13 years of remitting relapsing MS and today my neurologist said the disease has become a Secondary Progressive type

[Demishca]

Hello everyone

I have been using LDN since Jan. 17th 2019, I think that my best dose has been 3.5mg, I take it at night, been on that for the past two weeks now, there are subtle changes to the better.... I saw a neurologist today and after 13 years of having Remitting Relapsing MS he said the disease has become a Secondary Progressive type, and I meant to ask if anyone with SPMS here has tried LDN and whether or not it works for them or if there are any pieces of advice in that regard....

Appreciating your time and love in advance

[aredtigress Administrator]

I don't have MS, but I highly recommend going to the Trust's website and listening to some interviews. Here's a link, scroll down to Multiple Sclerosis, and then scroll through the many interview. Some differentiate between types, some don't.

ldnresearchtrust.org/ldn-vi...

Michelle

[Demishca in reply to aredtigress]

Thank you Michelle ❤️