March 1 2018 will mark 2 years in remission from Leukemia for Brandon. It’s been a slow and steady recovery from his treatment and stem cell transplant and making it to 2 years is a giant milestone. Over the course of his recovery we’ve seen him blossom into a funny, caring, cheeky and inquisitive 4 year old. I’m happy to report that he is attending school and our family life has largely returned to normal. Thinking back to where we were 2 years ago, Ingrid and I couldn’t imagine he’d be in the position he’s in. We are so blessed and grateful for his recovery and to be able to watch him do all the things children should be doing which is playing, laughing, learning and enjoying their childhood.

It’s hard looking back at the photos and videos of his treatment. The treatment for leukemia feels like you’re navigating a minefield blindfolded. Complications and infections among many other things can arise at any time which can result in Chemotherapy cycles getting delayed which could allow the cancer to come roaring back and it all spirals from there. If a stem cell transplant is required (which Brandon needed) finding a suitable match is similar to winning the lottery. And then you have the threat of relapse hanging over your head as you work through the recovery.  If that happens the whole process starts again only the stakes are much higher. I often think about all the families that i’ve never met that are going through a similar journey and it breaks my heart which is why I’m participating in the St. Baldrick’s head-shaving event again. St. Baldrick’s only funds research for childhood cancers with the aim of finding cures. Hearing a doctor tell you “your child has cancer…" and "we’ll do our best to save him...” is a horrifying thing for any parent to hear.  Supporting research for cures will help prevent other families from hearing those words.