Our Stories

The KCNA2 mutation affects families from around the globe. Each case is unique with its own challenges and triumphs. Click on the links below to read our stories

KCNA2 Epilepsy Treatment Stories

Damian's Story

Read Damians’s Story

KCNA2 Epilepsy Treatment Stories

Alex's Story

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KCNA2 Epilepsy Treatment Stories

Antonin's Story

 Read Antonin’s Story

KCNA2 Epilepsy Treatment Stories

Avery's Story

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KCNA2 Epilepsy Treatment Stories

Roman's Story

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KCNA2 Epilepsy Treatment Stories

Giana's Story

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KCNA2 Epilepsy Treatment Stories

Nya's Story

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KCNA2 Epilepsy Treatment Stories

Aggelos-Paisios's Story

Read Aggelos-Paisios’s Story

KCNA2 Epilepsy Treatment Stories

Madison's Story

Read Madison’s Story

KCNA2 Epilepsy Treatment Stories

Ilana's Story

Read Ilanas’s Story

KCNA2 Epilepsy Treatment Stories

Aaron's Story

Read Aaron’s Story

KCNA2 Epilepsy Treatment Stories

Paula's Story

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KCNA2 Epilepsy Treatment Stories

Fride's Story

Read Fride’s Story

KCNA2 Epilepsy Treatment Stories

Leo's Story

Read Leo’s Story

KCNA2 Epilepsy Treatment Stories

Nele's Story

Read Nele’s Story