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Content provided by Two Rare Mama Bears Podcast, Cure CMD (Matty Manley, and Megan Meyer). All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Two Rare Mama Bears Podcast, Cure CMD (Matty Manley, and Megan Meyer) or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
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008 - Team Stay Strong {Muscle Club Apparel & Love Bug Apparel with Jeff & Nicola Smith}

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Manage episode 210330527 series 2176784
Content provided by Two Rare Mama Bears Podcast, Cure CMD (Matty Manley, and Megan Meyer). All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Two Rare Mama Bears Podcast, Cure CMD (Matty Manley, and Megan Meyer) or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
The Smith family lets their son, Kaden, set the stage for their outlook on life with congenital muscular dystrophy - which is to stay strong and stay positive. Kaden doesn’t let his diagnosis of LAMA2 slow him down a bit - he keeps his parents on their toes while they are also busy running two successful home businesses, Muscle Club Apparel and Love Bug Apparel. Jeff & Nicola show us that finding your passions, capitalizing on them and relying your support system will be what gets us through tough times. Their community (Ruston, Louisiana) has rallied behind them to show overwhelming support in the face of difficult times the Smith family has had, full of hospital stays spanning many months and across multiple hospitals. This is a great episode to listen to in order gain a sense of perspective, as well as taking Kaden’s lead on staying positive!
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57 episodes

Artwork
iconShare
 
Manage episode 210330527 series 2176784
Content provided by Two Rare Mama Bears Podcast, Cure CMD (Matty Manley, and Megan Meyer). All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Two Rare Mama Bears Podcast, Cure CMD (Matty Manley, and Megan Meyer) or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
The Smith family lets their son, Kaden, set the stage for their outlook on life with congenital muscular dystrophy - which is to stay strong and stay positive. Kaden doesn’t let his diagnosis of LAMA2 slow him down a bit - he keeps his parents on their toes while they are also busy running two successful home businesses, Muscle Club Apparel and Love Bug Apparel. Jeff & Nicola show us that finding your passions, capitalizing on them and relying your support system will be what gets us through tough times. Their community (Ruston, Louisiana) has rallied behind them to show overwhelming support in the face of difficult times the Smith family has had, full of hospital stays spanning many months and across multiple hospitals. This is a great episode to listen to in order gain a sense of perspective, as well as taking Kaden’s lead on staying positive!
  continue reading

57 episodes

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