Hi Everyone, I would be really grateful if you would help me and the British Dupuytren's Society out by take a quick survey, it is only 6 Dupuytren's and Ledderhose related questions. We are just going to see if we can see any trends from the information, nothing formal and it is anonymous.
Please click here to take the survey
My experience with Ledderhose disease aka plantar fibromatosis. This information is not intended to replace your doctor. Information on this blog is provided for informational purposes only. You should not use the information on this web site for diagnosing or treating.
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