Meet Casey Jo!
She is my beautiful sister. She was diagnosed with Cystic Fibrosis as a baby.
She has been fighting this disease all her life.
Casey Jo's health has been gradually getting worse. Her doctor told her that she is close to being eligible for placement on the lung transplant list. We have decided to document and blog her journey together. This page is where all of Casey Jo's updates will be found.
In May 2013 Casey Jo started her round of transplant testing at UPMC. Here is her journey thus far:
(To read each blog post, click on the blue link below the pictures)
Wow! I had no idea that your sister had Cystic Fibrosis. I was truly meant to click on this page. For my final semester at UNCC, I put together a public relations campaign for an organization called The More than Just Me Foundation. The founder works closely with patients suffering from CF and is currently climbing 7 of the worlds largest peaks to raise funding for new programs, and hopefully a cure for CF. I hope that you reach out to them. Maybe they'll showcase your sisters journey or can be of assistance some way.
ReplyDeleteYour sister is gorgeous and a warrior! I'll be stopping in from time to to to check in on her. Thanks for sharing her journey.
Oh my goodness! That's crazy you clicked on this page! Thank you for informing me. We will definitely check it out! :) Thanks so much Theresa! You said this is your final semester, good luck and best wishes for graduation! :)
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