Join the MS Movement - National MS Society

[medad1]

What about the Gut Bacteria issue concerning MS? Is there any news about?!!

[jdavis1975]

This is my favorite MS video. It really explains what MS is, why we need research and why those of who have it so pray for a cure.

[omv08]

MS is now being linked to the newly retrovirus discovered in 2006 XMRV ....

[bluephilly29]

most beautiful message i ever seen i am a aspiring filmaker i know i am in he right feild of study iwant to send messages like this through film i am inspired to live my best life with ms thank you

[lroMStify]

@macrockettere

Depending on where you live, find the nearest MS center...get on nationalMSsocietyDOTorg for a list.  Do NOT go to just a general neurologist. You need a center that specializes only in MS and there are only a few in the country. Good luck

[macrockettere]

@lroMStify Thank you for your information. I would like to speak to ppl who have this disease, their symptoms and how they got help. Thank you alot. I am one of the millions of ppl who are uninsured unfortunately and trying to work on that as well. Any information or help is very much needed and appreciated. Kind regards!

[lroMStify]

@macrockettere

As you can see I'm slow in getting on the computer. I do know that several MS centers will give MRIs and other diagnostic tests for free, depending on your needs. It doesn't hurt to call and find out what assistance is available. Also check out the MS Foundation. They help people as well. Good luck.

[macrockettere]

@lroMStify You are very kind & your response has been well received. Thank you very much. I so hope I am wrong on this but so far...my symptoms coincide greatly with MS. Again...I thank you greatly!

[macrockettere]

I need assistance to find the proper services to diagnose my symptoms. Any facilitators with expert helpful resource information, please contact me. I am experiencing great difficulty walking, balance,. tremors, vision problems & excruiating generalized pain along with fatigue, muscle weakness, tightness and Ive been experiencing muscle cramping, incoordination, vertigo, extreme numbness, tingling with extremeties feeling "dead" and cold or hot. Please help. Thank you.

[SirFrostyWins]

I have had MS symptoms my whole life, wasn't diagnosed until last winter. I am 17♂ now and my tremors are getting worse can't feed myself without a straw, but i wont let it stop me from being best darn dietitian ever. :D

[pdye39]

You state you want to keep us moving. Why the ban on simple angioplasty? Why deny us the option of obtaining some relief when we have proof that our veins are stenosed. You can't keep us down forever. The National Money Sucker Society will be out of a job. Criminal negligence by no allowing us the option to obtain a simple procedure that has been approved since 1979 just because we have MS like symptoms. You would rather us continue on this slow-tortuous death. Pay that CEO $450,000 while we die

[aihtsisu08]

I was diagnosed in July '05.

[fiddler927]

This is a great video. It explains MS in a way that makes it a little easier ti understand. I don't think anyone who doesn't have MS can really understand completely, but this video helps some. Thanks, National MS Society for helping to bridge the gap.

[TheFAITHOUSE]

This is an excellent video. It explains the struggle SO well. It is so misunderstood and extremely hard to explain. You somehow explained so much in 3:36. The NMSS, is fantastic. You helped me through my diagnosis and have been a constant source in my constant shifting MS. God bless you. Peace out.

[sheltiebrat]

This is such a well done video, and I think I will pass this on to my former supervisor, whose argument was that she had met people with MS, but they were not that bad, so she wondered why I was having issues, and honestly, just did not believe me. I think I will send this to her during MS week in March.

PS:Dr. Jung, You ROCK : )

[rdbaldwin75]

MS just sucks. There's no easy way to explain it to people who don't live with it daily. The great hope is that there are so many out there looking for a cure. This video is an excellent reminder. Great job NMSS!

[rubberducky06592]

Thank you so very much. My father has this debilitating disease.

[nojuliachild]

Thank you so much.

[jwasko777]

To hard to explain - by far my favorite You Tube. This is the realist part off my life. Very difficult to live this way. Peace.

[indianamccue]

I have progressive MS! Its determination and a strong spirit and additude that I wont let it beat me DOWN! I HAVE BALANCE WALKING & HEAT PROBLEMS! I REFUSE TO USE A WHEEL CHAIR A MESSAGE TO ALL I TELL MYSELF THERE ARE OTHERS WITH MORE PROBLEMS THEN ME.I JUST WISH THAT MS COULD GET AS MUCH ATTENTION AS BREAST CANCER,HEART,ETC..

[YdotKidVE]

My sister has it. she was diagnosed when she was nineteen and then she had her first baaby when she was 22 and she couldnt take her medication so immiedieately after she gave birth, the MS triggered rapidly. on a wheelchair now, it affects her legs the most. but she doesnt regret her son and is on the road to recovery

[micah5five]

Wonderful!!! Lets Raise MS Awareness!! I was diagnosed Feb 2007!!! But took 7 YRS and after my 2nd child it got so bad my arm went paralized, my son was only 4 weeks. Thats when they figured what was happening to me all these years. I thought I was just a Klutz ROFL!!!

[RIProgressive]

I have had MS for 25 years and I haven't stopped moving!Ms helped meunderstand about moving and I exercise every day now and am on the Avonex treatment, once a week for 5 years. I can walk 2 miles now(every morning I do this).

[RocScatterbrain]

THANK YOU :-)

[RocScatterbrain]

Thank You :-)

[TEFFY357]

Very well done!

[jnjarboe34]

all we can do is keep trying and moveing jnjarboe diagnosed in 1994

[SHansord]

I wish more people would c this

[TerezzaMV]

Now THIS should be a commercial during Superbowl Sunday!

[brassandivory]

Amen!!

[odetoREDribbon]

I'm almost grateful to have MS after seeing the hope in this video.

[pwmarcia]

Very good video. Thank you.