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 | 2004-08-09 |
| Location |  |
| Message | good site with very useful information for ms sufferers and carers.  |
Private Message added 2004-08-07 |
| Date | 2004-08-03 |
| Location |  |
| Message | A MESSAGE FOR NICK MILLS Hi Nick Unfortunately we have no way of getting hold of you via the guest book - could you perhaps e mail us at info@msrc.co.uk with your phone number or your e mail address so we can contact you and see how we can hopefully help and support you? Alternatively,give us a ring on 0800 783 0518(press 2) or 01206 505444. Take care and we look forward to hearing from you Rachel |
| Date | 2004-08-02 |
| Location | |
| Message | Some advice please! Where can I get some info on how to deal with the tiredness, working for myself and dealing with family, especially children, with love and understanding. Thankyou! Nick Mills |
| Date | 2004-07-27 |
| Location |  |
| Message | I am a rehabilitation counselor for the state of West Virginia, USA. I am seeking information on a place to purchase a cooling vest for a consumer with my agency. We are well into our summer season here and our temperatures are 80-90 degrees F. The garment I seek presumably helps to protect a person with MS from the adverse effects of high heat and humidity. Can anyoune help me, please? |
| Date | 2004-07-19 |
| Location | |
| Message |  Well i was diagnosed back in '96 & to be truthful & honest i'm not at all bothered about this disease as i treat this as a life challenge.  I started out as RR but come 2000 they told me it had moved house to SPMS. Again, i'm not that bothered about it- ok i may look drunk & disorderly but thats funny to me, it says a lot about those who are some what bemused by my drunken state but {me} who can be more articulate & communicative then those people. I'm a guy yeah, but hate- no not hate as that is a to strong a term to use- dislike people who just cant be bothered speaking without swearing. So who are the more intelligent people here? I think we are. Listen yeah, i thought {how stupid was i} that the MS Society were god as well as the back office crew neurologists & MS nurses. But having witnessed their financial affairs~ listen its £27 million year on year but only 20% of that income comes or goes anywhere near us. I could carry on but i wont bore you. I dont understand girls liking boys, as i dont know one good looking guy DO YOU. So i suppose i'm a lesbian as girls sail my ship every time but their to beautiful to come near me. Dont cry its a laugh trying like. Always look on the bright side of life... Ambition? Is all about dreaming, the dreamer who dreamt of the wheel succeeded in turning that dream into reality. If we care to dream of a far better life this reality will happen too. Picture the dream, the dream will happen~ reality will take place. {{{{Welcome to your new world.}}}} If your not living on the edge, your not living.  |
| Date | 2004-07-17 |
| Location | |
| Message | Hello to all from a wet yorkshire in the uk,i am a carer my partner is called diane who is at this moment at woodlands york(respite) i think a welcome break for both of us.Diane was diagnosed with ms in 1986 and unfortunately now has to remain in bed but with all the difficuties we still have a good laugh together and god bless the talking books |
| Date | 2004-07-17 |
| Location | |
| Message | I have been a subscriber to Pathways for almost 10yrs now and I am so glad I found you guys. You offer hope and good advice. I am married to Terry and we will become grandparents for the first time next February, I`m not old and wrinkly. We are so looking forward to it. We are both members of The LDN Campaign Team and are working hard to get LDN recognised as a treatment for MS. We live in Irvine on the West Coast of Bonnie Scotland. I have had MS for 15yrs and am still fighting it every step of the way.  |
| Date | 2004-07-17 |
| Location | |
| Message | Thank you for your message Sue. Go for it! Yours Lawrence and all at MSRC.  |
Private Message added 2004-07-16 |
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