You are not alone.

Getting a rare disease diagnosis can be a scary time in a family's life.  Know that you are not alone. Those with CACNA1A variants have different sets of symptoms and no two patients are precisely the same. Early intervention, intensive therapies and appropriate seizure control are critical factors in patient outcomes. We are a small but mighty community, and we are in this fight together.

This is Emily with her siblings at her high school graduation. Emily has a CACNA1A variant.

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