Gavin had a weird night last night. Right after dinner, I got Gavin's IVIG infusion going. The weirdness started when he decided to stop eating dinner because he thought he…
The boys had a great time at their Grandparents house last night and today. They've been rather quiet since they arrived home. I haven't heard any fighting and that's awesome. …
I mentioned yesterday that Gavin's IVIG infusion supplies hadn't showed up. Thankfully, they arrived yesterday, right before the boys left for their Grandparents house. I showed Gavin how to make…
It's slated to be somewhat of a busy day. Gavin needs his IVIG infusion first thing in the morning, and then we have to go order his new glasses. We…
My son Gavin, has something called Primary Immunodeficiency. This means that his body doesn’t produce enough antibodies to fight off infections. What antibodies his body does produce, are defective. Thankfully, there’s a treatment for this life-threatening condition, and it’s called IVIG. Gavin receives his IVIG via subcutaneous infusion, directly into his belly, twice a week. IVIG is essentially donor antibodies. […]
Gavin's IVIG infusion is well underway and aside from a few hiccups, it seems to be going well. The hiccups I'm referring to are the result of one of the…
With everything that went on Monday, we weren't able to get to Gavin's IVIG infusion. He's supposed to receive these infusions on Monday and Friday, but sometimes it doesn't always work…
It's becoming more and more difficult to pretend that Gavin's not getting worse. I know he's never going to get better, and that's something both my wife and me have…