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Our Impact This Year

  • People Helped

    1497

  • Volunteer Hours

    2412

  • HS Speaks

    4

Are You Part of an HS Community?

The International Association of Hidradenitis Suppurativa Network (IAHSN) was developed with a passionate desire to be your trusted health and wellness information center to provide updated information on the latest research and trial treatments.

IAHSN rapidly growing desire to serve the needs of those accounted one million HS survivors and to reach the twelve million or more that are estimated not to have an official diagnosis. It’s reported that there will be more individuals diagnosed with the hidradenitis suppurativa disease.
You may not have hidradenitis suppurativa yourself, but IAHSN guarantee that you know someone who does. It may be your family member or friend, and they just don’t have a name for their condition.

  • Dr. Donna Atherton, Founder and Chief Mission Officer
    Dr. Donna Atherton, Founder and Chief Mission Officer

    “The International Association of Hidradenitis Suppurativa Network provides help you need while promoting research to find a cure.”
    An estimated 1% of Americans have hidradenitis suppurativa. Many will develop other comorbidities and/or symptoms of mental illness. For over 11+ years, we've provided advocacy, education, support, and community to millions of individuals impacted by this chronic skin disease. We won't stop until there is a cure."

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