Six Months of LDN

[Guest guest]

My name is Bill; I'm 56, was dx'd with RRMS in 1998, and changed to

Secondary Progressive MS in 2002. I have used A, C, and R of the

ABCRs, have had six months of Cytoxan (Chemo), plasma exchange, and

enough soly to float (Or pick up!) a battleship. All were mildly

successful by the standards put forth by the companies who promote

them, but I continued to go downhill. I became obese, confined to a

wheelchair, and on oxygen when I started taking LDN. At the same

time, I discontinued R.

Improvement was not immediate, but I was not experiencing any

episodes, and did begin to notice gradual improvement. I had already

been doing light exercises, such as leg lifts,foot raises, and

walking in a shallow pool; but I was able to gradually increase

exercise, and I also began doing work in my workshop from my

wheelchair. To speed this up, it has now been over five weeks since

I've used my wheelchair, and for the last week, I have not even had

to use a cane. I still do have numbness in my left leg, but I am

able to walk without a limp. I had my six-month check-up with my

neuro, two weeks ago and blew my functional composites away! My

neuro was blown away, too.

I feel better that I have in seven years.

I don't know if improvement will continue or what, but I am

overwhelmed by the results so far and cannot believe there is not

serious and fervant research being done with this medication.

Thanks, Bill