Where can I find support for Palmoplantar Pustulosis?
Join our forum for help!
Many sufferers of Palmoplantar Pustulosis are feeling lonely and at times depressed. Often the reason for this is due to the lack of understanding from the people around us, not many people know of nor heard of PPP before, and don’t realise how painful and disabling PPP really is. The information about this rare skin disease is scarce. Many of us are feeling depressed due to the constant pain and itchiness and the recurrent pustules outbreaks that never heals.
We have a global Facebook group, a forum for friends, family and sufferers of Palmoplantar Pustulosis, where we are able to ask questions and to give support and advice to each other when there's a need to talk. I highly recommend joining our group.
It doesn’t matter if you don’t want to be an active poster, it can be helpful just to read other sufferers postings.
There are many of us in this group who combated Palmoplantar Pustulosis and gone into remission using a natural approach, and we can all help if you have questions about that and what to do. There are also members in this group who are using conventional medicine, so there's a broad spectrum of knowledge
This group is closed so you have to first ask permission to join.
Welcome!
Åsa Kärrman
We have a global Facebook group, a forum for friends, family and sufferers of Palmoplantar Pustulosis, where we are able to ask questions and to give support and advice to each other when there's a need to talk. I highly recommend joining our group.
It doesn’t matter if you don’t want to be an active poster, it can be helpful just to read other sufferers postings.
There are many of us in this group who combated Palmoplantar Pustulosis and gone into remission using a natural approach, and we can all help if you have questions about that and what to do. There are also members in this group who are using conventional medicine, so there's a broad spectrum of knowledge
This group is closed so you have to first ask permission to join.
Welcome!
Åsa Kärrman