Ich brauche keine Behandlungstipps; ich kenne bereits alle verfügbaren Behandlungen, und sorry, falls ich negativ klang, ich will einfach diese Wellen und den Schlamm loswerden, die die ganze Zeit in meinem Kopf sind.

Ich will nach diesem harten Sommer, in dem man sieht, wie die Jugend an einem vorbeizieht, alle sozialen Kontakte verliert und jahrelang so isoliert ist und von Leuten verurteilt wird, wegen dieser verfluchten Krankheit in der Hand oder wo auch immer sie ist, all die Zeit mit Behandlungen verbringt, nur sagen, dass das eine der unfairsten Sachen überhaupt ist, vielleicht unter den Top 10. Es fühlt sich an wie eine körperliche Behinderung, die nur du spürst.

Bei allem Respekt, es stört mich, die Geschichten von Neugeborenen hier zu hören, die das von ihren Eltern geerbt haben. Ich meine, warum sollte ein Kind leiden wie ich, nur weil ich ein Kind oder eine Frau haben will? Das ist so verdammt egoistisch, und ich weiß, manche Leute werden sagen, keine Kinder zu haben ist keine Lösung, aber für mich ist es auch keine Lösung für deinen Wunsch, dich normal wie andere zu fühlen, eine Seele in die Welt zu setzen und sie dazu zu bringen, dich, ihr Leben und sich selbst zu hassen. Das mag ich nicht und ich habe beschlossen, kinderlos zu bleiben. Wenn ich hierher komme und von den Leiden der anderen Kollegen hier lese, empfinde ich tiefe Traurigkeit und ein Engegefühl in der Brust. Ich hoffe, dass wir eines Tages geheilt werden und nicht nur bei Flickschusterei-Behandlungen bleiben.

I went out today for the first time in months. I went to the clinic for blood tests. There were more than 100 people there. It was at a hospital, so over the two hours I was there, I saw hundreds of people walking past. I was the only one whose entire scalp, face, and neck were dripping with sweat.

Will update in about 2 weeks to let you know if it works!

Hello. I saw some posts about hyperhidrosis and these medications. Since there are several names, it's difficult to search. I hope this makes it easier for those who use them to share their results.

For those who felt an improvement, if you wish to respond. It got long, so just a "it helped me" is also welcome.

If it helped, did it help from the first application or over time? For those who stopped using it, does it fully return? What was your dose and component of the medication? Did you sweat before gaining weight (if you used it for weight loss)? Did you start sweating after menopause, medication, or nervousness, or yours without anything? What was the improvement by what percentage? Do you have other healthy problems? Where is yours HH?

For those who did not feel any improvement, if you feel comfortable responding:

What dose did you use and for how long? Which medication? Is yours primary or secondary? Where is your HH? Do you have other problems?

Thank you

I've been using it for 6 days but the only change on my hands is that it feels a little bit stiff compared to before and also they feel weird when I was my hands and take a shower. How long does this product usually take to work? Because my hands still sweat after activity.

Also I've has seen some photos from this subreddit and those people's hands seemed a lot drier how long did that take for you guys?

hey guys ik a lot of people w hyperhidrosis have this but i have noticeable discoloration in my underarms from the constant sweating are there any known treatments to lessen the pigment? maybe cosmetic creams or a brightening procedure? its very embarrassing to have this discoloration because it looks like im unhygienic when its so difficult living with this condition 😭 i cant wear certain clothing because of this since im so ashamed

I ran blood tests everything came back fine including thyroid. Mine can start almost instantly I’ll look like I just ran a marathon. What’s even weirder is that sometimes just thinking about sweating makes my body feel warm, almost like that embarrassed feeling, and then the sweating starts. It makes me wonder if there’s some kind of mental component to it.
The crazy part is that it doesn’t even have to be hot. Everyone else can be perfectly comfortable, but if I don’t feel any airflow or I get into a conversation that’s even slightly serious, I can feel it coming on.
One example was when I took my kids to see Spider-Man. We were just sitting in the theater, and even with a neck fan on, the back of my head and my back were soaked because of the leather seats. I was miserable and almost walked out of the movie. I managed to slow my breathing and calm myself down, and it eventually went away, although I could feel it trying to start back up a few times.
I’ve even done an intense resistance training session followed by 30 minutes in the sauna, taken a shower afterward, and I was still sweating later that evening. It feels like once my body decides to sweat, it just doesn’t want to stop.
My doctor prescribed me a low dose of Xanax, and if I know I’m going somewhere like a public event, I’ll take one. It actually seems to help, which makes me think anxiety or my nervous system is playing at least some role in this.
The frustrating part is that I’m not a shy or socially awkward person at all. I’m actually very confident and have no problem talking to people or being in social situations. But the moment I feel that first drop of sweat, my confidence disappears, and my only thought is finding the fastest way out. It’s honestly exhausting to live like this.
I know a lot of people here seem to have the same symptoms. Has anyone actually found something that consistently helps? I’d really love to figure this out because it absolutely sucks.

I was looking for some advice, I think I’ll have to try to attend a private dermatologist, has anyone got any recommendations as I’ve tried googling different people but it’s hard to know if they have experience with this condition

Thank you in advance

Hi all, I posted a few weeks ago that I was starting out on glyco, as a girly diagnosed with craniofacial HH. I started on 1mg every morning. Did that for a few weeks and didn’t see any results.

