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Gabriel Boyar's Fundraiser
Riding for CACNA1A
Every donation helps fund research and support families
Dave Price
"In honor of a good man doing good work. Go Gabe!"
$100
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Cory Zimmerman
"Great cause; great job!"
$54
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Brennan Reilly
"Thanks for riding for CACNA1A!!!"
$1,000
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David Weintrob
I donated in support of this campaign.
$250
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Randy Wolpert
I donated in support of this campaign.
$1,000
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The Couper Rothenbergs Couper
"Have fun!"
$50
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Eva Isaak
"Go Gabriel!!"
$50
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Deborah and Jerry Isaak-Shapiro
I donated in support of this campaign.
A supporter of Gabriel Boyar
I donated in support of this campaign.
A supporter of Gabriel Boyar
I donated in support of this campaign.
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Gary Schanzer
"Good Luck Gabe!"
$100
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Glenn Norrgard
"Happy to support you in your efforts!"
$100
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Jeff Boyle
I donated in support of this campaign.
$25
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Greg Kennedy
"Supporting Gabe Boyar"
$25
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Debra Hirsch
"Go, cousin! ❤️"
$50
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Robert Moraru
"Go team Gabe!"
$50
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Rick Bullotta
I donated in support of this campaign.
$500
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Misha Isaak
"Don’t embarrass your brother!"
$50
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Jonathan Sweedler
"Go Gabert! But the bike is still hotter than you."
$250
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Jeff Cohen
"Proud to support our fave MAMIL as you pedal for this important cause."
$180
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Jonathan Roth
I donated in support of this campaign.
$100
A supporter of Gabriel Boyar
I donated in support of this campaign.
$100
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Jim Brayton
"Go Gabe!"
$250
Hi friends,
On May 3rd, I’ll be riding 40 miles through all five boroughs of New York City in the iconic TD Five Boro Bike Tour as part of Team CACNA1A. I’m riding to support the Manaster Family, their daughter Emily and all the good work they do for CACNA1A.
I’m participating to help raise awareness and critical funds for the CACNA1A Foundation, which supports individuals and families living with rare, life-altering neurological disorders caused by mutations in the CACNA1A gene.
Last year we kicked some serious ass on the fund raising front and I’m hoping to do that again I even bought a bike this year so I can look even cooler on a bike …… I am still a handsome devil
CACNA1A-related neurodevelopmental disorders can include epilepsy, developmental delays, autism, stroke-like episodes, and speech and language, and movement and coordination challenges. For many families, diagnosis is complex, care is fragmented, and treatment options are limited.
The CACNA1A Foundation is working to change that by:
- Funding research aimed at developing targeted treatments
- Providing trusted education and resources for families
- Connecting patients, clinicians, and researchers to accelerate progress
I’ve committed to raising $2,000, and I would be incredibly grateful for your support. No donation is too small — every gift helps move this research forward and brings hope to families who urgently need answers.
Thank you for supporting my ride and standing with the rare disease community.
With gratitude,
Gabriel
40 miles. One rare cause. Endless impact.