Skraban-Deardorff Syndrome Foundation
SKDEAS Foundation
Team Leader / Family-Led Giving Campaign
Rally for Rare! The SKDEAS Foundation is on a mission to support individuals and families affected by Skraban-Deardorff Syndrome. Through research, advocacy, and building a strong community, we're committed to helping find answers, share hope, and create a brighter future for those living with this rare genetic condition. This Giving Tuesday, we are crowdfunding vital funds to accelerate research, provide family support, and ensure that no one faces this journey alone. Together, we can make a real difference!
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$7,813
Raised
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$1,500
Goal
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13
Supporters
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17
Days Remaining
Recent Transactions
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Robert and Robyn Moellenberg
$300.00 / 30 days ago
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Anonymous
$1,500.00 / 34 days ago
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Margaret Flanagan
$100.00 / 35 days ago
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Ludmila Zhuk
$51.38 / 36 days ago
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Marjorie Hille
$102.75 / 41 days ago
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Rasenfunk GmbH
$51.60 / 41 days ago
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Jennifer Eskola
$102.75 / 41 days ago
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Judith Flanagan
$102.75 / 41 days ago
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Jeffrey Skraban
$100.00 / 41 days ago
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Kathleen Skraban
$102.75 / 42 days ago
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Anonymous
$5,000.00 / 59 days ago
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Anonymous
$100.00 / 76 days ago
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Lynne Schlossberg
$200.00 / 103 days ago
About SKDEAS Foundation
The SKDEAS Family-Led Giving Campaign is a grassroots initiative powered by the families of individuals affected by Skraban-Deardorff Syndrome. This crowdfunding effort unites families across the SKDEAS community, each driven by a shared commitment to foster hope, advance research, and build resources for those impacted by this rare genetic condition.
Guided by love and determination, these families are reaching out to friends, loved ones, and compassionate supporters to help fuel the future of SKDEAS research and community support. Every contribution, no matter the size, strengthens our network and brings us closer to the answers, care, and connections that will uplift all individuals touched by SKDEAS.
Join us as we work together, family by family, to make an enduring impact on the lives of individuals living with Skraban-Deardorff Syndrome.