The cold seems to help me. The climate, snow, etc. Some people it doesn't, with more connective tissue illnesses additionally like arthritis, etc.

I have RRMS too and I track how I do with different weather, amongst other things. For me, I can actually handle pretty good heat (100*+) as long as humidity is low. Humidity for me is the real killer and I go downhill quickly. I do find that it takes me a while with each change of the seasons for my body to adjust. So for example, I struggle a lot in the spring and early summer when temps start to get into the 80's. But by mid summer I can handle it better and 80* feels almost cold! I have found that those transitions between seasons are my most vulnerable and when symptoms flare, (it's also the time of year I've had my two big MS incidents) so I try to up my self-care during those times. I do get cold very easily in winter - we get down to the teens so not too cold, but cold for California! - but I find the cold doesn't cause as many issues as the heat so I just bundle up in my fleece long underwear and cuddle with my pups! I love our Nest thermostat. SO easy to manage different areas of the house through an app on my phone. My happy place is 68* - we are getting solar installed next month to help with our summer cooling bill! XX

My body temperature is really screwy !!
I can’t take real heat (which sux since I live in Tx). So I pretty much stay inside.
I also can’t take the cold !!
If the barometric pressure changes, if some puts the a/c on near me, my body aches so badly!!!!
Inside my house it has to stay around 73 degrees.

Hot temperatures make my skin tingle all over and sometimes I pass out. Cold temps make me shiver uncontrollably. Not sure if that's MS, or just because I'm a Floridian lol

In the heat of the day it started to get to me, I used to love getting a tan in the sun. For me the less humidity the better :)