Added: 2 years ago
From: 2009liveit
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  • Well done! Very informative.

  • I'm 27 and have a mild case of 22q. It's wonderful to see and hear things from others who have this disorder especially since I don't get to see as many who do. Best of luck!

  • You are perfectly perfectly normal to me! My 7 years old kid has 22q11 and Global developmental delay and problems from head to toe.. Lucky you!

  • Hi Mackenzie i'm a friend on your facebook so just thought i'd say hi cause i was looking to make a page for Di George Syndrome! Lots of love katie xxx

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  • my son is 4 yrs i was just informed by a doctor that he has 22q11.2 deletion syndrome...he was operated VSD surgery when he was 5 months old... dont now my his doctor did not inform us then!!!!

    thank you mackenzie i will add your fb gruop ! i am very confused!!!!!!

  • Hello Mackenzie, Thank you so much for posting this.

  • i'm 21 and have 22q deletion and adhd pdd ocd add and get nervous easily uncomfortable talking with people and i have severe scoliosis lets talk about it ok my name is eric.

  • I can't find your group?

  • Math always sucked for me! I still have a hard time counting money and it's very hard for me to get a job because most jobs are cashiers. It always tears me up because it's so hard to live like thhis.

  • Hello! I'm 25 and my name is Nicole I also have 22q deletion. My symptoms are speech impairiment and learning disiablities. I've struggled through life and it's been very hard. I now have a 2 year old son whom also has 22 deletion, but is totally normal. I definately don't want him to go through what I went through. The toughest part of this was my speech impairiment and I still hate it.

  • Hello mackenzie my son has 22Q11 he is only 3. Thankyou for your words! I'm trying to understand more about him but it's very hard!

  • hi mackenzie Im brittany i also have vcfs I cant find you on fb but if you want you can email me at brittdixon@verizon.net it would be nice to talk to someone with the same problems as me. Wish you well.

  • I mackenzie Im brittany i also have vcfs I cant find you on fb but if you want you can email me at brittdixon@verizon.net it would be nice to talk to someone with the same problems as me. Wish you well.

  • I have never been embarrassed by my scars, I don't understand it. I guess some people are different. I have DiGeorge Syndrome. Math has always been a struggle with me. I'd like to talk if you can drop me a message. I'm 27 and was never diagnosed.

  • Makenzie, you are an inspiration. My granddaughter has this 22Q11.2 Deletion syndrome. She is 4 now, she is the brightest little person and the toughest. she has had multiple issues including heart surgery. I will be looking for your facebook page and hope to connect. Thank you again for sharing.

  • Hi thanks for the video I have a 2 year old boy he does not talk and we tried to find out what was going on and finally we took him to a Genetics specialist and she said he may have the same syndrome you have. I always say that God knows how to do things because all my friends had different problems and when I was in college I always helped disabled and other persons with problems. I was a math tutor and all my students passed their classes. God bless you

  • @jayvielo Can he talk he just doesn't want to?

  • @AmericanAussie12 He is finally talking now... he says mom, dad, mamushka which means soda, mameshe, which means leche "milk" in spanish. I can finally understand him and last time he said umizumi and pokoyo....

    :)

  • hi my name is McKenzie and i have this syndrom but i have never been in serguray for this. My Dad said im really lucky cause i dont have any of the stuff that other kids have.

  • omg i have it and suck ass

  • I can memorize numbers better than i do with my own past! I have 22q11 and i'm 27 years old. and my school life wasn't that great either! i was very slow at learning and i can never hold a job down! and i suffered with bad depression! and you don't look like you have a disability some people can be effected with the face and i consider my self very lucky. i have had many operations to do with my throat and ears. but thats all i can fit on here.

  • @JessicaKirbyshire hey i have it to is your adult life better than your childhood

  • i have it to

  • hi all--- i created a 22q group. go to facebook.com and and search

    22q11.2 deletion syndrome (Mackenzie Barnes) Boulder, Colorado

  • God bless you and your parents...I will show my son your video (he has 22q11)...he's 9 years old.

  • My husband and youngest daughter also have the deletion.

  • @davidNtonya (getting back to all of you on here. i have been offline for a while)!!! I have a face book page. go to (mackenzie Barnes) 22q.112 if u have face book. its a group.

  • You are an inspiration to parents, you know?! You give hope to us. Any more videos?

  • Thank you for making this video. My wife and I had a daughter (Ella Rockwell) born 3/5/10 with 22q11.2 deletion with truncus arteriosus. She had her first surgery at 4 days old and we have in in the ICU ever since. She is doing good but healing slowly. Your story is inspiring to us.

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