cure for hyperhidrosis?

klamm76

klamm76

Well-known member
Is ETS the only cure for hyperhidrosis? Or i will put it this way,yes you have dry hands permantly but it is a trade off.Because you have to sweat severe else where,so....

I take iontophoresis now and its working,but still not satisfaied.Still sweat and must spend a lot off time doing it + I have swellingproblems because of the hyperhidrosis.

All the things I have tried out to stop the sweating from my hands and feet:botox,different antiperspirants,bioenergiser,herbs(anti-sweat),and now ionto again.Idrostar and that works better than drionic i have tried out before.BUT still not satisfaied.I want to get totaly RID off the HH.Know it sound selfish off me because there are people out the that sweat a lot more than me,suffering from side-effects(ETS),ionto or nothing is working for them.And it is offcourse alot of diseases that are worse to.

Im just so frustrated,because I look at other people every day and envy them because of their healthy nervous system and dry hands/feet.

Much off bla,bla here now. Its just that everything we can do to help our self whit is things to stop the sweating glands,when the really proplem is in the nervous system.So tired of reading 100% guaranti for treating hyperhidrosis,I havent still read 1 post of someone who has get rid of hyperhidrosis on the forums by herbs,mind,diet and so on........

And i dont trust the sunshine stories from the sites that sells the products anymore.

I know that the nervous system is complicated,but why hasnt anyone come up whit a cure other than ETS??

Dont they know how,do they not want to because off all the money that it is in this HH HELL.Is there anyone/country who do sience to treat HH permanetly??Is ETS really the answer?

How diffcult can it be if someone spend money to find a cure.

One example.Why do I not sweat when I am drinking alchohol?Im never nervous when i do not drink but still sweating like hell in hot rooms.

There must be something that can carm down or balanse our nervous system like alchohol do.I cant drink everyday,and do not either.

Have a couple other example to,but my english is not that good so i cant go into details.so then its better to not write.

woahuirøgbkjiopkjioptgedhbjiopatejio5r90i420+y543u90hbpjmio there must be something do treat this f....... terribale ,cruel desise.

Would like some other opinium on this topic.

By the way im NOT drunk,just pisst off by this condition.

I WANT TO BE NORMAL.
Whish u all the best,happy eastern:)
 
A

April27

Member
klamm76 said:
Is ETS the only cure for hyperhidrosis? Or i will put it this way,yes you have dry hands permantly but it is a trade off.Because you have to sweat severe else where,so....

I take iontophoresis now and its working,but still not satisfaied.Still sweat and must spend a lot off time doing it + I have swellingproblems because of the hyperhidrosis.

All the things I have tried out to stop the sweating from my hands and feet:botox,different antiperspirants,bioenergiser,herbs(anti-sweat),and now ionto again.Idrostar and that works better than drionic i have tried out before.BUT still not satisfaied.I want to get totaly RID off the HH.Know it sound selfish off me because there are people out the that sweat a lot more than me,suffering from side-effects(ETS),ionto or nothing is working for them.And it is offcourse alot of diseases that are worse to.

Im just so frustrated,because I look at other people every day and envy them because of their healthy nervous system and dry hands/feet.

Much off bla,bla here now. Its just that everything we can do to help our self whit is things to stop the sweating glands,when the really proplem is in the nervous system.So tired of reading 100% guaranti for treating hyperhidrosis,I havent still read 1 post of someone who has get rid of hyperhidrosis on the forums by herbs,mind,diet and so on........

And i dont trust the sunshine stories from the sites that sells the products anymore.

I know that the nervous system is complicated,but why hasnt anyone come up whit a cure other than ETS??

Dont they know how,do they not want to because off all the money that it is in this HH HELL.Is there anyone/country who do sience to treat HH permanetly??Is ETS really the answer?

How diffcult can it be if someone spend money to find a cure.

One example.Why do I not sweat when I am drinking alchohol?Im never nervous when i do not drink but still sweating like hell in hot rooms.

There must be something that can carm down or balanse our nervous system like alchohol do.I cant drink everyday,and do not either.

Have a couple other example to,but my english is not that good so i cant go into details.so then its better to not write.

woahuirøgbkjiopkjioptgedhbjiopatejio5r90i420+y543u90hbpjmio there must be something do treat this f....... terribale ,cruel desise.

Would like some other opinium on this topic.

By the way im NOT drunk,just pisst off by this condition.

I WANT TO BE NORMAL.
Whish u all the best,happy eastern:)
Click to expand...

HH is hell.
 
Jezza

Jezza

Well-known member
I guess there is no way of knowing whether or not someone is working on a solution, I mean, we won't know till we know.

I too am hoping somebody will ultimately find out what is causing the nervous system to "go crazy". I strongly feel it's not just that the sympathicus is overreactive without an underlying reason, I think it's way too far out of the normal situation for that, and also there are too many variations of HH. (If it was genetic, wouldn't everyone have almost the exact same symptoms, instead of one person with axillary, the other facial or palmoplantar HH???)

As I've mentioned before in a topic, I think the best bet to find what's causing HH is for medical examiners to gather a group of HH sufferers and try to single out the common denominators among them, and then look what could be causing the HH. (DNA, bloodwork, maybe physiological pattern etc). I believe this would be much more effective than approaching it purily theoretical, with no real understanding of what HH means.

First of all, we should establish 100% certain what is the cause of HH. I think it's insane this still hasn't been achieved. How do you expect to find a cure when you are not sure about the cause?

Finally, I don't think there's a conspiracy going on to prevent finding a cure. Obviously some people will benefit if there isn't a cure but a lot of medical people/companies are ambitious, if they can solve a disease they will do it, even if only because they'll reap the benefits from that too...

Luckily I think lately there's clearly a tendency to give HH more attention. More people begin to realise how severe the problem is and that it's probably physical more than anything else, which means there could be a physical cure.
 
klamm76

klamm76

Well-known member
I agree.

But I think the reason why some people have axillery HH,some hands/feet HH,some all over body HH and some is blushing is that we do not have the same connections in our nervs.

There are milions of nervetreads in only the symphatic system and they maybe do not connect the same in all of us???

Maybe thats why some ETS pasients who have the same t1,t2,t3........cut have different side-effects.

I dont know, but this could be a reason.?
 
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