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
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?
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.
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.
