The British Dupuytren's Society would like to hear from anyone living in Scotland who has Dupuyten's or is a carer for someone with Dupuytren's.

We'd like to know how Dupuytren's affects your daily life - and if you've had treatment, what kind of treatment you had and what impact this has had.

If you post your reply here, then I'll see it, or you can contact me offline at Judith@dupuytrens-society.org.uk

The information may be included (anonymously) in a submission to the Scottish Medical Council.

Thanks,

Judith