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  1. Accepting Donations
  2. Accessibility of Tools
  3. Accountants
  4. Additional/Supplemental Resources
  5. Advisory Boards
  6. Advocacy
  7. Advocacy Organizations List
  8. Advocacy Resources
  9. Articles, Letters, and Other Media for Lay Publication
  10. Assistive Technology
  11. Attaining 501(c)(3) Status (Not-For-Profit Determination)
  12. Attending Professionals' Annual Meetings
  13. Audits
  14. Autopsies and Tissue Collection
  15. Available Resources
  16. Barriers to Rare Disease Research
  17. Basic Formatting
  18. Becoming the Organization You Imagine
  19. Benefits of Collaboration with Advocacy Organization Community
  20. Best Practices
  21. BioBanks
  22. Biobank Sample Collection
  23. Biobank and Registry External Relations
  24. Biobank and Registry Financial Management
  25. Blogging
  26. Blood and Tissue Banks
  27. Brochures and Fact Sheets
  28. Building a Website
  29. Bylaws and Articles
  30. Celebrity Spokesperson
  31. Characterize Condition
  32. Characterize Resources
  33. Charity Rating Listings
  34. Childcare
  35. Children's Hopes and Dreams Foundations
  36. Choosing Internet Service Provider
  37. Choosing an Internet Service Provider
  38. Clinician- and Researcher-Focused Materials
  39. Compare Goals and Resources, with the Characteristics of the Condition
  40. Conference Call Services
  41. Conferences, Workshops, and Meetings for Affected Individuals
  42. Connecting Individuals
  43. Connecting Organizations
  44. Considering Starting a Support Group for a Condition that Already Has One?
  45. Consumer Medical Information
  46. Consumers and Researchers: Making It Work
  47. Cool Tips
  48. Councils and Other Advisory Bodies
  49. Creating New Pages
  50. Creating a Natural History Survey

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