This is our journey of living with Cystic Fibrosis and navigating the wait for a double lung transplant. Our goal is to keep our friends and family aware of what is going on as well as help others who may be in a similar situation. Laura and Amy made a documentary to provide hope for parents, friends and family of other who have CF. Feel free to share and comment. Cheers from our family to yours.
Tuesday, September 25, 2018
A surprise happening
I have said this before but it really can't be reiterated enough. We have the most amazing support network. NOTHING is too much to ask and when we don't ask people take it upon themselves to do amazing things.
Here is the image and link to retail store for #teamlaura. A friend new we had discussed starting a foundation to help other transplant patients that are not as fortunate as we are. They went on their own to design t-shirts for all sizes and sell them to raise money. AMAZING!
We can't thank them enough. We are excited to help other as they move through their journeys.
Cheers,
The Z's
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