Health : Diseases, Disorders, and Disciplines

Osteogenesis Imperfecta Foundation

Helping people cope with problems associated with osteogenesis imperfecta

Rating

Overall Rating    
      (38.30)
Organizational Efficiency      
Program Expenses 58.0%    
Administrative Expenses 21.0%    
Fundraising Expenses 20.8%    
Fundraising Efficiency $0.22    
Efficiency Rating     0 Stars
      (18.30)
Organizational Capacity      
Primary Revenue Growth 10.5%    
Program Expenses Growth -0.1%    
Working Capital Ratio (years) 1.14    
Capacity Rating    
      (20.00)

Income Statement     (FYE 06/2008)

Revenue  
Primary Revenue $1,771,231
Other Revenue $139,280
Total Revenue $1,910,511
   
Expenses  
Program Expenses $1,093,824
Administrative Expenses $396,051
Fundraising Expenses $393,309
Total Functional Expenses $1,883,184
   
Payments to Affiliates $0
Excess (or Deficit) for the year $27,327
   
Net Assets $2,252,006

Charts

Expenses Breakdown

Expenses Legend

Revenue/Expenses Trend

Revenue-Expense Legend

Contact Information

Osteogenesis Imperfecta Foundation
804 West Diamond Avenue
Suite 210
Gaithersburg, MD 20878
tel: (800) 981-2663
fax: (301) 947-0456
EIN: 23-7076021

Mail donations to:
P.O. Box 630342
Baltimore, MD 21263

Contact Email
Visit Web Site

Leadership      (FYE 06/2008)

Name Title Compensation % of Expenses
Tracy Smith Hart Chief Executive Officer (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.) $125,000 6.63%

Donor Privacy Policy

YES, this charity has a written donor privacy policy.

Mission

The Osteogenesis Imperfecta Foundation (OI Foundation) is the only voluntary national health organization dedicated to helping people cope with the problems associated with osteogenesis imperfecta (OI). A genetic disorder known as brittle bone disease, OI is characterized by bones that break easily. Founded in 1970, the OI Foundation's mission is to improve the quality of life for people affected by OI through research, education, awareness, and mutual support. Since its inception, the OI Foundation has doubled funding for research every five years, for a total investment of almost $3 million. A biennial national conference provides more than 570 people with medical, research, and coping information.

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