Pages with the most revisions

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Showing below up to 198 results in range #1 to #198.

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

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