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a common hope | an uncommon bond

Pemphigus and pemphigoid are very serious, autoimmune diseases.  If left untreated, pemphigus, and sometimes pemphigoid, can be life-threatening.  The International Pemphigus & Pemphigoid Foundation is dedicated to providing information and support to the community of people living with pemphigus and pemphigoid; including family members, friends and medical professionals who care about and care for them, as well as pet owners with pets that have pemphigus or pemphigoid.

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Register for FREE and get access to more information and services! Why register for access? Read our Registration FAQ and find out more. You'll have FREE access to extra menu items and member-only information. Once you log in, look for the "*" next to site member-only areas!

The IPPF provides basic facts, frequently updated information about these diseases and helpful services, including:

In addition to the facts, you'll also find emotional support here. Those of us who live with and treat these relatively rare diseases share an uncommon bond, and the IPPF is the place to share personal stories, pose questions, and ask for and receive help, advice and guidance. Assistance is available both online, via our very active and caring email list, in person through our Heart2Heart program, and national and international support groups.

Because these diseases are so rare and often misdiagnosed, the IPPF is also dedicated to increasing awareness of pemphigus and pemphigoid within the medical community. This is of vital importance, since with proper diagnosis and the right therapies, combined with helpful support systems and a good attitude, pemphigus and pemphigoid patients can effectively deal with these life-threatening conditions.

Thanks to the caring support of its members and the medical community, the IPPF is here to help patients and caregivers alike.

Last Updated ( Thursday, 17 January 2008 )
 
Discussion Forums

Have a question? Better yet, have some answers? Join our interactive discussion forum and see what you have been missing.

Last Updated ( Tuesday, 24 July 2007 )
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Email Discussion Group

The very first support service that the IPPF introduced, about a year after the Foundation began, was our Email Discussion Group. It was the best and most direct way for us to bring together patients from all over the world to share experiences, information, advice and more.

Last Updated ( Friday, 06 July 2007 )
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IPPF Member Login

Newsflash
Take a Survey

The IPPF Survey page lists current surveys you can participate in. Check it from time to time and see how you can help by answering some simple questions.

So what are you waiting for? Let your voice be heard!

 

Polls
If you have pemphigus or pemphigoid, what is your blood type?
 

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