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…
During the information afternoon in Zwolle, on December 9, 2023, our Scientific Officer Annet gave a presentation on gene therapy. We also asked you about your thoughts on gene therapy.…
In May 2023, scientists worldwide left for Athens for the CURE-PLaN consortium. This group met annually to share new scientific insights and results from research. During the European consortium meeting…
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.…
