New to the site, just wanted to say hello.

I am about to start a site and your site gave me much hint how to do it. I really loved to visit your blog. Hope to see more inputs from you in your site.

Resume Writing   

For all visiting this site, are you registered to receive our weekly MS related e-Newsletter? If not, click the link found on the left of this page, under the Main Menu bar that reads: Register for e-Newsletter and site. 

You can exercise and lose weight without being hurt by building up core temperature...

Need to work-out if needed, in a very cool environment and drink plenty of water.

Read more here: http://wwwmsviewsandrelatednews.blogspot.com/2010/06/study-shows-people-with-multiple.html

and here: http://wwwmsviewsandrelatednews.blogspot.com/2010/02/exercise-has-protective-effect-on.html

Visit my Blog: http://wwwmsviewsandrelatednews.blogspot.com/ - use the search box. Type in exercise. click enter and see the articles that open.

Good Luck and let me know how it works for you. I am sure others will want to know too...

Since being diagnosed I have gained wieght. I have tried to workout but I am often very tired and when I work out. I easily get my core temp up which is what I need to do to loose wieght but causes problems with my MS so it either workout or gain wieght does anyone have a workout plan that will work ?

Choosing professional resume writers as a profession is the easy decision; the work begins when it comes to looking for freelance writing jobs and freelance writing gigs. As many freelance writers know finding freelance work can be time consuming and require a lot of effort and heartache. Numerous rejection letters, continuous query letters, and at the end of it all nothing is guaranteed.

how to convince my neuro to look at ccsvi as a fact and not a false hope for me?

hi...i am new to ths site and also recently diagnosed with ms. i am doing as much research as possible to try and calm my fears. i am very scared and dont know where to begin. i have no idea what my future has in store for me but i know i must keep a good outlook and hold my head high. strength comes within. i am open for suggestions on how to begin my new life with ms.♥

You are invited to attend a Talk MS LIVE! program in your area! Your questions will be ansered by leading physicians and nurses and you'll have the opportunity to connect with others living with MS. Call 1-866-756-0490 for more information and to reserve your seats!

Talk MS is taking the show on the road to the following cities:

• Kansas City, KS
• Dublin, OH
• East Syracuse, NY
• Denver, CO
• Allentown, PA
• Austin, TX
• Jacksonville, FL
• Scottsdale, AZ

Took me awhile to read all the comments, but I really love the article. It proved to be very helpful to me and I am sure to all the commenters here! It's always nice when you can not only be informed term papers, but also engaged! I'm sure you had fun writing this article.

it took me a while but i found a place to fit in i was dignosed with MS on holloween of 06 with no relapse since then and all the meds i have tried have made me sick after about 6 months i have considered stopping so i can feel "normal" i have 3 children under 12 and a hard working husband with epilepsy this is very hard on them too does any one have any suggestions emails would be great i do not now much about diet with ms either HELP!!!!

It amazes me that all the talk about CCSVI centers around the fact that it may help with MS and has helped many, but there is no absoluted proof.  One of the things that has been proven is that everyone !00% of those with MS have malformed veins.  Those without MS do not have malformed veins. 

My point is that it is not normal to have malformed veins.  If I have malformed veins causing a interuption of proper blood flow I want it fixed.  I want it fixed whether I have MS or not.  It may be causing several other things that I am not aware of.  If it were discovered that everyone with MS had a broken arm we wouldn't study that, we would fix the broken arm.

I am all for further study.  However, those that condem this because no study has been done make me question their true motives.  Do the studies but don't condem and stop the correction of repairing a defect in the body. 

Hi! i have MS since 1983 and it is nice to talk to different people who have different symtome but feel the same thing and feeling.god bless you

the "show must go on" video is absolutely great, i mean it's difficult to not put in the shoes of someone having MS... i really liked it... because now I understand how it feels... OMG... I'm about to cry... THANKS...

Thanks for the great info. I will visit again often.

it is a good site. interesting for me. and useful..Thanks.

Term paper

Sandra,

Being you are from Scotland, you may have heard of the McLaughlin family and of their famed son, Ryan, who is informing many of Vitamin D and it's need.

Contact Ryan's Mum, Kirsten -  at: kirsten.mcl1929@googlemail.com

I am sure that Kirsten will be able to guide you in your efforts to help your son.

