Address book

<p>A patient-run non-profit organisation founded in 1994 that supports individuals with Fabry across Australia.<span></span><br />
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<ul class="connect-tag">
<li><span><img alt="" src="/themes/custom/bemi/img/icon_mail.svg" /></span><a href="mailto:admin@fabry.com.au">admin@fabry.com.au</a></li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_world.svg" /></span><a href="https://www.fabry.com.au&quot; target="_blank" >www.fabry.com.au</a></li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_adn.svg" /></span>Rare Diseases<span></span></li>
</ul>

<p>A non-profit association with the mission to Improve the health and wellbeing of Australian and New Zealander Gaucher patients through community building, education, advocacy, and support of research.<span></span><br />
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<ul class="connect-tag">
<li><span><img alt="" src="/themes/custom/bemi/img/icon_mail.svg" /></span><a href="mailto:info@gaucheranz.com.au">info@gaucheranz.com.au</a></li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_world.svg" /></span><a href="https://www.gaucheranz.com.au&quot; target="_blank">www.gaucheranz.com.au</a></li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_adn.svg" /></span>Rare Diseases<span></span></li>
</ul>

<p>A tax-deductible registered charity, formed in 1988 to provide support and information for individuals and families affected by a genetic condition.<span></span></p>

<ul class="connect-tag">
<li><span><img alt="" src="/themes/custom/bemi/img/icon_phone.svg" /></span><a href="tel:+61(2)92958359">+61 (2) 929 583 59</a></li>
<li><span><img alt="" src="/themes/custom/bemi/img/icon_mail.svg" /></span><a href="mailto:info@geneticalliance.org.au">info@geneticalliance.org.au</a></li…;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_world.svg" /></span><a href="https://www.geneticalliance.org.au&quot; target="_blank">www.geneticalliance.org.au</a></li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_adn.svg" /></span>Rare Diseases</li>
</ul>

<p>A not-for-profit patient advocacy organisation dedicated to serving persons with hereditary angioedema, in Australia and New Zealand.<br />
</a><span></span></p>

<ul class="connect-tag">
<li><span><img alt="" src="/themes/custom/bemi/img/icon_mail.svg" /></span><a href="mailto:info@haeaustralasia.org.au">info@haeaustralasia.org.au</li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_mail.svg" /></span><!--%3Ca%20href%3D%22mailto%3Ainfo%40haeaustralasia.org.au%22%3E-->zoe@haeaustralasia.org.au&nbsp;</a></li>
<li><span><img alt="" src="/themes/custom/bemi/img/icon_world.svg" /></span><a href="https://www.haeaustralasia.org.au&quot; target="_blank">www.haeaustralasia.org.au</a></li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_adn.svg" /></span>Rare Diseases</li>
</ul>

<p>Rare Voices Australia (RVA) is the national peak body for Australians living with a rare disease. Established in 2012, RVA works with all key stakeholders to drive the best outcomes for Australians living with a rare disease.</p>

<ul class="connect-tag">
<li><span><img alt="" src="/themes/custom/bemi/img/icon_phone.svg" /></span><a href="tel:+61(0)499549629">+61 (0) 499 549 629</a></li>
<li><span><img alt="" src="/themes/custom/bemi/img/icon_mail.svg" /></span><a href="mailto:helpline@rareportal.org.au?subject=Testing out mailto!">helpline@rareportal.org.au</a></li>
<li><span><img alt="" src="/themes/custom/bemi/img/icon_world.svg" /></span><a href="https://www.rarevoices.org.au&quot; target="_blank">www.rarevoices.org.au</a></li&gt;
<li><span><img alt="" src="/themes/custom/bemi/img/icon_adn.svg" /></span>Rare Diseases<span></span></li>
</ul>