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<BiographyAUAnet ID="x23491" Name="Oxalosis &amp; Hyperoxaluria Foundation" IsComponent="true" Changed="20260902T17:56:14" Created="20260902T17:48:30" Published="20260902T14:01:52" SiteBaseUrl="https://www.auanet.org" Locale="" XPowerPath="/Home/Advocacy/Patient Advocacy/Coalition for Urologic Patients/Coalition for Urologic Patients Members/Adv_P-A_CUP_Members/Oxalosis &amp; Hyperoxaluria Foundation">
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  <Biography type="xhtml" UID="90596f3bfc69427f9f79d2727a8feaea" label="Biography" readonly="false" hidden="false" required="false" indexable="false" Height="" CIID="">&lt;p&gt;&lt;a href="http://www.ohf.org" target="_blank" title="Oxalosis &amp;amp; Hyperoxaluria Foundation" rel="noopener"&gt;The Oxalosis &amp;amp; Hyperoxaluria Foundation (OHF)&lt;/a&gt; is a global patient advocacy organization dedicated to improving the lives of people living with primary and enteric hyperoxaluria and ultimately finding a cure. OHF focuses on advancing research, educating patients and healthcare professionals, and increasing awareness of hyperoxaluria within the urology community, where patients may experience recurrent kidney stones for years without recognition of an underlying genetic disease. OHF advocates for earlier diagnosis, appropriate genetic testing, improved access to expert care and treatment, and policies that address the needs of people living with rare stone diseases. By amplifying the patient voice and working with clinicians, researchers, policymakers, and other stakeholders, OHF is committed to transforming the diagnosis, treatment, and care of hyperoxaluria.&lt;/p&gt;</Biography>
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