"I knew he was the one for me when he held my hand without flinching, even when I tried to pull away out of embarrassment. He told me he didn't care and continued to hold my hand." This early tender moment eventually led to love, an engagement and an unforgettable wedding day. But to Therese Hernando, it meant more than just a romantic gesture. It literally affected her skin-deep.
Therese has suffered with a dermatologic disorder called Hyperhidrosis since she was six years old, leaving her with perpetually wet hands and feet. Throughout her teen years, socializing was difficult since her condition made her shy about shaking hands with new friends or taking the hand of her dates. The moment her future husband held her hands, she hoped worries about her sweaty palms were behind her. They were, until she started to plan the wedding.
"I couldn't even touch my dress for fear of ruining it with my sweaty hands. I would hold my hands out to the side during fittings. I didn't know if I could wear these beautiful satin peep-toe shoes in a champagne color for fear the sweat stains would show through!"
Wendy Stewart, a dressmaker/tailor based in Wilmington, DE. has worked on her share of wedding gowns. After more than 30 years in the business, she knows first hand the unfortunate effect of sweat on garments. "Both satin and iridescent taffeta will harden when perspiration sets in, making for a very crunchy walk down the aisle!"
According to Dr. David Pariser, president of the American Academy of Dermatology and founding board member of the International Hyperhidrosis Society (IHHS), some 176 million people worldwide (approximately 3% of the population) are afflicted with this rare disorder which causes their bodies to secrete up to 5 times the amount of sweat that is normal or necessary to maintain a steady body temperature. People with hyperhidrosis sweat profusely nearly all day, every day. This usually occurs in focal areas such as the hands, armpits, feet and face. The good news is that medical help is easily attainable and often covered by insurance. The IHHS website www.SweatHelp.org provides education, support and medical resources to affected children, teens and adults worldwide. The site's Physician Finder database helps individuals locate doctors familiar with hyperhidrosis and trained by IHHS on treatment methods.