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.
So I have been in contact with the guy who runs the international Dupuytren's Society and my blog is now (and currently the only) link on their useful links page:
I am even happier with the statement that my blog is great :-)
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