In this episode of 'Where the Ramp Ends', host Summer Parrish and Bryce Wooten welcome Mike Dodd, a father and social media advocate for children with Down syndrome. Mike shares his personal journey of parenting his son Grayson, who has Down syndrome, discussing the emotional challenges and joys that come with the diagnosis. He emphasizes the importance of advocacy, representation, and the need for fathers to share their experiences in the disability community. The conversation highlights the significance of inclusion, understanding, and the shared humanity of all children, regardless of their abilities.

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Takeaways

Mike Dodd is a father and social media advocate for children with Down syndrome.

The emotional journey of receiving a Down syndrome diagnosis can be overwhelming for parents.

Advocacy and representation are crucial in the disability community, especially for fathers.

Social media can be a platform for sharing real-life experiences and challenges of parenting a child with disabilities.

Inclusion and understanding are essential for children with disabilities to thrive in society.

Parents should allow their children to experience failure as part of their growth.

The importance of patience and love in parenting children with special needs.

Mike emphasizes that all children, regardless of their abilities, want to be included and accepted.

The need for more fathers to share their stories and experiences in the disability community.

Building a supportive community can help parents navigate the challenges of raising children with disabilities.

In this episode of 'Where the Ramp Ends', hosts Summer Parrish and Bryce Wooten engage with Barbara Whinery, a passionate advocate for individuals with disabilities. Barbara shares her journey of founding '4RKids', an organization dedicated to providing employment and support for individuals with disabilities. The conversation explores the importance of community, innovative employment opportunities, and the impact of advocacy on personal growth and communication skills. Barbara emphasizes the need for a supportive village and the legacy she hopes to leave behind, inspiring listeners to take action in their own communities.

https://www.4rkids.com/

https://www.facebook.com/4RKids

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Summary

In this episode of 'Where the Ramp Ends,' hosts Summer Parrish and Bryce Wooten engage in a heartfelt conversation with Tyler Bond, a statewide disability advocate living on the autism spectrum. Tyler shares his personal journey, discussing the importance of individuality beyond labels, the impact of family support, and the misconceptions surrounding autism. He emphasizes the significance of advocacy, both for oneself and within the community, and offers insights on building confidence in social situations. The discussion also touches on the role of parents and educators in fostering inclusion, the experiences gained from the Partners in Policymaking program, and reflections on historical institutions that have shaped the disability rights movement. Tyler's story is a powerful reminder of the ongoing fight for disability rights and the importance of community connections.

Takeaways

Tyler Bond emphasizes the importance of individuality beyond labels.

Family support plays a crucial role in building confidence.

Misconceptions about autism often stem from media representation.

Advocacy begins with self-acceptance and understanding one's challenges.

Social skills can be developed through consistent practice and encouragement.

Parents should encourage their children to engage in diverse social settings.

Educators must do their research to create inclusive environments.

Partners in Policymaking provides valuable insights into disability rights.

Community connections are vital for personal growth and support.

Historical institutions highlight the ongoing need for advocacy and reform.