Current TV Presents ‘Dying Young’
Thursday, July 29th, 2010 at
5:34 am
CysticFibrosisUSA asked:
This documentary short explores the struggles of living with cystic fibrosis. Produced by and for Current TV.
Tagged with: Cystic Fibrosis • Documentary • Dying Young
Filed under: Cystic Fibrosis
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I pray for all the cystic fibrosis fighters out there and for a cure. I know two of them. God bless you all.
my best friend has it :’(
lovely, thanks
@djvampya im now 24 and am on the lung transplant list
I am a researcher and curing cystic fibrosis occupies most of my waking hours. I am fighting for you guys with everything I have. God be with you and I hope a cure comes soon.
I am praying for all who suffer and have been taken by CF
I am a father of three kids, two of which have this awful disease cf. With the current medical research and awsome people raising money such as walking for the cure and cff donations, their is hope for a cure. We have a Great Physician in Christ Jesus our Lord.
@mkw050791 This is just a brief overview of Cystic Fibrosis. If you’d like to know more you can always private message me and I can give you a run down of my day or you can ask any questions you may have. I’m not afraid or ashamed to talk about it so ask away. Much love and thanks for your support.
25 with Cystic Fibrosis and always grateful for each breath God gives me. It’s a crappy disease that screws up your entire body. I have arthritis, obstructions, lung damage that’s irreversible, gave up most everything I love, and am sick constantly. I don’t wish this horrible disease on anyone. I love you Siobhan.
be strong all of u guys who have cf…be strong always and dont lost hope to God…God is good remember that.
@mefobblog thank you for your condolences.
@kryan364 im sorry to hear this
hello,
my name is kristin, im 14, and I have Cystic Fibrosis. I would love to talk to someone else with this disease. Feel free to message/add me.
i´m looking up to all of u guys. you´re all so strong and don´t let your desease get you down. i hope you´ll all have a long and happy life and find someone you love and who cares about you. god bless
My mom recently died from CF, i knew it was bad but i didn’t think it was this bad…
i am also living with cystic fiberosis. i am only 12 years old, and my brother who is 15, also has it. but i was never told i could die from it
I’m 23 and have cystic fibrosis, and I’m having a lot of trouble with my finances. I don’t qualify for disability yet, but I am unable to work full time. I’m going to be aged out of my parent’s health insurance policy soon, and don’t know what to do about health insurance. What is everyone here doing about their health insurance?
Thank you very much, keep standing strong and God bless. .
This video really moved me it upsets me alos. I have CF im 42 this year. transplant is getting nearer to me now. FEV1 0.66.. stay strong people. xx
im 29 and have been diagnosed with CF from the age of 1. the one thing i can say to people here is dont let CF get u dwn, its something we must control and put up with but never let it dictate life!! those days when the lungs feel free, live life to the full, enjoy it! one thing ive noticed bout CF sufferers is that we all have the same smile on our faces, never let anything get us down! Im running a marathon in dublin in oct, if i can do it so can u!! Keep fighting and never give up!!!!
I found this so moving. Im 21 and have CF and I always worry want the future holds for me but we need to face each day with a smile on our faces.
im so sorry and sad to hear that this is happening with so many people. There so young. i’m so sorry for the suffering you go through. Love you. stay strong. God Bless
@TheSecretangel101
Thank you, she was very strong willed. Siobhan considered the live lung transplant, I have the same blood type she did, but she decided against it..I think it was too risky and her friend did it and then died just two weeks later.
my girlfriend has CF and it kill sme to think that i might not be able to spend my life with her like we talked about.
My bestfriends Sister, Sheana Danielle Blanchard just passed away from CF on March 28th, 2010. She had just turned 21. I wish she didnt have to go, but In a way i’m so happy she left us. She was suffering sooo badly. She couldnt go with out oxygen tanks. RIP Babygirl.
@lilro89 my friends hav cf, it scares me sometimes, but down deep inside i know all of you with cf can do it, just keep on fighting, one day there will be a cure, and jamie your 18 young and strong, you can do it, god is on your side, and we all have faith in you and everyone fighting out there, good luck jamie, god bless you your a great girl.