22q11 Deletion Awareness
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39 videosYouTube Mix for Mark Wills- 4:37
Olivia Visits the Mall - Part 2by dmlcotter13,336 views
- 3:48
Lane @ 29 months w/ Full Trisomy 18 is now able to pull himself up into a crawl positionby alihauber19,464 views
- 7:41
22Q11.2 Awareness Videoby richfarrant1,197 views
- 3:45
Mackenzie (22q11.2 deletion syndrome)by 2009liveit5,457 views
- 9:55
TERALYNNby davidNtonya9,651 views
- 1:35
joshua 4 years old speaking - di george syndromeby julietjie2,149 views
- 3:05
The Faces of Williams Syndromeby lspinney2006120,000 views
- 2:38
Cri-Du-Chatby jorgourita236,586 views
- 4:31
Jaxsonby jessykak2,666 views
- 2:02
Deb Broers and DiGeorge syndrome 22q11.2 deletion syndromeby YVMemorialHospital1,110 views
- 5:41
Chromosome 16 Deletion Ace's Storyby chromosome16disorder6,041 views
- 1:49
Anna Leighby AnnasGranny1,078 views
- 4:59
Frejas bildspelby josefinefreja845 views
- 8:25
Mackenzie's story: dealing with 22q deletion syndrome discussionby Kforever2011830 views
- 3:25
sindrome velocardiofacialby dgthomaz3,080 views
- 8:59
Prader-Willi Syndrome Explained by Mayo Clinicby mayoclinic12,648 views
- 8:04
Repair of the Tetralogy of Fallot with Absent Pulmonary Valvby gorgorito143010,122 views
- 8:56
Weak Syllable Deletionby speechpathstudent2,591 views
- 3:58
Chromosome Disorder Outreach (CDO) YouTube Videoby chromodisorder15,010 views
- 9:46
Balin- Pierre Robin Sequenceby PierreRobinAustralia13,219 views
My son Jayden whom is 2 years of age has vcfs such as I do (his mother) also has vcfs! I'm NIcole and I am 25 years of age. My mother found out I had VCFS when I was 3 years of age! We were are so scared, but no matter what happend in life we are all special in our own way! I've had some depressing moments in life with bullies, feelings, and ect.... Once I found out I was pregnant and knew it was 50/50 chance he could have vcfs I was terrified, but no matter what I'll always love my son! <3
LifeAsNicole 1 month ago
My son Joshua has Di george and when he was first diagnosed there was only two sites on the internet about the syndrome. I swore I'd do something and I did. The local paper came and did a story and before I knew it Joshua's story was on the internet...and in turn it helped raise awareness. I am sooo happy to see this video. It is truly amazing and now when people ask me I can refer them to this video...great job!!!
nicholebyers1 5 months ago
I'm 25 and have vcfs all my life! My son whom is almost 2 also has vcfs, but as for now he's completely normal! i'm so blessed to have a wonderful child like him! :)
LifeAsNicole 8 months ago
Amazing!
LifeAsNicole 8 months ago
Amaizing video!
I posted it on my facebook page,
I have the 22 chromosome as well.
Kerenl123 10 months ago
My son just got suspended 2nd time in grade four....he was consistently picked on in 2 different schools (his cupped ears and open mouth) and he (althought quiet) retaliates by hitting. My wife and I endure(d) a lot of his health and care...and now the nightmare continues.
vincevega0 1 year ago
@mrskiedis123 we have since found out my husband and 5yr old have it too
mrskiedis123 1 year ago
@mrskiedis123 we have since found out my husband and 5yr old have it too
mrskiedis123 1 year ago
My Son Has This Syndrome And I See In This Video All The Kids Ears Are A Lil Bent My Sons Are To But It Dont MAke SOmeone Differnt Just Cause They Dont HAve The NUmber 22
samspade19 1 year ago
Do you have an email address or a fb page??
Heather082574 2 years ago