dupuytren's contracture

[wantmorenow]

Having surgery for this next week. Anyone have some positive stories to help me feel less anxious?

Having to have the skin graft version to my little finger. Terrified.

I am a fellow DD sufferer but my contracture is fortunately still very slight. I would recommend the British Dupuytren’s Society website and its associated Facebook group as a source of information and support. People regularly post there before and after surgery and you should find lots of reassurance and encouragement there. It is well moderated and really useful. I am very glad I found it so soon after diagnosis. Good luck!
https://dupuytrens-society.org.uk/

Thank you. Mine was non existent 14 months ago and only had first diagnosis in July. Super fast deterioration. Will check out Facebook