Hello, my name is Annette Klinkert: 59 years old, PLN carrier, transplanted and volunteer at the PLN Foundation. As all…Read more
International Rare Disease Day
Today it is International Rare Disease Day. PLN is a rare disease. There are only 1500 carriers known in the…Read more
The PLN mutation is a hereditary disease and is therefore passed on from generation to generation. The mutation inherits an…Read more
The PLN Foundation in The Netherlands is looking for a scientifically skilled person for 16 hours a week. Read more…Read more
Sponsor the cycle tour of Daan!
Daan Obdeijn from The Netherlands is organizing a sponsor campaign for the PLN Foundation: he will cycle an “alternative Elfstedentocht”!…Read more
Dear reader, If someone had asked me about 2020 last year, I could never have predicted a pandemic. Full of…Read more