Added: 1 year ago
From: clairebarnwell
Views: 22,640
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  • i have cf and now asthma and eve in inspiration for all kids to keep holding on. iver had cf for 16 years now and im fighting to breathe everyday and this little girl has touched my heart(: thanks eve

  • so many people need help. I spend alot of my time in a hospital too but I have something not as terrible as cf....... pleez help spread awareness. Eve you are so brave

  • she is adorable, what a brave girl my heart goes out to you all <3

  • What a beautiful child! She has such a pretty face. All the smiles - she's an inspiration.

  • What a beautiful girl!!! Im praying for her, and hopes she makes it to 85!!!! What a princess:)

  • I had a neighbor who had CF but she didn't make it, she was 8 years old when she past but her family is selling merchandise to raise money for a cure It is called Anna's Army. Info is on their website.

  • OMG SHE IS ADORABLE.I CAN ONLY IMAGINE SEEING MY CHILD STRUGGLE WITH THIS.SHE IS A FIGHTER. PRAYING FOR YOUR FAMILY.GOD BLESS YOU.

  • loved the video she is such a sweetheart i also have cf and im 23 so i will keep her in my thoughts and prayers and keep your head up little one and keep fighting and we will beat this thing one day

  • hi..i just want to say that the video was really emotional and i hope eve gets better ..and God bless you all and best wishes for you all :)

  • My husband is 35 with CF.

  • She is a beautiful little girl and such a strong little fighter! I pray she is doing well and lives a long happy healthy life <3

  • This was sad and heart touching! I dont have cf but I do have asmtha and whenever it is chilly and I have to run track at school I can't breath and my throat burns! Stay strong EVE! We all believe in u ! Love you too ;)

  • I have cf, and I'm 14, I have to take over 80 tablets:(

    great video:) stay strong!-3

  • Wow , she is just breath taking gorgeous <3 , a strong little squirt you got there : )

  • dios te bendiga hija....

  • She is so cute. I hope she is doing well. Today is Janurary 20, 2012

  • Im crying as i logging on and making a donation. Btw i love the zebra skirt at the end

  • i dont know how i got onto here but im glad i did. my mom had cf so i know how hard it is. your daughter is truely a fighter!

  • Where did you get the shirt with the boxing cloves on them?

  • wow 1:08 is really inspiring i take it shes going thought treatment and still has that smile...

  • crying she did every little test with a smile on her face

  • i was crying

  • I was crying. Wat a little trooper. Eve, I will pray for u. Stay strong little one.

  • Eve I will pray for u everyday! Stay strong and u can overcome this demon!! -3

  • Eve is SO ADORABLE, Claire! I've seen you post on our group and now I have a beautiful little smiling face to go with her name :) -Katie, Lila's Mommy

  • this is very sad

  • She's beautiful! Your family will be in my prayers until there's a cure!

  • I have chronic lung disease I'm 12 and I fought for my life ever since birth , it hurts to breath I will donate as much as I can to help find a cure for CF . Eve is so cute !

  • Thank you everyone! Please share this video and help spread awareness of CF!!! <3

  • She is so cute :) she seems to be doing wonderful and i hope she lives a long happy life :) I luv her Smile :) il pray for her :) gods peace

  • i feel so bad it is very said

  • my brother has cf, i do as much fundraising as i can! :) he is the same age, she is gorgeous and i hope both and millions of others make it! DONATE! <3

  • i wish i clould give 100,000,000,000,000 dollers! but im just a kid so i cant get a job :( but im saving every penney! i hope she will surely live to 80! :)

  • What a beautiful girl and the smile she carries on her face is amazing for what she goes thru on a daily basis. I don't have CF but I have bad asthma and I know how terrible it feels not being able to breath so I couldn't EVEN IMAGINE what she feels like. What a trooper she is and I pray to God that a cure is found. God Bless you and your family.

  • Oh my gosh she is the best person in the world. This made me cry. I'm not joking this is so sad. I hope she lives a long happy life and they find a cure. You guys all should donate. I know that there are only about 3,000 people in America that have it but every life counts. WE LOVE YOU EVE!!!!

  • @venicegirl310 i dont think its only 3,000 cuz of the 200 kids in my school 4 have cf

  • she is impossibly beautiful, i wish her all her dreams xxx

  • A truly beautiful little girl :') I am inspired by her and she has a beautiful smile...Hope you are doing well and your family too!

  • //eng.wavegenetic.ru/

  • i have cf i know how she feels :)

  • aww shes lovley i am 19 and have cf ... hope 1 day they will be able to cure cf big well dont to this video you are a little star <3 xxx

  • Great video. Well done :) Gary Dillon

  • Thank you both!! She is a little fighter...just like all the other CFers out there!! We need a cure now!!!! <3

  • Stay strong Eve..

    All of the treatments and pills can sometimes be overwhelming..

    but you will fight this disease and one day be cured <3

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