.  Melissa
 

8:00? 8:25? 8:40?  Find a flick in no time
 with theYahoo! Search movie showtime shortcut.

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