#MyHhStory: True Life with Hyperhidrosis©

Meet an amazing and beloved member of your #hyperhidrosis community. In her own words, she tells the story of life with hyperhidrosis and the International Hyperhidrosis Society.

Please know: You are not alone. In fact, you are a member of a powerful tribe. Together, we are beating down the impact of hyperhidrosis and #ExcessiveSweating. Join us! We are happy you found us, and now you can #KnowSweat!

If you or someone you care about suffers from hyperhidrosis, you should know that treatments for excessive sweating are available. We’ve got information to help you understand hyperhidrosis and we can help you find the support and treatment you need to live the life you deserve.

#excessivesweating #hyperhidrosis #hyperhydrosis #miradry #botoxtreatment #KnowSweat #dermatology #dermadry #hiperhidrosis #sweatyhands #sweatyfeet #sweatypalms #sweaty #antiperspirant #healing #deodorant #deodorants #bodyodor #stigma #hiperhydrosis

[jodiecatlin]

I totally am with you. My life was ruined from this condition.

[andreherault]

Our life is weird...but we are strong enough...

[Alieve_Films]

Back when I was in school I used to put some papers or a some tissues on my book while writing I couldn't even hold the pen correctly and i used to believe when i grow up all this problems will be gone, but now I still have the same problem I can't text my phone, can't use the touchpad of my laptop it's like Tsunami both my hands and feet are wet, everyday I use different socks. I don't shake hands especially girls instead I put my hands on my chest and pow a lil to show them respect funny is people greet me back that way like I'm fucking chines, anyway I tried many times to go to surgeon but after i saw all those injecting needles I realized its too much risk bcoz they're dealing with nerves if anything goes wrong then you're done. So I let it go and I'm not ashamed to have a Hyperhidrosis.

[arushinainwal]

damn MY SCHOOL LIFE...was destroyed completely..no words...who will bring it back

[macropusrufus]

As a person with palmoplantar hyperhidrosis (sweating on palms and feet), I certainly wish that we could raise enough awareness so that people like us can wear gloves all the timw (even at home) without being perceived as weird.

[hibadas]

Oh god I'm not alone!!😢😭 It feels blessed to know, cause no one understands us like in summers also I need to wear socks!! This is so embarassing 😔 I can't live my life with this.

[sunnysilprium]

I understand completely. I suffer from palmer hyperhidrosis. It makes life very difficult and frustrating.

[kaneangle]

I recieved my Dermadry package yesterday in the afternoon, used it last night and again this morning. And im not going to lie to you guys its 3:29 pm and im already experiencing changes. Im so happy I finally decided to purchase Dermadry... NO REGRETS!!!!

[Sariine]

It makes me isolate from people and I was made fun of it in the past. I get jealous of the smallest things like someone rubbing their dry hands. :/
It made me so sad it gave me anxiety and depression, but I meditate :). I got a iontophoresis mashine today for my birthday and I'm 16.
Hold
On
Pain
Ends

[jodiecatlin]

It seriously affects absolutely every aspect of your life. Im an alcoholic because of it.

[kasubdivrttbn]

42 years old with hiperhydrosis and my 10 years old daughter have it too

[pritam_this_side]

I think I am suffering from more.. because I sweat alot either it's palm or feet, but my butts sweat too much so when I sit on any surface it gets wet, it's really embarrassing.. please suggest me something

[jieun]

I'm 19 now and I'm suffering with primary hyperhidrosis it's hereditary I got this from my mom .There ain't a single moment when I don't remember sweating it's really hard to live a normal life like others ... it's really embarrassing, I can't even express how frustrating it is everytime the paper gets totally wet, I'm afraid of holding things because of slipping through my hands ...there are literally many situations which I can't even explain .It's really hard to live like this ...

[mentality-uj]

This is so true. I couldn't even look at my friends cuz of this conditions.

[ichinikochiniseokjinie]

It sucks having palmo plantar hyperhidrosis. It really sucks.
Friends refuse to hold your hands and makes you feel left out. They don't take your pens and supplies.
You can't hold anything without getting it wet. It sucks even more when you have to take a seminar or something Infront of the whole class and you're socially anxious too. The book would've literally drenched in sweat.
I can't write examinations like normal students because the stress doubles the sweat. I never finishes it within the correct time. I can't take lecture notes and I also can't draw ( I am really talented at drawing. I was a state level competition winner. But sadly I can't draw anymore because the sweating has increased when I reached highschool ).
I can't type anything and it literally took me about an hour to write this and I am not even kidding.
When I consulted a doctor he told me that there are not much options other than surgery.
When I googled about some ways to help my condition, I read about iontophoresis machine but when I checked its price I realised that I couldn't afford it.
Even my parents and siblings gets grossed out seeing my wet hands.
And the worst thing of all is that it's not even included in the list of disabilities even though it should be..
.
.
.
I've just started living and I've already had enough..i wish everything would end already..

[viralmemes]

Same problem .... Can't write on paper .. can't play video games on mobile ...wtf 😢😢😭😭😭😭😭

[mapletree]

i just want to be able to hold someones hand

[sumayyakp]

i have been suffering from severe hyperhydrosis for 30 years..guys there is a treatment invest some money and buy an iontophoresis machine..we have to maintain the results..but you will get a new life for sure..i wish i had known it earlier..

[IncognitoDiabetic]

I feel like I have the same condition but my hands aren’t completely drenched they just have a sweaty film all the time. Idk if I have it or not. Anyway else feel me?

[shambhupandit]

I am also a part of international hyperhydrosis society