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Mowat-Wilson Syndrome

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Uploaded by on May 3, 2009

Chase was diagnosed with Mowat-Wilson Syndrome in March of 2004 at 3 1/2 years old.

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Nonprofits & Activism

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Uploader Comments (davendeby)

  • hola soy amy mama de vicente somos de chile y mi hijo hace poco le duagnosticaron SMW. ESPERO PODER TENER CONTACTO CON UD Y SABER MAS DE SU HIJO Y QUE TIENE UN SORPRENDENTE PARECIDO CON MI HIJO VICNETE

  • @TheAmy2505 Please contact us through our website mowatwilson. org

  • Dave, what a great video! Very informative for those who don't know or are new to MW world. Love it! Chase is adorable! Laura - Bella's mom

  • Hello Laura,

    We are glad you enjoyed the video. Thanks for taking the time to post a comment. Hope Bella is doing well.

    DavenDeby

  • my daughter has mowat-wilson syndrome too. me and my wife never heard of it until they told us she had it. we always thought that something was wrong when she couldnt sit up on her own until she was 15 months old. she is in a birth to 3 program now and shes going to be 2 on august 28th. she functions at the level of a 6 month old. god bless you and your family

  • FYI we have an email support group for MWS. Do you belong?

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  • My sister is 7 years old and she has mowat wilson syndrom. I didnt really know what it was except the obvious that she cant walk or talk. ILY lil sis

  • Adorable video you made of your son! He is very cute!! My son is 17 months and we just found out that he has MWS also. Hope Chase is doing good! God Bless!

  • hi dave i love the video watching him reminds me of nick, you and your wife should be proud of yourselves  and i love the slide show of faces with mws it's time the word gets out to the world i hope as many people see this and spread the word

  • hi dave i love the video and the faces ofmws slide show . seeing chase in the video reminds me so much of nicholas i never get a look from the outside i 'm always lookng in at him you and your wife have done a awsome job for your family and all the mws familys also it's nice to bring awarness about this syndrome it's time the world nows thanks for everything jasmin

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