Being rare: a patient tale of being diagnosed in an OSCE
14th December 2020 @ 5:30 pm
Wyburn-Mason syndrome. Ever heard of it? Dan Jeffries has, and his insightful talk explores what it’s like living with one of the world’s rarest medical conditions – to then discover you have another one.
Barts & The London Students for Rare Diseases are excited to invite you to their first online event of the year!
They’ll be hearing from Dan Jeffries, a well-known figure in the rare disease community. Dan is a Trustee for Medics 4 Rare Diseases, a Volunteer Ambassador for The Pituitary Foundation and has spoken at numerous rare disease events around the world.
The event will be hosted on Zoom – please sign up via the form below and we will send you a link.
This website uses cookies to improve your experience. We'll assume you're ok with this, but you can opt-out if you wish. Cookie settingsACCEPT
Privacy & Cookies Policy
Privacy Overview
This website uses cookies to improve your experience while you navigate through the website. Out of these cookies, the cookies that are categorized as necessary are stored on your browser as they are as essential for the working of basic functionalities of the website. We also use third-party cookies that help us analyze and understand how you use this website. These cookies will be stored in your browser only with your consent. You also have the option to opt-out of these cookies. But opting out of some of these cookies may have an effect on your browsing experience.
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.
Wyburn-Mason syndrome. Ever heard of it? Dan Jeffries has, and his insightful talk explores what it’s like living with one of the world’s rarest medical conditions – to then discover you have another one.
Details
Organiser
Venue