I was debating on whether or not to post this video…
I know that it will be hard for some friends & family to watch…
But this is the reality of Cystic Fibrosis. This is the reality of what this horrendous disease does to it’s young community.
And I believe that it is essential for the entire world to get a glimpse of Eva, her strength, her courage…her love.
The majority, if not all, of the CF community seems to have caught wind of this amazing video clip. This young woman is wise beyond her years and has somehow accepted her fate with a smile. She is much stronger than myself and there are many prayers headed their way from our household.
If you want to view the video I have posted it below, or click HERE to see her entire blog.
*Just a warning, she is saying goodbye, so make sure to grab some kleenex.*
Why do I post this video on Valentine’s Day you ask? Because Eva’s heart is filled with love, even in the most difficult of times…I don’t think I could find a better clip portraying love in a better way if I spent a lifetime searching…
Please donate to our cause. You will be helping not only our young son, but thousands of young lives around the world.
We NEED a cure for 65 Roses…
Wow, the last few times my computer has been letting me post comments! I saw this video, such a strong young women! We can all learn a little from her strength.
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