- Official Nonprofit
- 100 Actions
- $108,059 Raised
Credit Suisse MS Bike 2010 NYC
Hi All!
On Sunday, October 3rd, I'll be riding for the fourth consecutive time 66 miles around Manhattan and New Jersey in aid of the Multiple Sclerosis Society - NYC Chapter. Credit Suisse annually has one of the largest teams (258 riders last year!) - and …
The 26th Annual Ultimate Summertime Party presented by News Corporation at the Central Park Zoo on Thursday, July 22!
Hi everyone,
Here is a message from a fellow National MS Society supporter about a great fundraiser event in NYC. So please check it out!
Message from Hamill Serrant:
In the summer of 2008, my sister, Grace, was diagnosed with multiple sclerosis, which has …
World MS Day-May 26th!
To all members of the National MS Society:
This year on May 26, the world unites once more in the MS movement to highlight the international effects of multiple sclerosis (MS). Organized by the Multiple Sclerosis International Federation (MSIF) with the help …
Why is this campaign important to you?
Have been living with MS as a very unwelcome guest for over 15 years, will never get used to it, or give in to it!
No Janet , just too stubborn to give in!! But thanks x
Janet, you are mode than just a bit brave yourself !!x
Found out I might have ms
:'(
Not only am I a nurse and encounter this horrible disease everyday and see how it effects not only the person who has it but their families as well, but my mother has it. She is a brave woman who fights hard everyday, and is lucky to be in remission for almost 10 years. I look up to her for everything she has overcome and still does everything in life that she can. She doesn't let this disease knock her down, she is a fighter. I am so proud of her. I hope someday they can find a cure....
…Not only am I a nurse and encounter this horrible disease everyday and see how it effects not only the person who has it but their families as well, but my mother has it. She is a brave woman who fights hard everyday, and is lucky to be in remission for almost 10 years. I look up to her for everything she has overcome and still does everything in life that she can. She doesn't let this disease knock her down, she is a fighter. I am so proud of her. I hope someday they can find a cure. Someday I may have this disease but I know that I have my mother's strength and will to fight through it if it happens. <3
So happy to hear that your mom is a fighter. My sister-in-law was diagnosed around 2008 and my brother stuck be her the whole time taking good care of her. She lost her battle last year on February 3rd 2012. She was only 47 years old. I sure do miss my best friend. God bless your mom.
On July 7th of this year my daughter was hospitilized with severe problems with her eyes. After several days and many tests, Kara was told that she has M.S.. not the kind of news that you want for your 26 year old daughter who is set to graduate from college in December. it was a shock, but we decided to face it head on. Kara has been amazing throughout this entire situation. of course we wonder about the future but we both know, that we can only control the here and now. She has been an...
…On July 7th of this year my daughter was hospitilized with severe problems with her eyes. After several days and many tests, Kara was told that she has M.S.. not the kind of news that you want for your 26 year old daughter who is set to graduate from college in December. it was a shock, but we decided to face it head on. Kara has been amazing throughout this entire situation. of course we wonder about the future but we both know, that we can only control the here and now. She has been an inspiration to us all. For right now, the toughest part is the injections that she has to have every weekend. They make her sick, so sick she has to stay in bed for hours. We are hoping for the pill form to come out soon. But this is the face of M.S. You have one good day at a time.
Prayers going out for your daughter and your family
My husband Ray has MS he struggles everyday with normal tasks that each of us take for granted. Sitting up,turning over n bed,standing,walking,speaking,feeding himself. Normal everyday tasks that humans do to take care of themselves. As a caregiver it is also hard on me. Please support the Multiple Sclerosis Society to help find a cure. It is a very debilitating thing to happen to a family. Thank You!!
My brother and mother and step mother suffer(ed) from the disease.
I have RR MS. I am a single mother and work full time as a special education teacher. I get so tired and frustrated with this disease, but then u remind