Our son Phillip was diagnosed with Long QT Syndrome within hours of being born on 10/19/06.  As per Phillip's doctors suggestion, we contacted SADS immediately  and from that day forward, SADS has been the connection that we so desperately needed.  SADS is a community of people who truly understand what it is like to parent a child with Long Qt Syndrome.    SADS is a constant support system for our family and many families just like us.  With your support we hope to keep SADS mission strong and continue to advocate for people with SADS conditions.

  Thank you for joining our campaign to save lives by raising money to continue patient family support and SADS education programs. Several thousand young people die unnecessarily each year from SADS (Sudden Arrhythmia Death Syndromes) in the United States, and education is the answer.

Funds raised through the Climb to Conquer SADS will:

 

• Provide Family Support to assist patients and their families in making informed medical decisions and living with the challenges of these conditions
• Increase General Awareness of Warning Signs to recognize and prevent heart rhythm abnormalities
• Educate Health Care Professionals in early diagnosis and treatment of heart rhythm abnormalities
• Be Advocates to increase arrhythmia research and improve the quality of life for patients and their families.

Please see the link below for more information about Climb and the SADS Foundation. Climb and the SADS Foundation Information

 

With much love and appreciation,

Phillip's Parents

Jeanine & Daniel Breen