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.

Take action yourself πŸ’ͺ

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!

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