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-   -   Hot Baths (https://www.neurotalk.org/multiple-sclerosis/37788-hot-baths.html)

D_HOLLAND 01-31-2008 08:50 AM

Chris is the same way, heat just wipes him out and he has learned that. Sometimes he will still take a hot shower and then sit there and cool off before he gets out so that he doesn't fall to the floor.

I would assume since MS effects everyone different that the heat would also be different for everyone.

momXseven 01-31-2008 09:05 AM

Quote:

Originally Posted by Erin524 (Post 202467)
I've noticed problems in extreme cold. We've been having -15 and -20 degree temps here. I'll go outside and my feet will suddenly feel like someone dropped them in a bucket of water and I suddenly had giant ice cubes surrounding my shoes. (ice shoes) and I had to walk slower.

Wow, that's cold. I just have to be below 60 and my body hurts really bad and limbs don't want to work well. But the heat gets me also, I go numb, brain doesn't work well (I feel like I'm dreaming).

FinLady 01-31-2008 09:52 AM

Heat turns me into a ragdoll, and I get very weak. So standing in a hot shower is out for me. I still take hot baths on occassion to help with some of my muscle pain, but I only let myself stay for about 15 minutes and it's usually right before bed so I don't have to worry about moving around too much. I also never do this when I'm home alone, just in case.

When the cons get worse than the pros of doing this, I will definitely stop. ***knocks on wood*** Haven't gotten to that point yet, but I know it may come at some time.

Dejibo 01-31-2008 12:48 PM

sometimes I LOVE a hot bath! :circlelove:

Sometimes a hot bath makes me feel pretty sick :hit-safe:

Some hot days dont bug me, some make me limp like a noodle.

Carolynj 01-31-2008 02:20 PM

Hot Showers are the highlight of my day, can't get started without one and the hotter the better.....but they definately drain me. I just plan ahead and know that when I get out I will have to just sit for 15-20 minutes while I re-energize. Hopefully it doesn't get any worse - I would hate to have to give them up!!

Extreme cold - yep that too! Not always, but frequently, when I first go outside and it is cold - I do the Frankenstein walk. I have to stop and really stretch my muscles out to get them kick started.


the Bird 01-31-2008 02:41 PM

When I am FINE totally....then I can bath hot! However if there are MS things happening, forget the hot bath!

I too had those stars and never told anyone!!! (I'm a classic keep strange sx to myself person!!! BUT I'm learning to behave and call the doc!)

mommywms 01-31-2008 03:19 PM

Because is excerbats your sx.
I cant take hot baths,I cant be in the heat,And I can not drink my coffee in the summer months. Which sux big time. I drink NOS in the summer months,and if its cold out I can chance it and maybe drink one cup of coffee.

tovaxin_lab_rat 01-31-2008 04:59 PM

Here is some information about Heat Intolerance and MS from the National MS Society that you might find helpful as well.

http://www.nationalmssociety.org/sit...ourcebook_heat

Many people with MS experience a temporary worsening of their symptoms when the weather is very hot or humid or they run a fever, sunbathe, get overheated from exercise, or take very hot showers or baths.

cat265 01-31-2008 06:58 PM

I have been reading this thread and I have a question about the eye thing you were talking about. I get those sparkles, I always thought that was a sign that my b12 was low. Has anyone ever seen (I know this sounds weird) like and x-ray type of picture of an eye ball when you close your eye?? I don't know how to explain this sorry:o

KajunButterfly 01-31-2008 07:41 PM

I'm VERY heat intolerant...no hot baths or showers. If outside temps are above 70 degrees, I am a virtual hermit. When I get overheated my legs feel like walking on wet noodles, my eyes get blurry and cog fog sets in and I feel like all the blood has been drained from my body because I am so weak.


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