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Mom Captures Shocking Moment She Realized Her Baby Went Blind (Exclusive)
Mom Captures Shocking Moment She Realized Her Baby Went Blind (Exclusive)
A sweet birthday tradition with her daughter ended up becoming a heartbreaking moment for one mother. In a video shared on TikTok, Canada-based mom Amanda Burritt captured the moment she fully realized her daughter was likely blind.
Donate - KIF1A
Donate - KIF1A
We need your support to find a cure for KIF1A Associated Neurological Disorder and help children and families living with the disorder in the meantime.
5-year-old girl with rare neurodegenerative disease gets a robotic walker after Calgary community rallies to help pay for it
5-year-old girl with rare neurodegenerative disease gets a robotic walker after Calgary community rallies to help pay for it
All that stood between five-year-old Emma Shingleton -- who has a rare neurodegenerative disease that has rendered blind, and unable to walk, talk or crawl -- and a robotic walker that could make her life a little bit brighter was about $50,000 and with a little help from complete strangers, an A&W and the folks in Auburn Bay, and a lot of bottle drives, she got one.
Donate to Help Emma Walk with the Trexo Robotics, organized by Amanda Burritt
Donate to Help Emma Walk with the Trexo Robotics, organized by Amanda Burritt
4-Year-Old Girl Living With KAND, One of the Rarest Disorders in the World
4-Year-Old Girl Living With KAND, One of the Rarest Disorders in the World
KIF1A.ORG | KIF1A Associated Neurological Disorder
KIF1A.ORG | KIF1A Associated Neurological Disorder
KIF1A.ORG is dedicated to improving the lives of those affected by KIF1A Associated Neurological Disorder and accelerating research to find a cure.
www.kidspot.com.au
www.kidspot.com.au
Yesterday my disabled (almost) four-year-old got her first wheelchair.
Kamloops parents of child with rare genetic condition move to Calgary for therapy
Kamloops parents of child with rare genetic condition move to Calgary for therapy
Emma Burritt was born with a rare medical condition called KAND. Her parents are working hard with her to help her build strength twice per week at a therapeutic centre in Calgary.
7 Ways To Support The Special Needs Mama
7 Ways To Support The Special Needs Mama
"I am not the person I used to be."
‘You’re so strong…’ 3 little words I often hear as a parent to a very special girl.’ I don’t want to be, but here I am, giving the middle finger to her diagnoses.’: First-time mom shares special needs journey – Love What Matters
‘You’re so strong…’ 3 little words I often hear as a parent to a very special girl.’ I don’t want to be, but here I am, giving the middle finger to her diagnoses.’: First-time mom shares special needs journey – Love What Matters
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