Skip to main content

#OscarStrong

Our sweet Oscar will be 27 weeks on Wednesday, September 20. One thing Brian and I wanted to do was get bracelets to help individuals to remember to pray for Oscar and our family. We have partnered with Threads of Hope, Inc. to do a Love Project with Oscar's bracelets. This means that 100% of the funds from #OscarStrong bracelets will go straight back to the work Threads of Hope is doing in the Philippines.

You may be asking why Threads of Hope. Well...Threads of Hope was a booth at Bible Missionary Conference at Beulah Beach this summer.  If you read our story from the beginning at this conference on July 23, I said to Brian, "I think something is wrong with our baby" and then on July 24 my feelings were confirmed with a call that we needed our anatomy ultrasound bumped up and some additional appointments scheduled that day too. 1. to see the genetic counselor and 2. to have a consult with the MFM doctor as well. Threads of Hope not holds a place in my heart and is an organization I plan to support when I can.

 So how do you get a bracelet? We currently only have 75 and they will go on a first come basis. The bracelets are a $1.00 each, but if you would like to give more than a dollar you can and please know that a 100% of the money will go back to Threads of Hope, Inc.. Please reach out to Brian or I in person, text, email, FB message, or a comment on here.
If we run out of bracelets and you live in the Toledo area please attend Sylvania Fall Festival on Sunday, October 15, from 11am-4pm. Threads of Hope will be there with all of their products and Brian and I will be helping work the booth that day. Theodore and Chuck may show up too. :-) On October 15th, once all expenses are paid (booth rental, cost of goods, etc...) as a small fundraiser Threads of Hope is splitting their profits with us. The money our family receives will go towards paying for medical bills that are uncovered by insurance, travel expenses (we requested a referral to be written for Nationwide Children's Hospital HeartCenter in Columbus with hopes that when Oscar is stable and strong enough he will have heart surgery there), and finally just additional expenses with having a chronically ill child (one example is bottles for babies with a cleft palate are $25-$30 each).

Thank you for being on this journey with us and praying for our son to stay #OscarStrong.

Comments

  1. LeahSeptember 25, 2017 at 11:21 AM

    I am so thankful you emailed today and sent a link to your blog. I've been reading and reading your sweet blog since then. Somehow, I did not know at all about Oscar's story. I would truly love a bracelet. Praying so earnestly with you all.

    ReplyDelete

Post a Comment

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...
Post a Comment
Read more

Merry Christmas from The Kasers 2023

As the calendar inches closer to the end of the year we always enjoy seeing and hearing updates from our family and friends. No matter if we are fortunate enough to have our paths crossed or this greeting is our only interaction, know you are in our prayers and we hope you will enjoy this most blessed time of year. Our 4th child, Finneas McClish, graced us with his arrival on June 1st. It is hard to believe he is 6 months old already and lights up any room with his big smile. Brooks, now 4, started afternoon preschool at the elementary school across the street from our house. He has quickly blossomed into a social butterfly and is always looking forward to a playdate with new found classmates. Theodore, now a reading loving 3rd grader, thinks it is pretty cool having his little brother at school with him. Teddy also has really enjoyed being a part of Boy Scouts and is always looking for adventure. As you can imagine Julie has her hands full keeping everyone organized, but she tackles ...
Post a Comment
Read more

Day 29 - With Broken Hearts

It is with broken hearts we wanted to let you know Oscar went home to be with Jesus at 11:35am today, Saturday, December 16, 2017. Oscar as you know was taken off the endotracheal tube on Tuesday, December 12, and placed on a nasal endotracheal tube to see if he could maintain his airway with less support. We also were providing him with Versed to help him relax and rest during this transition. Oscar had a large drop in his blood sugars on Thursday, December 14, in the evening. Due to this they placed Oscar on continuous feeds and upped his calories to 28 calorie Elecare. It seemed this helped, but it was not a complete fix. After his low sugar of a 26 on Thursday night he had a hard time getting settled even with doses of the Versed every 6 hours. Then on Friday, December 15, we tried Oscar off the ventilator with no support this was around 12:30pm. He seemed to be retracting lots and having a hard time breathing. We then placed him on nose ram cannula with oxygen support. The...
Post a Comment
Read more