A Gift for Savannah’s Heart

by Ryan Hensler // December 14, 2014 // No Comments

Throughout much of this year, our blog posting discipline has been lax. This is not because important events and milestones have not happened, it’s just that life tends to get in the way of writing most days. In recent weeks,... Continue reading →

R.I.P. Sweet Noah

by Ryan Hensler // August 24, 2014 // 4 Comments

With heterotaxy being a fairly rare disease, those affected by it tend to stay fairly well connected. Especially with the advent of social media, we can share our life experiences across various continents as they happen. While the support and... Continue reading →

Cincinnati Trip

by Ryan Hensler // April 13, 2014 // No Comments

This past week has been quite interesting. The good news is that Savannah is doing quite well. The bad news is that Savannah has another surgical procedure scheduled in May. Our first appointment on Thursday was with an ears, nose,... Continue reading →

Another Big Day

by Lori // April 8, 2014 // No Comments

Thursday we will be going to Cincinnati Children’s for a day full of appointments for Savannah. While we don’t expect any surprises, I am still nervous! We will be seeing ENT to double check her airway issues, but we honestly... Continue reading →