Welcome to SADS Channel, the official blog of the SADS Foundation! SADS Channel is intended to be a place for sharing experiences, information, news, research opportunities, and other content related to SADS conditions such as LQTS, BrS, CPVT, and more.
This blog was created as a collaborative effort with SADS Foundation staff, volunteers, and supporters.
Nothing on this blog should be taken as a substitute for medical advice. It is for informational and educational purposes only.
Please keep comments respectful and be aware that this is a public space. We’d love to hear your ideas for topics to address in future posts. We want this blog to bring you the content that’s important to you and your family. If you have ideas, please let us know in the comments!
We are excited to have created this space to be an additional resource for SADS Families and we hope that you are too!
Jasmine – we are very excited to see this launch and hope it creates a safe and much needed space for our SADS community to express our thoughts, questions and fears. Let’s hear from all of you. What are some of your most unanswered questions?
I think Bruce should be the mascot of this group that is only because I find him to be very attentive