Looking back to when I was just starting out I was on about 3000 page views in March 2012 (now on more like 250,000) and I had just interview the British Dupuytren's Society.
http://ledderhose.blogspot.co.uk/2012/03/interview-with-british-dupuytrens.html
The other thing I wanted to mention was the activity on the Facebook groups. To my knowledge there are 4 Facebook groups for these conditions however the 3 below I am sort of active on.
1) Dupuytren's, Ledderhose and related conditions support group
https://www.facebook.com/groups/1462124944043779/
2) Dupuytren's Disease Support Group - In may I will be doing a 1 hour or so coffee talk on here (just answering questions)
https://www.facebook.com/groups/879351412113444/
3) DART
https://www.facebook.com/groups/1622748151282109/
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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