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"These two mama bears will leave no stone unturned, because failure is not an option!"

Matty & Megan

Two Rare Mama Bears, a Cure CMD Podcast
We discuss all things Congenital Muscular Dystrophy & Rare Disease.
All subtypes, ages, abilities and topics!

While participating in Rare Disease Week on Capitol Hill, the idea of a podcast was born 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.

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Connect with us on Two Rare Mama Bears social media - we want your feedback and topic suggestions!

Matty Manley, a Pacific Northwest mom to an adorable son with congenital muscular dystrophy.

Mama bear. Disability advocate.
Busy mom & wife. Believer.

Megan Meyer, a blessed
Midwest mom to a sweet girl with congenital muscular dystrophy.


Mama bear. Disability advocate. Higher Ed Professional. Foodie. 

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Disclaimer: The views expressed in this podcast do not represent the opinion of Cure CMD or your podcast provider. Medical, research, legal, or financial opinions or advice expressed in this podcast should not be substituted or interpreted as professional advice; please consult your healthcare provider or other appropriate professional regarding any health related or other concerns.

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