PEM Friends is pleased to announce the new PEM Friends website NEW website and logo! The new site is simple and informative.

The APPF was created in 2005 by patients. Its aim is to provide help, information and support to people suffering from rare autoimmune blistering skin and/or mucous membrane diseases such as Pemphigus, Pemphigoids, Epidermolysis Bullosa Acquisita, Linear IgA Dermatosis or Dermatitis Herpetiformis.

Take a look at the latest issue of Cutis Laxa Internationale's CLI-News N°34 from September 2020. Read about how the Covid-19 pandemic has changed the work happening at Cutis Laxa Internationale.

Isobel Davies, of PEM Friends, shares how COVID-19 has changed how PEM FRIENDS is connecting with their community.

Don’t get me wrong. I have nothing good to say about this awful disease. Like the curse attributed to Confucius though, we are certainly living in interesting times.