Best,  Stuart

im a mum of a 6 year old boy who has ms,sam was diagnosed when he was 5,can someone tell me if i need to give sam vit d supplements even though sams levels have been tested and are normal.thanks

The recent article on Richard Humphries' triumph over his MS ( http://repairstemcell.wordpress.com/2009/09/02/my-ms-pain-is-gone/ ) prompted this response from a concerned reader. "Posting was bright and filled with promise, but, alas, not a lot of information. - CJD"Good call CJD! I did some digging and would like to present the cumulative results to answer the question:

You decide. Here are 11 articles from my blog, 47 from donmargolis.com, 28,000 from google news and 20 clinical trials from clinicaltrials.govhttp://repairstemcell.wordpress.com/2009/09/02/multiple-sclerosis-and-stem-cells-need-more-info/

Hello,

I'm new here but certainly not new to MS; my diagnosis was confirmed in 1977.

Please write to me and tell me if any of you are being pushed into a Power chair when you want and your doctor prescribes a scooter. I'm in the middle of an investigation of Home Medical Equipment companies who advertise scooters that take Medicare Assignment but once you contact them, suddenly they want to give you a Power Chair instead. They haven't even met you and have no idea of your disability!

So far I've kept my independence because of my scooter!   It's important to me because I live alone since the death of my husband. In my case even my Neurologist filled out the Medicare form saying that I would benefit more from a scooter, I cannot tell you how many places will not help me unless I take their chair that cost twice as much as a scooter. The Scooter Store is one of the worse offenders!

At first I thought it was just the companies that were responsible but today I hit pay dirt when I found attorneys telling them how to get around Medicare saying, "We can make two three times the money with a Power chair than a Scooter." This is a fight that needs support of all patients who were pushed into chairs before they need them,

Our doctors order a scooter and have no idea why we end with chairs instead; they think it was our choice.  I know there has to be a great number of people out there that were lied to! Medicare never said after five years we can only get Power Chairs, that is a lie being perpetuated by companies that are supposed to help us! It is also Medicare fraud! Please come forward and tell me what happened to you; lets get these crooks exposed to Medicare and our physicians, Without us they would have no business; it's all about greed, the same kind of greed that has put our economy in the toilet. Thanking all of you in advance.

Sincerely,

corinnebegga@aol.com <

Hi Stuart:

Even during the holidays you take the time and think of us. Just wanted to let you know that all your efforts are greatly appreciated. Wishing you and your family a happy and healthy new year.

Karin in NW FL 

Today is the first time I have had a chance to check out, this website! I find it contains a lot of helpful information and resources! I wanted to thank Stu for all of his efforts and hard work!

Ms sufferers need more help! they need better treatment! They need better diagnosses processes. For this to happen, More reaseach is needed and more money, Much more money is needed to help research!

Ms Needs better goverment support for research and testing & treatments & care for MS sufferers. Stu's hard work will help in every way! God bless Stu for his hard work!..Jason

        Hello Stuart, i'm new to this site,but can't wait to start learning more, Thanks for all the neat info!!  I am having trouble dealing with all this, and times am overwhelmed.. Nice to know theres a place to go just to chat or vent. Thanks

Stu

   As a long time M.S. advocate and an M.S. Friends volunteer, thanks for the great job.  I hope in the future you will do a piece on M.S. Friends, as it is the most wonderful associatation I have ever had the pleasure of working with.  Every day we make a difference in peoples lives.  How many people can say that.  Keep up the good work

                                                    Howard Klein 

I have trafficked myself here from Merely Me's site.  I love her writing here and on her own site.  She rocks!

Stu, you have so much information here that I will have to slowly nibble a piece at a time.  I am hoping to start Tysabri in the next few months so I look forward to checking that information out on your site, also.

I am also a blogger with MS.  The link to my site is http://messystuffalifewithms.blogspot.com/ .

I'm a late 30s teacher diagnosed with RRMS in 2005.

I'll be around reading,  Weeble Girl

Thank you Stuart for being proactive and starting this amazing web site.  It is so current and informative and keeps all of us up to date on the latest in MS. The articles enlighen and empower us and present information for living with MS now and hope for the future.   The site brings us together as a community and makes us aware that we are not alone.  I for one am so appreciative that you've taken the initiative and put this together in a very user friendly environment.  Your site is truly a gift to all of us with MS.  Keep up the excellent work.

Your site is so incredible.  To me it is the perfect picture of MS helping MS.  Stuart you have moved an entire MS community for the better. I save every MS Views and Related News.  I feel with this information i am on the cutting edge of what is happening in the MS world.  What you do in invaluable and i am very grateful.  Thank you for this great site and for leading by example.  You prove to me... we are all here to help each other. KUDOS YOU!

Thank you for championing me in this national contest by ABC and Prevention magazine.  That makes you the champion here!!

 Keep up everything you do.  i am proud to call you my friend.