MS and warm...

Absolutely!
Here in Southern Illinois the temps are reaching the mid-90s and my MS is going crazy. My foot didn't bother me most of the winter and now climbing the five steps to my house is difficult, not to mention taking the laundry down to the basement.
I can't imagine how Shaun does it either...I'm looking to move north (though not as north as you).
Air conditioning helps, except that then when you go outside its like an immediate sapping of your strength and energy.

I'm sorry that you have to suffer like this, especially when the summertime is what most of us in the temperate climates live for! My sister-in-law has MS, and they had to sell their Jacuzzi tub because the heat of the water made her so weak and wobbly that she couldn't function. She also has trouble on really hot days, but it doesn't sound like her symptoms are as bad as yours. Is there any adjustment of your medication that could be made to help you out?

I have to stay in doors during the day with my air on and I also do get shaky but I have to take pills for it. Like baclofen and activan and i also have to drink alot of gatorade and water. I already found out earlier this year my electrolites are messed up beside shaking from ms. I hope your body doesn't shake like mine does sometimes it gets scary.

Hey Freebc, Oh it is so nice to talk to someone who suffers the same thing. I too have MS, and I do not handle heat well at all. The hear we are having right now, is taking its toll on me. It also affects me, like I am drunk. I stumble, and my coordination gets off. I also get this feeling like a fish out of water. I much prefer the cooler weather. Every time summer comes around I gringe the hot days, because it has such an effect on me.

related resource: water cooler

Well i do not have an health problem..tfu tfu tfu
But i can tell you that the very hot weather in this country during the summer does cause me to have those effects.
Weakness, headaches, and other things.
i do not think that hot weather is really healthy for anyone.

I Also have MS and the heat is the worst thing for me anymore I live with my Father and he says he understands about ms but will not turn the AC on untill its like 85 in the house andwhen it gets above 80 I start to feel it, Now yesterday I told him I need the AC and he said it was ok but if he keeps this up I will have to go live with someone else. He takes good care of me Except for this.
Have a Great Day/Night.

No I not been told of this at all,I did know a lady that had MS,i did her hair in my shop but she never related to me about the heat.I am sorry you are having a bad time,i wasn't aware that the heat had any bearing on MS,i suppose we learn something new everyday.Just be careful not to fall ...I don't have neurlogical disorder but my husband has menieres disease which makes him dizzy and he cannot take heat well either,I do try to make him stay inside during the hot weather though.I suppose we all have our demons to fight.I have crohns disease and it makes it tough for me to be anyplace that does not offer a bathroom,and i have been in many tight spots before.Well take care,and stay close to you a/c...

I suffer in the heat and humity. I was diagnosed 9 years ago with R/R MS. I know now why I was always weak in the summertime. The heat absolutly wipes me out. I would say that is my biggest gripe with my MS. I lived in Houston, Texas for 3 years and my MS explains alot of things. My falling and 'drunk' walking is always worse in the summertime. This year, the heat seems to bother me worse. I live in my air conditioning in the warm weather.