t’s been an interesting five months of heart checkups for Blaise. He hit the five year post-Fontan surgery this summer, and is entering the new “pre-adult” Fontan clinic that was established at children’s this summer. The goal of this new clinic is to follow the kids who’ve had fontan surgeries done and complete regular tests and exams to keep on top of their single-chamber fragile hearts to look for things that are starting to fail, don’t look right, liver damage etc.
So in July Blaise and I spent two long days getting him evaluated. EKG, holter monitors, echo, bike stress tests, liver ultrasounds, about 12 vials of blood and more. These tests all came out good, and we will repeat them yearly to continue getting baselines. I knew there was a good chance they’d “find something” as we are starting to dive pretty deep into looking at things closer then we ever had. A cardiac MRI was scheduled last Monday for Blaise, a first as well. Unfortunately a few things were seen, including one that’s a more pressing current issue. Today, we had an echo, to try and answer some questions from the MRI. His fontan is made with a plastic vortex tube/shunt. The blood flows sluggishly through this, and there is one area in here that is showing “something”. It appeared on mri, but was hard to determine. The echo today went the same way and hard to determine. They are concerned it’s a blood clot, or it could also be a fold in the shunt. So, we need to determine what it really is. Next step is to do a ct scan with dye contrast that is scheduled for next Wednesday. If that is still not conclusive enough, they will do the exploratory heart cath surgery to determine. They will also potentially fix a few other things noted in the MRI including coiling new arteries that have formed. If it is a blood clot, they will change him from his daily baby aspirin to Coumadin blood thinner the rest of his life (Not ideal at all) to remove the clot.
We are so grateful and thankful God continues to bless us with this miracle Blaise. We are praying that the CT provides answers and that there is not a clot! Thank you for our community of support and prayers- God continues to hear then!
Blaise you are a true warrior! You have our prayers! God is with you on this journey❤️
ReplyDeletePraying for answers to be found and the best outcome for Blaise.
ReplyDeleteBlaise, you are a champion and will do great things. We pray that answers will be found. God is good!! 💕
ReplyDeletePraying for no clot and easy fixes! Blaise has been such an inspiration to so many and has shown perseverance like no other. Continued prayers for Blaise and your wonderful family! ❤️
ReplyDeletePraying for good outcomes for Blaise! He is in great hands at Children's!! Thinking of you all!
ReplyDeleteHang in there, Hartwells! Praying hard that you find answers & that it is good news - NO BLOOD CLOTS!
ReplyDeletePrayers will continue for this sweet young man , and his wonderful family! His grandma Donna and I have been friends since grade school! Liz Foxhoven😊🙏
ReplyDeleteThanks so much have for update. I love that kid . Praying you get the answers you want.
ReplyDeleteBlaise you are such a warrior! We love you and miss you everyday! Lots of prayers for you bud! Heather and Ryker🤍
ReplyDeleteWe are and will continue to pray for Blaise. So grateful on your outlook towards Blaise as being a miracle! Keep that faith always!! -Aaron and Tawnya Meyer
ReplyDeleteWe are praying for Blaise & all his family!
ReplyDeleteBSF- Fremont
Wishing Blaise good news as you continue with the testing! Prayers for your family!
ReplyDeleteWe are praying for Blaise & your family, Erin! - Summy Family from MN
ReplyDeleteHugs and Prayers Hartwells! Please let us know if we can help, pick up kids or anything else! We love you! The Petersons (Clint, Brooke, and all!)
ReplyDeletePrayers for Blaise and all your family!
ReplyDelete