Skip to main content

Merry Christmas 2019

As the calendar turns over to yet another year it is time for a Kaser family update. We pray and hope this note finds you and yours enjoying time surrounded by loved one’s frolicking in all of your favorite traditions.
Over the summer we added to our ranks! Brooks Graham Kaser was born July 5th and his smile always brings joy to our day, even if it is followed by a river of drool. Currently, he is working on pushing his first teeth through and his best baby dinosaur roar impersonation. We also have a preschooler now! Theodore attends half days Monday through Thursday at the school right across the street. He always comes home with a good story or carefully manicured craft. Other big news for Theodore he just turned 5. We celebrated his birthday just over a month ago with his first all kid party. The theme was Star Wars and you might just say it was out of this galaxy. Our boys truly keep us on our toes, but we are always left wondering the adventures we would have if Oscar were here to join us. #OscarStrong #UntilWeMeetInHeaven
Julie has really enjoyed settling into her stay at home mom role. She continues to watch our nephews a few days a week which always adds major excitement at the house. The sewing machine or freezer is constantly being stocked with homemade creations that Julie makes with care. I have continued my position as the Attendance Specialist for Washington Local Schools. I really enjoy helping families in all kinds of situations improve student attendance. You may have noticed Chuck, our beloved slobber faced family dog, missing this year. We lost him in the spring and ever since Theodore has been asking what kind of pet we are getting next, including everything from a snake to a fish to a hamster.
We hope to connect with as many of you as we can over this Christmas Season. May God bless you during this busy time of year and we pray that you find time to rest in the peace and hope that comes from our Lord and Savior.
The Kasers

Comments

Popular posts from this blog

Pulmonary Atresia with Ventricular Septal Defect (VSD)

To everyone that has prayed for Oscar. Please keep praying. Today at his fetal echo cardiogram we found out he has Pulmonary Atresia with Ventricular Septal Defect (VSD). What this means is that there normally is a pulmonic valve that opens and allows blood to exit the heart through the right ventricle. Oscar's pulmonary atresia valve is permanently sealed or absent. Along with that, the main pulmonary artery is very small about 1/4 of the size it should be and it is much smaller than the Aorta. Oscar also has fluid surrounding his entire heart which was not there on the August 1 ultrasound. His heart function is okay, but it is not good. During the 2 hour fetal echocardigram there were also signs of fetal arrhythmia of Oscar's heart rate dropping lower and more quickly then it should. Going forward we need your prayers for our son's heart. We believe in a God that heals and does miracles. We don't know if Oscar being born alive is going to be that miracle we are gi...

3 years

3 years today since Oscar left us and went to Heaven. I can't help, but replay his last days in my mind and vividly recall certain details. For any parent with a sick child whether that child was an infant, child, teenager, or adult those last days, hours, and minutes are such a blessing to have, but still so painful when you allow yourself to really remember them. You look back and you can't help, but wonder if you made the right decisions, did you push them too hard, why didn't you see how sick they really were. Those are things that after 3 years I still wonder and I am sure always will.  To someone that hasn't lived through their child dying you are probably thinking that doesn't seem healthy, but for us that have lived through this I beg to differ that I think it is completely normal. You see as a parent you always want to do what is best for your child to make sure they are happy, healthy, and feel loved. My child is not here to think about those things prese...

Meeting some of Estella's Team

Brian and I headed for the MFM office Tuesday, August 1. Our appointment was at 10:45am and we got called back around 11:00am. Our ultrasound technician was wonderful. She was so kind and it turned out she lived in the same town we did. It was a long ultrasound and one where questions were asked, but answers were not able to be given. Estella was moving a lot during the first half of the ultrasound which was fun to see and good to hear her heartbeat (155 bpm). Throughout the ultrasound the technician had to leave from time to time to talk to the doctor and to see what remaining images he wanted. About 12:30pm the ultrasound was finally completed and into the room came the maternal fetal medicine specialist doctor and genetic counselor. The doctor told Brian and me that our baby had some significant birth defects: a bilateral cleft lip with possible palate involvement, a VSD heart defect, and Dandy Walker Malformation that affects the cerebellum in the brain. I sat on the ultrasou...