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Showing below up to 178 results in range #21 to #198.

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  1. Harnessing the Resources That Are Hard to Measure‏‎ (1 revision)
  2. Member Dues‏‎ (1 revision)
  3. Planning a Research Conference‏‎ (1 revision)
  4. Starting Points for Planning Materials‏‎ (1 revision)
  5. Working Full-Time on Nonprofit‏‎ (1 revision)
  6. Accessibility of Tools‏‎ (1 revision)
  7. Becoming the Organization You Imagine‏‎ (1 revision)
  8. Creating New Pages‏‎ (1 revision)
  9. Education of Members, Providers, and the Public‏‎ (1 revision)
  10. Health care Providers and Specialists‏‎ (1 revision)
  11. Mentors‏‎ (1 revision)
  12. Policy Tools & Resources‏‎ (1 revision)
  13. Research Model 1: Recessive Disorder‏‎ (1 revision)
  14. State-Specific Issues‏‎ (1 revision)
  15. Creating a Natural History Survey‏‎ (1 revision)
  16. Emergency Preparedness‏‎ (1 revision)
  17. Internet Services: Websites, Chat Rooms, and Newsgroups‏‎ (1 revision)
  18. NAC Best Practices‏‎ (1 revision)
  19. Preparing for and Handling Publicity‏‎ (1 revision)
  20. Research Model 2: Chromosomal Disorder‏‎ (1 revision)
  21. Additional/Supplemental Resources‏‎ (1 revision)
  22. History of Advocacy Organizations and Genetic Alliance‏‎ (1 revision)
  23. National Awareness Day‏‎ (1 revision)
  24. Press Kits‏‎ (1 revision)
  25. Research Model 3: Dominant Disorder‏‎ (1 revision)
  26. Choosing Internet Service Provider‏‎ (1 revision)
  27. Events‏‎ (1 revision)
  28. How to: Create a New Wiki Page‏‎ (1 revision)
  29. National Institutes of Health (NIH)‏‎ (1 revision)
  30. Promoting Research‏‎ (1 revision)
  31. Research Models‏‎ (1 revision)
  32. Advocacy‏‎ (1 revision)
  33. Choosing an Internet Service Provider‏‎ (1 revision)
  34. Determine Goals‏‎ (1 revision)
  35. Expertise‏‎ (1 revision)
  36. Genetic Alliance‏‎ (1 revision)
  37. How to Get Started‏‎ (1 revision)
  38. Knowing Your Community‏‎ (1 revision)
  39. Promoting Research on a Condition‏‎ (1 revision)
  40. Advocacy Organizations List‏‎ (1 revision)
  41. Biobank and Registry External Relations‏‎ (1 revision)
  42. FARA Patient Registry Q & A‏‎ (1 revision)
  43. How to Obtain Donated Office Space‏‎ (1 revision)
  44. Leadership‏‎ (1 revision)
  45. Nonprofit Organization Sample Templates‏‎ (1 revision)
  46. Protecting Member Privacy‏‎ (1 revision)
  47. The Kitchen Table Is a Good Place to Start: Klinefelter Syndrome and Associates‏‎ (1 revision)
  48. Advocacy Resources‏‎ (1 revision)
  49. Biobank and Registry Financial Management‏‎ (1 revision)
  50. Compare Goals and Resources, with the Characteristics of the Condition‏‎ (1 revision)
  51. Developing the Organization That Can Achieve Your Goals‏‎ (1 revision)
  52. FARA Q & A‏‎ (1 revision)
  53. How to Use This Guide‏‎ (1 revision)
  54. Legislation and Policy Advocacy‏‎ (1 revision)
  55. Protecting Message Boards from Spam‏‎ (1 revision)
  56. Results and Individual Follow-up‏‎ (1 revision)
