kelly manz
My blogs
| Gender | Female |
|---|---|
| Location | United States |
| Introduction | Chloe June was born 11/04/08. Her CHD was discovered nine hours after her birth (with a little help from mother's intuition and a Pulse Oximetry Screening). Chloe spent the first two weeks of her life in the NICU at CMH. She was finally diagnosed with Taussig-Bing (DORV, d-TGA, VSD, ASD). Since she had a VSD, she was able to go home and wait to have surgery. She was sent home on oxygen and an NG tube. She had a Balloon Atrial Septostomy at 2 months and her open heart surgery (Arterial Switch) at the Denver Childens Hospital at 4 months. She continued to be fed through NG tube until seven months, when she had the Nissen Fundo and Mickey Gtube surgery. She still suffers from GERD and continues to be tube fed 6x a day. She currently sees a PT and OT once a week. She is my Chloe-cakes and I LOVE HER! |