We are scientists very much committed to promote information to patients, families and the society as a whole about an ultra rare disease: Primary hyperoxaluria. We also support the European Primary hyperoxaluria advocacy group with our ideas.
The links below will guide you to gain in-detailed information about our ideas and projects related to Primary Hyperoxaluria. Have a look!
Europe is not only a continent. Europe is a rich variety of cultures and languages, with a strong historical background, which makes Europe a pleasurable place to live and to enjoy. These different cultures and languages need to be supported by a united European project, to
Please find a link to every current project in the specific language below.
In most of the pages we have produced so far you will find the information translated in-to six different languages. We are currently working to translate our projects even into more languages. Our challenging European project has indeed a positive side effect: we can also reach the big Spanish speaking community in Latin America, in the US and the Portuguese community in Brazil! It is a great advantage that they can also use our informations and read everything in their own language!
We are proud about our team and you are more than welcome to send your ideas, suggestions, comments to spread the voice among the international PH community. Our mascots, the running oxalates Oxy and Laty will be happy to help!