International Hyperhidrosis Society
 

The International Hyperhidrosis Society News Blog is the only publication dedicated solely to the needs of hyperhidrosis sufferers, their loved ones, and the physicians and scientists who care for them. Alerts and news are published throughout the year and conveniently delivered to tens of thousands of global subscribers by email. If you haven't already subscribed to this groundbreaking resource from the International Hyperhidrosis Society, sign up today!

 

 

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With the Chance to Win a Free Treatment, a More Comfortable Process & New freshEvents: There’s More to Know about miraDry 

miraDry is a non-surgical treatment for underarm sweating. Studies have shown that, for underarms, miraDry can provide 82% reduction in sweating – permanently!  Today, with the chance to win treatment, miraDry’s new comfort-enhancing protocol, and debut patient education events, there’s more to miraDry than ever before. 

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Breaking: Research Proves Delays in Hyperhidrosis Care, Treatment (Dis)Satisfaction + More

A newly-published research article in the Journal of Drugs in Dermatology shows that hyperhidrosis patients wait YEARS (3 to 10 years, in fact) before seeking treatment and that some of the most commonly recommended treatments provide the least satisfaction. Read the full blog to discover all the key findings. Thank-you International Hyperhidrosis Society community for participating in this eye-opening study.

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Shannon McLinden is Making a Difference (and So Can You)

Here’s a story about an “ordinary” person making a difference. Shannon McLinden, founder of Summer Soles and FarmHouse Fresh, is a member of our community (just like you) and she’s using her businesses, her story, and her Texas ranch for positive change. Life with Hh can be hard, but if each of us strives to make a difference… that can make ALL the difference.

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Patient-Focused Drug Development: We Shape the Future

It’s been just over a month since our Patient-Focused Drug Development (PFDD) meeting on hyperhidrosis (Hh), but the process is not over. Your – and our -- input will help shape the future of hyperhidrosis care. PFDDs are an important way for us to make our voices and needs heard by treatment developers, healthcare providers, and the U.S. Food and Drug Administration (FDA). Have your say and comment via a “PFDD Comment” email.

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Turning the Corner: Patient-Focused Drug Development for Hyperhidrosis

It’s Time for Everyone Affected by Hyperhidrosis to Speak Up & Speak Out

This is a watershed moment for hyperhidrosis. The International Hyperhidrosis Society hosted a Patient-Focused Drug Development meeting in Washington, DC on November 13, 2017 designed to ensure that those affected by hyperhidrosis can make their voices – and needs -- heard by treatment developers, healthcare providers, and regulatory professionals from the U.S. Food and Drug Administration (FDA). If you’ve ever wanted a better way to control your sweating – and to stop sweating from controlling your life – it’s time to speak up - OPEN COMMENT PERIOD NEEDS YOUR INPUT NOW.

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New Research Documents Quality-of-Life Burden of Hyperhidrosis

A new study details just how hard it can be to live with hyperhidrosis and how the condition can negatively impact nearly every aspect of a person’s life. From damaging emotions to not being able to go to the movies – if you’re feeling trapped by sweat, you’re not alone.

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Non-profit shout-outs

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International Hyperhidrosis Society has received the GuideStar Exchange Seal a leading symbol of transparency and accountability provided by GuideStar, the premier source of nonprofit information.


 

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International Hyperhidrosis Society has been awarded as a Top-Rated NonProfit for seven years in a row! Read the reviews and add your own.

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Hyperhidrosis Awareness Month Countdown

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