  57. The Power of Advocacy Organizations‏‎ (1 revision)
  58. Articles, Letters, and Other Media for Lay Publication‏‎ (1 revision)
  59. Blogging‏‎ (1 revision)
  60. Disease Advocacy Organization(DAO)‏‎ (1 revision)
  61. Facilitating Quality Research‏‎ (1 revision)
  62. Genetic Privacy‏‎ (1 revision)
  63. How to post a file on WikiAdvocacy‏‎ (1 revision)
  64. Obtaining and Maintaining Registry Data‏‎ (1 revision)
  65. Scholarships for your participants/families/members‏‎ (1 revision)
  66. Translational Science‏‎ (1 revision)
  67. Individual Speaker Recommendations‏‎ (1 revision)
  68. Maintaining Computer Files‏‎ (1 revision)
  69. Orphan Drug Application‏‎ (1 revision)
  70. Setting up Useful Systems‏‎ (1 revision)
  71. Travel‏‎ (1 revision)
  72. Attaining 501(c)(3) Status (Not-For-Profit Determination)‏‎ (1 revision)
  73. Getting Needs on Government and Legislative Agendas‏‎ (1 revision)
  74. Informal Offices or Regional Support Groups‏‎ (1 revision)
  75. Maintaining Your Membership‏‎ (1 revision)
  76. Publisher Recommendations‏‎ (1 revision)
  77. Sharon F. Terry‏‎ (1 revision)
  78. Using Search Tools to Get Found‏‎ (1 revision)
  79. Attending Professionals' Annual Meetings‏‎ (1 revision)
  80. Connecting Organizations‏‎ (1 revision)
  81. Financial Assets‏‎ (1 revision)
  82. Getting Needs onto the Research Agenda‏‎ (1 revision)
  83. Information about Rare Genetic Diseases‏‎ (1 revision)
  84. Matching Resources‏‎ (1 revision)
  85. Overview of WikiAdvocacy‏‎ (1 revision)
  86. Recruiting‏‎ (1 revision)
  87. Vision‏‎ (1 revision)
  88. Considering Starting a Support Group for a Condition that Already Has One?‏‎ (1 revision)
  89. Getting Your Community Interested‏‎ (1 revision)
  90. Media Access‏‎ (1 revision)
  91. Recruiting Celebrities‏‎ (1 revision)
  92. Celebrity Spokesperson‏‎ (1 revision)
  93. Getting Your Needs on Government and Legislative Agendas‏‎ (1 revision)
  94. Intended Goal‏‎ (1 revision)
  95. Media Tips‏‎ (1 revision)
  96. Patient's Bill of Rights‏‎ (1 revision)
  97. Functions of Advocacy Organization‏‎ (2 revisions)
  98. Start Using WikiAdvocacy‏‎ (2 revisions)
  99. Why Go There?‏‎ (2 revisions)
  100. Internet Services: Listserv Guidelines Netiquitte Help‏‎ (2 revisions)
  101. Charity Rating Listings‏‎ (2 revisions)
  102. Benefits of Collaboration with Advocacy Organization Community‏‎ (2 revisions)
  103. Childcare‏‎ (2 revisions)
  104. Working with a Lawyer‏‎ (2 revisions)
  105. Fundraising Appeals‏‎ (2 revisions)
  106. Internet and Web Resources‏‎ (2 revisions)
  107. Biobank Sample Collection‏‎ (2 revisions)
  108. Resources for Nonprofits‏‎ (2 revisions)
  109. Tax and Finance‏‎ (2 revisions)
  110. Clinician- and Researcher-Focused Materials‏‎ (2 revisions)
  111. Genetic Alliance BioBank‏‎ (2 revisions)
  112. Novel Meeting Formats‏‎ (2 revisions)
  113. Publications‏‎ (2 revisions)
  114. Assistive Technology‏‎ (2 revisions)
  115. Connecting Individuals‏‎ (2 revisions)
