Every month, committed supporters and loved ones start actions on our dedicated fundraising website. All money raised through this website is 100% dedicated to scientific research. Thanks to this research,…
On Saturday, April 20, 2024, we will host the first official PLN: You'll Have It Youth Day. This day is for young people ages 16 and up through young adults…
Gene therapies are a promising treatment option for genetic heart muscle diseases such as PLN. In such a disease, gene therapy can address the cause and then prevent the development…
On Saturday, April 20, 2024, we will host the first official PLN: You'll Have It Youth Day. This day is for young people ages 16 and up through young adults…
Researchers at UMC Groningen recently made a major breakthrough in their search for a treatment for the heart muscle disease PLN, a disease caused by an error or "mutation" in…
How do we look back on 2023 as the PLN Foundation? The short answer: good! We made fantastic breakthroughs and raised the visibility of the disease. The last days of…
Would you like to contribute to affordable treatment for the incurable orphan disease PLN? You can! We desperately need your support in our fight against the disease. You can do…
As the PLN Foundation, our primary mission is to find affordable treatment for PLN. No expense is spared to achieve this goal. In addition, we believe it is important to…
The news that you are a carrier of the PLN mutation comes to everyone differently. Whereas one person can disregard the news relatively quickly, for another it may take longer.…
Every month, committed supporters and loved ones start actions on our dedicated fundraising website. All money raised through this website is 100% dedicated to scientific research. Thanks to this research,…
