Ask A...Rheumatologist - Part One

We are pleased to share Part One of our new Q&A video, created in response to the many thoughtful questions submitted by our community. 

At the Hughes APS Trust, we know how important it is for individuals and families affected by Hughes Syndrome/Antiphospholipid Syndrome (APS) to have access to clear, reliable information and support. This Q&A series is one of the ways we hope to address common concerns, provide reassurance, and strengthen connections within our community. 

 

We would like to extend our sincere thanks to everyone who took the time to send in questions. The response was incredible, and we received far more questions than we could cover in a single video. 

Because of this, the Q&A will be shared in multiple parts. 

 

This video is Part One of the series. We are currently preparing Part Two, which will be recorded with Dr Kaul, and will address even more of the important topics raised by our supporters and patients. 

We look forward to sharing the next instalment very soon. 

 

You can watch Part One below 

 

Thank you, as always, for your continued support of the Hughes APS Trust and for helping us raise awareness and understanding of APS.