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Just had MRI - what will happen now?
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From:
![]() ![]() liltrubin
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Dear Maz:
Hello! It sounds like you are on your way to getting better. Which is
awesome-:) One thing that I have learned is that when we are in it and feeling
so awful we do not understand why docs do not get 'aggressive' and just replace
what is depleted. Does not make sense-:) I have found replacement can take a
while to start feeling the effects and more is not always better but it is your
illness, your symptoms and you are the one not functioning!!! I want you to know
I have been there, heard the same things and I am happy worth my current
progress after several years of treatment but it took awhile.
I did do Testosterone and I swear by it for women. I was never so happy as
when I was on it (so was my husband). You can approach the subject by asking the
endo if he would be willing to try a very low dose and what harm it would do
just to try it. If it were his drive that was gone you bet he would be on it-:)
A lot of tumors do not show up on MRI's. Just because they cannot see it
does not mean it is not there and they symptoms are all in your head. You may or
may not have one and either way it may not effect your treatment. For myself, I
am not operable so my treatment would not change even if the tumor was not
there.
What I can tell you and you will not believe it right now but I promise
you, you will have points when you do feel better. It is up hill (with a few
slides down ever now and again) from here. I never thought I would be feeling
better. I wanted everything replaced. I was such a mess, like you just
functioning was impossible and I am doing so much better even with a tumor in my
head. I wish you could see the difference in me for yourself. I know I will have
bad times again but it is so worth the fight to get better.
HUGS!!!!
Tina |
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- Re: Just had MRI - what will happen now? liltrubin
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