Reena loves a story, and she‘s fascinated by the people behind them. She loves to bring stories to life. Her appetite for storytelling has taken her from the Jerry Springer Show to the legal drama of the courtroom. From influential players to reality stars, nothing is censored here. Reena interviews people whose stories haven‘t been told, at least not through her unique lens, and then gets daddy‘s advice afterward like a good daughter does. Whether you have daddy issues or a father who‘s inspired your path, you will be able to tap into my daddy‘s wisdom, wit, and humor at the end of every episode. My daddy has been a guiding light my whole life and there‘s not much he doesn‘t know, as an entrepreneur for forty-plus years, a husband, a loyal son, and my number one supporter. He has learned lots of life lessons along the way and is here to share them with you. It‘s time to reminisce and reflect on the conversations you‘d like to have with your daddy and learn from mine. Come share in some good old-fashioned family bonding and help us up our wisdom rating. There is wisdom from four generations and I’m addressing what happens from childhood to adulthood!
Episodes
Friday Jun 06, 2025
Friday Jun 06, 2025
"It takes a village to raise a child. It literally takes almost a country to solve a complex disease like this one."
"The will to act is everything. If you want to change a very complex disease with very little resources, you have to keep going."
"It’s not just about fighting; at some point, you have to transition to more of a logic."
"Time is our most valued and precious resource, and for that reason, we’re not able to wait."
In this inspiring episode of Better Call Daddy, hosts Reena Friedman Watts and Wayne Friedman welcome Mazi Keyghobadi, a dedicated father and advocate battling muscular dystrophy. Mazi's journey is akin to flying through turbulence, filled with grit, heart, and the unwavering love for his son. He draws a powerful parallel between his experiences and the iconic film Top Gun, emphasizing the importance of courage and teamwork in the face of adversity.
Mazi shares the emotional moment he discovered his son's diagnosis and the subsequent journey of becoming an expert in muscular dystrophy. He discusses the complexities of the disease, the challenges of navigating medical conversations, and the critical role of collaboration within the muscular dystrophy community.
With a focus on action and determination, he highlights the necessity of building a support network, working with scientists, and advocating for research that could lead to breakthroughs for rare mutations. Listeners will be captivated by Mazi's insights on resilience, the importance of awareness, and the drive to make a difference, not just for his son but for others facing similar challenges.
His story is a testament to the power of community, the significance of open communication, and the relentless pursuit of hope in the fight against muscular dystrophy.
Join us for a heartfelt conversation that underscores the essence of fatherhood, the quest for knowledge, and the transformative power of love. This episode is a must-listen for anyone seeking inspiration and motivation in the face of life's toughest battles.
(00:00) Reena Friedman Watts interviews Mazi Keyghobadi about battling muscular dystrophy
(05:16) Talk about when you first found out that your son had muscular dystrophy
(10:36) The key here is collaboration. It literally takes almost a country to solve a
(16:34) Getting the scientists was not that challenging, but it required a little bit of bravery
(18:26) What would you tell other parents that find out that their child has muscular dystrophy
(23:16) So talk to me about how you've taken action and gotten attention for the action
(30:02) Have you talked to your son about muscular dystrophy? Yes
(35:21) Talk to me about consciousness and staying humble
(38:49) We plan to share data and research live as we go
(44:52) What is the probability of a cure if you do this study on mice
(52:49) That really is. Wow. What big blessing that is. And again we were introduced to that. And they gave it to us without asking for
(53:21) We currently need $4 million for a clinical trial
(01:00:30) PPMD's Advocacy Conference is scheduled for June in Las Vegas
(01:04:23) Tushar Tangsali is raising funds for muscular dystrophy research
(01:08:18) The Better Call Daddy Show focuses on helping people with rare diseases
Don't miss this enlightening episode that reminds us all of the strength found in community and the impact of relentless advocacy. Be sure to like, subscribe, and share this episode with anyone who needs a dose of inspiration!
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