Prisms, Inc.

Prisms, Inc. PRISMS provides support to families of persons with Smith-Magenis Syndrome (SMS)

Thank you to the Jean Bishop family and to everyone who came out to support the Nickels for Nico 2026 fundraiser in Loui...
08/22/2026

Thank you to the Jean Bishop family and to everyone who came out to support the Nickels for Nico 2026 fundraiser in Louisville, KY. The heat index was 108, but that did not keep supporters away. Fun was had by all who were there supporting Nico and PRISMS. Thank you for your support!

It is hard to believe it has been three weeks since we met in Minneapolis for the conference where hugs and high fives r...
08/20/2026

It is hard to believe it has been three weeks since we met in Minneapolis for the conference where hugs and high fives ruled! We are already looking forward to meeting again in 2028!

Earlier this summer, one of our International Partners, the SMS Foundation UK, welcomed families to their “Come Together...
08/17/2026

Earlier this summer, one of our International Partners, the SMS Foundation UK, welcomed families to their “Come Together” Family Weekend in Liverpool, England. Representing PRISMS were Board Member Diane Erth and her son, Max, who were honored to experience this incredible gathering of the Smith-Magenis syndrome community.

The weekend was a beautiful reminder that although oceans may separate our families, we are united by a shared journey, unwavering support for one another, and a common goal of improving the lives of individuals with Smith-Magenis Syndrome. The warmth, generosity, and collaboration between our organizations continue to strengthen our global SMS community.

Read about the event on the PRISMS blog:
https://www.prisms.org/building-connections-across-the-globe-sms-foundation-uk-come-together-family-weekend/

A heartfelt THANK YOU to the incredible PRISMS Professional Advisory Board! Your expertise, dedication, and commitment t...
08/12/2026

A heartfelt THANK YOU to the incredible PRISMS Professional Advisory Board!

Your expertise, dedication, and commitment to the Smith-Magenis syndrome community played such an important role in making our conference a success. From sharing your knowledge and research to answering questions, connecting with families, and helping us move the mission of PRISMS forward—you made a lasting impact.

We are so grateful for the time, talent, and passion you give to our community. PRISMS is stronger because of you! 💙

Thank you for helping us continue to Shine a Light and Ignite Hope for everyone affected by SMS.

08/10/2026

Join SMS Mom, Connie Bessette, on a guided group climb of Mount Kilimanjaro in support of the PRISMS and research into Smith-Magenis Syndrome (SMS).

This climb brings together purpose, community, and a once-in-a-lifetime experience on Africa's highest mountain. You do not need prior high-altitude or mountaineering experience — just commitment, training, preparation, and heart.

For more information, go to: https://www.tazamaafricasafari.com/prisms-hike?utm_source=-custom-by-source-0-

PRISMS would like to extend our deepest and most sincere gratitude to all of the amazing sponsors who supported our 13th...
08/05/2026

PRISMS would like to extend our deepest and most sincere gratitude to all of the amazing sponsors who supported our 13th International Conference

Your generosity, partnership, and commitment to the Smith-Magenis syndrome community made this unforgettable event possible. Thank you for believing in our mission and helping us create an experience that will have a lasting impact on our community.

From the bottom of our hearts—thank you for making a difference. 💙

Thank you to the parents, caregivers, siblings, medical professionals, researchers, speakers, donors, sponsors, Board, a...
08/03/2026

Thank you to the parents, caregivers, siblings, medical professionals, researchers, speakers, donors, sponsors, Board, and volunteers for making the 2026 PRISMS Conference unforgettable! Let's continue to build on the momentum and keep shining a light and igniting hope.

It was sad to see it come to an end, but we look forward to seeing you in Indianapolis, July 20-22, 2028! Check out our announcement video here: https://youtu.be/Grts5Apx914

Our hearts are full after an incredible night of celebration, generosity, and hope at our Light Up the Night Conference ...
08/03/2026

Our hearts are full after an incredible night of celebration, generosity, and hope at our Light Up the Night Conference Fundraiser.

Together, we raised critical funds to support our mission and ensure we can continue making a meaningful difference for the families and individuals we serve. Every guest, sponsor, donor, volunteer, auction bidder, and supporter helped make this evening an overwhelming success.

The night was filled with dancing, fun. laughter, meaningful connections, and a shared commitment to creating a brighter future. It was a beautiful reminder of what we can accomplish when a community comes together with purpose and compassion.

To everyone who attended, donated, volunteered, and cheered us on—thank you!

Some PRISMS conference attendees had an incredible time cheering on the Minnesota Twins while proudly raising awareness ...
07/30/2026

Some PRISMS conference attendees had an incredible time cheering on the Minnesota Twins while proudly raising awareness and showing our support for the Smith-Magenis syndrome (SMS) community prior to the opening night of the conference in Minneapolis. Thank you to everyone who joined us - it was a homerun!

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Herndon, VA

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+19722310035

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