Thursday, July 26, is Miracle Treat Day, and proceeds from Blizzard sales at participating Dairy Queen stores will benefit Children’s Hospital of Wisconsin.
Children’s Hospital champion Brea enjoying her Blizzard on Miracle Treat Day 2011.
My name is Jerry Schiefelbein. I’m the operator of three local Dairy Queen stores. I’m asking you to join me for Miracle Treat Day which supports Children’s Miracle Network Hospitals across the country.
I’m happy to participate in this great event to help out a hospital that has helped my family. Our community is lucky to have one of the nation’s top children’s hospitals. My daughter, Nicole, was a patient at Children’s for 10 years with type-1 diabetes. The care and education she and our family received was second to none. She is doing great to this day. We are very appreciative to the doctors, nurses and support staff for Continue reading →
My name is Mary, and I have scoliosis. I was diagnosed with it a few years ago. I wear my brace during the day now, but I used to wear one at night. Wearing a brace has affected my life in many ways, but don’t worry. You can still be the same you even with scoliosis.
I’m 14 years old and a freshman at Hampshire High School, in Hampshire, Ill. Let me tell you a little about myself. I love to read, and I love cats. I have one cat named C.C., and she is the cutest thing ever!
During this past school year, I got a daytime brace. Don’t be afraid to tell your teachers and Continue reading →
No one can tell the stories of children’s hospitals better than the patients and families that we serve. Every year, the Children’s Hospital Association hosts Family Advocacy Day in Washington, D.C.
This year, Claire Bevec, from Kenosha, Wis., is taking her story to Washington, D.C. She will join nearly 30 other child patients and their families from across the country to ask Congress to protect health care for children. National health care programs our kids rely Continue reading →
Prom night at Children’s Hospital of Wisconsin.
An Evening with the Stars was much more than just prom night at Children’s Hospital of Wisconsin. As a Teen Advisory Council member for Children’s, prom was about being able to give back to the community.
Seeing the patients of Children’s smile and laugh is something words can never describe. The thought that something we do could make such a large impact Continue reading →
Claire and Linda Bevec
On behalf of Children’s Hospital of Wisconsin our family will participate in the Children’s Hospital Association’s eighth annual Family Advocacy Day in Washington, D.C. next month.
Family Advocacy Day brings approximately 30 families from the nation’s top children’s hospitals to Washington each summer. While there, families educate members of Congress and the media about the quality health care that all children and families need and to address critical medical and health care concerns for children specifically in their home state.
Our daughter Claire was born six weeks premature Continue reading →
Jordan Miller with Donald Driver
I am so happy that Children’s Hospital of Wisconsin gave me the opportunity to meet Donald Driver and other Packers players earlier this month at the Donald Driver Charity Softball Game. It was truly the experience of a lifetime. I will never forget it.
I was picked because I go to Children’s Hospital of Wisconsin often because I have type 1 diabetes. I was diagnosed when I was 4 years old. If I’d never been diagnosed, I never would have been able Continue reading →
Our fourth daughter, Kendra, was born on September 29, 2003. My husband and I were very blessed to bring home another beautiful little girl. Kendra had a few minor issues right after she was born. She was sick a few times, but we were not overly worried about any major medical issues. Our oldest had been sick a few times when she was an infant, but I learned she was much better if I stopped nursing her and changed to formula.
We tried this for Kendra and it seemed to help for a little while. Unfortunately, she continued to projectile vomit. Soon after, she was admitted to the local hospital for a test to find out what was going on. We learned Kendra’s urine was going the wrong direction. If this hadn’t been detected, Kendra could have ended Continue reading →
Carmen responded immediately to a cost-effective prescription drug used to control cyclical vomiting.
“It’s the stomach flu” I said into the telephone receiver when I called Carmen’s school to inform them of her Thursday absence. “She should be feeling better tomorrow.”
“Great!” I thought to myself …. “how am I going to keep the rest of the family from contracting the bug?” I wiped down the bathroom with disinfectant wipes in hopes of banishing the 24-hour virus from our home. Little did I know this was just the start of our journey with Children’s Hospital of Wisconsin and a brilliant man named Dr. Li.
Looking back at that first day of illness, I remember Carmen complaining of an upset stomach in the weeks prior to her vomiting. It was nothing to be concerned about at the time … she was able to go to Continue reading →
Due to the many wondrous talents and skills by Children’s Hospital of Wisconsin physicians and nurses, I am alive today, and I will continue to live day after day after day. I have not been to every clinic and specialist (knock on wood, please), but I’ve been to quite a few over the last almost seventeen years of my life. From orthopedics to ENT to pulmonary functions to the Herma Heart Center, I’ve been down many hallways in the hospital.
What is especially promising and a relief to know is that my cardiologist, Dr. Earing, not only takes care of kids, but also has an adult clinic. This guarantees a knowledgeable Continue reading →
Mo and Kate Jurgens
My daughter Maureen (Mo) has Loeys-Dietz Syndrome, a connective tissue disease similar to Marfan syndrome. Loeys-Dietz syndrome is complicated. It affects the connective tissue that runs throughout the body—organs, muscles, and blood vessels. You name it. It’s present. When the tissue is weakened and defective, it is bound to wear down, be stretched to its limits and sometimes break. A major issue for Loeys-Dietz patients is they develop aneurysms throughout the body along with having many issues with the joints and other soft tissues.
Mo was born in 1995. Loeys-Dietz syndrome was not discovered until 2005. She has made many trips to Children’s Hospital of Wisconsin since she was born, visiting a number of clinics including orthopedics, ENT and neurology. Her first visit to Continue reading →