MIKE AND JILL:

 

I HAVE PUT YOU IN MY PRAYER BASKET AND WILL INCLUDE YOU IN MY PRAYERS.  IT
IS THE LOVE OF OUR FAMILY AND FRIENDS THAT GIVES US THE STRENGTH TO GO ON.
PLEASE KEEP US INFORMED.

 

PATTI - WISCONSIN

 

From: Jill Hammond [mailto:3jmhamm...@clearwire.net] 
Sent: Thursday, September 03, 2009 6:40 PM
To: tmic-list@eskimo.com
Subject: [TMIC] Update on Mike

 

Well, everyone, here is your first update.  Before I begin, however, I would
like to thank all of you who have kept me and my family in your prayers, it
means a lot.  Don't stop, though, as the  next 7 weeks or so are going to be
a little rough.  I especially want to thank my family, without their help
and support; I cannot imagine where I would be.

 

For those that like to be very specific, I found out I do not have what I
told you last time.  What I have is a tumor in the Maxillary Sinus.  This
tumor is a Neuro-endocrine type (small cell) of cancer.   There, that should
make it clear as mud.  

 

Went in yesterday to the Chemo doc, and when he heard that we had to wait
until next Thursday for our radiation Doc appointment, left the room, came
back and told us as soon as we were through with him, we could go downstairs
and talk to the radiation doctor.  The right people and a little help from
above just cut off another 8 days of waiting.  I can start fighting back.  

 

Today I went in to the doctor's office and got fitted for my "Hannibal
Lector" mask.  This mask ensures that you do not move your head at all while
receiving radiation. Radiation for this is received from a Tomography
machine which produces the rays electronically.  I will tell you that I
could not even open my eyes while wearing the mask.. Very claustrophobic, so
a little Xanac helped.  Now, I go back in for my very first radiation
treatment next Thursday.  During this 7 week, five day a week treatment, I
will receive at least 6,000 RAD (Radiation Absorbed Dose) to the cancer.
For those who are not aware, just let me say that 6,000 RAD is a LOT.
Unfortunately, my right optic nerve may receive much of this.  The optic
nerve begins to show damage at 4,500 RAD, So, I may loose some, or all,
vision in my right eye.  There are a lot of other little complications like
loss of salivary glands, loss of taste (Have that already), possible teeth
problems,  and hair loss (time for a Kojack shave).  

 

The Chemotherapy introduction session is tomorrow and I learn what I get,
when it will start, if I will need a port and lots of other questions I am
sure.  

 

So another update in a week or so.  Take care and be talking with you soon.


God bless us, everyone,

 Mike and Coach Jill.  

 

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