Sweating

I’ve had RRMS for 4 years and I’ve had 2 rounds of Lemtrada. For years I’ve suffered with extreme sweating and after Lemtrada it’s gotten worse! I literally can’t leave the house as I’ve only got to move and The sweat is pouring off me. I take small electric fans everywhere with me and I have a fan on at home 24/7! I actually feel hot all the time as well. I’ve mentioned it to my doctor and ms nurse and they don’t seem to think anything of it. I’m taking sage tablets as that’s meant to help but nope! It’s ruining my life! I can’t even go places with friends anymore! Does anyone else sweat like this?
@Mlgilber1

I actually have the opposite problem... I used to sweat super bad no matter what and right around the time I was diagnosed it stopped. I barely sweat now, but I have heard from other people with MS in general that now they sweat more. I’m really sorry you’re dealing with this. Have you tried asking your primary care about it to see if they take you more seriously?

@Danielle_Rogers-Atkinson

I’m going to mention it again to my ms nurse when I see her next and tell her how much it’s effecting me and my life I’ve given up going out now!