I have brittle diabetes type 1.. my bloodsugar can raise at an emotional upset or lower with being calm.. it can sink randomly but i have a worse case than most.. i test myself more than 10 times a day to stay under controll and take at least 7 injections.. it can make you dizzy or sick or faint or barf or tired or shake.. this was a question to sweating.. but in all honesty i was much more capable of a normal life freedom driving and working without epilepsy.. i cant monitor it daily or prevent the effects of it nomatter how hard i try.. i have a very severe case of epilepsy seizures and damage however i want to say to all of you. I am constantly upset and feeling hopeless do to the lack of help to people in situations not making enough to pay rent not allowed by doctors concerned to work not allowed to drive to somehow find a way to make it better and farther in life. I must say.. nomatter what help i dont have if I can’t find it i will make and find my own never give up but also one day i pray to make a difference and help and awareness for people like us. Money is an issue but if i die trying i will do my best to accomplish this and i think every day of somehow all of us doing this together. One day i will think of a plan to do this and sometimes I believe we all need to find a way to improve. Supporting having compassion and understanding advice and fellow awareness and safety and communication in our lives is a beginning and more of the world can use this. People with or without medical hinderances have hinderances every way they turn and i want to change that. People feel allone sad hopeless and even i do. I think every day and feel like a failure but i still see a ray of sun waiting to shine and it drives me crazy never finding a way to do it. Sometimes it takes a group of people to start one. Perhaps we should find ways to do this in other ways as well. Call me crazy but i speak my mind.

I saw a woman who had a sweating issue it wasn't menapause it was immune deficiency where she was allergic to certain enviorments. I also know my last bad big siezure, i was sweating and it was dripping down me never had veen like that before so I know what your saying. Hope you find some answers.

I never sweat! I am going through menopause and very rarely sweat now! Have you said anything to your doctor and what medications do you take?? One other thing. My ex husband sweat all the time too. Nobody noticed why but it was found out there was a genetic cause on his dads side of the family. It had not been noticed for a long time since his mother and dad had been divorced and he had to get the medical history. Sometimes stress can cause it. Just look at all the different cause around you because they can combine to make them. gOOD LUCK AND HAVE A SEIZURE FREE DAY!

You are not crazy if you're making sense. Its just people don't want to make the time to show compassion, understanding unless there is something in it for them. Otherwise, they don't see the point. It would be nice if we could find work with a company that we could work at home. I still feel bad I can't work anymore because of my seizures and stress. But I find myself having to be like you and find a way to get through the day. Find a doctor who can assist me and not tell me to take 2 and call me in the morning if anything changes. You always find a way to do it. Take care, and continue to speak your mind. Maybe someone will listen.

Wow, I thought I was the only one that goes through this. I too have night sweats. And sometimes it happens in the winter time. It also occurs on nights I don't sleep well. Right now I am averaging 3-4 hours a night. It's a strange feeling to just lay still and break into a sweat out of no where. I had to change out of my Iron Man shirt and comfy pants. Hope you get through this uncomfortable time and have a seizure free day, take care.