In the first part of our journey, we shared the initial struggles and uncertainties we faced as Andre was born and diagnosed with Pyridoxine-Dependent Epilepsy (PDE).

We wrote this story about Andre in 2014 when he was 3 years old. We wanted to post it as it was to be able to reflect back on where we were and where we are now.

One of our goals at CurePDE is to help families feel more connected and educated. While we hope that we can do a part of that, we also know there are other organizations that may resonate with you as well or have a local presence.

A recent study has shed new light on how PDE affects energy production in the body, offering fresh insights that could potentially lead to better treatments.

If you’re a parent or caregiver of a child with Pyridoxine-Dependent Epilepsy (PDE), you know how crucial early diagnosis and treatment are.

If you or someone you know is living with Pyridoxine-Dependent Epilepsy (PDE), you’re probably aware that most of the information focuses on children. But what happens when these kids grow up?

This article is based on a recent publication titled:Association Between Lysine Reduction Therapies and Cognitive Outcomes in Patients With Pyridoxine-Dependent Epilepsy

In this post, we will delve into the genetic underpinnings of PDE, shedding light on the diverse types of mutations associated with PDE.