The British Dupuytren's Society is a small UK charity for
people affected by Dupuytren's Contracture, Ledderhose Disease and Peyronie's
disease:
Today I am going to do a blog post on the above charity, as
you can see from the description I have posted they do work for people with
Ledderhose as well as Dupuytren’s and Ledderhose so I urge you to visit their
site.
Firstly I would also urge you to follow them on facebook and
twitter …
Facebook – http://www.facebook.com/britdupsoc
Twitter - @Dupuytren
Ok so I am not going to make a huge post as I am hoping to
do an interview type thing with them in order to get a better and more in depth
idea of what they do and where the money goes. For now though I do have the following
from an e-mail that my wife received.
“The British Dupuytren's Society will be giving a talk to
the British Chiropody and Podiatry Association later this month, hoping to
spark a dialogue on creating a national approved treatment protocol for Ledderhose.
This is an example of where we use donations…”
