The Multiple Sclerosis Resource Centre

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

Name	Shirley Renshaw
Date	2010-04-09
Location
Message	Hello from across the pond! This site is great! You need info you can get it here!

Name	Michael Sacco
Date	2010-03-10
Location
Message	Hello all. Writing from Chicago where there is no shortage of doctors and research on MS. I have been living with this for 22 years. I'm blessed that another MSer told me that early on--fight and learn to live the best you can. I still work, I still walk a bit, but not the 3-5 miles a day I used to. If I do 200 feet I feel its a victory...I take Copaxone and have had 2 infusions of novantrone. I use 4 AP to help with walking when I have it. It helps a little. My balance is crappy, so I sometimes use a cane... I am secondary-progressive, so the drama of a relapse is something I haven't had for 8 years and my docs say not to expect...Just saying hi and encouraging people to not let the beast defeat you. MS won't kill you (so they say), so learn to live the best lives we can! Love, pray laugh, help, work, care, touch, cry, share, fight injustice, sing, read, teach and love some more! Peace, Michael

Name	Joanna
Date	2010-02-26
Location
Message	I think the website is very good. I still feel however, that MS and other disabilities need far more exposure. I have therefore added to my site, an area for "Disabled Parents" to join in discussions and add their thoughts. We welcome people from across the globe. www.fullnappy.co.uk Jo

Name	dot
Date	2010-02-10
Location
Message	dx 99...most of the time I tolerate it. sometimes it fights me..

Name	Jeannie Lambert
Date	2010-02-05
Location
Message	Thank you for giving us this site! I will be back soon.

Name	Georgiana
Date	2010-02-05
Location
Message	Hi to everyone im Georgiana from Romania,just find about this site and im very happy about it.My brother has MS for 17 years now and he tried every single treatment in the world;i can see that there is some hope with the LDN treatment i will be very happy to hear any opinions if you try and how does it works and maybe my brother will have more strenght to walk.Lately he is really bad, i want him to be better for his family and daughter......but i think these things kept him alive and with the power to survive.He is only 37 years old i really need him next to me......hope for the best

Name	Helen
Date	2010-01-22
Location
Message	At last, a place to natter about MS. Have been afflicted for 14yrs (PPMS) plus Type1 diabetes (45yrs),a diabolical mix. Anyone else with the same combination? Any tips please?. Must be among the oldest-----will be 72yrs in March. As so far pain is rare, I'm able to cope most days---some days are very GRIM. I read a lot for escapism which works well for me, also listening to music---well loved pieces of light classcs nothing too heavy it doesn;t lift my spirits enough. Shall be pleased to read any comments. Keep smiling!

Name	Elizabeth Haran Caplan
Date	2009-12-08
Location
Message	Greetings all, this is a well conceived site, highly accessible, informative, balanced and user friendly. Further it does not depress me to read through it, very solution, self determined wellness oriented. Very nice. Thank you. My one request: please make the verification a bit darker! Best wishes all.

Name	Martin Scott
Date	2009-12-03
Location
Message	Your site is great as is your new video. To Elizabeth Wardlow and anyone else needing MS help in the US, try contacting National Multiple Sclerosis Society 900 South Broadway Street Second Floor Denver, CO 80203 The National Multiple Sclerosis Society is a source of information about multiple sclerosis. You can reach your local chapter in the U.S. by calling 1-800-FIGHT-MS (1-800-344-4867). www.nationalmssociety.org as it is a great resource for additional information. There is also MSAA Multiple Sclerosis Association of America National Headquarters 706 Haddonfield Road, Cherry Hill, NJ 08002 Telephone (856) 488-4500 \| Fax (856) 661-9797 \| Toll Free (800) 532-7667 E-mail msaa@msassociation.org There is also MSLifelines whose contact info I don't have. I know what a pain it is to have no support and I do hope this helps you.

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