A ray of hope for potential users - Secondary Progressive MS user

[Guest guest]

I have been diagnosed with Secondary Progressive MS. My first onset

was at 18 years of age with double vision. Now is some 30 years

later.

I have been in a wheelchair for about 5 years now. I still work

full time and carry on pretty much as normally as possible (driving,

shopping, etc) as long as there aren't stairways.

I could not tolerate the CRAB drugs (I won't go there). Anyway, I

started LDN 5 months ago at 3.0 mg.

I was beginning to lose dexterity in my right hand. This would have

been a real problem as typing is a mainstay of my job. I am pleased

to say that using LDN reversed that trend. I can even " flip people

off " again, a gesture I was only able to do with my left hand for

several months.

This brings up a point. The benefits of this treatment are probably

measured in small but significant changes. Here were mine after 3

weeks. I tried to stay very objective and note all changes, even

those that didn't seem to be MS related:

Increased Right Hand dexterity (to almost normal strength)

Less numbness in feet

Improved mental attitude, concentration and stamina

Increased strength and balance

Improved complexion (I have rosacia)

Improved continence (dramatic improvement)

Fewer episodes of constipation

Reduced appetite (feeling full trigger seemed to happen earlier in a

meal)

Less facial hair growth (I'm female so this is good)

Vivid dreaming

Protruding eyes have diminished

Now at 5 months all of the above have remained except:

Improved complexion

Increased strength and balance

I am going to call my doctor and ask for a 4.5 mg script for my next

rx.to see if the two I lost will come back. I am very hopeful about

this treatment. Good health to all.