About Baby Cathryn Color .pdf

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Title: About Baby Cathryn Color

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Baby Cathryn’s Craniosynostosis Journey
About Cathryn Bay Aulino

Lifelong Lindenhurst residents, Eddie
and Jenifer Aulino, have four children,
3 boys, ages 12, 11, and 8; as well as
a beautiful little girl, Cathryn Bay
who is now 6 months old.
Cathryn Bay Aulino, at 5 months old,
was diagnosed with craniosynostosis,
a rare congenital birth defect.
that causes one or more skull sutures
to close earlier than normal. If left
untreated, craniosynostosis can cause increased intracranial pressure,
seizures, visual abnormalities, skull deformity & developmental delays.
The only way to correct this is through reconstructive surgery of removing
her skull and remodeling it. What lies ahead for the family is a long
processof many doctor visits, highly invasive surgery and and a lengthy
recovery. The out-of-pocket cost just for the surgery Cathryn so
desperately needs is $50,000. While the family is financially struggling,
they are doing all that they can to pay for Cathryn’s surgery. They are a
big family and have even bigger hearts. Their remarkable family has always
given back to the community- Jen founded Adopt A House and helped
countless Sandy affected families for 22 months- and now need help
themselves- and for their precoius daughter.
“Never underestimate the difference
one person can make in improving
Consider making a contribution
the life of another. Kindness is
the most valuable gift you can
Ask your employer about a donation
ever give someone.” -Pablo
matching program

Ways to help:

Please consider donatiing:
Gently used clothing & shoes
Baby Items
Sporting Equipment

Anything item in good condition!

Post in your workplace
Get your school, PTA, community organization,
church, or children’s teams or groups involved
Get the word out to your friends and family
Start your own creative fundraising effort
Crowdrise site https://www.crowdrise.com/
To send a check, made out to Cathryn Aulino:
44 Liberty Avenue,
Lindenhurst NY 1157

Follow Cathryn’s Craniosysntosis Jorney
on facebook at
]“Our Girl : Cathryn Bay's Craniosynostosis Journey”
Keep informed on upcoming
fundraisers, visit “Team Cathryn”
Contact info: CathrynsCause@gmail.com
or 631-560-8474.

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