matthew1100-400

WELCOME
TO THE OHF

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.
katie

PLEASE JOIN US

To raise awareness amongst the general public
and decision-makers about rare diseases and
their impact on patients' lives.
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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 http://t.co/S5FanwJUfd1 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! http://t.co/J7ejyJBuHu #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 http://t.co/6G0qKFdOo7… #RDD20152 days agoReplyRetweetFavorite

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