PIPERSVILLE, Pa., Nov. 10 Just as the holiday season brings relatives together to relive fond memories, it's also a perfect time to share that most vital bit of knowledge - your family health history. One organization promoting more 'health talk' around the family table is the International Hyperhidrosis Society (IHHS).
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IHHS knows that many hereditary skin conditions like hyperhidrosis (excessive sweating) are often passed on within families from one generation to the next without much acknowledgement or discussion, each generation learning to cope in isolation. Studies have shown that as many as 65% of individuals with hyperhidrosis have family members who are also affected. Yet many people suffering from excessive sweating are unaware of their family members' affected status or feel too embarrassed by the physical, emotional and social discomfort of constant wetness to bring up questions about their condition.
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As the leading authority on hyperhidrosis, IHHS puts substantial medical muscle behind its website, www.SweatHelp.org. The site provides information and hope to affected individuals and families looking for answers on dealing with this debilitating condition.
"Simply put, the website has the tools you need to help live the life you want," says Dr. David Pariser, president of the world-renowned American Academy of Dermatology and founding Board member of IHHS.
"The site is dedicated to answering all your questions about hyperhidrosis management. It teaches you about treatment options, helps you find a dermatologist, and even offers material to share with family and friends to build a more educated and understanding support network. "
The holidays are also a good time for families to discuss the option of participating in the Genetics of Hyperhidrosis study currently being conducted at the Albert Einstein College of Medicine. Researchers are attempting to isolate the gene or genes responsible for this skin condition, subsequently using the information to develop more effective treatments. Families wanting to participate or receive more information should contact the project's genetic counselor/research coordinator Betsy Vibert, MS, CGC, toll free at 877-444-2525 or mailto:[email protected] [email protected] .
Dr. David Pariser is available for interview opportunities. Please contact Tita Cherrier for further information and to schedule a date/time.
The International Hyperhidrosis Society is committed to reducing the symptoms, anxiety and social stigma associated with excessive sweating by offering education, support and medical resources to an estimated 176 million affected children, teens and adults worldwide.
International Hyperhidrosis Society(R) is a registered trademark of the International Hyperhidrosis Society.
SOURCE International Hyperhidrosis Society
