Added: 2 years ago
From: Thomas84pl
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  • I have cf and I am 28 yrs old I sing and play in a band from raceland,la...I really would like to play this song..how would one go about getting a copy of the chords are something!!!

  • How can I get a copy of this song? I am putting together a video for a friend of ours that has past from CF and would love to play this song?

  • I am gathering resources to bring a CD to light as a benefit for Cystic Fibrosis. I live in the Hudson Valley (NY) and am calling this out. I have a very close little girl in my life who me and my family adore. She has CF and I am calling this out in hopes that someone "out there" will offer up something to help manifest this vision. Help me with this project in any way you can. We will help the strides towards the cure, together. Email me: Natashalynnalthouse@hotmail.co­m

  • Thanks to everyone who put this song together. This truly a blessing to be able to hear. My daughter Kaitlyn has Cystic Fibrosis & she is a fighter. You will never see her without a smile. It keeps my faith alive that yes, one day there will be a cure. My prayers are sincerely with all our Cfer's around the world & their loved ones.

  • Can somebody give me the chords of this sonng! PLEASEEEE

  • WOW this is Amazing Work. Thanks for this

  • This is Tess from the remix of Breathe. It's amazing to see how many people's lives this has touched. It was a wonderful experience, and I'm so lucky I was able to participate.

    Let the memory of Matt live on, and let's continue the search for a cure!

  • @tessdunn

    Tess, This songs remind me my son Brian, who died 26 months ago, and every time a listen to this song, i can´t stop crying. Really beutiful. Hugs!!!

    Gustavo D

  • I live with CF and my main dream is a cure to be found :} "I know the answers out there,wont you HELP me PLEASE!"

  • I love this song and it makes me cry every time I listen to it and I am 26 and I have CF!

  • This song hits home My son has CF it is the hardest thing in the world to watch him take meds all day and do breathing treatments and wear his vest please help us find a cure

  • i want to raise awareness of CF and i want people to remember tommy...he was a pretty good friend of mine who passed away becasue of CF so im going to sing this sometime at a summer camp this year! RIP tommy! i miss u soooo much!!! <3

  • this video hits home to me i have a 7 year old son and a 17 year old niece living with cystic fibrosis. I'am so greatful for people like you posting this. life is so precious

  • i love this song im 13 and have cf

  • aaw :( my fiance just passed from cf last month! i told his mom im going to try to share this and let everyone more aware of what cf is! i hope they find a cure someday!!!!!!! Breathe Easy my love!

    RIP Jonathan Arledge!

  • R.I.P. Matt, thanks for the great music x Lewis

  • Great Song, brought tears to my eyes!!! My son has Cf, he is 18 . much of his days are filled with medications, treatment or being in the hospital. He still stands strong and is an Inspiration to many others.

  • Our best friend Haley has Cystic Fibrosis. We love her very much and we know she's strong. She's healthy for a CF kid. She's 16 and such an amazing person. She knows she's not alone with her illness even though she's the only person we know who has it. We love you Haley! :)

  • I also have Cystic Fibrosis. And love this song!

  • LOVE this song and video!!! What a fantastic job the singers did:) My niece Hannah who is a very mature 5 has CF and I can't wait to share this song with her!!

  • I have CF and I'm 20 about to be 21. I try to keep hope and I used to hate my illness but I've learned to embrace it cause I wouldn't be who I am today without it and everyone says I'm mature for my age, but you have to be. No one realizes how fast you have to grow up when dealing with an illness. I've come to realize I see the world differently than most ppl. Everytime I see a new med I know we're getting closer to a cure and that's what keeps me going.

  • I have Cystic Fibrosis am 15 and i hope one day they will find a cure i don't mind having it, i wouldn't be the person i am today if it wasn't for my CF i see life with a positive attitude and i am looking foward the future to going to college and getting married, like i always say I Hope, I Believe, i Dream, i Know so to everyone who has CF think positive everyday!! even if its those days when your down!!!!! <3 Stephanie

  • RIP and breathe easy Matt Scales.

  • Everyone Loves This Song. Most Of The People Don't Know What CF Is. All My Friends Who Listend To This Song Started To Ask Questions And Triet To Find Out About CF On Their Own.

    Everyone - Make All People You Know Aware Of The CF.

