livingwithms

Our MS Space
Living with MS Stories, Poems, Struggles, etc...
Living with MS

My name is Gina and I am from
Alaska.
I was diagnosed December 31,
2007 with RRMS. I have been
having problems with my knee
giving out and know that a Cane
might help me in the near future. I
was kind of reluctant because I am
only 31, until I saw your wonderful
creations. I Googled canes and
found your site. I know when the
time comes I will for sure order
from you!!!
Thank you for being so PRO
ACTIVE!!!! I found wonderful
support on MSWORLD.ORG and
have received lot's of information.
Until then take care and thank
you! Gina
Anchorage, Alaska
Betaseron, 1/1/08

Hello, My name is Rita,

I am 57 years old, married 39 years,
have one daughter that is 35 and I
was diagnosed with MS in October
of 1979.

I do well other then I use a
wheelchair. I am STILL Me I am just
a lot slower and shorter..haha....
anyway, here is a picture of me.

We live in Ohio and we are AVID
Ohio State football fans.

Lets get the word out, we need a
cure...:)...I take daily injections of
Copaxone, have a Baclofen pump
for spasms.

Lets beat this Monster.:)

Thanks,
Rita

Hi
My name is Michelle Pelleteir i live
in the small town of Mexico, Maine.
I was diagnoised with MS last Feb.
i have been having symptoms for 4
years before i was diagnoised. i am
the mother of 4 great kids. i to feel
left behind do to this illness. i am
so tired all the time. I am glad that
my Husband is so supportive. he
realy got more then he bargined
for. i think that the hardest thing is
being 30 and on my bad days i feel
like i am 60.
I am lucky i have found a job that
they are very understanding. i
work as a team leader for a socail
services company. we work with a
wide varity of people.i love it, i
love helping people but i find that
i never take the time to help me. i
guess it is if i don't address it then
it is not there. i know that this is
denial but sometime i can't get out
of the poor me thing and i hate
that. anyway thanks for the small
chance to vent...lol not to many
people want to hear it you know. i
always say i have the disorder no
one believes because you can't
always see the sffects.