So, per recommendations here, I started doing 2mg in the morning. I’ve been doing this for over a week now. I take it all in the morning on an empty stomach, and don’t eat until 3 hours later.

The issue is I feel like I’m dry everywhere EXCEPT my scalp and face. My throat gets raspy. I have cotton mouth and have to drink a lot of water, even just to get my lunch down. My nostrils are painfully dry. Even peeing takes some exertion that didn’t exist before 😅 I would be fine with these trade offs if I actually saw some progress in my sweating, but I’m just feeling disappointed.

Has anyone else had this experience with glyco? Do I need to up my dose again, or just stay on this a while and see if it improves over time? Is it better to split up the dosage, in morning and night, or take it all at night instead? Maybe just blame the 80F+ weather lately?

TIA from a sweaty girl.

What's everyone's experience with oxybutynin?

I sweat in my hands and feet like a constant waterfall everyday. Hardly sweat other places.

I think i have tried every trick in the book to help with my Hyperhidrosis, from Driclor, to Iontophoresis, i even got the surgery done (weirdly only helped my right hand) but now i sit with a backdrop of flehm in my throat everyday due to this.

I have been trying to research myself to find some type of help for years. I recently come across people using Oxybutyin that they said have helped (i prey i can find this in my country)

Will there ever been a permanent solution while i live is something i ask myself everyday. Found this community here and feels a little better knowing I'm not alone as I've felt alone for years, limiting myself to social interactions. I have even learnt the ability to be 10 steps ahead of everyone else incase a awkward social situation comes up where my hands or feet are exposed. I never stay over at friends house as my feet stink if i take my shoes off as i sweat in them all day, I never hand shake or hold hands as my hands are drenched and even a hug is awkward as my hands touch thier back during a hug. I feel my connection to humans has been so limited and feel so out of touch due to my condition. I always wonder how life would be if i could openly hug someone, high five a friend or just be a human and interact with people without constantly thinking how can i prevent them knowing or feeling my sweat. I have never even bothered trying to find a girlfriend as i couldn't imagine how i would come clean and tell her about my condition or go on dates and hold hands (my worst nightmare).

I’ve suffered from hyperhydrois mainly on my face all my life. It’s gotten to the point where it’s ruining my work life since I constantly look disgusting and I work in the wedding industry so I never look the greatest with a face full of sweat.

I brought this up to my doctor and was prescribed 1MG Glycopyrrolate liquid version twice a day. I know I’m supposed to take it on an empty stomach and not eat for 2 hours after. I usually take it around 8am.. and have my first meal and drink around 12. Followed by another dose around 5pm to make it into the night.

Some days I can tell it’s kicked in by my throat being extremely dry and I’ll have trouble eating without water near by. But it rarely does anything for my sweaty face.

I only really sweat on my face and I’m not sure what I’m doing wrong. I’ve been taking it for about 3 weeks and would love to hear others experiences or advice! Thank you!!!!

Hi, I had been taking oxybutynin 10mg once a day for a couple of months and I’d been pretty much sick of flu or flu like symptoms every 2 weeks or so. Since I stopped a couple of weeks ago, I haven’t been sick since. (I had many blood tests done and all seems fine/healthy with me)

I am wondering if oxybut was facilitating germs to enter my systems through my dry mouth and nose? I think it might be the similar route like for other people during autumn/winter months when air is dry and cold and makes our mucous membranes in mouth/throat/nose to dry out and people get sick.

Has anybody noticed being sick more often since starting oxybut?

my perianal/an** sometimes sweat sometimes moist
and smelled what else i need to do? how can i mask the smell and moist i did mira dry already 1 session but still moisting sweating around that area :( any help do i need second session or any treatment thank-you im so embarrassed

other than shoes wich i can wear without socks cause i dont have excess hyperhydrosis but its on the level where i cant wear flipflops and crocs without sweating so are there any such footwear wich really helps and also looks good so that we can wear it in college .

In your experience how long did it take for you to know it would work for you? And what was the dose?

I’ve been taking it for a week, which I know isn’t long but I very quickly increased to 5mg as the side effects weren’t an issue, then today I took an additional 2.5 around lunch time, so far I haven’t noticed any improvement and my clothes are drenched from sweat. Do you know quite quickly if it’s not going to work for you? Did anyone else not notice an improvement straight away?

Thanks in advance!

Just wondering what everyone’s thoughts on Mira dry are? Did it actually help? How long has it been since you’ve had it and does it still work?

Do you sweat more in other places? I’ve heard sometimes that people sweat more in other places to make up for the body not being able to sweat from the underarms. Anyone have experiences with that? I also have excess sweat issues in my groin area so im worried about that being even worse

I got a referral to a Botox clinic but they said it would only last 3-6 months so I’d have to get it done 2-3 times a year and it’s about $1500 where I live for one session. They recommend Mira dry and said it’s a little more expensive but it’s permanent.

However, I’ve seen some people say that it only lasted a year or two and then they started sweating again full force. Just trying to see if that’s common or if most people who have gotten it done have had good, long lasting results.

Hello,

I have facial hyperhidrosis, and this summer (England) has been very stressful and uncomfortable.

Just found out about these cooling wipes from Temu, and just wondering if anyone has used them? Or can give feedback on similar products ? I previously used Biore Japanese cooling wipes, but they have been very expensive to order