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 | 2011-07-23 |
| Location |  |
| Message | Hi all. just passing through and signing the book  Love the website, its very informative. For the record, i am a partner/carer for my partner Jennifer who has RRMS..  |
| Date | 2011-07-16 |
| Location |  |
| Message | We are from Sri lanka and wish to know whether you wish to voluntarily give your ideas to set up one of the following activity in your country initially limiting to targeted area or consult to us 1.to deliver wholesome tropical vegetarian lunch for aged unable to move or indepedenlty living aged persons 2.to provide meals free of charge for bereavement families at least for 5 days as prevailing tradition in sir lanka and other support as far as can The said activity will benefit such persons in sri lanka too The above services to be provided by the income generating from mobiles sales in counties by disadvantaged persons 3. to provide accommodation and meals and medical care free of charge at monastries for those who are interested in study and practice of meditation and with a visit to places of archaeological interest. The participant will have to bear only the cost of air ticket to sir lank and inbound travel cost only We wish to know ideas from you , and you may even assist us in setting up the above even by ideas at least Thanking you if you have any interest in this proposal pals email to exchange ideas further Thanking you Ernest Tele 0094112896400 Mobile 0094712329449 Email [email protected] |
| Date | 2011-07-11 |
| Location |  |
| Message | I am a 72 year old female with MS for more than 30 years. I live in U.S. I've recently started hyperbaric oxygen therapy. I've had 11 sessions. I'm trying to find anyone with MS who has experience with HBOT and to learn of their results. So far I have not seen any change. I am hopeful for change in the area of mobility. I appreciate any response. Sincerely, Lynn Wolf |
| Date | 2011-06-28 |
| Location | |
| Message | Hi, I have had progressively bad MS for over 15 years while I lost balance, appetite, energy, strength, coordination, and so many body functions, I no longer was the one who could say, "I have MS, MS doesn't have me." I have tried it all to the point of humiliation, and now we find out it's a cut off vien in our neck?!!! I lost a lot but didn't lose my big smile and we all need smiles... CCSVI is what is hurting us. I wish us all healing and blessings now with the rest of our physical lives. With love always, me  |
Private Message added 2011-06-02 |
| Date | 2011-05-28 |
| Location |  |
| Message | Hi. I'm 36 and would love to chat/moan about anything and everything. I live in Aberdeen with my husband and 6 year old son. I was a chartered account but I feel I am even streching the truth saying I am a accountant now. Please just say hi. |
| Date | 2011-04-27 |
| Location | |
| Message | hi im corinne,i have had ms for 11years,i try to read as much as i can bout ms and treatments,the stem-cells and ccvi etc,it affects mainly my balance so standing and walking i cant do for long now,i have a walker sticks not much good now i look more drunk and trip lol,scooter for shops and a wheelchair when legs very bad,and have not alot of feeling in my finger tips,so buttons,zips paper,money etc hard to pick up etc,i used to love danceing but legs dont go with the music lol,swiming i do now and again as legs like jelly and need to sit fast for bout 20mins,like us all we have odd good days and alot of bad days hey?and i admit?i do cry easy at times,emotional at films or cry for no reason like round shops for 10 mins about,then im ok again,feet are always cold and cant feel my left side alot at times too,wow this as got abit long lol,sorry,my families great,i have a partner over 2years now,hes great too he understands me and ms,and me him has hes a dieabetic,spelt wrong i know,i do get trouble with spelling and sometimes talking,well?thats a long read hey?take care everyone,and lets try not to let it beat us without a fight |
| Date | 2011-04-04 |
| Location | |
| Message | HI All,My name is Tracy and ihave M.S. I was miss diga.for at least the first 7 yrs.&I then got pretty bad after my daughtjer was born Nov.1999&after alot of doctors and tests we found out that i have M.S. I can no longer work since 2005&on S.S.D. I am married to a wonderful person he has stood by me threw everything To make along stroy short i live by a saying I HAVE M.S.But M.S Doesnt Have ME!!! I push thru everyday and my husband&daughther help me stay strong. I wish everyone good blessing in their journay with MS&Stay strong!Trust me i have good days &bad days but we all know thats MS.I am now starting to losse my vision and the leftside of my body is going downhill but hey i take it day by day.. Thank you all for reading&Hang in there i have been fighting for almost 11yrs ¬ stopping anytime  !!!Thank You&Have a great day, Tracy Maynard    |
| Date | 2011-04-03 |
| Location |  |
| Message | Hi, Following Andies very recent diagnosis we were and still are very new to this, needless to say very uninformed and uneducated on M.S. Despite being advised by lots of people "Whatever you do don't go on the internet looking" we decided to anyway!! On finding this site all we can say is we are pleased we had a look. There is so much positivity and advice from people with M.S. and also practical and medical information from the resource centre. Thank you all and i am sure we will be regular visitors. |
| Date | 2011-04-03 |
| Location | |
| Message | Hi again everyone, I posted a message today regarding hyperbaric oxygen and L.D.N. treatments for M.S. If anyone would like to contact me and chat about those treatments or M.S. in general my e-mail address is: [email protected] Take care x |
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