Health : Diseases, Disorders, and Disciplines

HHT Foundation International, Inc.

Dedicated to finding a cure

Rating

Overall Rating    
      (59.26)
Organizational Efficiency      
Program Expenses 67.6%    
Administrative Expenses 29.0%    
Fundraising Expenses 3.2%    
Fundraising Efficiency $0.03    
Efficiency Rating    
      (29.26)
Organizational Capacity      
Primary Revenue Growth 12.0%    
Program Expenses Growth 15.2%    
Working Capital Ratio (years) 2.10    
Capacity Rating    
      (30.00)

Income Statement     (FYE 06/2007)

Revenue  
Primary Revenue $855,747
Other Revenue $151,938
Total Revenue $1,007,685
   
Expenses  
Program Expenses $502,456
Administrative Expenses $215,803
Fundraising Expenses $24,009
Total Functional Expenses $742,268
   
Payments to Affiliates $0
Excess (or Deficit) for the year $265,417
   
Net Assets $1,784,045

Charts

Expenses Breakdown

Expenses Legend

Revenue/Expenses Trend

Revenue-Expense Legend

Contact Information

HHT Foundation International, Inc.
P.O. Box 329
Monkton, MD 21111
tel: (800) 448-6389
fax: (410) 357-0655
EIN: 22-3115041

Contact Email
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Leadership      (FYE 06/2007)

Name Title Compensation % of Expenses
Marianne Clancy 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.) $90,000 12.12%

Donor Privacy Policy

NO, this charity does not have a written donor privacy policy.

Mission

The HHT (Hereditary Hemorrhagic Telangiectasia) Foundation International is dedicated to finding a cure, the best available treatment, and education to the medical community and to those with Osler-Weber-Rendu Syndrome. HHT is a genetic disorder, which affects blood vessels. Our mission is to find a cure for HHT while saving the lives and improving the well-being of individuals and families affected by HHT. To achieve this mission, the HHT Foundation will: fund research to find better treatments and a cure, educate families and physicians about HHT, provide linkages among people affected by HHT, collaborate with multidisciplinary HHT Treatment Centers worldwide, advocate for and support those with HHT, and engage the scientific and medical community.

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