crystalina0814
New member
<a target=_blank class=ftalternatingbarlinklarge href="http://www.youtube.com/watch?v=fMGUXOtFxjc
">http://www.youtube.com/watch?v=fMGUXOtFxjc
</a>
This documentary will be airing in Canada...what a touching story that hits so close to home for most of us on this site. I can't wait until it becomes available for purchase or aired in the US.
"This personal and touching journey takes an unflinching look into the life of Eva Markvoort as she battles a fatal genetic disease called Cystic Fibrosis (CF). At 23, Eva needs a double lung transplant to live. Unable to be around other patients with her disease, Eva turns to the internet where she forms a strong connection with two American girls named Meg and Kina. The girls also have CF and are in different stages of transplant. Now at a critical turning point in their lives, the film travels the distance the friends cannot go themselves, capturing the compelling and often heartbreaking realities they face just trying to take each breath."
Pray the Eva.
">http://www.youtube.com/watch?v=fMGUXOtFxjc
</a>
This documentary will be airing in Canada...what a touching story that hits so close to home for most of us on this site. I can't wait until it becomes available for purchase or aired in the US.
"This personal and touching journey takes an unflinching look into the life of Eva Markvoort as she battles a fatal genetic disease called Cystic Fibrosis (CF). At 23, Eva needs a double lung transplant to live. Unable to be around other patients with her disease, Eva turns to the internet where she forms a strong connection with two American girls named Meg and Kina. The girls also have CF and are in different stages of transplant. Now at a critical turning point in their lives, the film travels the distance the friends cannot go themselves, capturing the compelling and often heartbreaking realities they face just trying to take each breath."
Pray the Eva.