I have MS and will be starting LDN for the first time tonight. I just stopped Tecfidera as it gave me leukopenia (severe drop in WBC) and was too toxic (also have a HUGE concern it would eventually cause cancer). For those who take LDN for MS... what dose do you take? I'm trying to see how many take 3 or 4.5mg rather than ONLY 1.5mg.

I am VERY confused what dose would do the best job at preventing MS progression.

How many here went off all MS drugs and are ONLY using LDN like myself?

Thanks!