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BDS blog

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BDS blog

Postby Gary1987 » Mon Nov 05, 2012 10:35 pm

The British Dupuytren's Society now has a blog so we can all keep up too date with the efforts made to help Dupuytren's and ledderhose patient in the UK. http://dupuytrenssociety.blogspot.co.uk/
Gary1987
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Re: BDS blog

Postby White Stone » Thu Nov 06, 2014 4:28 am

Hello Gary,

Thanks for the link. Found your Blog there, too. Very interesting. I guess, since I can still stand they didn't offer me the Radiotherpy. Maybe, a few years down the road. Strange, the condition is called two different things in our two Countries, and we speak the same language. Cheers,
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Re: BDS blog

Postby Gary1987 » Mon Dec 08, 2014 1:08 pm

The condition is called both things in both countries just mostly Ledderhose in UK and PF in the States.

You will probably not get offered radiotherapy as most people have not heard of it, other than those that use it. Doing research yourself, as you have, is important for this.

Thanks,

Gary
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Re: BDS blog

Postby White Stone » Mon Dec 08, 2014 4:45 pm

Dear Gary,

Thank you for your reply. It gets a little lonely here on this forum. <Big Grin> After seeing your Blog it is clear you are a very busy man. I truly appreciate your efforts. This forum has been a help to me.

Kindly,
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Re: BDS blog

Postby Gary1987 » Tue Dec 09, 2014 12:38 pm

Hi,

As I have said elsewhere the Facebook group is more active. You should also consider the international Dupuytrens society forum if you don't have Facebook, great Ledderhose section with decent activity.

Thanks for the kind words. Busy yes but always happy to help, I know how isolating the condition can be.

Thanks

Gary
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