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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NameElizabeth Wardlow
Date2009-11-14
Locationclick picture for more information
MessageYour video was inspiring, especially when so far I've felt despair and have found no hope out there in the world. I was diagnosed in hospital that have no neurologist on staff, and so I have a diagnosis but not health care. The specialists in my home town and surrounding area of Dallas will not even see me as I have no health insurance or income. What can a person do to help themselves?

Thank you for this website and the optimism I viewed on the video. smilie


NameJean Davis
Date2009-11-09
Locationclick picture for more information
MessageHiya. My first attemot at "chat-rooming" ... with SOME success!?! Regular emailer and www-trawler, but a chat-room novice! Wheelchair-reliant MS sufferer for 11 years now ... a mum, currently working part-time ... and keen to interface with local MS sufferers with a view to e-connecting and possibly face-to-face-social-connecting locally ... e.g. Sarah P in Scunthorpe (which I'm near) found on the Tysabri Diaries link. smilie


NameContrary Mary
Date2009-10-23
Locationclick picture for more information
MessageHi there,
Just introduced to your website through "Stu's news&views on MS". I'm 54, was diagnosed in 2005, & live in Florida. August & September's heat suck the life out of me, but now that October is here, the extreme humidity has subsided.
Been ready alot about Vitamin D & possible connection to MS.
Enjoyed your website, including the video! : smilie smilie smilie


NameJessica Howland
Date2009-10-12
Locationclick picture for more information
MessageAloha!
I'm on the island of Maui in Hawai'i. I found your site by following a few links, and will have to check out your Facebook page. Too bad I can't afford to pay for your airfare here, that'd be great. Oh, well, thanks for doing what you do; the information here in the US can be very biased, even the national organizations have some strong biases (e.g. against medical marijuana or denying that people can die from MS). Keep up the good work! smilie


NameVita
Date2009-08-09
Locationclick picture for more information
MessageHi everybody! I'm Vita, I'm 20 and I have MS for 3 months. Actually my MS is not so hard for limitation of my live. But I wanna be ok forever and do something for my "ok", I mean I feed with Embry diet, try to be in regime and so on.
The most interestin for me in MS is Embry diet. I now a lot but not all the details.
Guys, I need this details like everybody of us!
So I'd like to connect with everybody about it)
Good luck, Vita smilie


NameJasmina Russell
Date2009-07-13
Locationclick picture for more information
MessageThankyou for all the information you provide. It's just recently been disclosed in the media here about the correlation between Vitamin D and MS. Interestingly enough, it's been suspected by scientists as long as 33 years ago.(!)
Having recently been diagnosed with Relapse-Remitting MS, being 32, just returned to work after having my first baby and pretty much knowing nothing about MS, I am very interested in the developments in medicine and science regarding MS. I hope the future (preferably in my time!) holds the secret to curing MS. Til then, I will take my needles and remain POSITIVE. smilie


NameJasmina Russell
Date2009-07-13
Locationclick picture for more information
MessageThankyou for all the information you provide. It's just recently been disclosed in the media here about the correlation between Vitamin D and MS. Interestingly enough, it's been suspected by scientists as long as 33 years ago.(!)
Having recently been diagnosed with Relapse-Remitting MS, being 32, just returned to work after having my first baby and pretty much knowing nothing about MS, I am very interested in the developments in medicine and science regarding MS. I hope the future (preferably in my time!) holds the secret to curing MS. Til then, I will take my needles and remain POSITIVE. smilie


NameLynda Lube
Date2009-06-24
Locationclick picture for more information
Messagesmilie It has been over 2years since I have changed my diet. I was diagnosed with MS in 1996 which included IBS, restless legs syndrome, unexplained hip/leg pain, debilitating fatigue. After following a diet free of my food sensitivities and known MS trigger foods I am symptom free. I also discovered that most of the trigger foods ie: diary, grains containing gluten, are processed foods which contain hidden processed glutamic acid or MSG. MSG, aspartame and other chemicals in processed foods are known brain excitotoxins which destroy brain cells. MSG is hidden in processed foods under other food labels such as any hydrolyzed protein,gelatin, yeast extract, calcium caseinate, carrageean, broths, any flavourings, many fermented products.
It is vital that people with MS and other neurological problems avoid hidden MSG or free processed glutamic acid


NameLauren
Date2009-06-05
Locationclick picture for more information
MessageHi
This is a great site smilie javascript:SetSmiley('%20smilie%20'smilie

I am 45yrs and have had multiple sclerosis for 29 years. Since I was 16. I can no longer walk, use a suprapubic catheter, get tired pretty quickly but all in all, am supremely grateful. I can no longer type but use Dragon NaturallySpeaking. There are so many losses with ms, but strangely enough there have been so many gains. Unbeknowns to me, my life has been predicated by ms. I was only diagnosed when I was 28. Lots of damage had been done. But in the 12 years I had been to university, got a couple of degrees. Lived overseas for four years on my own. I am not married and do not have children, which is my greatest sorrow. But take courage, all who might be newly diagnosed. Your treatment options are wide. The world of ms is changing.


NameJ
Date2009-06-01
Locationclick picture for more information
MessageFirst time here n excited 2 learn of a place where I can share my feelings n thoughts, ask questions n possibly have something 2 add or say 2 someone like me! Full of questions, fears,hopes,anxieties,uncertainties,couragesness and above all these (and ness) FAITH! I have M.S but thank God, MS doen't have me. It has certainly won a few (too many) battles with me but 4 sure, thanks 2 God, I AM THE VICTOR! I am planning 2 get stem cell therapy n I would be so gratefull 4 any advice, comments,thoughts n feedback in general. I am a 53 yr youmg woman, full of life n ideas whos legs cant (or wont)catch up with my brain! HELP PLEASE God bless n encourage you.


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