Health : Diseases, Disorders, and Disciplines

Fanconi Anemia Research Fund

Dedicated to finding effective treatments and a cure for Fanconi anemia

Rating

Overall Rating    
      (58.63)
Organizational Efficiency      
Program Expenses 89.8%    
Administrative Expenses 3.6%    
Fundraising Expenses 6.4%    
Fundraising Efficiency $0.11    
Efficiency Rating    
      (36.00)
Organizational Capacity      
Primary Revenue Growth -1.1%    
Program Expenses Growth 10.5%    
Working Capital Ratio (years) 1.81    
Capacity Rating    
      (22.62)

Income Statement     (FYE 12/2007)

Revenue  
Primary Revenue $1,313,423
Other Revenue $711,863
Total Revenue $2,025,286
   
Expenses  
Program Expenses $2,020,526
Administrative Expenses $82,802
Fundraising Expenses $145,667
Total Functional Expenses $2,248,995
   
Payments to Affiliates $0
Excess (or Deficit) for the year $-223,709
   
Net Assets $4,116,658

Charts

Expenses Breakdown

Expenses Legend

Revenue/Expenses Trend

Revenue-Expense Legend

Contact Information

Fanconi Anemia Research Fund
1801 Williamette Street
Suite 200
Eugene, OR 97401
tel: (888) 326-2664
fax: (541) 687-0548
EIN: 93-0995453

Contact Email
Visit Web Site

Leadership      (FYE 12/2007)

Name Title Compensation % of Expenses
Mary Ellen Eiler Executive Director (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.) $81,800 3.63%

Donor Privacy Policy

YES, this charity has a written donor privacy policy.

Mission

Founded in 1989, the mission of the Fanconi Anemia Research Fund is to find effective treatments and a cure for Fanconi anemia and to provide education and support services to affected families worldwide. Fanconi anemia (FA) is one of the inherited anemias that leads to bone marrow failure (aplastic anemia). Family Support Services provided by the Fanconi Anemia Research Fund include education to FA patients, their families, and treating physicians about the genetic causes and effects of FA and state of the art life-extending or life-saving treatments. Information is provided through publications, the Annual Family Meeting, regional meetings, and through consultation with our family support coordinator.

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