InfoBedingungenDatenschutzKontakt
 
Wird aktualisiert
Raising Rare

Raising Rare

Veröffentlicht: 2025-10-14
© Copyright 2020-2024 Salem Oaks LLC
Raising Rare - QR Code
97 Folgen
Audio
Anhören auf Apple Podcasts
97 Folgen
Audio
Anhören auf Apple Podcasts
Veröffentlicht: 2025-10-14
© Copyright 2020-2024 Salem Oaks LLC
Aktuelle Folge
Rare Mamas: THE Field Guide for Navigating Your Child’s Rare Disease

Rare Mamas: THE Field Guide for Navigating Your Child’s Rare Disease

Five years ago, we first spoke with Nikki McIntosh. In this episode, Nikki returns to share her journey as a mother of a child with spinal muscular atrophy (SMA) and the profound impact of clinical trials on her son’s life. Miles is growing up and h
Länge: 32:06
Five years ago, we first spoke with Nikki McIntosh. In this episode, Nikki returns to share her journey as a mother of a child with spinal muscular atrophy (SMA) and the profound impact of clinical trials on her son’s life. Miles is growing up and has started playing wheelchair tennis. Nikki shares the joy this brings to her.
Nikki also discusses the emotional roller coaster of navigating rare diseases, the importance of community support, and her new book, 'Rare Mamas: Empowering Strategies for Navigating Your Child's Rare Disease.' The conversation and the book highlight resilience, advocacy, and the need for actionable strategies for parents facing similar challenges.
https://raremamas.com
Folgen-ID: 1000731840314
GUID: 2f11f65d-cfe8-4a19-a413-f6cc96f8a4cb
Erscheinungs­datum: 14.10.2025, 15:00:00

Beschreibung

Imagine the excitement of becoming a new parent and then within hours finding out your child has a serious developmental disorder.
That is exactly where Sanath Kumar Ramesh found himself in the summer of 2018. One year later, on his son’s first birthday, they found out that their son, Raghav, had an extremely rare mutation of the GPX4 gene. At the time, doctors told them that Raghav may be the only one on the planet with this genetic variant who had lived beyond one month of life. The prognosis is completely unknown.
They were alone.
They were scared.
And then they went into action.
And now they want to share their story.
Every couple of weeks Raising Rare will give you an update on baby Raghav as he grows up. We will also share how Sanath and his wife Ramya are driving toward a treatment for their son. We will explore the science that Sanath is initiating, their efforts to fund that research, and the people they meet along the way. We will also hear how the family adjusts to challenges and changes that they are faced with. Most importantly, we will share the wisdom they gain along the way so that other Rare Parents can learn from their steps and missteps.
We don’t know where this story will go. We do know we want you to join us for the journey.

Apple Podcasts: Kundenrezensionen

Kein Eintrag