Kids & Family
We are very thankful for moms like Erin Hartzell, who share their story and help us gain perspective into the world of congenital heart disease. Those who have never walked in CHD shoes, will never fully understand all of the emotion and trauma associated with diagnosis, surgery, recovery, and strength required by these amazing families.
Today you hear Erin share her 13-year-old daughter's journey from diagnosis to surgery, amazing supports, as well as help identify other real-life struggles families in the CHD community face daily.
Erin shares some very valid and real conversation identifying emotions some families have as they rush through or avoid February and Heart Month. Many families struggle to celebrate and reflect because of how hard it is to remember their difficult journey; and it's hard to acknowledge there are others who have buried their babies/children because of a CHD diagnosis.
We are thankful to have Erin's voice provide perspective, awareness, conversation and education about Congenital Heart Disease/Defects (CHD).
#CHD #CongenitalHeartDisease #CongenitalHeartDefect #TotalAnomalousPulmonaryVenousReturn #TAPVR #AtrialSeptalDefect #ASDCHD #HeartMonth #MendedLittleHearts
More Episodes
RARE Diagnosis: Angelman Syndrome, Episode 01
2021-08-05
186
2021-08-05
186
Dad Discussions, Episode 1: Jeff Roby
2021-06-17
74
2021-06-17
74
CMV Awareness Month - Episode Two: Linden Priddy
2021-06-10
69
2021-06-10
69
CMV Awareness Month - Episode One: Cara Gluck
2021-06-03
60
2021-06-03
60
Stroke Awareness Month (Part Two): Stephanie Tachell
2021-05-21
138
2021-05-21
138
Stroke Awareness Month (Part One): Stephanie Tachell
2021-05-20
256
2021-05-20
256
Maternal Mental Health: Emily Clark Shares Her Story
2021-04-29
88
2021-04-29
88
Get this podcast on your
phone, FREE
