Are there any people with Multiple Sclerosis here who have heard about oral fumarate and perhaps have even tried using it? Is there any news about this? From what I have heard oral fumarate can make a real difference and will reduce MS activity. I'd really love to hear more about it.
I have never tried oral fumarate but would really like to. I got the same information that you did, and it does sound like oral fumarate has a good chance of making life with MS a bit easier. I would first like to know what the possible side effects of oral fumarate are, because there are bound to be some.