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It’s crazy how much can change in such a short time. I am dedicating this blog post to my thoughts on the corona virus that has become a pandemic. I want to begin by saying that I hope everyone is staying healthy and calm during this time. It is easy to read the media for […]
Read moreFebruary 12th of 2016 is a day I remember very vividly. This was the day that Wyatt was diagnosed with Cystic Fibrosis. First, let’s jump back to the day before. On February 11th we were getting dinner ready when I got a call from the pediatrician. Of course my ringer was off and we received […]
Read moreHi everyone! This is my first official blog post so please be patient with me as I learn how to share my thoughts and experiences with you all. The topic for this first post is a typical yearly cystic fibrosis appointment. Wyatt is required to go to the cf clinic every three months (when healthy), […]
Read moreBy Tony Zerucha An Oak Bank Elementary School student is doing everything he can to find a cure for cystic fibrosis, and his most recent step was educating his classmates about the disease. The cause is a deeply personal one, nine-year-old Lucas Filipchuk said Dec. 12. “Cystic fibrosis is the most common genetic disease,” he […]
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