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Our WHY
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About us Perri section
Perri Marie-Dorothy Poggio,
Distal 18Q Deletion

Perri is our
reason why!

We are the Poggio family, and we are proud advocates for individuals affected by rare Chromosome 18 conditions—including our daughter, Perri, who was diagnosed with Distal 18q-. As a result, Perri experiences total hearing loss along with other unique medical challenges.

about us

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Perri's
imPERFECTIONS

Distal 18q Deletion (Learn More)
Distal 18q- is a genetic condition characterized by the deletion of a part of the long arm (q arm) of chromosome 18. This deletion results in a range of health and developmental concerns. Distal 18q- manifests differently in each individual, with some common problems including heart defects, developmental delays, hormonal abnormalities, seizures, and immune system changes. The condition is usually diagnosed through blood tests in infants or children with health and developmental issues.
Distal 18p- (Learn More)

See Perri's Path

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perris imperfections
What is
Trisomy 18p
This happens when a person has a duplication of the entire short arm of chromosome 18.
Our Sweet Perri, has both Distal 18q- & Trisomy 18p, which is incredibly rare and, we have been told, she could be the only person in the world with this unique anomaly
Distal 18p- (Learn More)
Get
Involved
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Pennies for Perri is our annual fundraising event that we founded to raise awareness and funding for the ONLY organization in the world dedicated to Chromosome 18 research – the Chromosome 18 Registry & Research Society, an official 501(c)(3) non-profit organization. To date, we have raised over $215,000 & counting. The difference between hopeless and hope is research.

About the event

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My Pear Lady
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