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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Namelynn mcdonough
Date2012-05-17
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Messagevery good site,will visit again.
do you need any volunteers?
I have had relapsing remitting ms for
30 years,


NameShirley Tucker
Date2012-05-01
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MessageHi
This my second visit to your site and both visits I have found very valuable information, in particular information pertaining to MS in African Americans and other people of color.
I have R/R MS and I was d'x in 1996.I have had my share of relasps, the most severe just this past April.Even though at my age it is thought that MS has pretty much smoothed out in regards to relasps, my issues in April really don't bear that out.
I love your site, it is indeed very user friendly, and it also provides great information.
Thanks MSRC smilie


NameLynn Weaver
Date2012-04-30
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MessageJust discovered your website. Have had Primary Progressive since 2002. Found the website most informative. A real good resource. Thank you


NameTenesia Sargent
Date2012-04-26
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MessageI was diagnosed in 2007 with Relapsing MS. I found this site very informative and user friendly.


NameMichelle D
Date2012-04-19
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MessageThank you for the great information regarding BG-12. As an MS patient with a fear of needles it has been extremely hard for me to accept the fact that at this point I had no other choice but to have injections. I am doing ok on them but still would rather have something that is not invasive. Although I am aware that there is another pill form that can be taken my insurance denied the approval because of the side effects and tests that had to be done before I could even start. I am also not comfortable knowing that there were some noewly reported deaths. But I am excited about BG-12 and so is my neurologist. I can't wait. smilie smilie


NameAngie Garza
Date2012-04-05
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Messagesmilie My daughter Emily was diagnosed with MS 2 years ago after a long battle of many different diagnoses. From Transverse Myelitis to ADEM to MS and shortly after she permanetly lost her vision in her right eye. She just turned 9 years old on Veterans Day this year. She is the strongest person I know. Thank you for this website. This information in it is priceless!



Private Message added 2012-04-04


Namekathy tompkin
Date2012-03-12
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MessageJust found the site


NameMatthew (herbie) Roberts
Date2012-03-05
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MessageI've haad MS Relapse Remiting for appox 11 years. And since 2008 I've not been working. And I've found this article on CAF most interesting smilie


Nameamanda alexander
Date2012-02-27
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Messageforgot to mention
my Mom and generations before her, were born in Nuneaton, is there any one from that area?


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