by Patrick Dunn, IPPF Executive Director I’m happy to introduce you to the new IPPF Communications Manager, Geoffrey Waring! After conducting a nationwide search, we found that Geoff’s impressive mix...
by Fred Wish / Guest Contributor Hosted by Dr. Kyle Amber of Rush University, the IPPF 2026 Patient Education Conference took place from August 28-31 at voco Chicago Downtown-Riverwalk by...
Living with pemphigus or pemphigoid can feel unpredictable but identifying your personal triggers can make a big difference. For some of us, triggers can include stress, certain foods, illness, medications,...
Are you passionate about making a real impact in the lives of those affected by pemphigus and pemphigoid? The IPPF is looking for dedicated volunteers to help, support, educate, and...
By Becky Strong There’s something that happens when you walk the halls of Congress and say, out loud,” I’m here because of the IPPF Community”. It’s equal parts nerve-wracking and...
Receiving a diagnosis of pemphigus or pemphigoid (P/P) can feel overwhelming, and it’s natural to search for meaning in a journey that may seem uncertain at first. While these conditions...
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