Latest Articles
Cruise4Life – „Ship Ahoy, Cast Off!“
Finally, on 27 August 2024, the time had come for us, the PCH FAMILY, to set sail from Kiel on…
Embrace the colorful journey
Artist with PCH2 “My name is Damien and I am a disabled artist.” This is how 29-year-old Damien from Canada…
CZI Funding of PCH2cure Continues
The Chan Zuckerberg Initiative (CZI) is now officially funding the PCH2cure project for a second round.
1st 2025 PCH2cure Research Meeting at KIT
On January 20, the core scientific team of PCH2cure met with scientists and physicians from Tübingen, Freiburg and Karlsruhe at…
Video for Rare Disease Day: Living with PCH2
February 28, 2025 was Rare Disease Day. To mark this day, the University Hospital of Tübingen made a short video…
Family Portrait “PCH Angels”
In this interview, Judith talks about her older daughter Lotti, who passed away shortly before her 7th birthday.
Family Portrait “PCH Angels” and Adult PCH Patients
“What helped most was the endless love for my children”. Brigitte from Germany is the mother of Leonard and Kilian,…
Family Portrait Toddler
“He won't be able to play football with you, but he will cheer you on!” These are the words with…
Meeting of the “Rare as One” network in Nevada, USA
In June 2025, Dr. Julia Matilainen, representing the PCH2cure-project, attended the “Rare as One” meeting of the Chan Zuckerberg Initiative…
2. PCH Research Network Meeting in Karlsruhe, Germany
The 2nd PCH Research Network Meeting took place at the Karlsruhe Institute of Technology (KIT) in May 2025. International researchers,…
