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
Sign Guestbook Back to The Multiple Sclerosis Resource Centre
| Date | 2004-06-08 |
| Location |  |
| Message | Life generally tests us, but when one is tested by being asked to cope with the extra burden of M.S. it becomes difficult. Stay positive - have something to look forward to each day - no matter how small or seemingly unimportant it is to others. Learn to realise your limitations, but do not give up.  |
| Date | 2004-06-06 |
| Location | |
| Message | I live in Chesterfield, Derbyshire. I have SPMS. I find the MSRC extremely helpful and supportive |
| Date | 2004-06-03 |
| Location | |
| Message | Hello Nice People I have just discovered your site and can't wait to explore more. I have secondary progressive MS, but have made considerable progress and improvement by modifying my diet. I now want to take things further (blood tests etc) - and am completely convinced that there is a solution out there for every one of us. I heard about Stephanie Sang's achievement and was inspired. Best wishes Dee |
| Date | 2004-06-02 |
| Location |  |
| Message | I am a 31 year old male who is currently going through the drawn out process of diagnosis. MSRC has / is providing me with invaluable information and sometimes a bit of a reality check. I am married and have a four year old son and life can be pretty hectic, just being able to log on here for a quiet ten minutes and learn things, get strength from others and sometimes laugh is just wonderful. Many thanks  |
| Date | 2004-06-01 |
| Location | |
| Message | Greetings from the Yorkshire land. It's a privilage and an honour for me to be involved with MSRC. Although I don't have MS I take great pride in learning more about it each day. The MSRC office is just one BIG hype of activity,, no one has one particular job.Everybody mucks in and gets on with it,,,wether it's making the coffee or answering a counselling call,,I don't know how they do it. Without them MSRC would not be here. I salute everyone of you,,,,and give you my FULL respect. Keep the Faith Skinny Legs  |
| Date | 2004-05-31 |
| Location | |
| Message | i;ve been living in linboland with possible ms for some years. Having explored many avenues with a postive approach the msrc has everything i have looked at and more. Its postive approach gives help and support with so much help and information. The mag and website are brill. As the motto says home of the free.Its important to me as there's still a negative attitude out there but here eveyone supports one another and a postive approach is number one! |
| Date | 2004-05-30 |
| Location | |
| Message | Hi, My name is Pam, I am 48 and I have been married to my wonderful supportive husband for nearly 26 yrs. We have 3 children, all in their 20’s,and we live in West Yorkshire. I trained as a nurse nearly 30 yrs ago and worked in nursing for about 20yrs. With hindsight I have had MS for approx.17yrs but it “kicked” me in a big way in 2000 and I was diagnosed in 2001. I spent a year “surfing” the internet looking at anything I could find about MS and then eventually came across this site in 2002 ……and I haven’t really bothered with any other sites since. This site has EVERYTHING!!! It is definitely the most informative, friendly, unbiased, supportive site I have found …..and, as I said, it has everything you could ever need all on one site. Keep up the good work MSRC and a big thankyou to everyone.  Pam (spam) |
| Date | 2004-05-30 |
| Location | |
| Message | Hello, I am one of the older members of the MSRC, having started life 61 years ago on the East coast of Yorkshire. I gradually moved South and have lived in Winchester for 32 years. Despite spending two thirds of my life playing various sports in my spare time, I now spend all day in an electric wheelchair, due to PPMS. My wife of 38 years, who is now my carer, has been my best friend for 41 years. When my MS was confirmed in 1991, the Neurologist suggested that I picked up a brochure about the MS Society as I left his office, and I have been a national member ever since. It was only in 2003 that I stumbled over the MSRC. It was a breath of fresh air! As soon as you use the Message Board, you can’t help being impressed by the friendliness and supportiveness of the members. It is like being in an enlarged family of friends, and in my experience you learn far more from other members than you ever learn from your doctor or Neurologist. The MSRC publishes a bi-monthly magazine, New Pathways, which I saw described recently by a reader as the best MS magazine in the world, and I don’t doubt this for one minute. It now has a distribution list of around 6000, and is mailed across the world. Finally, I must pay tribute to the small group of people who allow MSRC to function. Under the CEO, Lawrence Wood, the staff perform weekly miracles to support a very large web site, a 24 Hour Telephone Counselling Service, a busy email operation, and a free phone service. |
| Date | 2004-05-29 |
| Location | |
| Message | Hi All You really are the wonderous group of people anyone in the world could wish to know. The MSRC rocks! All new people visiting this guest book, come on over to the Message board and get a very worm welcome for the crew :O) I love you all :O) squiffs :O) |
| Date | 2004-05-29 |
| Location | |
| Message | Where would we be without the MSRC? The MSRC gets on with the all important job of helping people with MS to help themselves. They are a bunch of crazy workaholics!!! They do so much with so little finance. And why because they have a vision! I know all about living well with MS nowadays, having lived badly without before I discovered the power of self-help info, and the all important positive attitude which follows. I still have ms but I no longer live my life in fear of it! The MSRC stand for everything I live and breath for. What am amazing webpage and magazine, New Pathways. Knowledge is power in this game and the MSRC are ensuring that we get access to the information we need and all the help we could ever need. Long live MSRC...and if anyone has any contacts which can help raise their profile or boost their financial position please get in touch, a life-line to so many, their work must go on... Sylvie x http://www.lifeafterms.com        |
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