This community is a safe space where you can share your experiences, support one another, and become better informed about ADPKD (Autosomal Dominant Polycystic Kidney Disease).
There’s several ways you can use this community:
* Ask a question – and we’ll do our best to answer as quickly as possible or other community members may well have answers for you from their experience.
* Start a blog and share your thoughts and opinions. This could be anything relating to ADPKD and how it affects your life – your family or work, the impact of drugs you take or how you feel (emotionally and physically). The blog can be as short or long as you want. Just post what’s on your mind.
* Or you could post about some useful information that’s helped you.
Enjoy the community and keep well.
Tess
PKD Charity CEO (and polycyster)
Recently diagnosed...under-informed...full of questions that I am sure I don't actually want the answers too
Feeling worried....
Hi Its Snow Castles Here after 3 years.
Just diagnosed