So this year, I'm diving head first into fundraising for the Cystic Fibrosis Foundation. I've been wanting to be proactive in my kids health and research since Izzy was diagnosed, and now I have the time to devote to it. So, I'm building a team for the walk in Pensacola, on May 26. And I'm planning several events through the year. I know that not everyone can participate or donate, but if you can do either that would be great!
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| Tristan when he was just an itty bitty, and yes my friends he too has CF. |
Ok, so I'm moving on now, and going to add stuff to my page about the walk specifically. So,
PLEASE PLEASE share this info. The more awareness the more likely funds will be raised and better therapies developed.

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