Anyone else have Mucoepidermoid carcenoma "MEC" as primary lung?
Hi, My name is Abe and im one of the new kids on the block..
im two weeks post op from a lobectomy and resection of my rt lung.. I know mucoepidermoid carcenoma is ultra rare as primary lung but im wondering if anyone else is a survivor of it?
Comments
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thanksdennycee said:Was hoping that someone would
Was hoping that someone would check in. Perhaps you could contact other patients through the website at cancergrace.org
i think im asking for too much with under 200 documented cases... ill just keep reading and also visit the other site everyone seems to talk about.
Thanks!
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AdviceFreightTrain said:thanks
i think im asking for too much with under 200 documented cases... ill just keep reading and also visit the other site everyone seems to talk about.
Thanks!
Take the advice and ask all the questions ( one at a time of course) over at cancergrace.org , they have a cancer Dr that answers your question , so it is not someone guessing an answer and it is FREE, so ask till you truly understand the answer you get , Dennycee told me to go there and I am very happy I did !!! Let us all know what you learn as this is a journey that we can all learn from each other !! Sending WARM AND POSITIVE THOUGHTS YOUR WAY , MAY YOU GET THE ANSWERS YOU NEED!!! HUGS
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