still have the numbness and tingling in the legs and arms, worse when I lay down. MS hug is better in the day and worse at night too. Same with the burning legs and feet.

So I guess LDN helps in the day, but wears off a few hours before I take it again, hence the worsening at night.

They say blocked jugulars are worse when laying down so maybe I will get a surprise with the CCSVI. However, it all remains to be seen as time passes. I will continue taking the LDN. It helps my balance. I stopped running into walls.

Nothing sensory has worsened on LDN, some got better, like my thighs pain and spasms. I had only one relapse when I usually get two a year.

@Carol, so happy to hear you're doing okay. Your energy and eye is better, that's great. Do you live in a year round warm/ hot location?

It's so cold here I don't remember my heat problems, but I don't sweat so I can't tell right now anyway.

My energy was better until I got zapped with the Flu and now a cold. I'm glad your dry eye is gone. I have dry eye in my right eye too. With this cold it is not dry, nor is my nose.

I haven't had a cold in two years. I have been on LDN two years. I started Dec. 2008. I think I'm a bit holiday stressed, or overwhelmed. I think of snow and cringe. Nice to hear from you.