I have been meaning to post about Stellan again for days, guys. Stellan is still in the PICU, still dealing with frequent bouts of SVT, and still very, very sick.
There has been some big hope the past day or so. He has a new "fancy" electrophysiologist in Boston directing his care. He has a new medication regimen. And... if he continues down the same path through the weekend, MckMama and Stellan will be airlifted to Boston for an ablation... a surgery relatively common in older children and adults, but very fragile and scary to perform on a heart so small.
Please, please keep this family in your thoughts and prayers.
Also, there is a prayer blog that has a link to a fund set up for the MckFamily. Take a look.
Then, the great sellers of etsy have banded together once again to help support this family! Any listing that includes "Praying for Stellan" is set to donate the proceeds to the family fund. Clicking on the button below will take you directly there. I even have a couple treats listed this time, and I will be adding more after our trip to MN this weekend!
One last thing- seriously go check out Stellan's name gallery! It is really, really neat to see!