Cheriz: My life with Cystic Fibrosis

Yes, Money, the topic people don't like to talk about. However, I think CF and money obviously affect each other. For instance, we have an out-of-pocket maximum of $4,000 per person (8,000/family).  Luckily Andrew is very healthy, so we don't ever (usually) pay on him (except dental). However, I always will hit my full $4000. It's just a matter of how I will spend it. It doesn't matter whether it is over 6 months over the course of my prescriptions (co-pays) and doctors appointments, or if I pay it all at once with a hospital stay. I have to be prepared, we never know when I will end up on IVs. Plus I go to CF clinic every other month and it costs $200 per visit. I ended up paying my final $1,400 of my out-of-pocket this last week for my hospital stay in October. So I should be 100% covered (since met my out of pocket) until Jan 1, 2018, and then it starts over... How? How can we afford that? We certainly can't take it out a lump sum of paycheck (he gets paid every

I have a lot of feelings going on, for many, many, many reasons. It all centers around my health and family. On August 4th we received 3 Foster kiddos, let's call them "Cajun, Barbie, and Shoes" (that is what I refer to them by on FB). It was a very big Roller Coaster ride for the last 3 months. If that isn't enough worry and emotions to have going on, we can throw my hospital stay and lower lung function into the mix. I knew my lower lung function was not a result of the kids (even though many believe it was)... Yes, I was run down from pulling all the "all nighters" with the kiddos- they are adjusting to a new home and its hard on them. BUT, I have been struggling with lung function for the last year now. I was 60% August 2016. I started Orkambi in Sept and 5 weeks later I was in the 20s.. I was admitted (my family did thanksgiving with me at the hospital last year). When I went home I was between 38-45 for months that followed. Not even getting to 50 was