This Is MS Multiple Sclerosis Knowledge & Support Community

I'm sorry you're having a hard time with LDN. Haven't ever heard of a reaction like that, but anything's possible. I've certainly had my share of unusual responses to meds! What I mainly want to say is that quite a few people are starting out on 1.5 mg and titrating slowly upward, say by .5 mg incre...

Hi, Jake, and welcome from another newbie! This looks to be a really good board. You'll find a variety of strong opinions on diet and MS, and since not much is really proven to be of benefit in that area, it all comes down to doing some research yourself and making an educated guess. Swank, Best Bet...

Radical dietary change is one of the hardest things a human being can do. We eat what we do for so many reasons other than nourishment: convenience, comfort, recreation, tradition, etc. Plus, we live in countries where the markets are stuffed with an incredible array of choices, and we're subjected ...

I do take the DL-Phenylalanine; it keeps my mood from bottoming out when the LDN is out of my system. I also take Milk Thistle at night with my LDN; I'm at 2 mg of the latter now, after having increased spasticity at 3 mg, and titrating slowly back up to 3 mg (hopefully). By the way, Milk Thistle is...

Arron, thank you for the welcome! Kasuku, I've been on LDN for four months now. I started at 1.5 mg, increased to 3 mg, then dropped back to 2 mg because of increased spasticity. Now I'm titrating slowly back up to 3 mg (hopefully). I haven't had any new symptoms during that time period, but some of...

Just trying out my signature.

bluejay

Hello; I'm new here. I've visited &/or been a member of a number of MS boards, and I'm very impressed with the level of inquiry and commitment here. I hope, over time, I'll be able to contribute as well as read. I have SPMS, diagnosed 3 years ago when it was still (barely) RRMS. My history indic...