I know that I have been affected  by the loss of my dear friend, and hope
that I haven't offended  anyone.  I love you all so much and could not live
my life without  any one of you.  Each of you have made a difference to me
and helped  me through the times I was in the hospital and when I broke my
legs.   You will never know how I feel about each and every
one of you.

Pam was not the only friend I have  here on the List...that is for sure.  I
love all of you and I mean  that with all of my heart.

Maybe it might not seem like it,  but it is true...From the bottom of my
heart,

FTBOMH,
Judy


In a message dated 6/17/2009 10:01:02 P.M. Eastern Daylight Time,
[email protected] writes:


I  HAVE ALWAYS FELT VERY WELCOME BY EVERYONE ON THIS SITE, EVEN THOUGH  I
DO NOT SUFFER FROM SO MANY OF THE PAIN AND SUFFERING SO MANY OF  YOU DO.  I
DO HAVE PAIN BUT NOTHING I CAN’T LIVE WITH SINCE I HAVE  NO CHOICE.  IT IS
THE COMMUNICATION WITH ALL OF YOU THAT HAS HELPED  ME SO VERY MUCH.  I WANT
TO SAY THANKS TO YOU ALL.  I MYSELF  HAVE FOUND THAT SINCE WE LOST PAM, I
HAVE BEEN DOWN IN THE DUMPS WHEN I  REALLY HAVE NO REASON TO BE.  I THINK A
LITTLE DEPRESSION HAS  SETTLED ON ALL OF US.  I KNOW IT HAS ME.  I FIND MYSELF
FEELING MORE SORRY FOR MYSELF THAN I HAVE IN A LONG TIME.  I MISS  MY DAILY
E-MAILS FROM PAM WITH HER FUNNY JOKES.  I THINK AS A  RESULT WE ARE ALL A
LITTLE TESTY WITH EACH OTHER.  I KNOW PAM WOULD  WANT US ALL TO GET ALONG.  I
HOPE THAT TIME WILL HEAL US ALL.   AT LEAST I SO HOPE SO.
BLESSINGS  TO ALL OF YOU.
***************TIAD**************   AND LET’S HOPE IT IS A BETTER ONE FOR
US ALL.
PATTI  - WISCONSIN

From: Jill Z  [mailto:[email protected]]
Sent: Wednesday, June 17,  2009 6:05 PM
To: [email protected]; [email protected];  [email protected]; Tracey
L. Black
Subject: RE: [TMIC]  Transverse Myelitis Network

Well said  Tracy!

Jill

---  On Wed, 6/17/09, Tracey L. Black  <[email protected]>  wrote:


From: Tracey  L. Black <[email protected]>
Subject: RE: [TMIC]  Transverse Myelitis Network
To: [email protected], [email protected]_ (mailto:[email protected])
,  [email protected]
Date: Wednesday, June 17, 2009, 1:14  PM


As a  caretaker/mother of a daughter who has had TM for 4 years now;  this
saddens me to read this. I am also a member of the one  Yahoo TM site b/c
for me it seems like it involves more children  than adults and I can identify
more with their issues. Since my  daughter was inflicted at the age of 11
and is now 15 ½, I get  lots of answers from the other site but also stay on
this one                 b/c I want to know what the future may hold for my
daughter as  an adult. I know that we&  ALL have been saddened by the
passing of Pam but this should not be a time to bicker and a  time for people to
quit the site b/c they feel as though they  are traitors for checking out
another site. There have been  numerous times that I have tried to unsubscribe
and for some  reason, it never works. Maybe I am supposed to stay on this
site  for another reason. I know I don’t write very much and maybe  this
email will just be taken with a grain of salt. Fortunately,  my daughter seems
to have a much lighter case of TM than a lot  of others on this site. With
that in mind, I still continue to  read everyone’s emails b/c they make me
feel so much more  blessed that my daughter didn’t get inflicted as badly as
others  although she does deal with one or two of the symptoms. I can’t
imagine what most of you feel on a daily basis with the pain,  fatigue, banding,
sweats, cold feelings etc. My daughter hasn’t  had any pain, other than at
onset, and that was more of the  tingling than anything. She is the typical
15 year old and  walks, with assistance through high school every day (except
for  now b/c school is over) and she still hangs out with her  friends, she
helps me around the house and she even babysits the  4 year old and 1 year
old boys next door. She was confined to  her wheelchair at one time but
thanks to Dr. Kerr for helping us  get into the Kennedy Krieger Institute for
Spinal Cord Injuries,  she has been walking for about 2 years. Time has flown
by over  the last 4 years that it is hard to remember life before TM. I 
hope that everyone continues to stay on this site b/c it is full  of great
information and great people that are willing to answer  any question that is
ever asked. No one judges anyone for asking  questions.
As Pam would say  !!!!!!!!!!!!!!!!!!TIAD!!!!!!!!!!!!!!!!!!!!!!!

