Primary progressive multiple sclerosis: A patient's perspective

Craig Milverton shares his experience of living with primary progressive multiple sclerosis (PPMS).
More about Roche in multiple sclerosis: www.roche.com/ms
More videos from Roche on: / roche

[@incontroldiapers]

Stay Strong! We are always here to help! 💙

[@lenlevasseur1355]

This was a wonderful example of someone living with thiis distructive disease! Well put together my friend! Leonard LeVasseur Utah USA.

[@Nina_Olivia]

Thanks for sharing your story. What an amazing pianist and what an amazing attitude. Hope you’re still playing up a storm!

[@jeathtunes769]

Its very brief. I would have liked to hear about the symptoms and how it affetcs your personnal life

[@roche]

Thanks for your feedback. You can find more information about living with MS here: www.roche.com/ms

[@juliewiegel8418]

Listen again. He mentions several. 😎

[@alibengali7745]

Hi, a german women write that she became 1994 PPMS and than 2000 in Wheelchair. 2001-2003 she becam a therapie MITOXANTRON and after that her progression stilled. No becoming worser. Maybe other PPMS patients must try the same. Why the doctors do not try this?

[@tag7941]

Great story. Would love to hear your music.

[@ernietollar407]

Thanks for sharing my jazz/MS brother.

[@jamesgeerlings9113]

Well Done. Keep playing. You are amazing.

[@orbitingdecay6797]

I wonder how he is now 😢 I have severe onset ppms

[@budfredrick964]

I've had PPMS since 1988. At one time I was so bad that I was using a power chair. I found something that re-mylinated my nerves and now I don't have ant symptoms. I cant't say I'm cured, but I don't have any symptoms anymore.Amybody suffering with MS can do it with this.

[@Enoughsenoughnomas]

what did you find?

[@kleifschmistiansen3145]

He should meet up with Brendan Kavanagh for some boogie woogie

[@luisfernando-mm3jt]

I was whacting this and really relate to this aand thought to coment but them i sawl big pharma add ...Better not

[@lindaalice891]

I was diagnosed with Multiple Sclerosis (MS) in October 2011, at the age of 44. I woke up one morning with numbness in my lower back and legs, I couldn’t feel my feet touching the floor and I also suffered from Anosmia & Tinnitus🦻🏼🦻🏼. I saw my doctor and had an MRI to see if I had a disc problem, it was negative and she told me she feared MS. I was sent to a neurologist, had two more MRIs, and was told that night that I have four lesions on my spine MS. I tried every shot available but nothing worked. In 2015, my neurologist and I decided to go with natural treatment and was introduced to Dr Madidia natural organic MS Herbal formula, i had a total decline of symptoms with this treatment, the numbness, terrible back pains, stiffness, body weakness, double vision, depression and others has subsided.