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,…
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,…
From Venlo to Amersfoort, from there to Boston, then back to Groningen and now working in Wieringerwerf! Our new Scientific Officer Annet Linders joins our team since September 2023. Thanks…
Every month, committed supporters and loved ones start actions on our dedicated fundraising website. All the money raised through this website is 100% allocated to scientific research. Thanks to this…
We are working hard to increase awareness of PLN: by creating more awareness around the disease, people can anticipate more quickly when they have symptoms. In addition to raising awareness…
Growing up in Friesland, with Groningen parents. PLN has its origins in this province. This is how Job Hamming's personal connection to the disease arises. In June 2023, he will…
Last week our colleagues Pieter (Chairman), Corné van Dam (Scientific Advisor) and Luuk Kerckhaert (Scientific Officer) visited the researchers at Heart Research Center, Universitätsmedizin in Göttingen. "PLN research is critical…
"Every lap, Foundation PLN roars across the lake again!" one of our volunteers is told via WhatsApp. What an incredible achievement. Danny Jong from Wervershoof skated the Alternative Elfstedentocht for…
