Re: [MOL] tongue cancer/radiation [08451] Medicine On Line


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Re: [MOL] tongue cancer/radiation



Dear Friends:  Sally and Charlie on this line will best be able to speak
with you with first hand experience and information.  Please keep checking;
as I know Sally will respond to you query.  Most Sincerely, Lillian
-----Original Message-----
From: Patricia <pnpvanier@globalserve.net>
To: mol-cancer@lists.meds.com <mol-cancer@lists.meds.com>
Date: Friday, May 22, 1998 2:17 PM
Subject: [MOL] tongue cancer/radiation


>My DH has metastatic tongue cancer and did 7 weeks of radiation.
>He is feeling
>confused about the healing process from that point.  What is
>normal?  When can he
>reasonably expect to eat again (he's been on a feeding tube for 2
>months)?  He would like
>to hear from others who have been through this experience.  His
>cancer was in the throat
>part of his tongue (not an oral cancer).  It spread to the lymph
>nodes on both sides.
>INput appreciated!
>
>Patricia and Phil Vanier
>
>
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---- Begin included message ----

>
>Welcome to the mol-forum.  You will find lots of support here as well
>as great information and uplifting posts including some good jokes.
>
>I want to give you a short bio of some of the molers so you can
>put names and posts together.
>Lillian is our jewel, she answers every post and gives all good resources
>to find answers.  She is funny, sends lots of jokes that sometimes we
>have to censor. (just kidding )
>Marty & Barb are wonderful, Barb is a cancer survivor, Marty is the
>caregiver.  Now he has become all our caregivers, his posts are full
>of hope and positive ways to beat the cancering journey.
>John is a cancer survivor, who sends really bad jokes, but is warm
>and wonderful andyou can feel these great  qualities thru cyberworld..  He
is
>always there for you when you have a problem and we all love him.
>Charlie is on the cancering journey, we call it a rollercoaster ride, he
>is a singer and his wife Sally is the caregiver and some days it's so
>hard to watch someone you love go thru the battle, but Sally & CHarlie
>will make it thru this. We love them both, they are our inspiration to
>keep on going.
>Ron, another one on the cancering journey, is in the hospital, but we
>expect him home this week. He takes us on beautiful trips thru
>Manhattan and you almost think you're beside him.  He is also
>an inspiration to all of us.
>Carla gives us calm in the middle of the battle.  She always sees
>both sides of situation, passes on to us the peace and love she
>has found since starting the cancering journey. She is another
>survivor.
>Ross is going thru radiation right now and is a remarkable person.
>He loves nature and long walks.  He has a great sense of humor
>and shares lots of information with us.
>The caregivers are numerous, Cindy, Susan, Lori, and lots of
>others that I'm sure I've missed.
>Les is a newer member and he is a riot.  He will keep you laughing
>and that's so important, to be able to share sad as well as lighthearted
>banter.
>Betty, Ruth and Jeanne K are also on the cancering journey.  We
>are so lucky to have such wonderful people on the mol-forum.  JeanneK
>has lots of good information on herbs and vitimens that she shares with us.
There's Mel who gives allot of very important information.  Syvlia who has a
friend cancering and lends loving support to everyone on line.  Others
cancering are Corinne, Sylvia, Christine,Tina, Foisy, Mary Ann and so many
more wonderful people.  And ofcourse last but not least is me, Diana who's
brother is cancering.  I am known for my research work and sending important
updated information.
                                                        God Bless your
friend,
                                                                   Diana























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Welcome Ca..doc