Most linked-to pages

From WikiAdvocacy

Showing below up to 155 results in range #1 to #155.

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

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