• The DISC trial still needs more patients, they put out a call for people to contact them.
  • The International Dupuytren Society had it’s AGM in January, and Prof D Warwick held a slideshow presentation how his treatment of Dupuytren’s has changed over the years, first when collagenase became available, then when it was taken off the market, and finally when Covid reared it’s ugly head. In short, he is doing a lot more PNF (= NA, needle release) now than he did before.
  • New webpage: https://dupuytrens-society.org.uk/seeing-a-doctor-during-the-covid-19-pandemic/ on why it may be difficult to get your Dupuytren’s (or Ledderhose, Peyronie’s) treated during the Covid crisis