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 OHFIt's #RareDiseaseDay2015!! How's it going for everyone?! It's been a great day so far!! #OHF1 day agoReplyRetweetFavorite
The OHFRT @BioMedCentral: Rare Diseases impact more people than AIDS and cancer combined - More info this #RareDiseaseDay2015 in our blog: http://…1 day agoReplyRetweetFavorite
The OHFRT @rarediseasefdn: Parent: “Miracles happen – my #raredisease child, living today is one of them” #RareDiseaseDay20151 day agoReplyRetweetFavorite
The OHFCheck out the team from the #OHF Annual Meeting yesterday!! Just in time for #RareDiseaseDay2015 day agoReplyRetweetFavorite
The OHFRT @rarediseaseuk: Two short films launched by #HEE highlight the need of patients with #rarediseases for genomics to make a difference htt…1 day agoReplyRetweetFavorite
The OHF@RareDayUS Thank you for the RT!! #RareDiseaseDay20151 day agoReplyRetweetFavorite
The OHFRT @rarediseaseday: Today is #RareDisease Day 2015! Find out what's happening all around the world! #RareDiseaseDay22 days agoReplyRetweetFavorite
The OHFIt's officially #RareDiseaseDay 2015!! Show us what you're doing today!! #OHF #RareDisease @RareDayUS2 days agoReplyRetweetFavorite
The OHF.RT @rarediseaseday: Images from #RareDiseaseDay2015 events in 30 countries: this is what global looks like… #RDD20152 days agoReplyRetweetFavorite

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