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In our association you will meet like-minded people who are affected by PSSD and want to change something about the condition. Our work includes contacting authorities, publishers and clinics, informing doctors and other specialist staff, preparing and holding lectures and much more. You can be an active member or a silent member, but joining definitely helps keep PSSD going!
We run a WhatsApp group where we exchange information and support each other. Please send us an email with your mobile number so we can add you to the group.
Please read the section on WhatsApp groups (especially the group rules) in full before doing so.