262. 45 Years of Advocacy: A Conversation w/ NDSS President Kandi Pickard

We’ve been so grateful to have had the opportunity to collaborate with National Down Syndrome Society (NDSS) over the last few years. Today, we’re chatting with Kandi Pickard, the President & CEO of NDSS, and celebrating their 45th Anniversary coming up on June 20th! Kandi is sharing the organization's journey from a support group that has grown into a major policy and advocacy organization, she shares her experience from becoming a volunteer to taking over as President & CEO, and what the future holds for NDSS! We chat about the honor of learning from and advocating alongside self-advocates, and the commitment NDSS has to representing the beauty and diversity of the Down syndrome community. We’re so grateful for the vital work they do to support and create opportunities for the community, tune in and be inspired by Kandi’s dedication and vision for the future of NDSS!

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SHOW NOTES

• Learn more about the National Down Syndrome Society (NDSS)

• Find NDSS on Facebook, Instagram, X, Tik Tok, YouTube, and LinkedIn

• Learn more about the history of NDSS

• Learn more about this year’s 30th NYC Buddy Walk

• Learn more about the NDSS Policy Program

• Learn more about ABLE Accounts

• Learn more about this year’s Adult Summit

• Learn more about the first Barbie with Down syndrome

• Download the New And Expectant Parent’s Guide

Check out our past episodes with Kayla McKeon & Charlotte Woodward:

• 17. Self Advocacy - Down Syndrome in DC with Kayla McKeon!

• 92. Politics & Down Syndrome w/Kayla McKeon & Ashley Helsing

• 160. Organ Transplant Discrimination Against People with Disabilities (ft. incredible advocates!)

• 204. Self-Advocates On Capitol Hill w/Kayla McKeon, Matthew Schwab, & Charlotte Woodward

• Check out our episode from last year’s Buddy Walk: 225. NYC Buddy Walk Highlights

• Learn more about the National Down Syndrome Congress (NDSC)

JOIN THE MOVEMENT

Join us in celebrating and supporting The Lucky Few Podcast! For just $0.99, $4.99, or $9.99 a month, you can help us continue shouting worth and shifting narratives for people with Down syndrome. Your support makes a difference in our ability to create meaningful content, enable us to cover production costs, and explore additional opportunities to expand our resources. Become an essential part of The Lucky Few movement today! 

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