First off I'd like to thank the sweet Lord above for this forum, came across this recently and until then thought I was one of 5 people with severe HH. Reading all your posts and comments has been very uplifting to me and I hope to learn from those of you who have tried different solutions to combat this condition. I hope that you guys can take some time to read my story (might mimic a lot of other people on here) and give me input on some questions I have, this would mean the world to me as I have just recently found the courage to finally get up and do something about my hyperhidrosis instead of feeling unhappy at times and sorry for myself.
Keeping this as short as possible, I'm 22 years old and have severe hyperhidrosis in the hands and feet with armpits sometimes also being an issue (palmar, plantar, and axillae). I have had this since I was maybe 13-14 years old, the condition never got better or worse where I've had abnormally sweaty hands and feet for the last 8-9 years with some sweaty pits too (I have to watch what color/material shirts I wear quite a bit). Living through the teenage years, high school, and college was tough and I have no idea how I actually survived but I know it involved some embarassment, shying away from certain situations, wiping my hands a lot, and avoiding physical contact unless I was under the influence and drinking.
It wasn't until a couple months ago when I was finishing up my undergraduate studies that I decided that this condition was severely affecting the quality of my life and dominated it from the moment I woke up to the moment I went to bed, constantly being a worry in my mind. That is when I decided to really do something about it. I had seen a dermatologist awhile back as a freshman in high school complaining about my hands (the main thing I, or we
, care about) and she seemed to not really understand the severity of my condition and perscribed me drysol. I tried following the directions for my hands applying them on at night after I showered then wearing gloves for a couple weeks and nothing happened. Then I thought there was no solution, until recently.
After I decided that I was going to look into solutions for hyperhidrosis and really get serious about it, I perused over all the listed treatments online and one that stood out to me was the Mayo Clinic's sympaTHOTOMY, not the ETS but a different version where they simply cut the connection between the nerves instead of removing them or clamping them (http://www.mayoclinicproceedings.com/content/78/2/167.full.pdf). This procedure has had great success, the study currently out being a sample size of only 10 but a new one is coming out in August with a size of 150. I think it was 148 people were happy with the operation with minimal CS and dry hands, basically a miracle operation with minimal risks. I even had the chance to speak to someone who had the surgery 3 years ago and amazingly his hands are still bone dry to this day, using them to wipe sweat off his brow and other areas when exercising. I still had my doubts as I know to take everything in with a grain of salt. I flew to the Mayo Clinic in Rochester Minnesota with my father and heard from the surgeon himself. They were all very understanding, professional, and honest (no pressure). I was very close to electing to do the surgery, but after talking with my family we decided that it would be best to try other treatments first.
So here I am with some questions and praying that a solution out there can work for me like it has for some other people, dry hands (and if possible feet and armpits) would mean the world to me and I would give up so much for it (within reason of course!!). Living with HH has been such an impediment on my life and I feel that if I could just get this addressed and put to the side I could really move forward in life and get to experience new things.
My questions:
I think that Iontophoresis is going to be my first plan of attack and fortunately for me money is no problem in regards to buying a machine that gives me the highest probability of sweat reduction in my hands, feet, and possibly armpits. Because there are a lot of machines out there, I was looking at the Idromed 5 PS, Idrostar Pro Pulse, and Hidrex 500 PS. I was wondering what you guys thought of those 3 machines and which (if you know) has delivered the best results.
Also, these machines claim to be able to treat both hands and both feet at the same time, how is that possible when they only come with 2 trays that detach from being a briefcase?
They also claim to be able to treat armpits with some type of pad, I was wondering if anyone has tried this out or has any thoughts on that.
I am not very educated in terms of electricity and how it works but after reading some stuff I came across the issue of polarity and I was wondering how that plays into those machines and what I will need to do to ensure the best chances for results.
After the iontophoresis questions I was also looking into taking Robinul Forte after reading about the success people have had with taking that, not sure if I should do ionto first then take Robinul or vice versa, etc. I've read here that some people take the pill year round, bear the side effects, and have happily experienced dramatic sweat reduction.
