[LS]

Hi again Ed-tobias. I would like to let you know, I’m still following Coimbra Protocol. No new lession or diasese progression in 4,5 year. Many of my symptoms are gone. I have an Exopulse Mollisuit, a neurostimulation suit, great invention, I wear for 1 hour every day and it reduces the little spasm that I have and therefore reduce my fatique. Read more here https://www.ottobock.com/en-gb/product/28XP1000

So no MS-drugs and lots of vitamin d and control with my protocol-doctor every 6 months .

ottobock.com

Exopulse Mollii Suit | Reduces spasticity, activates muscles.

Intended for spasticity reduction, weak muscle activation and related pain relief

[LS]

Yes, I take vitamin D in high dose.
I live in Denmark, and follow the Coimbra Protocol and I consult a protocoldoctor in Germany. I was diagnosed whit MS(RRMS) in january 2019, my sympthoms started a year ago in september/october 2018. I was dizzy, had fatique, numbness, weak muscles, problems walking, burning sensation in my hands and feet, problem with eyesigth, pain etc
In the beginning I took only 2000 IU a day, and then 4000 IU. During the summer and before Coimbra Protocol I took 10.000 IU a day, I felt improvement and slowly many of my symptoms disappeared.  In september I started the Coimbra Protocol, taking very high dose vitamin D, under care and support by my protocoldoctor. And I am feeling so good, the healing process is speeded up. My fatique is gone, I don´t sleep during the day anymore, I can walk a long distance again. My MRI from june showed  my lesions in the brain has shrunk and the neurologist wrote MS regression in my journa, and that was on 10.000 IU a day.
As I sit and write this morning in Denmark my MS-symptoms are: numbness in 3 finges on my left hand. When I stand up and walk around, I feel some small electric tingling in legs . Sometimes I still have Lhermittes sign, when I bend my neck, but it is almost gone.
I´m on Aubagio prescribed by my neurologist to suppress my lymphocytes but my plan is to quit the Aubagio, when I feel ready.
Thats my story for now. Please feel free to ask any questions.

[LS]

Hi Ed
I’ve been using Aubagio since mid-february. I think I was taking 2000 IU Vitamin D at that time, and slowly increased the amount of vitamin D, as I read about it on the internet and I felt a little improvement everytime I increased. You get 10.000 IU vitamin d from the sun alone, by sunbathing in the middle of the day in the summer by the way.
I think that the vitamin D is helping me, by regulating and modulating my immune system and it improves myelination. Viamin D is actually not a vitamin but an steroid hormon. There is receptors (VDR) for vitamin d in nearly all cells in the body, and vitamin D regulates minimum 4000 genes in our body. So it is a powerfull hormon, and not good to have deficiency.
On the Coimbra Protocol, we increase the amount of vitamin D a lot more than 10.000 IU a day, but only under the care of a medical doctor, that is very important!
My knowledge of Aubagio is, that it inhibits the immune system and delay the progression of MS.
The neurologist dr. Cícero Coimbra that created the protocol said it puts 95% of MS patients in total remission.
I am convinced my improvement is due to Vitamin D.

Try to google Coimbra Protocol and read about it and search facebook for Coimbra Protocol groups.
LS