Kaleidoscope: The Cortical Visual Impairment Podcast
Kids & Family
Cheyanne Marcy has been an advocate on big stages, on everyday social media platforms and in day-to-day life on behalf of her son, Archer (5). She values action and advocacy – and has navigated not one, not two, but three state education systems.
She writes, “… I learned I was not doing enough to advocate for my child’s needs. Advocacy begins in your home, with our family and friends. It is all too easy to clam up and keep quiet. Sometimes feeling like you are explaining things over and over, then these people are close to you, so offense is taken. The challenge exists consistently.”
We sit down to talk about overcoming the fear of speaking up, vital services and resources for kids with CVI and NeuroMovement.
Resources:
Lighthouse Guild Tele-Support Enrollment or email moderator Judith Millman
NeuroMovement practitioner Sylvia Shordike
Find a NeuroMovement practitioner near you
NeuroMovement
sparkingtheneurons.blogspot.com
Sweet Valentina | Cindy Younan | 17
Hindsight and Insight | Kira Brady | 16
The PhD and the IEP | Barbara Lopez Avila | 15
Grace Unfiltered | 14
This Mom With a Blog | Mia Carella | 12
Word Bubble Much? | Tommy Szalapski | 11
Rosalie, Small but Mighty| Stephanie Kung | 10
Emma’s Renaissance | Lynn Elko | 9
Helping River Read | Judy Endicott | 8
Mini-Episode | Year of the CVI Advocate | 7
When Your Daughter Has a Visual Impairment, and Your Niece Does Too | Anna Ault & Lori Kinney | 6
Life With CVI and Perfect Pitch | Dagbjört Andrésdóttir | 5
What Happens When Things Go Right? | The Rastogi-Wilsons | 4
Going All In: From Phase I to Phase III | Alisha Waugh | 3
The Early Days: A Mother's First Year on the CVI Journey | Rachel Bennett | 2
Testing. Are CVI Parents Out There? | The Marquardts | 1
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