Health : Diseases, Disorders, and Disciplines

The National Marfan Foundation

Serving the Marfan community since 1981

Rating

Overall Rating    
      (65.52)
Organizational Efficiency      
Program Expenses 80.2%    
Administrative Expenses 8.0%    
Fundraising Expenses 11.6%    
Fundraising Efficiency $0.04    
Efficiency Rating    
      (35.52)
Organizational Capacity      
Primary Revenue Growth 68.7%    
Program Expenses Growth 15.6%    
Working Capital Ratio (years) 3.61    
Capacity Rating    
      (30.00)

Income Statement     (FYE 06/2007)

Revenue  
Primary Revenue $7,822,754
Other Revenue $345,507
Total Revenue $8,168,261
   
Expenses  
Program Expenses $2,409,393
Administrative Expenses $241,833
Fundraising Expenses $349,320
Total Functional Expenses $3,000,546
   
Payments to Affiliates $0
Excess (or Deficit) for the year $5,167,715
   
Net Assets $11,640,332

Contact Information

The National Marfan Foundation
22 Manhasset Avenue
Port Washington, NY 11050
tel: (800) 862-7326
fax: (516) 883-8040

Contact Email
Visit Web Site

Leadership      (FYE 06/2007)

Name Title Compensation % of Expenses
Carolyn Levering 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.) $161,256 5.37%

Donor Privacy Policy

YES, this charity has a written donor privacy policy.

Mission

Founded in 1981, the National Marfan Foundation (NMF) is dedicated to saving lives, and improving the quality of life for individuals and families affected by the Marfan syndrome and related disorders. The Marfan syndrome is a heritable condition that affects the connective tissue. Because connective tissue is found throughout the body, the Marfan syndrome can affect many body systems, including the skeleton, eyes, heart and blood vessels, nervous system, skin and lungs. NMF educates patients, family members and the health care community about the syndrome; advocates and funds clinical and molecular research into the syndrome's detection and treatment; and provides support services for patients and relatives to share experiences and improve their medical care.

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