Tracey  L. Black
Certified  Insurance Service Representative
Hockley  & O'Donnell Insurance Agency
Phone-  717-334-6741, x 29
Fax-717-334-3414
My  hours:  9:00 a.m. - 5:00 p.m.
Thank  you for providing information to us. Please be aware that no
coverage is bound and no change to your insurance program is  confirmed until
verified by a licensed agent during regular  business hours. If you do not hear
from us within 1 business day,  please re-contact us in case your
information has not been  retained

From:  [email protected] [mailto:[email protected]]
Sent:  Wednesday, June 17, 2009 1:03 PM
To:  [email protected]; [email protected]
Subject: Re:  [TMIC] Transverse Myelitis Network

Jude,

First of all, I  never said I PREFER the paraplegic/quadriplegic site. I
said I  IDENTIFY more. I feel as though I offended you by saying this.  There
are issues and concerns of being a quad they are not  addressed in the TM
site and I would imagine it's because most  people on this site are not
quadriplegics. I go where I can find  the information that helps me. If I did 
not
want to be on this  site, I could simply delete it from my contacts. There
is nothing  holding me back. I have asked questions on here regarding
autonomic dysflexia, only to have no one respond. Because I later  found out 
that
it's a medical condition for quadriplegics, so I  went to the
paraplegic/quadriplegic site to get the answers I  needed. I'm sure Jim uses 
these sites,
HE CREATED THEM! Where is  his hostility?? He knew that there would be a
need for additional  information, and that's all it is, is additional
information.

I have been a member  of this site, since I came home from the hospital in
2006, but I  am always looking for any and all information that could be of
help to me (as I'm sure all of us would be). There are people that  use
this site that are also members on the Yahoo Transverse  Myelitis site. Should
they just pick one or the  other.

I have met many  people through this site, one who has become my best
friend who  has TM. I would not trade that for anything, but your e-mail makes
me feel as though I am unwelcomed or a traitor of sorts. This  brings me to
tears. As I have poured my heart out on this site  (reluctant to make my
personal problems public), but felt  comfortable enough to share with others who
are, also suffering  with relationship problems, pain and depression. That
won't happen  again.



-----Original Message-----
From:  [email protected]
To: [email protected]
Sent: Wed, Jun  17, 2009 4:26 am
Subject: Re: [TMIC] Transverse Myelitis  Network



Then  what is holding you back?  Why don't you simply quit  this site and
use the other one that you say you  prefer?  What's the big  deal?




Jude




In  a message dated 6/15/2009 2:11:29 P.M. Eastern Daylight  Time,
[email protected]_ 
(http://us.mc343.mail.yahoo.com/mc/[email protected])
  writes:



I  am also a member of the paraplegic/quadriplegic website  that Jim has
started. Although I have TM, which left me a  quadriplegic, I identify more
with the members of the  paraplegic quadriplegic site then with the members of
the  TM site.




Naomi
C-4  Quadriplegic, since July 2, 2005
Due to Transverse  Myelitis




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