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    You are here : Home » Useful Resources » Personal MS Web Sites

    Personal MS Web Sites

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    One of the best ways to learn about MS and how to come to terms, face it and learn to live with it, is from fellow people with MS. Their knowledge and real life experience is dealing with and managing MS day to day can give you a great starting point on which you can build. Knowing that you are not alone, and whatever you are going through, you can bet others have been through it too, and come out the other side as survivors, often stronger for the experience, is very reassuring and empowering.

    Do you know any inspiring MS webpages? If you do please Tell Us.

    Sharing that which makes us strong strengthens everyone. Your recovering begins here with a simple Click of the Mouse.

    Matthew Grace
    Matthew Grace's recovery from severe MS is simply remarkable.

    Check out this website to discover more about this man! You can also read Matthew Grace's personal Account of his Recovery on this site.

    Matthew Grace
    Betty Iams
    According to this inspiring lady, we have a choice. We can be either Victims or Victors over MS and the choice is ours!

    Her main message is that there is life after MS!

    Betty's House Logo
    Andy Deek's homepage is about his life with MS; including his trip to England, his lovely dogs and his experiences in Chemotherapy treatment for MS.

    Be ready for a very cool intro page with Flash animations and music. To visit this webpage click on the link above.

    For those of you who cannot tolerate moving images you can skip the intro and go straight to his Homepage by Clicking Here

    Dog Picture
    Eva Marsh
    This lady is living-proof that Self-Healing and Recovery from MS may be possible.

    Eva Marsh
    Karan

    "Either you have MS, or MS has you…"

    Karan was diagnosed with MS in 1981. Here she discusses her journey to healing and acceptance, the various therapies she has tried, what works for her, and what doesn't. It is a spiritual and inspirational site filled with lots of love and encouragement.

    If you want Proof that Persistence Pays, Attitude is Crucial and Faith can Move Mountains visit this site!

    Karan
    Here at Life in Spite of MS you will find a view of MS from two perspectives - a man with MS and his wife and caregiver. 

    We hope you will find information as well as inspiration.  We welcome your contributions as well. 

    Together we can help others learn to cope with MS one day at a time.

    Website: http://www.life-in-spite-of-ms.com/

    Written & Compiled by Paul Hattersley

    MS: MY PERSONAL EXPERIENCE

    "I am a 47 year-old male and have had Multiple Sclerosis since 1985. The diagnosis was confirmed due to my inquisitiveness after my first symptoms, which was the limping in my left leg followed by slight blurring vision..."

    Paul's personal site contains a lot of information on MS, diet, exercise and fatigue. It is comprehensive and clearly written to aid anyone reading it to more fully understand the condition that he has, and how it affects his world.

    Take a look at this monthly online MS Magazine written by and for those with MS. The content of the magazine changes on a regular basis and there are many useful tips, stories etc. editied by Carolyn Reynolds.

    MSMusings Logo
    Our Mission:  MS Views and News is dedicated to the global collection and distribution  of current information concerning Multiple Sclerosis. In collaboration with other organizations, MS Views and News uses state-of-the-art communication channels to provide information for those affected by, or interested in MS.

    Website: http://www.msviewsandnews.org/ 

    The Stu's Views & MS News Blog: http://wwwmsviewsandrelatednews.blogspot.com/

    Follow Stu's Views & MS News on Twitter: http://twitter.com/MSViews_andNews

    MS Chat, designed by Lee Hession - "mschat is a unique Multiple Sclerosis website. Designed for people with MS, we bring people closer together..."

    A great place to meet other MSers and talk, a place to make new friends and learn more about MS.

    The MS-multiple-sclerosis-symptoms web site is my way of connecting and hopefully help other MS’ers like you and me.

    I know exactly how you feel.

    It’s frustrating trying to make people understand what you’re going thru and what you’re feeling. The truth is that the frustration disappears only when you meet and talk to someone else with multiple sclerosis (MS).

    Someone like you!

