Sweating and Parkinson’s : If you or your... - Cure Parkinson's

Cure Parkinson's

25,478 members26,800 posts

Sweating and Parkinson’s

jcavana profile image
11 Replies

If you or your person with Parkinson’s has excessive sweating issues (afternoon and evening) what did you do to deal

with it? Does your sweating come with lots of involuntary movements too? Did you change meds or timing of meds? I have read that sweating could be a sign of meds wearing off.

Written by
jcavana profile image
jcavana
To view profiles and participate in discussions please or .
11 Replies
pvw2 profile image
pvw2

mayoclinic.org/symptoms/nig...

Enidah profile image
Enidah

Yes, I get that during the day from dyskinesia. ...especially if the day is warm.I have lots of fans in my house and I dress in light breathable clothes.

Hikoi profile image
Hikoi

mayoclinic.org/diseases-con...

We have autonomic disfunction which leads tp the problems in this link.

Hikoi profile image
Hikoi

For me i get really hot when my meds wear off but also at 5am! I dont sweat though. If it happens with dyskenesia ( involuntary movement) it is probably a peak dose problem. Sorry cant help more.

Tilly56 profile image
Tilly56

I get hot flushes day and night then cool down

eschneid profile image
eschneid

I go through periods with the sweating, it comes and goes for weeks at a time and then it's gone for months at a time... Same with extra saliva and some other things that I can't remember right now. Can't explain it....

DianeF profile image
DianeF

Thanks for bringing this up. If the temp is above 70, I sweat profusely with the slightest exertion. Just going for a walk will do the trick. My hair and clothing will be dripping wet. Although I never tolerated heat well, this is a new development and can be embarrassing. I’m also a gardener and this impacts my work as perspiration will literally drip from my face. It doesn’t appear to be related to off time. My doctors just shrug and say it’s related to Parkinson’s. I’m afraid to do much in public now in the summer months.

134A profile image
134A

Sweating excessively wether PD related or not, could be a sign that the body is eliminating an excess of toxins either food, medications or environmental.

FMundo profile image
FMundo

Its seems that I sweat at appropriate times (Exercise, under pressure, etc.) but what is different is that since I've had Parkinsons I experience a lot more "facial" sweating. My solution is to wear a sweat band around forehead. Problem solved. I can see again !

horsplay profile image
horsplay

I suffer from excessive sweating and heat intolerance (plus I live in SC). My dermatologist prescribed me glycopyrolate. This drug has been a great addition to my regimen.

Cbgs profile image
Cbgs

I’m 53……actually 54 tomorrow !!🎂🎉🎂PD and menopause🤷🏼‍♀️

Oh the joy of it all !!!!

I do find tho, the hour stretch of dripping sweat is correlated to meds.

Be well all

C!

You may also like...

Travelling with Parkinson’s

counting the off times when you struggle to take your coat off/put on or fumble through your...

autophagy and Parkinson’s

I’m not saying I’m curing my Parkinson’s, but I believe soon I’ll be off meds....

Tapeworms and Parkinson’s

salivating all night and ‘went to the loo’ about 10 times. His torrid night ended with him...

Metformin for Parkinson’s?

drugs. Are any of you taking it for PD off label or for Diabetes? Thank you

The key to fighting Parkinson’s is a Autophagy

improved drastically. I talk as fast as I did before Parkinson’s. Michael J Fox foundation...