Health : Diseases, Disorders, and Disciplines

CFIDS Association of America

Working to make CFS widely understood, diagnosable, curable, and preventable

Rating

Overall Rating    
      (40.58)
Organizational Efficiency      
Program Expenses 80.8%    
Administrative Expenses 7.4%    
Fundraising Expenses 11.6%    
Fundraising Efficiency $0.11    
Efficiency Rating    
      (33.08)
Organizational Capacity      
Primary Revenue Growth -4.4%    
Program Expenses Growth -8.6%    
Working Capital Ratio (years) 0.91    
Capacity Rating    
      (7.50)

Income Statement     (FYE 12/2008)

Revenue  
Primary Revenue $1,900,404
Other Revenue $17,698
Total Revenue $1,918,102
   
Expenses  
Program Expenses $1,476,639
Administrative Expenses $136,675
Fundraising Expenses $213,084
Total Functional Expenses $1,826,398
   
Payments to Affiliates $0
Excess (or Deficit) for the year $91,704
   
Net Assets $1,667,607

Charts

Expenses Breakdown

Expenses Legend

Revenue/Expenses Trend

Revenue-Expense Legend

Contact Information

CFIDS Association of America
P.O. Box 220398
Charlotte, NC 28222
tel: (704) 365-2343
EIN: 56-1683450

Contact Email
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Leadership      (FYE 12/2008)

Name Title Compensation % of Expenses
K. Kimberly McCleary President, CEO (The person identified as holding the highest position of management, and therefore who would normally be responsible for carrying out the mission of the charity and leading the organization on a day-to-day basis.) $157,701 8.63%

Donor Privacy Policy

YES, this charity has a written donor privacy policy.

Mission

The CFIDS Association of America is the largest and most active charitable organization dedicated to chronic fatigue syndrome (CFS), also known as chronic fatigue and immune dysfunction syndrome (CFIDS). Since 1987, the Association has invested more than $26.8 million in initiatives to bring an end to the pain, disability and suffering caused by CFS. Our mission is for CFS to be widely understood, diagnosable, curable and preventable. The CFIDS Association offers information and resources to patients, family members, caregivers, support groups, media professionals the general public and health care professionals. The Association is proud to lead national efforts in research, public policy and communications that will advance understanding, diagnosis, treatment and prevention of CFS.

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