A world without PLN!

PLN Foundation was established to fund scientific research into the genetic heart muscle disease PLN. We also work hard to find carriers and raise awareness around the disease.

🫀 What is PLN?

♥️ For carriers of PLN

🤝 For loved ones of PLN carriers

😘 For peers & stories

🫶🏻 Sign up for the PLN Youth Day

📆 Check out our events in the calendar

Take action yourself 💪

The foundation funds scientific research thanks to the donations we receive. 100% of money raised to scientific purposes. As a result, nothing sticks to the bow. Support one of the ongoing actions or start your own for a world without PLN!

🎶 Singer-songwriter performs for PLN

♥️ Alice & Nikki run for a PLN-free world

👋 Margriet says goodbye to her work!

🕯️ Francisca makes bright spots

➡️ I am starting an action myself

About PLN Foundation ♥️

Want to know more about PLN? We would be happy to tell you more about the mutation and its possible significance for carriers.

🔬 What do you guys think about gene therapy? 5 x frequently asked questions

🫀 Roxanne participates in the PLN Youth Day

🫶🏻 This is the PLN Foundation team!

🤵 The PLN gala in 2023 with proceeds exceeding 250,000 euros

🧬 All about scientific research on PLN

💪 The latest news on our website

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