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      Since the middle of March most of us have been staying home and socially distancing.  COVID-19 was alrighty on the rise before many cities and states responded. Has anyone in our community dealt first hand with COVID-19?

      Have you or your pALS been diagnosed with ALS. If you are the primary or only caregiver were you able to get help? How did you adjust your life? Was leaving for the recommended 2 weeks an option?

      If you are a pALS, what kind of support were you able to get from your doctors and the ALS Association? Were admitted to the hospital? Were you encouraged to stay home and recover?


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