“Adaptive Equipment and Therapy Strategies for Children with Severe Developmental Delays” is the third in our 6-part series on Optimizing Therapies for those Living with DEEs in partnership with our friends at the CACNA1A Foundation.
About this Webinar
This webinar focuses on the more severely affected children and how adaptive equipment and positioning can greatly impact their ability to function in daily routines. We look at preventing ongoing deformities, how to get your equipment covered/funded including the importance of a strong Letter of Medical Necessity and a good DME (Durable Medical Equipment) provider.
We also explore strategies to build natural routines in the day that utilize positioning for participation and function in the school/home environment.
This session and the entire series is led by Theresa Spong MED, PT, CBP who has decades of experience working with complex children and is a CACNA1A grandmother.
For more DEE resources, check out our resource center
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