Patients, families, healthcare professionals and supporters came together for an afternoon of information, shared experiences and connection. Our guest speakers shared valuable insights into antiphospholipid syndrome (APS), and members of our community had the opportunity to ask questions and meet others who understand the realities of living with the condition.
Events like this are an important part of our work to support patients, reduce isolation, improve understanding of APS and bring our community together.
We aim to make the Patient Meeting an annual event, with a full hybrid setup to provide an inclusive and accessible experience for both in-person and online attendees.
A special thank you to our volunteer filmmaker, Anish, for generously giving his time to create this video, and to our speakers, trustees, attendees and everyone who helped make the meeting possible.
Please subscribe to our channel and share this video to help raise awareness of APS.
Find out more about Hughes APS Trust:
https://www.hughesapstrust.org
Contact us:
hello@hughesapstrust.org
Please note: This video is provided for general information and support and should not be considered a substitute for individual medical advice. Always speak to an appropriate healthcare professional about your diagnosis or treatment.
#APS #AntiphospholipidSyndrome #HughesAPSTrust #PatientSupport #PatientMeeting #RareDiseaseAwareness
This content will only be shown when viewing the full post. Click on this text to edit it.
Share this post: