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<div class="book">AN INTERACTIVE GUIDE TO BUILDING ADVOCACY GROUPS</div>
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<div class="part">Part II</div>
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<br />
<a href="/InteractiveGuide/PartI/">Part I</a><br />
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<a href="/InteractiveGuide/PartII/">Part II</a><br />
<a href="/InteractiveGuide/PartII/Pages/cat_assessment.html">Assessment</a><br />
<a href="/InteractiveGuide/PartII/Pages/cat_structure.html">Structure</a><br />
<a href="/InteractiveGuide/PartII/Pages/cat_resources.html">Resources</a><br />
<a href="/InteractiveGuide/PartII/Pages/cat_support.html">Support</a><br />
<a href="/InteractiveGuide/PartII/Pages/cat_education.html">Education</a><br />
<a href="/InteractiveGuide/PartII/Pages/cat_research.html">Research</a><br />
<a href="/InteractiveGuide/PartII/Pages/cat_advocacy.html">Advocacy</a><br />
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<a href="/InteractiveGuide/PartIII/">Part III</a>

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<h3>Recruiting: Healthcare Providers and Specialists</h3>

<p>
<p>Clinicians and specialists who deal with your condition can be very helpful. They can help you find affected individuals to become members. Clinicians cannot give you the name and contact information of affected individuals. This violates patient confidentiality. But if you give them information that is easy to distribute, such as a brochure, they can tell their patients about you. Don't depend on busy clinicians to make a pitch for you - make sure your materials explain themselves. Try designing an eye catching postcard or brief notice that invites individuals to contact your group. Then they can receive your patient packet directly from you - this serves a number of functions - you get their interested individual's contact information and you also can centralize your materials (keeping the costs down and availability easier to manage).</p>

<img src="" alt="PXE Postcard" />

<p>Three common ways to connect with clinicians are:</p>
<ul>
<li>Direct mailings</li>
<li>Professional journals</li>
<li>Annual medical or research meetings (international, national, regional and state, of professional associations)</li>
</ul>

<p><b>Mailings</b></p>

<p>One effective method for recruiting affected individuals is direct mailing to a healthcare provider. You can usually purchase, for about $200 and up, lists of members from the medical and professional societies. Prepare a direct mailing that includes information clinicians can distribute to their patients. </p>

<p>Remember to tell the healthcare provider if you are creating a registry. This is important because a clinician might not think his or her patient needs support, but he will understand the need for all patients to be registered in one central registry and will help you in that endeavor.</p>

<p>May doctor's offices are still not using digitized databases for patient information, Thus they are often unable to sort their patient database with reference to your condition. Healthcare providers may have to wait until a patient returns before they can offer them your materials. Consider sending a postcard announcement when you have a small bit of news (maybe at the same time you send out press releases) - use any reasonable excuse to keep your group in the clinician's mind with a periodic mailing.</p>

<p><b>Medical Journals</b></p>

<p>Medical journals can provide information about your group to health providers and researchers. Look for journals that relate to your condition. For example, if your condition affects the neurological system, consider putting a notice in a journal associated with that specialty. There may be a cost involved in placing an ad or notice about your group. And if your goal is recruiting members, you may want to target a clinical journal, but don't neglect the research journals - various laboratories have registries of small groups of individuals or families affected by the condition. Although researchers cannot release individual's names, they can inform the study participants of your group.</p>

<p>What kind of information can you submit to a medical journal? Acceptable items include announcement of a registry, a research or medical meeting, a request for grant applications, or the announcement of a research project with a call for participants. See the section on educational functions for more information about using journal articles to promote your group.</p>
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<a href="http://geneticalliance.theanteroom.com/InteractiveGuide/PartII/Pages/000056.html">&raquo; Recruiting: Attending Professionals' Annual Meetings</a>
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The Interactive Guide to Advocacy Groups was written by Sharon Fontaine Terry and Caitlin Burke, with contributions from Genetic Alliance members. The Interactive Guide to Building Advocacy Groups is made available under a Creative Commons license. You may make and share copies of this work for noncommercial purposes without modifications and with this acknowledgement included in full. More information is available at <a href="/InteractiveGuide/About/">About the Interactive Guide to Building Advocacy Groups</a>. </p>

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<p class="nav"><b>SEPTEMBER 2004:</b> This is a preliminary installation of the Interactive Guide to Advocacy Groups. We need your feedback. Make comments on specific pages (you may see error messages, but comments should still post), or <a href="mailto:caitlin@marmoset.com">send email</a>. Is something missing? Can we make it easier to navigate? This Guide will change regularly over the next few months as we incorporate changes and fine tune the site. Thank you!</p>

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<a href="http://geneticalliance.theanteroom.com/InteractiveGuide/PartII/Pages/000054.html">&laquo; Recruiting: Celebrities</a> <br /><br />

<a href="http://geneticalliance.theanteroom.com/InteractiveGuide/PartII/Pages/000056.html">&raquo; Recruiting: Attending Professionals' Annual Meetings</a>

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