I just wanna share my experience with d3.
I live in Europe but I discovered this treatment on internet actually..one day I saw this video http://www.youtube.com/watch?v=erAgu1XcY-U
, I begun to talk with pacients who are doing this protocol, on facebook or mail, I discovered the treatment, I made an appointment with the doctor. His name is Cicero Galii Coimbra, he is neurologist and lives in Brasil, Sao Paulo.
I am taking a really high dose d3 (60 000 ui d3 daily..the dose is calculated for me, in base of my situation, my disease history, my simptoms, my weight, my pth level, my tests result).To avoid hypercalciuria, I must drink daily 2.5 lts water (these higher quantity of liquids assures a urine volume around 2500 ml which allows calcium dilution eliminated in the urine and avoids excessive concentration of urinary calcium - as when calcium is diluted it does NOT get deposed in the kidney, preserving renal function), I must not eat dairy products, not take calcium supplements and not take nephrotoxic drugs. And I must avoid stress and infections.
U must understand that vitamina d is not toxic, the problem is the calcium, who must be controlled. I make more tests, but the most important is the calcium in the urine in 24 hours. If someone tells me that he took d3 and had no effect, I will tell him that he did not took the right dose, not mainteined a certain d3 level.
In 2012 I had new lesions, new simptoms, I could barely walk, I had big equilibrium problems, I felt so tired,my edds was 4.5.
I am following this treatment by more than 16 months, and I had so many improvements. Actually in july this year I was able to go alone in Brasil to my appointement, I don t have equilibrium problems anymore, I don t wake up tired anymore, I can walk without help where I want..who sees me, does not think that I have MS or any disease...I have a normal life again...
This december, on 11 december, I did my MRI. Result: no new lesions, no active lesions, so no relapses. It's my first MRI with such a short answer. Every day I just feel better. This is my first December, since I discoverd MS, when I am not in the hospital doing 3 or 5 grams of cortisone. In general in the past I had every year 3 or 4 relapses.. This is the first time when from more than 16 months I had no relapses..I just did not knew in all this years how is not to have relapses, I just got used to those..
I DON'T suggest anyone to take such a big dose without a doctor's supervision, but I suggest to do more research on vitamin d. I also did a facebook page with good studies and articles https://www.facebook.com/pages/Vitamin- ... 70?fref=ts
please do the test 25 oh d3 to see the d3 level, because u would be surprised how many of u are deficient. and pls do more research on PubMed or Scirus.com
this is my experience and I ask u to respect it.. http://mscure.aussieblogs.com.au/the-bl ... eatment-3/
this is a blog in english of a pacient of Coimbra who lives in Australia..
wish u all all the best and a happy new year!!!:)