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New Message on Pituitary Chat

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From: nedaTN
Message 3 in Discussion

The only medication change in at least the last 6 mths is the increase from 
20mg to 30mg of somavert. And it's only with the increase that he's had these 
severe headaches. An occassional headache maybe but not these all day every day 
things. Also there is no tumor remaining that can be seen on an MRI. The latest 
one was just done in January. They also removed his pituitary gland itself, 
something funky about the normal cells behaving abnormally. If I remember and 
am explaining this correctly his normal cells were telling themselves to 
release more and more GH. I may be explaining that badly. The dr called it 
Neurogenic Acromegaly. I think I did a better job explaining it in one of our 
older posts. His endo is awesome and really takes everything into consideration 
with Bill. He's the one when we mentioned the Diahrea he was like "This is not 
acceptable. We have to try and figure out the cause and what we can do about 
it." I feel confident he will help us uncover and deal with these headaches. 
It's just frustrating because 2 months ago his blood test for thryoid cancer 
markers came back elevated and he had another neck ultrasound and they repeated 
the blood work last teusday so we are also waiting on that. Sometimes it seems 
like we climb one hurdle to smack straight into another one. The endo said the 
elevated marker might had been influenced by being off the somavert and having 
elevated growth hormone levels and IGF1 levels for a month so he wanted to 
retest and do the ultrasound before doing anything else.    Annetta and Bill

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