New reasons for special needs parents to worry about healthcare

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. […]

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I had to reapply for @makeawish

I told you the other day that I sent Gavin's information into Make-A-Wish, after waiting for him to decide he would be okay with possibly having a wish granted.  I replied to…

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