Do you or does someone you know have either Dupuytren Disease, Ledderhose Disease, or both? Here’s a message from the International Dupuytren Society:
“The International Dupuytren Society, the Ledderhose Blog, and the British Dupuytren Society have jointly developed a questionnaire targeting patients suffering from Dupuytren and/or Ledderhose disease. Please share your experience with these diseases, treatments and consultations!
The questionnaire is available at https://dupuytrens.org/DupPDFs/2017_Schurer.pdf
The individual results are strictly confidential and the summary results will be used to evaluate patients’ experience with treatments and patients’ needs. Researchers often speak about what patients need but this is rarely evaluated. Please help us to document patients’ experience and needs! “
I’ve taken the survey. It’s painless and fun. Online surveys are increasingly important in understanding conditions such as Dupuytren and Ledderhose disease, which can vary so much from person to person. Results of this survey will be presented at the 2015 International Conference on Dupuytren Disease http://DupuytrenSymposium.com
– Charlie Eaton
