I'm a 22 year old girl from Spain and have hyperhydrosis on my hands and feet. When I was 17 I looked into doing the ETS surgery, I researched it extensively. I came across a site where there were sections for positive reviews and negative reviews, as well as a discussion board. After reading all the available evidence, I finally decided to go ahead with the surgery, crazy as that may sound to some of you. I guess you can understand what it's like to be that desperate though. Anyway, I promised the people on the board I'd let them know how it went for me, but I can no longer find it, so I though I'd let you guys know.
It's been 5 years now since I got the clamps put in at the T3 level, and I have to say that overall I am very very happy with the results. Not everything is perfect of course, I do have compensatory sweating, pretty much all over, but it's not too bad and definitely far better than not having adequate use of my hands. I have been able to study car mechanics, something I'd never have considered before.
It's taken me this long to get back in touch with fellow hyperhydrosis sufferers because I've been too busy enjoying life, I guess that's what happens when things go well with you...what things were like kind of move to the back of your mind, and you forget how well you really have it.
I just want to say, for those of you for whom ETS has gone wrong, I am really, truly sorry. I cannot fathom just how awful your situation must be. I saw that possibility of having to share your plight, and hoped with all my might that it wouldn't be so. I have been so, so lucky.
I know a lot of you are filled with rage and bitterness at your situation and how you got there, and I understand that. I'm guessing if I were in your shoes I would feel exactly the same way towards the surgeons, and I even did my homework!
But I feel I need to say that it is not always bad. My life has changed so much, and for the better. It wouldn't be this way if I hadn't been able to have the surgery. I also think there are more good stories out there than you realise. The people for whom it has gone well aren't giving their hyperhydrosis a second thought, or the surgery for that matter. It's probably at the back of their minds like it was for me. The people for whom it has gone wrong though...well they have their suffering as a constant reminder, they're the ones on the Internet, trying to find solutions, or just a sympathetic stranger with whom they can share their woes. So I think it seems like there's more of them because they're here condemning the surgery and the surgeons, understandably so.
So I guess what I'm trying to say is let's not forget all the people who have benefited from this surgery. All the people whose lives have changed for the better because of it. Much as I feel for your case, I do not wish for the surgery to be banned, because I would be robbing other people of the opportunity to share my happy story.
What I would like is honesty, transparency and prudence from the surgeons. I researched everything about the surgery, but I guess not everybody does that, and they shouldn't have to pay for it. The surgeons are supposed to be the highly informed individuals, and should therefore be completely honest about every single thing that can go wrong with this surgery, something which I don't think EVER happens. My surgeon did not mention anything to me. That is really despicable. At the end of the day, there are still people undergoing this surgery even whilst knowing the risks, I am a shining example of that. Everybody should be given that choice, and not a completely unrealistic, rose-coloured version of what goes on.
Well I don't really know why I've come to tell you all this. I just felt that I needed to keep my word and give a report on the long term effects of the surgery for me. I hope that maybe this will be useful to someone out there.
I wish the best to all of you.




