As many of you will know I have had a lot of contact with the British Dupuytren's Society and have recently helped them with a few comments on their website and I have also helped them rewrite the Ledderhose treatment of their website. Specifically the radiotherapy and Surgery parts. See
Surgery for Ledderhose
and
Radiotherapy for Ledderhose
to see what information they now have. They are only a small and new charity so any help they can get is appreciated. Please also support them on facebook, twitter and Google +. Also feel free to follow me on twitter or google plus by hitting the buttons the right.
As always remember if you have any questions or want to share your story then please get in touch and share.
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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