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- Date and time Fri 17 Jun 2022 from 9:00am to 5:00pm
- Location Online
- Organised by Medical Genetics
This is a live stream. To attend this event in person please click here.
Join us at this live stream which will provide a valuable overview and a broader understanding of hypermobility syndrome and the care of these patients. Experts in their field will present a series of talks that will inform delegates about practical guides for the assessment and management of this condition and will explore how community care can make a difference.
Hypermobility spectrum disorder and hypermobile Ehlers-Danlos syndrome (hEDS) are often ill-understood and inadequately managed which can lead to more complications for the patient.
This series of talks will provide a detailed understanding of the multisystem nature of the condition, which will enable general practitioners and specialists to better assess problems and develop practical advice and management plans for patients.
Understand the many varied symptoms and signs of hypermobile patients
Increase knowledge about the different methods of treatment
Provide practical suggestions for care in the community
When to consider genetic testing in hypermobility syndrome
A CPD certificate with 6 CPD credits will be issued to those joining the event live as well as those who watch the recording afterwards. Certificates will be issued 7 days after the event to those who watch it live and after 60 days for those that watch the recording.
A CPD certificate with 6 CPD credits will be issued 7 days after the event.
View the programme
Registration for this event will close on Friday 17 June 2022 at 08:00am. Late registrations will not be accepted.
The agenda is subject to change at any time.
All views expressed at this event are of the speakers themselves and not of the Royal Society of Medicine, nor the speaker's organisations.
We are only able to share presentations that we have received permission to share. This is at the presenter and the RSM’s discretion.
This event will be recorded and stored by the Royal Society of Medicine and may be distributed in future on various internet channels.