Cool Cars For Kids

CCfK is a nonprofit that organizes the Philadelphia Concours d’Elegance and NY car events to support research & care for children with genetic conditions 🏎️🧬

[Cool Cars For Kids @CoolCarsForKids]

NEW YORK, GET READY TO ROLL! 🗽🚘 The FIRST EVER Cool Cars for Kids Car Show is hitting New Hyde Park on August 10th! Join us for amazing cars, food trucks, and family fun, all while supporting research and care for children with genetic conditions @NorthwellHealth

[Cool Cars For Kids @CoolCarsForKids]

From all of us at CCFK, Happy 4th of July! 🇺🇸🎆🎇

[Cool Cars For Kids @CoolCarsForKids]

From all of us at CCFK, happy #fathersday! Thank you for all you do for your children. ❤️

[Cool Cars For Kids @CoolCarsForKids]

Today officially marks 1 WEEK until our Sixth Annual Concours d'Elegance!

Buy your tickets today!
https://t.co/rhAKGvsQJG

[Cool Cars For Kids @CoolCarsForKids]

Today officially marks 2 WEEKS until our Sixth Annual Concours d'Elegance!

Buy your tickets today!
https://t.co/rhAKGvsQJG

[Cool Cars For Kids @CoolCarsForKids]

Thank you, Love, Tito's, for sponsoring our Philadelphia Concours Gala. We look forward to the great event made possible by your support! #LoveTitos

[Cool Cars For Kids @CoolCarsForKids]

Happy Memorial Day from all of us at CCFK. Thank you to all that have served and given the ultimate sacrifice! 🇺🇸 #memorialday

[Cool Cars For Kids @CoolCarsForKids]

Today officially marks 1 MONTH until our Sixth Annual Concours d'Elegance!

Buy your tickets today!
https://t.co/rhAKGvsQJG

[Cool Cars For Kids @CoolCarsForKids]

Happy Mother's Day from all of us at CCFK! Thank you for all you do for your children. ❤️ #mothersday

[National Organization for Rare Disorders (NORD) @RareDiseases]

That’s a wrap on the 2023 #RareImpactAwards! Thank you to all who joined us tonight to celebrate our 40th Anniversary and honor the many individuals and organizations doing remarkable work on behalf of #RareDisease patients and families.

[National Organization for Rare Disorders (NORD) @RareDiseases]

Congratulations to Bernie Williams (@bw51official), a voice, advocate, & champion for patients and families impacted by #IdiopathicPulmonaryFibrosis, on your #RareImpactAward! 🏆

[National Organization for Rare Disorders (NORD) @RareDiseases]

Congratulations to @MarinusPharma on your #RareImpactAwards Industry Innovation Award for Ztalmy® to treat #CDKL5 deficiency disorder (CDD)!

[National Organization for Rare Disorders (NORD) @RareDiseases]

Congratulations to @MNK on your Industry Innovation Award for Terlivaz® to treat #HepatorenalSyndrome (HRS)! #RareImpactAwards

[National Organization for Rare Disorders (NORD) @RareDiseases]

Congratulations to Ada Hamosh, MD, PhD, a creator of a tool for collection of phenotype & genotype data, as well as website connecting clinicians & researchers with interest in the same gene, on your #RareImpactAward.

[National Organization for Rare Disorders (NORD) @RareDiseases]

Congratulations @Novartis on your #RareImpactAwards Industry Innovation Award for Vijoice® to treat #PIK3CA-related overgrowth spectrum (PROS) disorders!

[National Organization for Rare Disorders (NORD) @RareDiseases]

Our host, @PeterAlexander, introduced a few special guests to #RareImpactAwards attendees!

[National Organization for Rare Disorders (NORD) @RareDiseases]

Congratulations to @alliancetocure on winning the #RareImpactAwards Abbey S. Meyers Leadership Award! Thank you for your work to raise awareness, drive research, & provide support for those impacted by #CavernousMalformation.

[National Organization for Rare Disorders (NORD) @RareDiseases]

Wishing a huge congratulations to NORD’s founder, Abbey S. Meyers, on the #RareImpactAwards Lifetime Achievement Award! Meyer’s founding of NORD 40 years ago will forever impact the #RareDisease community. 🏆

[National Organization for Rare Disorders (NORD) @RareDiseases]

Check out the Shine a Light on #UsherSyndrome portraits here!
https://t.co/7WEfbAVKTz

[National Organization for Rare Disorders (NORD) @RareDiseases]

Thank you @PeterAlexander for shining a light on #UsherSyndrome, the leading genetic cause of #DeafBlindness, at tonight’s #RareImpactAwards, and for sharing your sister’s story. And thank you to @UsherCoalition for displaying patient portraits throughout the Portrait Gallery!