Welcome to the MSRC Guestbook.

We would welcome your comments about the site and the services of MSRC in general.  

Completing the location part of the guestbook will also enable us to see just how many countries MSRC is reaching.

Thank you for your time.

The MSRC 


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NameHans
Date2008-11-19
Locationclick picture for more information
MessageHello everyone,

Congratulations with the very nice website.
I have also multiple sclerosis [for twenty year]
and Iam on TYSABRI without any side effect.
The results are spectaculare.
read my story on: www.hmhanse.nl

smilie Hans.m.Hanse


Namemaurice sullivan
Date2008-11-10
Locationclick picture for more information
Messagemy wife was diagnosed in Nov. 2006, after bad falls she had the MRI scan which confimed she had 'it'. she was offered Avonex and steroids. we researched and found the swank site and now the MSRC site, she has stuck to the diet rigidly, never once giving in, in may of this year her neuro said he was so pleased with her he did not want to seen her again. she has had no relapses for 2 years, not one day off sick, goes to work in london is out 11 hours per day and we have normality, please anyone who reads this DO THE DIET, and take the vitamins, she is on no meds. THANKYOU ALWAYS DR EMBRY..maurice


NameDennise R
Date2008-10-23
Locationclick picture for more information
MessageYour site was very informative! I've had MS for 26+ yrs - most of my adult/married life. I found out that a problem I've been having & thought was just needing a new glasses prescription/getting older, when now I'm wondering if it is optic neutitis (yet again) just with a different 'flavor' of symptoms. I was actually a bit relieved that maybe I could put a name to the changes in my vision that I'd been battling! I do needlework, photography, and music, so my eyes are crucial to all of those. I cherish being able to still do the things I love, with a few modifications, & I'd hate to loose what I do still have. I really enjoyed your site & found it easy to use & very informative. Thank you!! I hope you'll be able to continue it for a long time. I've bookmarked it so I can find it again whenever I need to.


NameBelinda
Date2008-10-23
Locationclick picture for more information
Messagesmilie
I am so glad I stumbled on this resourceful site. I am a fifty year old women who was only diagnosed one an a half years ago. Thanks so much for such useful information.


NameTony
Date2008-10-22
Locationclick picture for more information
Messagesmilie smilie smilie Hi all,
What a great web site I have had M.S.for
15 yrs and it is only with sites like this that
we can realise that we are not alone. I have
recently moved home to Cumbria and have joined
the local M.S.group in Whitehaven I have never
been made so welcome and they are a great bunch.
If you have never attended your local group
meetings please give it a try I am sure you will
be most impressed and try to remember that the
glass is always half full.
Tony.


NameTony
Date2008-10-22
Locationclick picture for more information
MessageHi all,
What a great web site I have had M.S.for
15 yrs and it is only with sites like this that
we can realise that we are not alone. I have
recently moved home to Cumbria and have joined
the local M.S.group in Whitehaven I have never
been made so welcome and they are a great bunch.
If you have never attended your local group
meetings please give it a try I am sure you will
be most impressed and try to remember that the
glass is always half full.
Tony.


NameKaz Overton-Smith
Date2008-10-18
Locationclick picture for more information
MessageHi,

Just been browsing through the site & am very impressed. I was diagnosed with Secondary Progressive back in 2005, (eventually after about 3 years of Doctors telling me they didn't know what was wrong with me - I am sure most of you have had similar experiences!)Whilst I have I have learnt to deal with the limitations that MS brings, my husband has found it very hard to accept/understand. Has anyone got any advice on how I can help him to accept the 'new' me?

Kaz - Southampton, Hampshire - UK smilie


NameTony Rooney
Date2008-10-14
Locationclick picture for more information
MessageThe Tysabri Diaries of fellow MS sufferers, I find, are truly courageous & extremly helpful. My point is, I'm not alone in this! I'd love to be able to give a hug to the ladies & have a beer with the blokes. The many Diary entries have truly moved me to tears - the braveness & guts of you all is truly outstanding.
Keep well everyone & good luck to all.
- Tony Rooney, Melbourne / Australia


Namejamie stirzaker
Date2008-10-12
Locationclick picture for more information
MessageHello, and congratulations on a site that remembers sufferers are still humans!!

I was diagnosed with MS this last week (October 2008) and after a little bit of blind panic, now is the time to take stock and work out the hows and whys that i have to implement, and how to change things without my children seeing too much difference, a challenge!!

However with the help of sites like this it will be sorted!!!

smilie


NameDenny Jo
Date2008-10-07
Locationclick picture for more information
MessageA big HELLO from Utah USA. My father died from complications of MS. My oldest son has MS, he is a patient advocate and travels everywhere speaking about MS.


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