British Dupuytren's Society
@british-dupuytrens.bsky.social
Raising awaresness of Dupuytren's, Ledderhose and Peyronie's. Supporting patients and research.
Sadly we are familiar with that problem!
October 9, 2025 at 6:49 AM
Sadly we are familiar with that problem!
He wants all patients to have a chance to hear about the option and discuss it.
So if you live in Mid or South Essex, and are willing to get involved, please message me your contact info, or email me anna@dupuytrens-society.org.uk
So if you live in Mid or South Essex, and are willing to get involved, please message me your contact info, or email me anna@dupuytrens-society.org.uk
July 2, 2025 at 2:45 PM
He wants all patients to have a chance to hear about the option and discuss it.
So if you live in Mid or South Essex, and are willing to get involved, please message me your contact info, or email me anna@dupuytrens-society.org.uk
So if you live in Mid or South Essex, and are willing to get involved, please message me your contact info, or email me anna@dupuytrens-society.org.uk
He wants to set up a group to raise awareness of radiotherapy for these condition among GPs and surgeons, maybe through meetings or a webinar. He said at the moment patients only get referred to him if they have read about the radiotherapy option or our website. (2)
July 2, 2025 at 1:32 PM
He wants to set up a group to raise awareness of radiotherapy for these condition among GPs and surgeons, maybe through meetings or a webinar. He said at the moment patients only get referred to him if they have read about the radiotherapy option or our website. (2)
It was a great conference
June 9, 2025 at 7:01 PM
It was a great conference