Re: [MOL] so many questions... [01082] Medicine On Line

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Re: [MOL] so many questions...


	Welcome to the greatest forum there ever was from me, a new member,
also.  I've been on a week, although it seems like forever and that I've
known these people forever.  I'm sure someone will get something to you
that will lead you in the right direction to answer your questions.  You
are right in that we are a faith-oriented group with a strong belief in
God and all that He can do for you.  While we try to help ourselves and
make use of what's out there, medically, we all accept that His Will is
always done.

	May I suggest that you, personally, write-email-etc. MD Anderson, or go
on-line for info from a major clinic and perhaps you can glean
information or even a second opinion option.  While the "patient" needs
to be in charge of their own bodies, it never hurts to "offer" them
additional information.

	Also, I'm sure your doctors that you are using wouldn't mind your
inquiring as to where they were schooled, who they trained under, whether
they are in contact with an outside facility re your father's cancer
(especially since it's rare) and which facility it is.  It might ease
your mind.

	At any rate, we are pulling for you and hope to help in any way we can. 
I'm sure Miss Lillian will forward some "sites" for your research.  God

Carol in Memphis

On Fri, 11 Aug 2000 07:19:58 -0600 "Winn" <>
> This is my first morning as a member of MOL-cancer... seems to be a 
> wealth of knowledge out there, perhaps you can help us!
> My Dad, age 58, was diagnosed last week with nasopharyngeal 
> carcinoma.  As you all must be aware of the many tests that are 
> performed, we now know he is in stage III (T3N0).  How much your 
> life can change with only a phone call!  The American Cancer Society 
> states that only 0.25% of American with cancer have this type - 
> fairly uncommon.  Anyone have any information or know anyone with 
> this type of cancer?
> I just moved home from Houston, TX where the world renowned MD 
> Anderson is located.  Now we are in a small area in Colorado.   
> Dad's doc's seem wonderful and we are all crazy about them, but you 
> can't help but question if they could be as good as a large medical 
> center would be.  Dad doesn't seem to open to a second opinion.
> Treatment will begin next week and involve radiation 5x week, 7 
> weeks.  Chemo (cisplastin) every 21 days, then 3 months of 
> cisplastin and 5FU.  
> We are trying to educate ourselves as much as possible.  Any 
> information you have or anything you wish to share is greatly 
> appreciated.  We are a family of FAITH and so many of you appear to 
> lean on Him for your support -  Thank you.
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