    Every Day Scientists Find Something New, Hopefully They Will Discover A Cure For The CF Very Soon.

  • I thank all of you for making CF known. May 29, 2010 CF took my second mom. She was an amazing person and the world is so much emptier with out her. I know that she can breathe and do everything that she couldn't do. This song will come true one of these days. CF needs to be CURE FOUND

  • I lost my darling nephew, Matt DeGregory, to CF 2/21/08. I know he's breathing free now. I pray that this song will come true and CF will finally stand for CURE FOUND.

  • does any1 know where to get the sheet music for this song? i wanna sing it for my school talent show but i need the sheet music! please help a fellow CFer thx :)))

  • My mom found the site about this song and she had tears in her eyes.

    I love the song and share this with everyone!

    I have CF too and 16 years old.

    R.I.P. Matt.

    I hope they find a cure for us soon.

  • Josh voice is great!!!! *o* all them are wonderful...thanks!

  • This is Josh from the Remix of Breathe. It was an amazing experience to be a part of this project. Thank you Matt Scales for sharing this with the world. Peaceful things.

  • @welcometojoshland

    Good to see you here, Josh. Thank you for posting comments. You have a great voice, and this song - yes, it is amazing, moving, and touches all the senses.

  • @welcometojoshland Hey Josh it's Leelee from Australia

    I still listen to this everyday

    Whether I'm in my salon at home

    or doing housework, my CF songs give me hope

    They bring out the goosebumps, a tear to the eye, and

    make us that bit stronger on the inside!

  • @welcometojoshland @welcometojoshland Hey Josh it's Leelee from Australia

    I still listen to this everyday

    Whether I'm in my salon at home

    or doing housework, my CF songs give me hope

    They bring out the goosebumps, a tear to the eye, and

    make us that bit stronger on the inside!

  • @welcometojoshland

    Im trying to put together a cd of CF songs for our fundraisers how can I download this song and do you have any suggestions for other songs?

  • This is Josh from the Remix of Breathe. It was an amazing experience to be a part of this project. Thank you Matt Scales for sharing this with the world. Peaceful things.

  • My dad found the Breathe project online and passed it on to me. You forget sometimes that there are other people out there dealing with this every day, so I come back to watch this every once and a while to remind me I'm not alone.

    And one day we will breathe.

  • My cousins wife Wendy, aged 32 just died with CF. She was a beautiful woman and left us with loving memories of her. I never once seen her without a smile, didn't matter how bad thing were at the time. She had to leave behind her loving husband Neil and a beautiful son Louis(11), who she managed to conceive naturally, which she was told she couldn't do! Hear death is such a loss to so many people it made it to the front page of our local news paper.(Inverness Courier). Miss you Wendy.xx

  • i love this song/video,, very touching .. i have a 14 yr old with cf.. i hope someday soon CF stands FOR CURE FOUND!..

  • @nikki6977 well said, im a14 year old with CF too. I wish we were allowed to mix, sometimes all you need is another person who understands it. Not doctors or nurses, just friends who get it.

  • @nikki6977 I like your thoughts on what should CF stand for. I agree. I'm a living testimony that doing treatments and working hard you can live a good life. Not saying I've not had my struggles. God bless and keep the faith.

  • I watched this everyday. It's just inspirational!

    Lee Mum to Joel 8 with CF xx

  • @Leelee0z I still listen to it everyday

    it gives me hope

  • Oh my goosh i love this (L) how can i get a copy?? <3

  • Thanks everyone for watching and commenting. I watch it few times a day. Love this song and Video, and can't get enough of it. Share this video with your friends, maybe it will make them learn more about Cystic Fibrosis. Hopefully there will be a cure in the near future.

  • This is so beautiful...how can i get a copy of this song???????

  • I love the song, the people, i love it all, i have cf too so i get it.

  • what a beautiful song. i lost my sister 5 months ago to cystic fibrosis it has been so hard for all of us the only thing that keeps us going is knowing she is finally breathing easy!

  • Thank you for this wonderfully touching song and video. I couldn't stop crying. We need everyone to know about this horrible disease and that we need a cure TODAY! I want my 8 year old son to live to be 108. I want him to breathe like you and me.

  • Comment removed

  • super good video 2nd coment!!

  • This is so GREAT!

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