Maddie's Joy: An Angelman Journey

Maddie's Joy: An Angelman Journey

Our daughter Maddie was diagnosed with Angelman Syndrome at 18 months old. This podcast explores her Angelman Syndrome diagnosis. We try to connect with the Angelman Syndrome Community at large and we touch on topics that all special needs parents can benefit from. Come and join our journey. We're all in this together.

Tämä podcast on lisätty Podme-palveluun avoimen RSS-syötteen kautta eikä se ole Podmen omaa tuotantoa. Siksi podcastin jaksot saattavat sisältää mainontaa.

Jaksot(26)

Episode 8 Preview: We're Back On February 3rd

Episode 8 Preview: We're Back On February 3rd

Maddie's Joy: An Angelman Journey podcast is back on February 3rd. We'll be going back to basics and talking about what Angelman Syndrome is, and how rare it is compared to other syndromes.

27 Tammi 20231min

Episode 7: Sleep

Episode 7: Sleep

Sleep issues affect 20-80% of children with Angelman Syndrome. Based on my experience, that number is on the higher side. See some simple tips that can make a world of difference in your child's life.

16 Joulu 202218min

Episode 6: Caregiver Burnout

Episode 6: Caregiver Burnout

On today's episode I build upon last week's episode and talk about caregiver burnout. I talk about the article "Why Self-Care Is Essential to Parenting" by Juliann Garey. I hope you enjoy this episode...

9 Joulu 202217min

Episode 5: Build Your Community

Episode 5: Build Your Community

In Episode 5 I describe how I built a community of support around our family.

2 Joulu 202219min

Episode 4: The Clinic Visit

Episode 4: The Clinic Visit

We visited an Angelman Syndrome specific clinic for the first time. We detail our experience at Children's Hospital Colorado.

18 Marras 202223min

Episode 4: A Preview

Episode 4: A Preview

We went to the Angelman Syndrome specific clinic in Denver this week. Here's just a preview of what's to come in the next week.

11 Marras 20221min

Episode 3: ASF CEO Amanda Moore

Episode 3: ASF CEO Amanda Moore

The Angelman Syndrome Foundation CEO Amanda Moore joined the podcast to talk about a variety of resources available to caregivers of all ages.

4 Marras 202227min

Episode 2: Maddie's Story

Episode 2: Maddie's Story

In this episode I take you through Maddie's road to diagnosis. I also discuss the advice that shook me from my post diagnosis fog.

28 Loka 202231min

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