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Less than an hour until our SADS Live with Dr. Mike Ackerman and he will be joined by Georgia Sarquella Brugada, MD, PhD. This is a live you won't want to miss! Click the link below to watch it on our YouTube or watch it on our Facebook page. youtube.com/live/b5NM4GjZQ…

We are so excited to announce our "101 Series". This series will explain and showcase common terms, condition, anatomy, medical equipment, and more that are related to SADS Conditions. If you want something explained or showcased in our 101 Series, comment it down below!

Share to spread awareness! Brugada Syndrome is a rare cardiac condition that affects less than 0.02% of the population in the West. For more information about #Brugada, visit sads.org/sads-condition….

May the Fourth be with you today! Enjoy these Star Wars Memes from all of us at The SADS Foundation! 🏷️ #MaytheFourth #LQTS #CPVT #Brugada #ARVC #ARVD #SADSCommunity #SADSFamilies

The Cardiac Conduction System 101 by the SADS Foundation If you want something explained or showcased in our 101 Series, comment it down below! We would love to add it to our content.

Do you ever feel overwhelmed knowing there’s still so much work ahead to improve treatment of our SADS conditions? You’re not alone. That’s why each year we make it easy to create change through our No Ball At All campaign. Save lives today right here - sads.org/donate/no-ball…

In this webinar, Dr. Sears will talk about how we can find joy even during difficult times. Join this webinar and discover what truly matters to you to live a long and happy life - despite your diagnosis. Register at sads.org/what-now/livin….

One hour until our Mother's Day SADS Live! Tune in on our Youtube Channel, Facebook Page, or on our Instagram Live to watch this special SADS Live. youtube.com/watch?v=jHjGKa…

The journey after being diagnosed with a SADS condition is filled with uncertainty - and one of the things that helps most is those who support you along the way. Tag one of them, or all of them, in the comments to let them know that you appreciate them. sads.org/get-involved/c…

Happy #MothersDay from the SADS Foundation! We are committed to supporting every kind of SADS mom - by providing resources to help you and your kids, and creating a space where you can meet other moms who understand. If you need support, please contact [email protected].

Are you the parent of a child with a rare heart condition? We've got a new support group starting in June - SADS Parent Connection, where parents of kids with SADS conditions can connect to share tips, support each other, and make lifelong bonds. sads.org/what-now/suppo…

Introducing The Cardiac Conduction System 101. Our 101 series explains and showcases common terms, condition, anatomy, medical equipment, and more that are related to SADS Conditions. If you want something explained in our 101 Series, comment it down below!

If you have a question, or if you’re feeling scared or alone because of your diagnosis – give us a call or text! Our hotline is open from 11 AM – 7 PM ET from Monday to Friday (and you can also leave us a message outside of business hours).

ATTENTION!! WE HAVE CHANGED THE DATE! We want all the SADS parents to be involved with this Parent Support Group, even if they are involved in one of our other groups. Because of this we have changed the date to the SECOND TUESDAY of each month. sads.org/what-now/suppo…

Who are we at The SADS Foundation? Swipe through these photos to read more about who SADS is, our mission, our goals, and our values. 🏷️ #SADS #SADSCommunity #SADSLive #LivingwithaSADSCondition #LQTS #CPVT #Brugada #ARVC #ARVD #ICD #LCSD

The SADS Foundation is here is to save the lives and support the families of children and adults who are genetically predisposed to sudden death due to heart rhythm abnormalities. Our main goal is support you. sads.org/what-now/suppo…

Introducing EKG 101 by the SADS Foundation! This post is apart of our "101 Series". This series explains and showcases common terms, condition, anatomy, medical equipment, and more that are related to SADS Conditions.

This year’s No Ball At All is in memory and honor of Bella who was only 12 when she suffered a SCA. Through genetic testing her family learned she had ARVC To save lives like Bella’s, simply donate AND share our posts with your community. sads.org/donate/no-ball…

We would love to take time to appreciate and thank all of first responders and EMS teams around the world. EMS teams are often tied very closely to SADS families. We’ve heard so many stories of EMS and the lives they’ve saved. We are always thankful for them.

This Friday we have a SADS Live Q & A Session with our favorite Dr. Ackerman! Click the link below or head to our Facebook page to watch it. youtube.com/live/dQjCR5sZm… 🏷️ #SADS #SCA #SuddenCardiacArrestAwareness #SADSLive