Has Anyone Out There Sweat Contineusly , I Mean Really Bad And If I Do Any Activity Is Gets Worses.? | MyParkinsonsTeam

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Has Anyone Out There Sweat Contineusly , I Mean Really Bad And If I Do Any Activity Is Gets Worses.?
A MyParkinsonsTeam Member asked a question đź’­

Sweat,sweat,sweat, it's all I can think of because it all I do besides tremors, and severe constipation. These sweats m ake me so weak and faint.
PLEASE ANY HEIP!!!!!!!!!

posted October 8, 2016
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A MyParkinsonsTeam Member

I too sweat when active. After showering and getting ready to go somewhere I need to shower again. Whew. Exercising is a major meltdown needless to say.

posted October 9, 2016
A MyParkinsonsTeam Member

The sweating is driving me crazy. It just never stops & is so embarrasing, I have an appointment with my neuro in 2 weeks. He better come up with a medication to help me. I think I will mention it to my internist too.

posted January 14, 2017
A MyParkinsonsTeam Member

I have to keep going to cool off in the shower........ always have a bottle of waterin my hand to drink.

posted October 9, 2016
A MyParkinsonsTeam Member

I'm with you. Just one of the many gifts of PD. I haven't found a fix but drinking lots of water helps. Staying hydrated can make a difference in a lot of areas. I'm not good at doing it though..

I thought hot flashes were bad. But I sweat so much more now. Think I'll just carry around a beach towel and pretend I just came from the sauna, pool, or gym.:)

posted October 8, 2016
A MyParkinsonsTeam Member

My sweating was so severe, it ran down my back & down my face. My neuro couldn't help me. I told my internist about it. She prescribed Venlafaxine ER 37.5 MG, which I take in the AM & again at 4 PM. I haven't had a bad sweating episode since I began taking this. It's a mild antidepressant used for hot flashes. It also comes in stronger forms but this works for me. Good luck

posted March 28, 2017

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