What Life is Like for Special Needs Families during the Coronavirus Pandemic
For most of us, the Coronavirus Pandemic is an inconvenience: Our dining and entertainment options are limited, we’re figuring out what homeschooling our kids looks like (and appreciating their teachers more and more each day), and we’re still trying to understand why everyone is stockpiling toilet paper. Life looks really different these days.
The way we’re living our lives today is the way many special needs families live their lives every day.
Leah Deason’s son Ozzie is a remarkable fighter who lives with a rare diagnosis, epilepsy, and hydrocephalus. Leah recently shared this perspective:
In this season when we are tempted daily to practice negativity, let’s open our eyes and look for the opportunity to practice empathy. Let’s offer our support to families who are not just inconvenienced by Coronavirus but are vulnerable during this season—and other seasons. Let’s put others first by enduring some temporary inconveniences that protect these vulnerable ones from a dangerous virus.
During this unprecedented season, the Who Is Carter Foundation is privileged to do our part to support special needs families with the resources available at TheBrainPossible.com. In particular, we’re offering some advice on stress relief for parents and caregivers during the Coronavirus epidemic and natural ways to boost your family’s immunity. Please share these resources—and this blog post—with families who could use the support during this trying time.