Cystic Fibrosis · Family · Life

Help Keep Levi Crazy!

It’s that time again, folks. I will be riding in the CF Cycle for Life fundraiser next Saturday, September 15. If you want to skip all the fol-de-rol and go straight to donating, here’s the link.

Cystic fibrosis is a currently uncurable genetic disease. Improved treatments and medicines have lengthened the predicted lifespan of CF patients dramatically in recent years, but we are still waiting for a cure.

Right now Levi does between 90 and 120 minutes of treatments and takes many, many pills every day, when he is healthy. If he gets sick, it’s much more. We are so grateful that these treatments and meds have helped keep him as healthy as he is, but more research is needed in the future to lengthen his lifespan, and that of other CF patients, and to make their lives easier and better.

Levi and me at one of his recent doctor appointments.

If you are able to make it even a small donation to the CF Foundation to help with research tour to cure, we would be so grateful.

I will be riding in the Cycle For Life event on Saturday, September 15. Paul will be working, so he’s not able to come, and cousin Amanda has stepped up to help watch the kids. (Levi is not able to attend this event because of cross-contamination concerns.)

You can donate to my ride here, if you’re so inclined.

Thanks for helping keep Levi crazy!

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