International Pemphigus & Pemphigoid Foundation

The IPPF publishes new report on urgent needs of patients and the importance of advocacy

The Sy Syms Foundation has awarded a $100,000 grant to the International Pemphigus & Pemphigoid Foundation (IPPF) in support of the IPPF's Biopsies Save Live Campaign.

Continued funding to support dental education, outreach, and awareness of pemphigus and pemphigoid, two rare autoimmune diseases.

Grant to Support Successful Early Diagnosis Awareness Campaign

Funds to Support Awareness Campaign for Rare Autoimmune Diseases

Join rare disease patients, caregivers and other health care advocates in California on March 2, 2015 to raise important awareness for rare diseases as part of Rare Disease Day®.

The public is invited to show their support at the California State Capitol on February 27, 2104 for the millions of people affected by rare diseases living around the world, across the county, and down the street.

The International Pemphigus & Pemphigoid Foundation (IPPF) will be joining the National Organization for Rare Disorders (NORD) and other rare disease organizations around the world in observing Rare Disease Day on February 28, 2014.

The International Pemphigus & Pemphigoid Foundation (IPPF) today announced that it has joined the National Organization for Rare Disorders (NORD) and dozens of rare disease organizations asking the United States Budget Conference Committee to protect.

The International Pemphigus & Pemphigoid Foundation's Board of Directors has elected Dr. Badri Rengarajan as President of the Foundation. He replaces Dr. David Sirois who will remain on the Board.