8 episodi

Spinal Muscular Atrophy and my experience as a mother of a type 1 baby. A mother to a kid with a rare genetic disorder.

The fault in our genes Maggie Moore

    • Salute e benessere

Spinal Muscular Atrophy and my experience as a mother of a type 1 baby. A mother to a kid with a rare genetic disorder.

    Rare Disease Day

    Rare Disease Day

    On this episode I talked about Rare Disease Day that was held on February 28th 2021.

    • 27 min
    Newborn Screaming in ALabama

    Newborn Screaming in ALabama

    On this episode, I talk about what is new born screening and our efforts to implement it in the state of Alabama.

    • 15 min
    Self care and caregivers.

    Self care and caregivers.

    On this episode I talked about the importance of self care as a caregiver and my journey, as well as tips of what has worked for me.

    • 26 min
    Illnesses and underlying conditions

    Illnesses and underlying conditions

    On this episodes I talk about our experience with illnesses and how they affect people with underlying conditions.

    • 18 min
    Care and support for diagnosis

    Care and support for diagnosis

    On this episode I talk about care and support, and what we do in a day to day basis.

    • 36 min
    Treatment Options

    Treatment Options

    This episode is a celebration for the approval of a new treatment for SMA. I will be talking about the different treatment options and our experience with them!

    • 20 min

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