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www.HereditaryColonCancerFoundation.org and www.HCCTakesGuts.org are informational and support websites for those affected by hereditary colon cancer syndromes. The website does not provide medical advice, recommend or endorse health care products or services, or control the information found on external websites.

 

Hereditary Colon Cancer Foundation and the Familial Adenomatous Polyposis Foundation are registered charitable organizations in Illinois and Utah, and tax-exempt under Internal Revenue Code Section 501(c)(3). Mailing address: 3519 NE 15th Avenue, Unit 518, Portland, OR 97212  |  info@HCCTakesGuts.org

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Hereditary Colon Cancer Takes Guts

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Attenuated FAP, Cowden Syndrome, Familial Adenomatous Polyposis, Gardner Syndrome, 

Hereditary Mixed Polyposis, Juvenile Polyposis Syndrome, Lynch Syndrome, Muir-Torre Syndrome, MYH-Associated Polyposis, Peutz-Jeghers Syndrome, Turcot Syndrome

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    Best Practices in Genetic Screeing

    for Hereditary Colon Cancer

    NOVEMBER: Research Highlights

    Webinar Series Overview

    OCTOBER: Extracolonic Manifestations

    AUGUST: Current

    Screeing Protocols

    DECEMBER: Genetic Screening

    SEPTEMBER: Successful Colectomies

    Identifying and interpreting the specific genetic mutation of a patient’s hereditary colon cancer syndrome is extremely valuable in developing a personalized care plan. In stark contrast to genetic testing for hereditary breast cancer, this tool is sorely underutilized in the HCCS community.

     

    This webinar will teach medical professionals when to screen, which test to use, and how to interpret the results. We will specifically cover:

     

    • Genetic causes of HCCS

    • Genotype/Phenotype relationships in HCCS

    • Benefits and risks of genetic testing

    • Social and emotional aspects of genetic testing

    • When to test, which test is appropriate, and cost of genetic testing

    • How to work with a genetic counselor 

    • Interpreting results and the limitations of testing

    • Developing a care plan based on genetic testing results

    • What age is appropriate for testing children

    • Direct-to-consumer genetic testing

    • Health insurance coverage of genetic testing

    • Genetic discrimination and Genetic Information Non-Discrimination Act (GINA)

     

     

    Target Audience

     

    Clinicians, including primary care physicians and gastroenterologists, physician assistants, and certified gastroenterology registered nurses interested in enhancing their knowledge of polyposis conditions; colorectal surgeons interested in broadening their understanding of polyposis conditions and how they relate to bowel diversions; basic and translational researchers and fellows in the fields of gastroenterology and gastrointestinal oncology; genetic counselors who provide care to patients with polyposis conditions or are interested in expanding their scope of care to genetic bowel cancers.

     

    Course Presenters

     

    • Carol Burke, MD, of the Cleveland Clinic

    • Brandie Leach, MS, LGC, of the Cleveland Clinic

     

     

    Learning Outcomes

     

    At the conclusion of this webinar, participants will be able to:

     

    • Identify when genetic screening for a colon cancer syndrome is needed.

    • Determine which type of genetic test to use.

    • Interpret genetic test results.

    • Recognize when to involve a genetics professional.

     

     

    Registration Information

     

    CEUs for Genetic Counselors

    5 Part Webinar Series by 8/28: $40*

    Individual Webinars: $10/each*

     

    Non-Credit for DO/MD/PA/RNs:

    5 Part Webinar Series: $40

    Individual Webinars: $10/each 

     

     

    CME/CEU Information

     

    NSGC CREDIT: The National Society of Genetic Counselors (NSGC) has authorized the Hereditary Colon Cancer Foundation to offer up to 0.5 CEUs or 5.0 contact hours (Category 1) for Preparing to Treat Polyposis Conditions. The American Board of Genetic Counseling (ABGC) will accept CEUs earned at this program for the purposes of certification and recertification.  *At the time of registration, a one time $25 fee will be added for the individual's application to the NSGC for CEUs.

     

    Refund Policy

     

    Registration fees cover the cost of CMEs, CEUs, and promotion of the webinar series. Proceeds benefit the Hereditary Colon Cancer Foundation. If you would like to receive a refund, please email TravisHBray@HCCTakesGuts.org 24 hours prior to the first webinar(s) start time. Refunds will exclude a 10% processing fee.

     

     

     

    December 11th, 1:00 - 2:00 p.m. EST
    ON-DEMAND available after live event
    Genetic Testing

    We would like to thank 

    Ambry Genetics

    and 

    Cancer Prevention Pharmaceuticals

    and

    Myriad Genetics

    for their generous grant support of this educational activity.

    CEU Registration
    Register w/out CME/CEUs

    ALL Webinars are available

    ON-DEMAND