Added: 3 years ago
From: rebcade05
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  • I have a friend with cerebral palsy (except it's a mild form) and he is a really cool guy. He's in my weight training class and I went to preschool with him. He does a lot for himself and doesn't let anything slow him down. And he's even missing a leg, he had to have it amputated when he was a baby. But he's amazing. And NO ONE has ever made fun of him. Everyone who knows him is his friend.

  • Great video! God walks with us in our journey. From one person with cp to another. Don't loose heart, you're going to make it

  • I know she can do this journey coz she have you. I have a CP too. I know God will guide us.. God nless.

  • she is absolutely adorable so proud of the progress she has made for herself. keep up the work tai and dont let anyone tell you arent special or are diffrerent cause u r o ne awesam girl

  • i Know what it fells Like to Be Laft a For any resons ! I am Adopted2 I have Reading Disabilitys And That is Just Some Of Them and I have a Close FriencWith CP

  • My granddaughter has Cerebral Palsy also and she cant even do some of the things I see her do,thats wonderful to see.My granddaughter was in a housefire in 2003,born normal,but now has Cerebral Palsy due to the smoke....thank God she didnt get burned...I know how it hurts inside to see them suffer.....I am soooooooooo devoted to Ilana,my granddaughter......I am with u on raising more attention on what life is for these children....

  • Very touching video! I have CP and I know how much it hurts to be laughed at by people who don't understand. I'm working on a series of books about a Cheyenne boy living with CP.

  • I'm a proud mom of a very special girl who lights up everyone's life....she too has CP

  • Not trying to be mean or anything, becaause my sister has CP but its 1 in every 400 kids.

  • I know exactly what you're saying because I have Cerebral Palsy too. When I was younger I couldn't walk so I bum shuffled around . When I was 3 I walked unassisted for the first time and had to wear AFOs as well.

    I have a mild for of Cerebral Palsy Hemiplegia and affects the left side of me body.

  • Hey There, I'm 15 years old. I have Cerebral Palsy and Epilepsy I know what you are going through. Stay strong hun Take Care xx

  • @300horselover Thank you for being a voice for these children! I have a beautiful niece with Angelman Syndrome and a 24 year old son with epilepsy. I wish my son had your attitude. It's so hard to keep him upbeat!!!

  • I'm not sure who you think your audience is... most likely if we're watching this we're already on your side or neutral. People that "laugh at someone with CP" wouldn't likely click on this, so the tone is a bit off. But she's beautiful and I wish her much strength.

  • Thank you

  • The road ahead is a challenge but with hard work from the parents and child and the help of therapists will achieve the goal to have a better life. My son is 7 with mild left hemiplegia.

  • I love this story. my best friend, Amanda had cerebral palsy. she passed away in 2006. but she was always happy and she always made me happy. but this is a great video.

  • @kellyfan25 Amanda will always be in your heart and thoughts

  • @titaniumtori yes she will. :)

  • She is so cute. My best friend Reccbca had cerebral palsy and die last year when i was in 6th grade. Now i am in 7th grade and now i have a new friend with cerebral palsy her name is maggie and i love her so much> Anway she is every cute and i love her for being strong

  • @babeinlove123 Your best friend Reccbca will always be with you in your heart and thoughts.

  • wow. my mom's friend's daughtter has it, and i help take care of her :)

  • cerebral palsy definently effects the family. its not the child but the disablilty that negativly effects the child and the family. my uncle has had cerebral palsy all his life and my grandmother has taken care of him for over 40 years. its sad it really is but if you make the best of the situation they can live happy lives. all the best to tai she's beautiful and i'm sure she'll make it through. support is the most important thing:)

  • Eye opening truth..I have twins with cerebral palsy...I love them more everyday and want so bad to protect them from evil people..love and hope keeps us going..Thanks for posting it helps me get through my fears

  • my brother has cerebral palsy and is bedridden for 23 years..i know he hears,see and feel us..i love him so much and he gives me strength..be strong and keep up the good work!!

  • RIGHT ON! Daniel is in high school. He can't talk or do anything on his own! His IQ is so low, he doesn't even know abc or 123. NO ONE IN HIS HIGH SCHOOL EVER MAKE FUN OF HIM, because everyone know his family love him. His parents got to know some these kids while Daniel goes out shopping. These kids introduced themself to his parents, because Daniel can't tell anyone who they are. Keep up the good work!

  • Your cousin Tai is so beauiful & awesome. I have Hemiplegia Cerebral Palsy, 4'8 tall & 16 years old. My best friends & cousins don't laught at me.

  • your cousin, tai, is beautiful. This video is astounding and really brought tears to my eyes. It's so sad to know the struggles that another person goes through. I pray for you and your family.

  • i have cerebral palsy too and i have the worst kind so i always get made fun of and life with cerebral palsy is extremely hard for me!:(

  • Cerebral Palsy pulse dance!

    chachacha!

  • No offense, but I found that having a pity party didn't help things, so stop whining about it, it is always going to be a a part of life, CP is, but you can still live a active life. CP sucks, yes, but have fun, we ain't getting out alive. xD

  • its hard for me to get through life with CP

    All the physical therapy, being fed, being wheelchaired

    how am i gonna get through life having Cp?

    I need as much support as i can get

    also to the people saying that im making fun of people with cp, im not!!

    I have cp so if I did make fun of people wirh cp then that means im making fun of myself so im not making fun

  • What you call a pity party we call awareness! My son has CP he is 5, he cannot walk, talk or do things for himself. Can he still live an active life? Educate yourself before you dictate a prescription! There is a beauty and pain when you know somebody with CP I adore every moment with my angel! So you should stop whining and be proactive instead of reactive!

  • Lady, I have CP. There is hardly any beauty to CP, but as you say, there is pain and humiliation. And believe me, I am educated about cerebral palsy. But I was hardly whining. I was encouraging him/her about the situation. Proactive? I'm on my school's football team. And might I ask you to keep your nose in your own business?

  • CP is my business, sorry if you were offended but, I didn't take this as a pity party. The beauty I was referring to was KNOWING someone with it, I have learned a lot and I adore him...

  • wow, i dont have words

    its a great video, nice job, my respect for all the people with cp, never stop guys, never!!!!!! dont listen the bad comments cause that kind of people dont understand, they dont have a good life full of love thats why the say stupid things.

    latinosssss say hi to you

    bye have a nice day!!!!

  • I have to wear AFOS too on my left leg to help me stand and walk

  • I have Cerebral Palsy too its hard to live with but i'm learing to live it it. But its very hard when people make fun of me. All the best. xx

  • @chontelle01 Chontelle-people that make fun of other people are quite frankly, Idiots. Usually, they're people with VERY low self-esteem, and making somebody else feel bad is the only thing that makes them feel good...and honestly, I believe so many of those "ugly" people feel guilt later. Sometimes I think they say things in front of friends because they think it makes them look "big". It doesn't. You're an amazing person....don't let ANYBODY tell you different, ever!!!

  • i have cerebral palsy 2 its hard 2 to live with but i am stronger because of it love alicia

  • I like what you said in this video. I too have to wear AFO's and also know the fight that people have to go through to get medical equipment paid for. I wish you the best of luck with your cousin Tai.

    Much Love,

    Alicia

    Concordia KS

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