Familial Adenomatous Polyposis Foundation

Organization Overview

Familial Adenomatous Polyposis Foundation, operating under the name Hereditary Colon Cancer Foundation, is located in Portland, OR. The organization was established in 2013. According to its NTEE Classification (G70) the organization is classified as: Digestive Diseases & Disorders, under the broad grouping of Voluntary Health Associations & Medical Disciplines and related organizations. As of 12/2017, Hereditary Colon Cancer Foundation employed 4 individuals. This organization is an independent organization and not affiliated with a larger national or regional group of organizations. Hereditary Colon Cancer Foundation is a 501(c)(3) and as such, is described as a "Charitable or Religous organization or a private foundation" by the IRS.

For the year ending 12/2017, Hereditary Colon Cancer Foundation generated $49.3k in total revenue. This represents a relatively dramatic decline in revenue. Over the past 3 years, the organization has seen revenues fall by an average of (30.1%) each year. All expenses for the organization totaled $61.6k during the year ending 12/2017. As we would expect to see with falling revenues, expenses have declined by (25.5%) per year over the past 3 years. You can explore the organizations financials more deeply in the financial statements section below.

Mission & Program ActivityExcerpts From the 990EZ Filing

TAX YEAR

2017

Describe the Organization's Program Activity:

Part 3

HIGHLIGHTS FROM OUR 2017 PROGRAMS: PATIENT SERVICES INCLUDED: OUR INFORMATIONAL WEBSITE, HCCTAKESGUTS.ORG, SERVED OVER 12,000 UNIQUE INDIVIDUALS. OUR "EXPERT CARE FACILITY" LIST HELPED OVER 2,000 PEOPLE FIND A PROVIDER. THE PATIENT'S GUIDE TO LYNCH SYNDROME WAS DISTRIBUTED TO OVER 500 INDIVIDUALS TO BE USED PERSONALLY OR SHARED WITH THEIR FAMILIES. THE PATIENT'S GUIDE TO FAP WAS DISTRIBUTED TO OVER 900 PATIENTS TO BE SHARED WITH THEIR FAMILIES. SERVING AS PATIENT NAVIGATORS AND ADVISORS, WE GUIDED PATIENTS TO CREDIBLE RESOURCES AND COACHED PATIENTS ON HOW TO NAVIGATE LIFE WITH A HEREDITARY COLON CANCER CONDITION. WE RESPONDED TO EMAILS AND PHONE CALLS FROM INDIVIDUAL PATIENTS, ON AVERAGE, ONE OR TWO TIMES PER WEEK. MEDICAL PROFESSIONAL SERVICES INCLUDED: OUR SEVEN-HOUR EDUCATIONAL WEBINAR SERIES ENTITLED "ADVANCING CARE FOR ADENOMATOUS POLYPOSIS CONDITIONS" WAS ATTENDED BY OVER 350 PROVIDERS. THE PATIENT'S GUIDE TO LYNCH SYNDROME WAS DISTRIBUTED TO OVER 600 PROVIDERS TO BE USED PERSONALLY OR SHARED WITH THEIR PATIENTS. THE PATIENT'S GUIDE TO FAP WAS DISTRIBUTED TO OVER 400 PROVIDERS TO BE SHARED WITH THEIR PATIENTS. WE PROVIDED OVER 250 COMPLEMENTARY BROCHURES AT THE REQUEST OF PROVIDERS FOR DISTRIBUTION IN THEIR CLINICS. WE ATTENDED AND EXHIBITED AT THE COLLABORATIVE GROUP OF THE AMERICAS ON INHERITED COLORECTAL CANCER ANNUAL MEETING. WE WERE SELECTED TO PROVIDE INPUT TO TWO SETS OF CLINICAL PRACTICE GUIDELINES DEVELOPED BY THE NATIONAL COMPREHENSIVE CANCER GUIDELINES: "GENETIC/FAMILIAL HIGH-RISK ASSESSMENT: COLORECTAL- AND "COLON CANCER SCREENING." ON A MONTHLY BASIS, WE SUPPORTED PROVIDERS BY CONNECTING THEM TO EXPERTS AT HIGH RISK CENTERS. WE ALSO SERVED PROVIDERS BY HELPING TO CONNECT THEIR PATIENTS TO OTHER AFFECTED FAMILIES.


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Financial Statements

Statement of Revenue
Total Revenue from Contributions, Gifts, Grants & Similar$49,113
Total Program Service Revenue$0
Membership dues$0
Investment income $0
Gain or Loss$0
Net Income from Gaming & Fundraising$0
Other Revenue$0
Total Revenue$49,312

Grants Recieved

Over the last fiscal year, we have identified 1 grants that Familial Adenomatous Polyposis Foundation has recieved totaling $5,202.

Awarding OrganizationAmount
Network For Good Inc

Washington, DC

PURPOSE: Unrestricted

$5,202
View Grant Recipient Profile

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