    In MS-multiple-sclerosis-symptoms you have a place designed with you in mind by someone just like you.

    Website: http://www.ms-multiple-sclerosis-symptoms.com/

    A brilliant site - highly amusing but highly informative MS site. Also home to the 'PlainTalk Communities', a very good set of MS Discussion Boards

    From the site  - "How to Suffer From a Chronic and Incurable Disease Without Appearing to be a Total Loser "

    Multiple Sclerosis Sucks Logo

    "My Odd Sock is a funny look at life with a limp.  An obtuse angle on Multiple Sclerosis, life and everything in between.

    Most of My Odd Sock is nonsense. It's my calling card! But it is also what is bouncing around in my head like a peanut in a tin can. So I use this Internet thingy that Al Gore invented to spew my dumb thoughts about MS and a whole lot of other stuff that gets my knickers in a twist. Hop on and enjoy the ride." - Doug Ankerman

    Doug Ankerman created the Web site, My Odd Sock, to raise awareness about multiple sclerosis and shed light on his humourous moments.

    The whole website is guaranteed to bring a smile to your face and make people wonder what you have been up to.

    Website: www.myoddsock.com.

    Jock McTavish
    This is a webpage rich with insight, information, and thought provoking reading.

    Jock is wise man indeed and the way he views life is just plain inspiring!

    Jock McTavish
    Rachel's MS Blog - A pas de deux with MS

    Hi, I’m Rachel and I have relapsing remitting Multiple Sclerosis.

    I was diagnosed in November 2007, at the time I was planning my wedding and buying a house for the first time. After the initial shock of the diagnosis, I decided to read lots to see if there was anything I could do to help. I read lots about MS and diet and I made some fairly major changes to my diet. I no longer eat any dairy or gluten and try to have a healthy diet . I try to keep active, in my youth I trained as a ballet dancer for 10 years, so I love dancing although I’m not sure if MS and pirouettes go together, I am attending some ballet classes soon, so will find out!

    I have tried alternative therapies and often go for reflexology and acupuncture, which I believe help and are a lovely treat! My main thing is to try and be positive, I think a positive attitude helps. It’s been nearly five years since my MS started, although I didn’t know what it was at the time.

    Fingers crossed, touch wood, and all those other things, I am doing OK or as the neurologist said recently, very well.

    I work at the local University and live with my husband and two mischievous cats, much of our spare time is refurbishing our house, which is very much stuck in 80’s decor!

    Rachel.

    You can read Rachel's blog here: A pas de deux with MS

    MAKE MS YOUR VICTIM, NOT YOU  - this simple message says it all for Sandy's site. It is well laid out with lots of interesting facts, not only about his own life with MS but also where he lives, etc.

    "Since I first started work on our family site in June 2005 it’s always been my intention to have a section on MS. Multiple Sclerosis (MS) is an illness that affects some 80,000 people in the UK so it’s certainly not rare. There’s a lot of invaluable information on the web, information not only for sufferers but for those close to them. I’ve added a page to this area of the site and will put links to the places I consider to be well worth a visit on there............."

    Sandy McGregor's Logo
    What's this site about?

    This site is dedicated to all those, who, like myself have Multiple Sclerosis.

    I hope through the laughter contained on this site to lighten the load of those with MS, to entertain those without the disease, and in the process to raise much needed funds for The Multiple Sclerosis Resource Centre.

    Squiffy's House of Fun Logo

    It is clear to nearly everyone that has Multiple Sclerosis (MS) or is close to someone who has it, that there are often many physical challenges associated with this condition.

    Exercise and diet are extremely important factors influencing the physical and emotional well-being of everyone, regardless of their health situation.

    However, this is especially true for people with MS. Appropriate diet and exercise will go a long way to improving the quality of life of people who have this difficult disease, and these are the two primary components of the program described here.

    The program offers both exercise and dietary resources (including exercise DVDs and specific recipes incorporating appropriate dietary ideas). Links to information about other exercise/physical therapy programs as well as general lifestyle adaptations can also be found here.......

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