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.
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.
This was a wonderful example of someone living with thiis distructive disease! Well put together my friend! Leonard LeVasseur Utah USA.
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.
Thanks for sharing your story. What an amazing pianist and what an amazing attitude. Hope you’re still playing up a storm!
Stay Strong! We are always here to help! 💙
Its very brief. I would have liked to hear about the symptoms and how it affetcs your personnal life
Thanks for your feedback. You can find more information about living with MS here: www.roche.com/ms
Listen again. He mentions several. 😎
Thanks for sharing my jazz/MS brother.
Great story. Would love to hear your music.
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?
Well Done. Keep playing. You are amazing.
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.
what did you find?
He should meet up with Brendan Kavanagh for some boogie woogie
I was whacting this and really relate to this aand thought to coment but them i sawl big pharma add ...Better not