The Only Foundation In The World
Dedicated to improving the care and treatment
and finding a cure for Oxalosis, Primary
Hyperoxaluria and other hyperoxaluria related
stone diseases.


To raise awareness amongst the general public
and decision-makers about rare diseases and
their impact on patients' lives.

SINCE 1989...

The OHF has been uncovering the secrets of
Primary Hyperoxaluria, investing millions of
dollars in research to find better treatments
and cure.


The OHFKidney stones that form in children and teenagers are likely to be caused by an underlying condition, such as hyperoxaluria. #TheOHF1 hour agoReplyRetweetFavorite
The OHFThere are only hours left to make a difference #constantcontact hours agoReplyRetweetFavorite
The OHFACTION ALERT!! Please read and take a moment to help Veronica if you can!! #TheOHF #WeAreFamily #RareDisease16 hours agoReplyRetweetFavorite
The OHFLet the world know you're #TeamOHF!! Download and post an OHF #facebook cover photo on your page! hours agoReplyRetweetFavorite
The OHFVisit #TheOHF at the Patient Advocacy Hub at the 2015 AUA American Urological Association!! #AUA15 #raredisease6 days agoReplyRetweetFavorite
The OHFNIH Rare Disease Day | NIH Intramural Research Program weeks agoReplyRetweetFavorite
The OHF#Cures2015 Legislative Phase Continues via @GovDelivery4 weeks agoReplyRetweetFavorite
The OHFApril 2015 E-NEWS via #constantcontact1 month agoReplyRetweetFavorite
The OHFNo matter how big or small, your contribution to the #OHF will go a long way. Donate today. #raredisease1 month agoReplyRetweetFavorite


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