I've been volunteering at IHHS ever since I was in high school and Lisa and the staff always treated me with care and respect. They go to great lengths to get the word out about hyperhidrosis and raise awareness about this disorder. I've known this organization almost since the beginning and seen them grow and do great things. Thanks to the work that is done, HH treatment and insurance coverage for it has come a long way. They're always in the know about upcoming treatments and work hard to facilitate progress in the field by interacting with scientists and companies that develop treatments for hyperhidrosis. There really is no other organization like this in the world.
This is the ONLY organization that understands WE are out here and need their help. They continue researching and always share any help they can to hyperhydrosis sufferers. I've had this condition since I was a teenager... now 38 and I've tried everything over the counter and many prescriptions. Over the counter products do not work and most prescription solutions have nasty side effects. There are medical solutions out there but many are temporary and not covered by insurance. Without the International Hyperhydrosis Society - we wouldn't be getting anywhere and the information wouldn't be out there in the world letting everyone know - THIS IS A REAL CONDITION and those who are suffering ... you are NOT ALONE.
Really the only place I have found ( and I rigorously have been searching)that is aggressively trying to help and address relief from this ignored and debilitating condition.
being in a stressful situation waking up perspiring before my brain was awake I went to the doctor and luckily a rep had just left and the doctor caught up with him and took one of his samples and gave it to me it was driclor it was wonderful it helped my stress levels and was effective from the start irene
I have been suffering with hyperhidrosis for the past few years. It just came out of nowhere for me. I don't know if it was because i got older or because of my hypothyroidism. I, of course, at first didn't know anything about this problem or that anyone else suffered from it, like me. When I went to my primary doctor I don't think he knew that much about it either. He referred me to a dermatologist and they gave me this prescription spray that burned my underarms and made them worse. I went back and told them of the burning and they told me to keep using it but also prescribed a hydrocortisone cream. The hydrocortisone cream worked to take away the rash that came from the burning but the spray kept burning my skin. I finally stopped using the spray and went out on my own to find something that works. Through a google search I found the hyperhidrosis Society website and got some samples. I also got something called pit paste and tried out and am still using a number of things just to make it through the day at work so people won't smell me and I won't feel uncomfortable wet. On the Hyperhidrosis website Christine Fleckenstein got in touch with me and kept in touch with me to link me with different websites and tell me about the Botox seminar coming up. Unfortunately, the seminar has been cancelled but I felt like I gained a friend in hyperhidrosid through Christine.
I've been begging physicians for help with severe hyperhidrosis since I was 8 yrs old...50 years of my life begging for help only to be unheard and dismissed as having a psychosomatic issue. Talk about defeat. The International Hyperhidrosis Society webpage is the first of it's kind to recognize that the problem is real, reaching out to those of us who silently suffer, with current information about who, how, what and where we might find help.
Praying that this godsend of a nonprofit will continue to forge a path of discovery in finding new treatments and practitioners to help.
I have nothing else but good things to say about this organization. They are very supportive with people suffering from HH and they continue to strive day in and day out to find THE CURE! Thank you so much for everything!
I'm from Germany and I'm really suffering from distinctive excessive sweating all over my body, no matter which part - you name it, I sweat it.
Therefore I'm deeply grateful that there is such a great nonprofit organisation which is engaged with this topic!
Hope to hear more and more good news in the future and maybe someday, there will be a cure even for myself.
Thanks a lot!
I have friends and acquaintances who suffer with Hyperhidrosis. I tell all my friends about SweatHelp.org. It is very helpful and informative for those with the disease. I appreciate all the help this gives those with the condition.
The transparent Mission of the IHHS is a refreshing motivating tool for all of us to become more attentive and active in the advancement of the quality of life for people of all ages; both women and men.
As an Engineer, I appreciate the informative and enjoyable format of the IHHS Newsletter.
It always sets forth a logical, well prepared message that clearly defines their Mission to help others.
This nonprofit is superb. Both Lisa Pieretti and Christine Fleckenstein epitomize the utmost professionalism, care and diligence in assisting both public as well as private individuals on combating hyperhidrosis. I'm GRATEFUL the IHHS serves as an effective, professional liaison and I have zero qualms recommending them. Thank you everyone!