Blue Lobster - Rare is Cool

05/08/2026

Williams syndrome isn't one story-it's thousands. No one way. No one size. Every journey with Williams Syndrome is its own. Follow along this May to learn more about WS. ♥️

09/26/2024

Love this!

09/22/2024

2024 Jack’s favorite day! 🩵💙🦞🩵💙 Thank you to and for all your hard work!

09/04/2024

Kindergarten! 📚🖍️📝

09/24/2023

2023 Walk! Thank you for all the Blue Lobster purchases and donations! 💙🦞💙

09/18/2023

2023 Boston Walk for Williams is 1 week away! 🤯

Jack wants to give you all a high-five for your donations to the Boston Walk for Williams! Every single dollar that's raised is like a splash of joy in the lives of families touched by Williams syndrome.

Thanks to your support, the WSA been able to dive into groundbreaking research, hook families up with super-helpful resources, throw awesome parties, host the coolest camps and conventions, plan awesome regional events, and even provide some life-changing scholarships.

Thanks a bunch for your support. We're making waves and making a real difference, and it's all because of you!!!

Stay Cool,

Team Blue Lobster

09/13/2022

1st day of school!!! Woohoo!!!

08/22/2022

Get them while you can! Roller Rabbit for Blue Lobster available now at www.teambluelobster.com All profits are donated to Williams Syndrome Charitable Foundation USA 💙🦞💙🦞

06/30/2022

Blue Lobster x is finally here!!!!! Words cannot express my excitement - RR was so amazing to work with and I’m so grateful to the entire team! Major shoutout to ! Couldn’t have done it without you guys! 💙🦞 snag your Blue Lobsters while you can! Rare is Cool!!!!

05/16/2022

Check out this article about Jack's friend, Luke!

METHUEN — Of all the lessons that come with parenthood, Stephanie and Matt Turmel never expected to have to learn the signs of sudden heart failure first.