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My neurologist, who first thought and treated for MS, had some special tests done and discussed them with his buddies. They are pretty sure my brainstem lesion is a glioma.
I'm to see a neurosurgeon next week to see if there is a way to do some type of biopsy without sticking a needle in it. Taking a piece of tissue would cause something to no longer work as the area in question is where our cranial nerves originate that control sight, hearing, swallowing breathing and other stuff I'd like to keep working. Then the following week I'm to see a radiation-oncologist for gamma knife. When a doc says brain tumor, cancer, and inoperable all in the same breath, it kind of lets the air out of you. Posted on 01/11/12, 11:09 pm |
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Speaking as one who has heard the three together...and is still here after 4 years...
Big Deep Breath... Then start enjoying whatever is left of your time here :) (((hugs))) Carla
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My husband recently passed away from glioblastoma multiforme, so I certainly hope that your tumor is not a glioma. The good news is that when you have an inoperable primary brain tumor your diagnosis is usually on the compassionate allownace list for social security dissability benefits, and your case is fast tracked. So the first thing I would do is apply for SSDI benefits. Have hope, and live life to the fullest. I don't know where you are located, but if you have the option of going to either the Mayo Clinic, Duke University, or The Huntsman Cancer Institute for treatment I'd do it. My husband saw a neuro oncologyst at the Huntsman, and we wouldn't have done anything differant with his treatment if we had gone to Duke. Talk to as many neuro oncologyst as possible about treatment options, and never, never give up hope!
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Good luck with the treatment anyway and

