Hyperhydrosis. --over sweating and excessive blushing. Someone please help me.?!
Question: i sweat under my arms way more than normal. I've tried every anipersperant ever made and nothing works. right now i use drysol (its a prescription anipersperant) and it works great, but it gives me nasty chemical burns, and i can't shave 'under there' for 2 days before i use it. does anyone know of something else that may help me? Also, hyperhydrosis makes my face turn bright red a lot. It looks like im MAJORLY blushing, but im not even embarassed when it happens, i could just be talking to someone and my face turns all red. I try so hard to avoid presentations at school because of this. I have no clue what to do about it. Does anyone have any suggestions? Please help, I'm so desperate.
Answers: i sweat under my arms way more than normal. I've tried every anipersperant ever made and nothing works. right now i use drysol (its a prescription anipersperant) and it works great, but it gives me nasty chemical burns, and i can't shave 'under there' for 2 days before i use it. does anyone know of something else that may help me? Also, hyperhydrosis makes my face turn bright red a lot. It looks like im MAJORLY blushing, but im not even embarassed when it happens, i could just be talking to someone and my face turns all red. I try so hard to avoid presentations at school because of this. I have no clue what to do about it. Does anyone have any suggestions? Please help, I'm so desperate.
I don't know about blushing but for the sweating you can use the new deodorant called Degree Clinical Protection for men and women. It works like a prescription but its not of talk to your doctor about the side effects.
I, too, sweat way more than others, not so much from anxiousness arising out of social situations but rather from warm weather. Mine is primarily on my head, face and upper body. Surprisingly, my underarms sweat very little and my hands and feet stay very dry. I, too, have tried everything including strong antiperspirants that seem to attack my skin and only make the condition worse. I greatly sympathize with you and hope you can find some solution but, after may years of this and many "solutions," believe this malady is unchangeable.