Does anyone else have trouble regulating ... - Cure Parkinson's
Does anyone else have trouble regulating their body temperature? I was told that Parkinson's sometimes attacks our Autonomic System.
Not as bad as when I went through menopause!
LOL!!! I know what you mean! I had an early onset Menopause due to a hysterectomy and that was really bad. But this is different....I used to not sweat very much, but it seems now I sweat with evey little movement cause my body temperature rises. Do you know any rememdies?
Jerri, My husband does this also. Haven't found an answer yet, but still searching. If I find something I will definitely share. His gets so intense he gets a cold cloth for his face and head. Take care, Ludie
If we go somewhere in the summer, I keep a cold cloth in a cooler with an ice pack so I can cool my face and neck. This is really not very becoming for anyone....but I deal with it.
Yes, I have also found this a problem. Sometimes I am very hot and sweating and other times cold.
Even a little exertion and my faces breaks out in sweat and I look like a lobster.
Not very attractive and sometimes embarrassing. Have not found an answer yet, but am sure someone will be able to help. One of the reasons I love this site.
Me 2 i find after my sinment i break out in a hot sweat then at night i freeze but cannot turn my air off, if i can get out of bed i warm a wheat pack or shiver until i can get out of bed..
If i turn the air off i cannot breath.
I hate nights get frightened because my meds seem to ground me still dont no what i'm meant to be doing with meds.
I break out in a sweat if I have forgotten my meds by 15 mins.. Also if under stress.
Can soak a shirt in 3mins flat
I just grin and bear it until I can change.
No I have problem with water. Legs swell then meds kick in and I have to run to the bathroom. Even pre-PD did not sweat much. It was a problem when jogging in the summer!
When I do strenuous work, like in my yard, during summer I sweat like a pig. Never had this problem before PD. I asked my neurologist, who said this is a normal problem for PWP. Sorry, no meds, no cure; just have to learn to live with it.
Hubby tends to be cold especially his feet and hands. They are a bit better since he started taking B Complex vitamins though. He is always wearing a sweater or jacket because he feels chilled.
Me too. My hands and feet get very very cold
I he been sweating profusely over the past 3 or 4 months. It is mostly my head and face,. I was told it had to do with my autonomic system, I gues it is a
Part of Parkinsons. I did try Drysol. It worked for a while, but you must keep applying it,
Pittgirl