Ask the Experts Introduced-Ground Breading Tool to Ask Experts About Heart Rhythm Abnormalities
The Sudden Arrhythmia Death Syndromes (SADS) Foundation has teamed up with Mayo Clinic to launch the ground-breaking program of “The Heart of the Matter – Ask the Experts." This resource serves as a crucial tool for worldwide professionals and community members to share their expertise and concerns on heart rhythm abnormalities that could cause sudden death in children and young adults
Salt Lake City, UT, May 11, 2012 --(PR.com)-- Heart of the Matter – Ask the Experts
Ground-Breaking Tool to Answer Questions on Heart Rhythm Abnormalities
The Sudden Arrhythmia Death Syndromes (SADS) Foundation has teamed up with Mayo Clinic to launch the ground-breaking program of “The Heart of the Matter – Ask the Experts." This resource serves as a crucial tool for worldwide professionals and community members to share their expertise and concerns on heart rhythm abnormalities that could cause sudden death in children and young adults.
The SADS Foundation is an organization dedicated to saving lives and supporting families of children and young adults who are predisposed to sudden death due to heart abnormalities. The Foundation provides information, support and hope to thousands of families with children living with the health threat and is a leader in education, research and advocacy for people with genetic heart arrhythmias that can cause sudden deaths.
"Ask the Experts" features questions regarding Long QT syndrome and other SADS conditions with answers from some of the world’s most respected professionals. Physicians, health care providers and affected families can submit their questions online, and the top-ranked questions will be answered by a SADS physician expert.
“Supporting families is what we do at the SADS Foundation, and this is an amazing tool,” says Laura Wall, Vice President of Development and Marketing. “At SADS Foundation, we are continually looking for ways to improve our field of knowledge and are making tremendous strides toward providing resources and support for those who are living with SADS conditions.”
One question will be answered once a month, and videos are available online at www.StopSADS.org.
About SADS Foundation
Formed in 1992, the SADS (Sudden Arrhythmia Death Syndromes) Foundation’s mission is to save the lives and support the families of children & young adults who are genetically predisposed to sudden death due to heart rhythm abnormalities. We are committed to promoting the early detection and treatment of these conditions throughout the world. The Foundation distributes materials internationally through grass roots efforts in order to teach families, educators and medical professionals about SADS conditions. For more information visit www.StopSADS.org or call .800.STOP-SAD (800.786.7723). Find us on Facebook at www.causes.com/causes/225843 and follow us on Twitter at www.twitter.com/SADSFoundation.
-StopSADS.org-
Contact: Laura Wall
VP, Development & Marketing
Office: 801.531.0937
Cell: 801.641.7148
E-mail: laura@sads.org
Ground-Breaking Tool to Answer Questions on Heart Rhythm Abnormalities
The Sudden Arrhythmia Death Syndromes (SADS) Foundation has teamed up with Mayo Clinic to launch the ground-breaking program of “The Heart of the Matter – Ask the Experts." This resource serves as a crucial tool for worldwide professionals and community members to share their expertise and concerns on heart rhythm abnormalities that could cause sudden death in children and young adults.
The SADS Foundation is an organization dedicated to saving lives and supporting families of children and young adults who are predisposed to sudden death due to heart abnormalities. The Foundation provides information, support and hope to thousands of families with children living with the health threat and is a leader in education, research and advocacy for people with genetic heart arrhythmias that can cause sudden deaths.
"Ask the Experts" features questions regarding Long QT syndrome and other SADS conditions with answers from some of the world’s most respected professionals. Physicians, health care providers and affected families can submit their questions online, and the top-ranked questions will be answered by a SADS physician expert.
“Supporting families is what we do at the SADS Foundation, and this is an amazing tool,” says Laura Wall, Vice President of Development and Marketing. “At SADS Foundation, we are continually looking for ways to improve our field of knowledge and are making tremendous strides toward providing resources and support for those who are living with SADS conditions.”
One question will be answered once a month, and videos are available online at www.StopSADS.org.
About SADS Foundation
Formed in 1992, the SADS (Sudden Arrhythmia Death Syndromes) Foundation’s mission is to save the lives and support the families of children & young adults who are genetically predisposed to sudden death due to heart rhythm abnormalities. We are committed to promoting the early detection and treatment of these conditions throughout the world. The Foundation distributes materials internationally through grass roots efforts in order to teach families, educators and medical professionals about SADS conditions. For more information visit www.StopSADS.org or call .800.STOP-SAD (800.786.7723). Find us on Facebook at www.causes.com/causes/225843 and follow us on Twitter at www.twitter.com/SADSFoundation.
-StopSADS.org-
Contact: Laura Wall
VP, Development & Marketing
Office: 801.531.0937
Cell: 801.641.7148
E-mail: laura@sads.org
Contact
SADS Foundation
Laura Wall, Vice President
801-641-7148
www.StopSADS.org
Laura Wall, Vice President
801-641-7148
www.StopSADS.org
Contact
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