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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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NameBecky West
Date2007-11-11
Locationclick picture for more information
MessageThis website is great! I was diagnosed with MS back in 1995 when I was 17 years old, and I was never given any hope of getting better. This is the first time I have ever had a chance to take control of my health. I have been on the diet for 111 days now, and I have never felt better!! I am anticipating full recoverysmilie Thank you, and I hope anyone reading this with MS finds encouragement and hope! smilie smilie smilie


NameRebbeca Going
Date2007-11-11
Locationclick picture for more information
MessageHey Everyone smilie

Just Wanna Say That The Firewalk Today Was Excellent, My Dad Was One Of The Firewalkers And Im Extremely Proud Of Him. Congratulations To Everyone Else That Did The Firewalk And All Those Who Helped. It Was A Joy To Be There. Hopefully In A Year Or So When I'm Old Enough I Can Do Something Like It smilie ... Or More Extreme smilie

Rebbeca
smilie


NameTheresa
Date2007-11-06
Locationclick picture for more information
MessageHi,

I see many things that MS nurses can do. I am an RN who is being worked up for MS and so far most tests and MRI are leaning toward that DX. The symptoms are going from annoying to troublsome. The jerk of my hand causes difficulty in typing and writing.

Well even if it something else, when all my body parts stop jumping around at will, I think that I will have more compassion for people with neuro. disorders...I have compassion now, but having the disease itself gives me a very new perspective.

Theresa


NameKimberly R.
Date2007-10-31
Locationclick picture for more information
Messagesmilie Hello Everyone! My name is Kimberly and I have had MS since 1978. I woke up one morning to excruciating pain in my legs and just could not stand up...or walk. Doctors did not have MRI's back then so they diagnosed me with Erythema Nodosum and Sarcoidosis. This was just the beginning. I was in a wheelchair for about 6 months or so and I gradually improved to normalcy.
In 1985 I had a C-section and a beautiful 9 pds 8 oz baby boy. Everything was fine. In 1995 I gave birth to another baby boy through C-section and he was 9pds and 7 ozs. Twelve days after this birth...I suddenly lost my vision, my ability to move and to respond to anyone or anything. VERY SCARY!!! Lots of testing done but no confirmation of a neurological deficit. I was there for 3 weeks and then sent home with a diagnosis of postpartum psyhcosis. And yet they stuck nitroglycerine tablets under my tounge every 3 to 4 hours. Go figure? So I had to endure learning speech and cognitive therapy all over again, cant go back to my job of 19 yrs cus I couldnt drive and wouldnt know how to get there. So relearning life was a challenge for me, my husband and children. Because MS mimic's strokes, and can paralize you in body and mind and then take your sight too. I was very fortunate...I survived a major relapse with every symptom possible.
To conclude my story...after several Doctor visits and several years, I finally was diagnosed with Secondary MS in 2001. I am a walking testimonial that we will survive! smilie


NameKathee Haigis
Date2007-10-27
Locationclick picture for more information
MessageThis is a very good site. I sent this site to all my family and friends so they could find out more about this disease with becoming overwhelmed or feeling like they were reading a medical book. It even helped me because it's down to earth terminology. Thanks so much!!!!!!!! smilie smilie


Namecora
Date2007-10-21
Locationclick picture for more information
Messagegreetings. just happen to slip into this web site and i think that it is great. wish we had something similiar in the us. the ms site in the usa is good but i like this one better. bonjour . smilie smilie smilie smilie


NameAlyson T
Date2007-10-15
Locationclick picture for more information
MessageHi,
I was dxed with ms in febuary 07,on copaxone march 07,and im happy to say no new lesions,and the old ones r gone!



Private Message added 2007-10-14


NameGlen
Date2007-10-04
MessageMS is rubbish but thanks for your news page !


NameLynda Lube
Date2007-10-04
Locationclick picture for more information
MessageI apologized to Mr. Embry in an email yesterday.
I was diagnosed with MS in 1996. Several MRI's to confirm this.
I did research back then and found articles regarding the Swank diet and I found an article Ashton wrote. I called him back in 1997 and listened to his enthusiasm and dismissed his claims.
You see, new symptoms started to invade my body, rashes, joint pain, etc. Neurological symptoms, numbing, tingling continued, BUT this rash started me on a journey.
I have shared my journey with friends, constantly sending them emails. Most thought I was nuts! Anyways, I thought I was developing arthritis, given the swollen, stiff hands. The rash was puzzling. I remember getting this same type of rash as a kid.
This rash forced me to wake up.
I started keeping a food journal (sept 19 1907)
Eureka,so I thought, I have Celiac disease and MS>
Gluten free diet since Sept 19/07
Neurological symptoms (restless legs,numbing, tingling, spasms were leaving my body)
Tests for Celiac disease can back Negative
WHY? The lab must have made a mistake.
Do you know a friend bought me the book, the 'Swank Diet' in 1997 and I returned it to the store
I will be 50 next March and I will be reborn by following the Best Bet Diet. smilie
ps I have just shared this with my 13 year old daughter, she had tears in her eyes. She will be following this diet,given her food allergies are identical to mine.


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