Where can I find support?

Many sufferers of PPP are feeling lonely and depressed. This is due to not many people know of or heard about this disease and the information out there are scarce.  Many are feeling depressed due to the constant pain and itchiness and the recurrent outbreaks that never heals.

I have started a global Facebook group for friends, family and sufferers of PPP who are able to give support and advice to each other when there's a need to talk.  I highly recommend joining this one. If you don't want to be active it can be helpful just to read other sufferers postings.

This group is closed so you have to ask permission to join.

​Welcome!

Åsa
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