The last question is in regards to the Diltiazem pills and whether those are worth trying or not before the Robinul due to what appears to be milder side effects.
This is my first post (of many I'm sure) and I can't thank you guys enough for being there for all of us with HH and taking time to post your comments on this board. Any opinions or thoughts would be greatly appreciated, the more the better. Thanks again!!!
Keeping this as short as possible, I'm 22 years old and have severe hyperhidrosis in the hands and feet with armpits sometimes also being an issue (palmar, plantar, and axillae). I have had this since I was maybe 13-14 years old, the condition never got better or worse where I've had abnormally sweaty hands and feet for the last 8-9 years with some sweaty pits too (I have to watch what color/material shirts I wear quite a bit). Living through the teenage years, high school, and college was tough and I have no idea how I actually survived but I know it involved some embarassment, shying away from certain situations, wiping my hands a lot, and avoiding physical contact unless I was under the influence and drinking.
It wasn't until a couple months ago when I was finishing up my undergraduate studies that I decided that this condition was severely affecting the quality of my life and dominated it from the moment I woke up to the moment I went to bed, constantly being a worry in my mind. That is when I decided to really do something about it. I had seen a dermatologist awhile back as a freshman in high school complaining about my hands (the main thing I, or we
After I decided that I was going to look into solutions for hyperhidrosis and really get serious about it, I perused over all the listed treatments online and one that stood out to me was the Mayo Clinic's sympaTHOTOMY, not the ETS but a different version where they simply cut the connection between the nerves instead of removing them or clamping them (http://www.mayoclinicproceedings.com/content/78/2/167.full.pdf). This procedure has had great success, the study currently out being a sample size of only 10 but a new one is coming out in August with a size of 150. I think it was 148 people were happy with the operation with minimal CS and dry hands, basically a miracle operation with minimal risks. I even had the chance to speak to someone who had the surgery 3 years ago and amazingly his hands are still bone dry to this day, using them to wipe sweat off his brow and other areas when exercising. I still had my doubts as I know to take everything in with a grain of salt. I flew to the Mayo Clinic in Rochester Minnesota with my father and heard from the surgeon himself. They were all very understanding, professional, and honest (no pressure). I was very close to electing to do the surgery, but after talking with my family we decided that it would be best to try other treatments first.
So here I am with some questions and praying that a solution out there can work for me like it has for some other people, dry hands (and if possible feet and armpits) would mean the world to me and I would give up so much for it (within reason of course!!). Living with HH has been such an impediment on my life and I feel that if I could just get this addressed and put to the side I could really move forward in life and get to experience new things.
My questions:
I think that Iontophoresis is going to be my first plan of attack and fortunately for me money is no problem in regards to buying a machine that gives me the highest probability of sweat reduction in my hands, feet, and possibly armpits. Because there are a lot of machines out there, I was looking at the Idromed 5 PS, Idrostar Pro Pulse, and Hidrex 500 PS. I was wondering what you guys thought of those 3 machines and which (if you know) has delivered the best results.
Also, these machines claim to be able to treat both hands and both feet at the same time, how is that possible when they only come with 2 trays that detach from being a briefcase?
They also claim to be able to treat armpits with some type of pad, I was wondering if anyone has tried this out or has any thoughts on that.
I am not very educated in terms of electricity and how it works but after reading some stuff I came across the issue of polarity and I was wondering how that plays into those machines and what I will need to do to ensure the best chances for results.
After the iontophoresis questions I was also looking into taking Robinul Forte after reading about the success people have had with taking that, not sure if I should do ionto first then take Robinul or vice versa, etc. I've read here that some people take the pill year round, bear the side effects, and have happily experienced dramatic sweat reduction.
The last question is in regards to the Diltiazem pills and whether those are worth trying or not before the Robinul due to what appears to be milder side effects.
This is my first post (of many I'm sure) and I can't thank you guys enough for being there for all of us with HH and taking time to post your comments on this board. Any opinions or thoughts would be greatly appreciated, the more the better. Thanks again!!!
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