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Hi everyone! My name is Stephanie, I am a health educator currently conducting a research project on Dupuytren’s Contracture. I would love to get a better understanding of what it is like to live with DC and how it affects your daily life. What kind of limitations, if any, do you experience? What type of emotions, if any, do you experience regarding the appearance of your hand(s)? Where do look for information and what type of information are you looking for? How were you diagnosed? What was the process like? What type of conversations do you have with your doctor? Have you heard of the new drug Collagenase that is currently in trials?
Any information you can provide about your experience with DC is greatly appreciated. Thank you so much for your time!
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