Zoey's medical fund

$1,750 of $5,000 goal

Raised by 21 people in 26 months
Toni Power Wagenaar
on behalf of Brooklynn Power
 Brantford, ON
Hi, this is Zoey Hammond (Mom is Brooklynn Power & Dad is Tyler Hammond) and this is her story.  She is 5 1/2 months old and has been through so much in just a short amount of time. 

 She was born with a genetic disorder so rare that 1 in 10,000 children are born with it. This genetic disorder is called XP22.31 Microduplication that creates many complications such as Hypotonia/low muscle tone, bilateral clubbed feet, focal localized seizures, Microcephaly(abnormal brain growth/failure to thrive.)

Zoey requires an NG feeding machine/tube to get her daily supply of food. With their new found challenges they face numerous trips to McMaster Children's hospital for visits to see her team of specialists including Neuorologists, Genetic specialist, Neuromuscular specialist, Orthopaedic  surgeon, Occupational Therapist & also testing for metabolic, chromosomal & mitochondrial syndromes etc. Zoey will also have to attend Landsdowne children centre for ongoing physiotherapy, occupational therapy, and visits with her infant & child developmental specialist. 

With these challenges comes a tremendous amount of financial stress & worry. With your help we can relieve some of this worry and strain and allow the focus to be on Zoey where it should be. We can't thank you enough for all of your love and support.
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$1,750 of $5,000 goal

Raised by 21 people in 26 months
Created February 5, 2017
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corinne parsons
26 months ago

Wish you all the best !

Lorrie Drassich
26 months ago

Thinking of you all xoxo

Calvin Holloway
26 months ago

All the best

Lorraine French
26 months ago

Our prayers are with you & your family

Kelly Lewis
26 months ago


Becca Haes
26 months ago


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