Know someone who got in on the group able to try this. Unfortunately it did not help BUT find the research hopeful. Even if it doesn’t move forward fast enough to help me it could help my children who I’ve potentially passed MS to genetically.
Dr. Boster, are you familiar with the research of OTC antihistamine repairs nerve damage caused by MS... PLEASE ADVISE IF YOU HAVE ANY THOUGHTS OR KNOWLEDGE OF IT....thank you
I have had antihistamines in the past and I’m looking to take them again; I used Tavegyl (Clemastine Fumarate) in 2021. It helped at the time but I didn’t fallow it properly. Do your own research before. I’m not sure if my neurologist will of approved of me taking this pills, but I was walking a bit better. Was short lived benefits as I didn’t had the money to keep doing the treatment and also a year later after a new relapse I was struggling again. Going forward to 2023, I am seriously thinking to do those treatment again and this time do it properly for a few months with breaks in between each corse of treatment. I need to go back and read on it again properly.
