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

Read Nya’s Story

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

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KCNA2 Epilepsy Treatment Stories

Paula's Story

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KCNA2 Epilepsy Treatment Stories

Fride's Story

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KCNA2 Epilepsy Treatment Stories

Leo's Story

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KCNA2 Epilepsy Treatment Stories

Nele's Story

Read Nele’s Story

KCNA2 Epilepsy Treatment Stories

Sacha's Story

Read Sacha’s Story

KCNA2 Epilepsy Treatment Stories

Ines' Story

Read Ines’ Story

KCNA2 Epilepsy Treatment Stories

Emerson's Story

Read Emerson’s Story

KCNA2 Epilepsy Treatment Stories

Cory's Story

Read Cory’s Story

KCNA2 Epilepsy Treatment Stories

Amaia’s Story

Read Amaia’s Story

KCNA2 Epilepsy Treatment Stories

Siyeon Kim's Story

Read Siyeon Kim’s Story