Callan is the 2012 Herma Heart Center Hero.
At 1-month-old, Callan was diagnosed with pulmonary atresia, a congenital heart condition that makes it difficult for blood to flow to the lungs. His doctors in Madison gave him a dismal prognosis, but his parents refused to give up hope. They reached out to the Herma Heart Center team at Children’s Hospital of Wisconsin in Milwaukee as a last resort for treatment options that might save Callan’s life.
Within a few hours, Callan was rushed to the Herma Heart Center, where physicians recommended a series of three open-heart surgeries. The surgeries took place over several months, and Callan had his ups and …Continue reading →
February is heart awareness month, and it’s a great time to increase awareness of cardiac emergencies in schools and homes. Knowing the causes and warning signs of cardiac arrest and the importance of calling 911 during these emergencies are useful messages for parents, teachers and students.
It’s recommend to have an emergency plan in place and know where the automated external defibrillator (AED) is located, if available. Having a plan and discussing it with …Continue reading →
February is heart awareness month, a time when we encourage adults to reflect and make changes in their lives for healthier hearts. This is also a good time to raise awareness of congenital heart disease (CHD) and children who start their lives with heart conditions.
CHD is the most common birth defect, and it is present in eight of out of every 1,000 births. Some forms of CHD cause few problems in health, growth and development. Other …Continue reading →
Recently there was a segment on the TODAY show about a young girl in Texas who was saved by the quick thinking of her teachers and the automated external defibrillator (AED) in the school. I encourage you to watch this interview with her parents about the rescue, caught on camera. …Continue reading this post
When I was 4, I was diagnosed with an ostium primum atrial defect, a hole in the area between the two upper chambers of my heart. I had open-heart surgery at Children’s Hospital of Wisconsin to repair the heart defect. My brother, Jim, passed away at age of 20 from complications of congenital heart disease, and my daughter, Cassie, 5, had open-heart surgery …Continue reading this post
Children’s Hospital of Wisconsin-Fox Valley is celebrating its 10th anniversary in 2011. As a pediatric heart specialist, I have seen real growth at the hospital during that time. I came here from Chicago. The adjustment from the bustling city to the quiet community of Neenah took me some getting used to, but I love it.
When I started at Children’s Hospital-Fox Valley in January 2002, the clinics had about 160 patients and all of the clinics’ charts could fit on one rolling cart. Now, the charts fill a …Continue reading →
I’m proud to say I’m the father of three athletes. I’m lucky to say that none of my children have fallen victim to sudden cardiac arrest. But, what if this did happen? What if I wasn’t there? Would someone know how to help?
In addition to my role as dad, I also am a cardiologist at Children’s Hospital of Wisconsin. One of the programs we offer is Project ADAM, an initiative that helps schools recognize …Continue reading →
You may have noticed a red hue illuminating the Children’s Hospital of Wisconsin hallways this month. You also may have noticed employees wearing red throughout Children’s Hospital and Health System. These efforts support the fight against heart disease and stroke.
Heart disease is the number one killer of both women and men. The Go Red initiative draws awareness to this and encourages people to take action to decrease their …Continue reading →
Jenni, 39, was born with ostium primum atrial defect (a hole in the heart) and her daughter Cassie, 4, also was born with a heart defect. Both are patients at Children’s Hospital of Wisconsin’s Herma Heart Center.
I was first diagnosed with a heart defect in 1975 when I was 4 years old. I had open-heart surgery to repair a large hole between the two chambers. I grew up a very normal kid and never considered myself to be someone with a heart problem.
More than three decades later in 2008, it was discovered through an employee of mine that I had very high blood pressure …190/100! I tried to justify it with being a mom working third shift and chasing three kids around. At the urging of my family and the employee, I went to see my primary care doctor who immediately said I needed to see a cardiologist. I have not been to one since I was a child. I remembered my mom telling me about the Adult Congenital Heart Disease Program at Children’s Hospital of Wisconsin. She said Dr. Michael Earing was the person to see.
…Continue reading →
When people are forced to live with the fact of their mortality every day, they have two options. They can give up – after all, what’s the point in planning for the future when doctors predict that you don’t have long to live. Or, they can live with it, accept some limitations, but refuse to give up on their dreams. Dr. Pip Hidestrand, a resident at the Children’s Hospital of Wisconsin, is an example of the latter case. This is her story.
I was born with a congenital heart defect and lung disease. By the age of 4 I had undergone three open heart surgeries and, as a result, I have spent my entire life aware of my precarious existence. While many physicians told my parents that I would not live past my teenage years, I did not let this deter me from my ambition to pursue a career in …Continue reading →