  116. Family Health History Initiative Guidelines‏‎ (2 revisions)
  117. Sibling Support‏‎ (2 revisions)
  118. Autopsies and Tissue Collection‏‎ (2 revisions)
  119. Consumer Medical Information‏‎ (2 revisions)
  120. Registries‏‎ (2 revisions)
  121. Medical Records‏‎ (3 revisions)
  122. People and Roles‏‎ (3 revisions)
  123. Webinars‏‎ (3 revisions)
  124. Barriers to Rare Disease Research‏‎ (3 revisions)
  125. Educating Membership about Research‏‎ (3 revisions)
  126. Registry and Biobank Weekly Tips‏‎ (3 revisions)
  127. Internet Services: Mailing Lists‏‎ (3 revisions)
  128. Accountants‏‎ (3 revisions)
  129. Helping Your Membership Help Your Group‏‎ (3 revisions)
  130. Children's Hopes and Dreams Foundations‏‎ (3 revisions)
  131. Defining Our Terms‏‎ (3 revisions)
  132. General Resources‏‎ (3 revisions)
  133. Joint Fundraising‏‎ (3 revisions)
  134. Conference Call Services‏‎ (3 revisions)
  135. Blood and Tissue Banks‏‎ (3 revisions)
  136. Family Health History‏‎ (3 revisions)
  137. Bylaws and Articles‏‎ (3 revisions)
  138. Financial and Summary Statement‏‎ (3 revisions)
  139. Volunteer - Peer Coaches‏‎ (3 revisions)
  140. Finding a Lawyer‏‎ (3 revisions)
  141. Volunteers‏‎ (4 revisions)
  142. International Offices‏‎ (4 revisions)
  143. Best Practices‏‎ (4 revisions)
  144. BioBanks‏‎ (4 revisions)
  145. Taking Credit Cards on the Web‏‎ (4 revisions)
  146. Genetic Alliance(GA) SOP‏‎ (4 revisions)
  147. Resources for School Success‏‎ (4 revisions)
  148. Brochures and Fact Sheets‏‎ (4 revisions)
  149. Insurance and Policies‏‎ (4 revisions)
  150. PEER Portal‏‎ (4 revisions)
  151. Challenges of 'Splinter Groups'‏‎ (5 revisions)
  152. Support for Individuals and Families‏‎ (5 revisions)
  153. Newsletters and Bulletins‏‎ (5 revisions)
  154. Setting Up A National Conference‏‎ (5 revisions)
  155. Working Remotely‏‎ (6 revisions)
  156. State Registration‏‎ (6 revisions)
  157. Ensuring Cultural Competence‏‎ (6 revisions)
  158. Getting Grants‏‎ (6 revisions)
  159. Donations from Canada/Outside the US‏‎ (6 revisions)
  160. Drug Development‏‎ (6 revisions)
  161. Fundraising/Third Party‏‎ (7 revisions)
  162. Your Organization's Name Is Important‏‎ (7 revisions)
  163. Advisory Boards‏‎ (7 revisions)
  164. Audits‏‎ (7 revisions)
  165. Youth to Adult Transition Issues‏‎ (8 revisions)
  166. Publicity and General Media‏‎ (8 revisions)
  167. Staff‏‎ (9 revisions)
  168. Dealing with Death‏‎ (9 revisions)
  169. Developing a Governance Board‏‎ (10 revisions)
  170. Fundraising‏‎ (14 revisions)
  171. Disease Advocacy Organization(DAO) Manual‏‎ (15 revisions)
  172. Building a Website‏‎ (16 revisions)
  173. Conferences, Workshops, and Meetings for Affected Individuals‏‎ (21 revisions)
  174. Donations‏‎ (25 revisions)
  175. Social Networking‏‎ (36 revisions)
  176. Main Page‏‎ (41 revisions)
  177. Overview‏‎ (65 revisions)
  178. Disease Advocacy Organization (DAO) Manual‏‎ (438 revisions)

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