Cystic Fibrosis Foundation Video Podcast: Cassalina family

The Cystic Fibrosis Foundation video podcasts present the stories of CF patients, families and volunteers. The Cassalina family shares their experience of losing their daughter, Jena, to CF and encourage others to help find a cure for CF patients like their son Eric.

Category:

People & Blogs

Tags:

• Cystic
• Fibrosis
• Foundation
• CFF
• video
• podcast
• patients
• families
• disease
• care
• volunteer
• Cassalina

[charlesthepoet2004]

DO A WEB SEARCH ON:

charles h. miranda  OR:

charlesthepoet2003

THANKS.

[traceylabelle]

I have CF and I am 33 soon to be 34. This video was awesome. Breathe easy Jenna!

[marinna205]

@marinna205 God bless you all, =]

[marinna205]

@marinna205 i also have a feeding tube and port so i can get anibiotics i used up all my vanes. and i get boost through my tube. i hate it though. :(

[marinna205]

I have cf im 13, i cough alot in school and everyone stares at me. i hate having it i go the the hospital every 3 monts =[ i hope i can live long and strong rip jenna

[Maddogpowerful]

:( I have CF... I'm fine so far, haven't gotten the Pseudomonas so I'm fine now... I'm 20 and I'm fine...

[AngelGirlCFF]

R.I.P Jenna I have cf and i am 12 and still fighting i am now fighting it and hating it!

[Loveableteen17]

i have CF and i am 19 R.I.P to jena

[ILY2ALL]

my sister died of cf and she and jenna can be strong together

[tttayler]

my boyfriend has CF and i hope someday we will find a cure<3