From Phoenix to Norway, love and resilience speak the same language. Tashana Dees talks with the parents of a 10-year-old girl living with Rett Syndrome about diagnosis, daily life, faith, and global advocacy-reminding us that courage knows no ...

From Phoenix to Norway, love and resilience speak the same language. Tashana Dees talks with the parents of a 10-year-old girl living with Rett Syndrome about diagnosis, daily life, faith, and global advocacy-reminding us that courage knows no ...

In this special episode of Rayana’s Voice, I sit down with my younger sister — the youngest in our family — to explore what it’s really like growing up with an older sister who has a disability. We’ll talk about early memories, everyday ...

🎙️ Episode 3 – Breaking Barriers: Accessible Healthcare for Special NeedsIn this episode, host Tashana Dees, founder of Rayana’s Voice Podcast and New Birth Diagnostics Laboratory, explores the systemic barriers that families ...

In this heartfelt and empowering episode of Rayana's Voice: A Rett Syndrome Journey, host Tashana Dees opens up about what families need to know after receiving a Rett Syndrome diagnosis.Through her personal experience as...

In our first official episode, we share the story of living with Rett syndrome through the eyes of a mother and advocate. We dive into what Rett syndrome is, how it connects to the MECP2 gene, and why this gene plays such a crucial role in the ...

🎙️ Rayana’s Voice: A Rett Syndrome JourneyThis powerful podcast shares the inspiring story of Rayana, a young girl living with Rett Syndrome, and the family who refuses to let her voice go unheard. Through heartfelt con...