severe HH sufferers: can you provide any hope?
Posted: Mon Nov 18, 2013 1:48 pm
Please assist me in formulating ideas in my mind about my hyperhidrosis (HH):
We both know that there are no cures in the near future, so please dont start with the Ionto, botox, ETS, Drysol, yoga, accupuncture, over-intake of water, under-intake of water, voodoo, etc, etc.
Me:
I am in my early 20's and living with HH for 15 years. Until a few years ago it was simply a part of me that I thought was normal. Now however it is making my life un-livable (as I move into adult-hood).
I am especially looking for posts from those who have the following in common with me:
- you suffer from HH in hands AND other areas which are visible to others (face, feet, butt, etc)
- your HH is amplified when your attention level is amplified; ie excited at a party = more sweating; watching an action movie = more sweating;
- you have had episodes of "panic attack" where the sweating was so extreme that a puddle was left on a chair or so visible that anyone with eyes would notice
Please give me some encouragement that this is not a "death sentence" - ie not really death, but makes everyday life so miserable.
I use Iontophoresis and have done botox in the past for hands. Botox efficacy degrades each treatment, and is reduced to nill after 5 or 6 treatments (3 years or so) and risks permanent muscle atrophy at about the same time.
ETS is maybe OK for those with a bit of hand-sweating; but for severe HH it is obviously a disaster (the good thoracic surgeons wont perform ETS for us although the bad ones will).
So with all that junk, here is my question for you:
Is there anyone reading this who is able to get out of bed each morning, go out into the world and be productive, hold a job, marry a spouse (or date others), and have say a minimum of a handful of good times each week?
Or is everyone with moderate to severe HH condemned to be a recluse - stay in our house, not venture out for fear of all that HH has to offer? Always afraid to hold hands, always afraid of a panic attack that will unleash a flood.
The HH cant be stopped - I realize that I have to come to grips with this fact. But how can the devastation of knowing what great a life could have been lived without HH holding me and you back?
I am looking for someone to say (in their own words and mean it)
"Yes - I have HH and it is severe. I have had panic attacks and left a flood on the floor/chair/ceiling. I sweat all the time. But I finally learned to say - the heck with the gawkers - I go into the world now and yes I sweat - then I freeze - and then I sweat some more. I can't do alot of things that I want to do because my hands dont have the grip that others take for granted. But I do enjoy something about every day - and I can say that I am happy enough times throughout the week to be satisfied with my lot in life."
Is there someone out there suffering from severe HH that can say the above in their own words and mean it?
Thanks!!
We both know that there are no cures in the near future, so please dont start with the Ionto, botox, ETS, Drysol, yoga, accupuncture, over-intake of water, under-intake of water, voodoo, etc, etc.
Me:
I am in my early 20's and living with HH for 15 years. Until a few years ago it was simply a part of me that I thought was normal. Now however it is making my life un-livable (as I move into adult-hood).
I am especially looking for posts from those who have the following in common with me:
- you suffer from HH in hands AND other areas which are visible to others (face, feet, butt, etc)
- your HH is amplified when your attention level is amplified; ie excited at a party = more sweating; watching an action movie = more sweating;
- you have had episodes of "panic attack" where the sweating was so extreme that a puddle was left on a chair or so visible that anyone with eyes would notice
Please give me some encouragement that this is not a "death sentence" - ie not really death, but makes everyday life so miserable.
I use Iontophoresis and have done botox in the past for hands. Botox efficacy degrades each treatment, and is reduced to nill after 5 or 6 treatments (3 years or so) and risks permanent muscle atrophy at about the same time.
ETS is maybe OK for those with a bit of hand-sweating; but for severe HH it is obviously a disaster (the good thoracic surgeons wont perform ETS for us although the bad ones will).
So with all that junk, here is my question for you:
Is there anyone reading this who is able to get out of bed each morning, go out into the world and be productive, hold a job, marry a spouse (or date others), and have say a minimum of a handful of good times each week?
Or is everyone with moderate to severe HH condemned to be a recluse - stay in our house, not venture out for fear of all that HH has to offer? Always afraid to hold hands, always afraid of a panic attack that will unleash a flood.
The HH cant be stopped - I realize that I have to come to grips with this fact. But how can the devastation of knowing what great a life could have been lived without HH holding me and you back?
I am looking for someone to say (in their own words and mean it)
"Yes - I have HH and it is severe. I have had panic attacks and left a flood on the floor/chair/ceiling. I sweat all the time. But I finally learned to say - the heck with the gawkers - I go into the world now and yes I sweat - then I freeze - and then I sweat some more. I can't do alot of things that I want to do because my hands dont have the grip that others take for granted. But I do enjoy something about every day - and I can say that I am happy enough times throughout the week to be satisfied with my lot in life."
Is there someone out there suffering from severe HH that can say the above in their own words and mean it?
Thanks!!