Whats more important, the Dose or the Response??

[Guest guest]

Ive been on ldn for 12 months now

for progressive MS (had for 6 years)

Im only 24, and starting 3mg in January with inital great results -

better strength , better balance, better bladder for the first 4-6

weeks, however the last 10 months have been awful.

Symptons became much worse than before starting ldn, weker legs, worse

balance. the only thing that has remained is my bladder.

Ive tried from 2mg - 6mg , and i have felt the best when on 2mg, my

walking is best on this dose.

I have read 3mg is the minimum to stop/slow down progression, so my

question is what is more important, the dose, or the response?

As on 2mg i feel best (mobility), i have also tried 6 weeks on 4.5mg,m

but it just makes me less mobile.

Is it best to go for 3 - 4.5mg , but my mobility/leg

strength/balance/bladder suffers.... or shall i go back to 2mg and

have sympton relief?

I havent tried 1.5mg yet, but it would probably help more.

Thank you for reading, and any knowledgable replies