On Saturday, March 23, 2024, we will host another information afternoon on behalf of the foundation. This is the first afternoon of information this year. With the information afternoons, we…
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…
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,…
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,…
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…
Thanks to the support we receive from C&W de Boer Foundation, we have a fine partner in our midst that helps us achieve our goals thanks to financial support for…
