Where can I find support for Palmoplantar Pustulosis?
Join our forum for help!
Many people with Palmoplantar Pustulosis (PPP) feel lonely and depressed due to a lack of understanding from those around us.
PPP is a rare skin disease that is not well-known and can be painful and debilitating. The limited information available on PPP can further contribute to feelings of isolation.
To combat this, we have a private global Facebook group for PPP sufferers, their friends, and family. This group provides a platform to ask questions, offer support, and give advice to one another. Joining this group can be beneficial, even if you don't wish to be an active poster.
We have members within the group who have gone into remission using natural approaches, and others who have used conventional medicine, providing a broad spectrum of knowledge. If you have any questions, members are happy to help.
To join the group, you will need to ask for permission first, as the group is a private members only.
Welcome!
Åsa Kärrman