Rights Upfront δημόσια
[search 0]
Περισσότερα
Download the App!
show episodes
 
Artwork

1
Rights Upfront

Chandy & Rights Upfront

Unsubscribe
Unsubscribe
Μηνιαία
 
Welcome to the Rights Upfront Podcast, where every story finds a voice. Join us as we delve into the world of disability rights and inclusion, amplifying diverse voices and advocating for change. From personal experiences to expert insights, each episode explores the challenges, triumphs, and ongoing efforts to promote equality and accessibility for all. Whether you're passionate about disability rights or simply curious to learn more, tune in to be inspired, informed, and empowered. Join th ...
  continue reading
 
Loading …
show series
 
Join me on an emotional and insightful journey as we explore the transition from creating humorous TikTok videos to becoming an advocate for mental health. In this episode, Rachel shares their personal story of coping with the loss of their mum seven years ago and the recent diagnosis of OCD. Discover how social media became a platform for serious …
  continue reading
 
In this powerful and emotive episode of our podcast, we sit down with an inspiring advocate for disability rights who began her journey at Leeds Uni in 2016. With the evolution of her blog into a force for societal transformation, she challenges us to rethink our perceptions of disability. Join us as we delve into topics such as Down Syndrome Day, …
  continue reading
 
In this episode, Pete's Ascent Beyond Boundaries in Para climbing, where we delve into the extraordinary journey of Pete, an athlete with cerebral palsy who defies all odds in the competitive world of climbing. Pete's story is not just about scaling physical walls but also about overcoming societal attitudes and financial challenges that athletes w…
  continue reading
 
"Embracing Differences and Finding Community With Neurofibromatosis" is a podcast episode that brings to the forefront the inspiring stories of individuals living with neurofibromatosis (NF). Join me as, I speak with Kristen, a personal trainer / senior manager at an advertising agency, from New York City, whose life has been shaped by the conditio…
  continue reading
 
In this episode, I speak to Kiera about being diagnosed with a brain tumour. Immerse yourself in our conversation which looks at the challenges in getting support and the impact of diagnosis on friends, family, and how to live well and embrace disability. highlights of each Podcast episode: The onset of headaches & the path to diagnosis Coming to T…
  continue reading
 
Join me as for this episode of the Rights Upfront podcast as I speak to Kelly Gordon, a wheelchair user, mother, and a trailblazer in advocating for disability inclusivity in creative industries. Kelly shares her transformative journey from the competitive world of football to becoming a voice for change in advertising and creative production. Epis…
  continue reading
 
In this episode, I sit down with Joe, the inspiring force behind Dystrophy Dad and Sons of Dystrophy, to explore his transformative journey through the world of muscular dystrophy. Joe candidly shares how his personal experiences with the condition evolved into a global mission to connect and empower others affected by different forms of dystrophy.…
  continue reading
 
In this episode I meet Madelyn, a 21-year-old advocate from Minnesota, bravely living with postural orthostatic tachycardia syndrome (POTS) and Ehlers-Danlos syndrome (EDS). Madelyn shares her intimate battle with these invisible chronic illnesses, revealing the day-to-day adversities she overcomes and the triumphs that define her resilient spirit.…
  continue reading
 
Join us for this enlightening episode with Danielle from Boston, who shares her vibrant journey as a disability advocate. Despite living with an unidentified muscle disease, Danielle's narrative is one of humor, resilience, and empowerment. We delve into the evolution of disability rights, the influence of films like "Crip Camp," and the digital er…
  continue reading
 
In this epiosode, I am joined by Amit Ghose, who opens up about his life with neurofibromatosis type 1 (NF1), a condition that's shaped his identity and advocacy journey. Amit shares the highs and lows, from the stinging stigma he faced growing up to the unconditional support from his family and wife, which has been a cornerstone of his resilience.…
  continue reading
 
Loading …

Οδηγός γρήγορης αναφοράς