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H&HP-team the European advocacy group for patients with primary hyperoxaluria welcomes you!
The pages you will visit are based on
individual input of
medical professionals, patients, parents, translators, artists, IT
specialists and friends of PH Europe. All the content presented is
independent of any outside sponsoring, with the exception of grants received from the German PH Self-support group so far. Our page is the
source of first information about a rare disease and guidance for patients wherever they live in Europe. The
input from patients and parents telling their individual stories is here of paramount importance.
Nobody has received any earnings or reimbursement for her/his input. The
idealism to help has been the main driver, which should remain, as it is the best motivator for such a great project.
Hence, many, many thanks, for all who have helped so far! Let us move forward together and please,
remain supporting us!
What is Primary hyperoxaluria?
