49 episodes

Two Rare Mama Bears, a Cure CMD Podcast - where we discuss all things Congenital Muscular Dystrophy and Rare Disease...All subtypes, ages, abilities and topics with the intent to connect the CMD community. This podcast is about bringing together affected individuals, their family, researchers, clinicians, industry, and policy-makers to have conversations with the goal of moving the needle on the mission of Cure CMD. Hosts: Megan Meyer and Matty Manley.

Two Rare Mama Bears Cure CMD (Matty Manley & Megan Meyer)

    • Health & Fitness
    • 4.9, 22 Ratings

Two Rare Mama Bears, a Cure CMD Podcast - where we discuss all things Congenital Muscular Dystrophy and Rare Disease...All subtypes, ages, abilities and topics with the intent to connect the CMD community. This podcast is about bringing together affected individuals, their family, researchers, clinicians, industry, and policy-makers to have conversations with the goal of moving the needle on the mission of Cure CMD. Hosts: Megan Meyer and Matty Manley.

Customer Reviews

4.9 out of 5
22 Ratings

22 Ratings

C to F ,

The voices of my tribe!

So grateful to hear your rare mama voices in the land of podcasts! As a rare mama myself, I LOVE the topics and the opportunity to feel a little less alone in this unique journey. I am in awe of your advocacy and energy! Keep up the fantastic work of telling CMD stories and building our community! #thankful @MaddiesRYR1tribe

LariDiego ,

Educational

I am so thankful to theses “Two Rare Mama Bears” for taking the time out of their busy schedules to bring all this great information to the CMD community. I really enjoy listening to the struggles and triumphs that they discuss, it reminds me that
I’m not alone out here. I have also been very educated in the many topics they discuss. Thank you ladies! -Larisa Valenzuela.

rsunris ,

Great Resource for Rare Disease Families

Megan and Mathea have a great show specific to this of us dealing with rare diseases. They cover a wide range of topics and bring on some interesting guests. Definitely worth a listen regardless of what type of rare disease your kids are dealing with.

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