Podcast thumbnail for Raising Rare

Raising Rare

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by Raising Rare

5.0(8 reviews)
102 episodes
Updated Weekly
Accepts GuestsHas SponsorsLocation 🇺🇸
52

Podcast Authority

Beta
FairBased on show quality, social media presence, reviews, charts, and more
Pod Engine
Quality65
Social0
YouTube68
Engagement32

Podcast Overview

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.

Language

🇺🇲

Publishing Since

2/26/2020

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52

Podcast Authority

Beta
FairBased on show quality, social media presence, reviews, charts, and more
Pod Engine
Quality65
Social0
YouTube68
Engagement32
8
Excellent Areas
0
Good Performance
11
Growth Opportunities
excellent
Episode Length
33 minutes
Performing excellently!
needs improvement
Publishing Consistency
Every 21 days

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Recent Episodes

Episode thumbnail for Jessica Patay - Offering a Lifeline

May 27, 2026

Jessica Patay - Offering a Lifeline

<p>“I didn’t realize how alone I was.”</p><p>For Prader-Willi Syndrome (PWS) awareness month, we are sharing a discussion with Jessica Patay, founder of We Are Braver Together. PWS requires 24/7 vigilance over a child whose appetite is unsatiable. This can become isolating, exhausting, and overwhelming to even the strongest moms. Jessica has turned her experience into a lifeline for other rare moms.</p><p><a href="We Are Brave Together" rel="noopener noreferrer" target="_blank">We Are Brave Together</a> emerged from the recognition that the girlfriend retreats she was hosting would be very helpful to moms who are caregivers. As these retreats have grown, she has helped many women feel like they belong. We Are Brave Together is built on the idea that human beings deserve to be seen, heard, understood, and validated. The retreats, the podcasts, the books all work to bring these moms together to share their stories.</p><p>Her first book, <a href="https://www.amazon.com/Becoming-Brave-Together-Extraordinary-Caregiving/dp/B0CY8PP1K4/ref=sr_1_1?crid=21Y6JNRFGJJM3&amp;dib=eyJ2IjoiMSJ9.lbV9aLQkZnDS4N4S5WWYqnyAPMuOO4qBZ2pzRWA7vGGFgFYglUAfgSvf056Av4pXFha_YomGkVbSJOqRBTlQ-P5Hzc1TE4bvoDb6U0UK2ro8ZCqPlOnv2-YQ3KKqTqOJp1leK2KEWYbUDoJ_UhFMFRSiWKJj3_2jjSCAqzE_DwG0ikilllq5iRo_m3wKstMg.a8TZ4OCWMKLJpmSzNpS_xVWyAflcRfF5SBeyBAh10TI&amp;dib_tag=se&amp;keywords=becoming+brave+together&amp;qid=1779814261&amp;sprefix=Becoming+Brave+Together%2Caps%2C240&amp;sr=8-1" rel="noopener noreferrer" target="_blank">Becoming Brave Together</a>, was to share stories. The new book <a href="https://www.amazon.com/Suddenly-Brave-Together-We-Are/dp/B0GW2WKS7Q/ref=sr_1_1?crid=27DHWK7D7V4AH&amp;dib=eyJ2IjoiMSJ9.ON-jscU8yOlTs71UQmFidMFBSct2oPEft3yThYuG0Aq_tZ1iBmRmpIR5u9_47LWahKNCDWQglahOki5EWYImp63Pew1T4laTHxuvQskEqvk.dU57CVPb2OCdkdSjiqcCwAFqP5QRwAt2dmu_W1UbRFM&amp;dib_tag=se&amp;keywords=suddenly+brave+together&amp;qid=1779814360&amp;sprefix=suddenly+brave+together%2Caps%2C134&amp;sr=8-1" rel="noopener noreferrer" target="_blank">Suddenly Brave Together</a> is a collection of letters from moms who have adult rare children to the new moms who have just gotten a diagnosis. Many hands and hearts reaching out across the universe saying, “You are not alone.”</p><p></p>

Episode thumbnail for 100th EPISODE  A New Season, A New Era

April 27, 2026

100th EPISODE A New Season, A New Era

<p>100 EPISODES!!!</p><p>It is hard to believe that over 6 years ago, we started Raising Rare as an experiment. How would people react to following the life of a young family affected by an ultra-rare disease? The response has been wonderful. The experience has been transforming. We thank Sanath Kumar Ramesh for sharing his stories all these years.</p><p>And with our 100th Episode, we start a new era for Raising Rare. Brittany Ratke will be my partner, riding solo in the co-host seat. Brittany and Sanath have shared the co-host role since 2022. With this change, we are going to focus more on Brittany’s family and slowly shape the show to her story and her style. Laughter, tears, and heartfelt questions.</p><p>Our hope is that our conversation will bring more people from the rare disease community together. As we reflect, we realize how many amazing people we have met along the way.</p><p>Brittany shares some positive developments in their care team, Everleigh’s school, and family life. They even celebrated Rare Disease Day at school.</p><p>We also touched on the impact on and of siblings of kiddos with a rare disease. They grow up faster than a lot of kids. They share in ways most people would not realize.</p><p>We are looking forward to a great season.</p>

Episode thumbnail for Leaving a Legacy - Sanath Kumar Ramesh

January 5, 2026

Leaving a Legacy - Sanath Kumar Ramesh

<p>Almost 7 years ago, Sanath Kumar Ramesh found out his son had an ultra-rare mutation.</p><p>This began a journey that would force him to grow into a man he never imagined. Part of his journey was this podcast, Raising Rare. Now, after completing our sixth season, Sanath is going to step back from this microphone.</p><p>In this episode, we reflect on our beginnings, our favorite conversations, and the deep connections that we have developed with each other and our co-host Brittany Ratke.</p><p>And with that... we close Season 6.</p>

102 total episodes available

Recent guests on Raising Rare

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Jessica Fein

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Jill Wood

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Frequently asked questions

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What is Raising Rare?

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.

How often does this podcast release new episodes?

This podcast updates weekly.

Where can I listen to this podcast?

This podcast is available on 10 platforms including Apple Podcasts, Spotify, and more. You can also use the RSS feed directly.

Does this podcast accept guests?

Yes, this podcast regularly features guests.

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