Live: October 5, 2017 @ 1pm ET
On-Demand: October 9, 2017
Voices of De Novo: A Q/A-Based Panel Discussion
with FAP Patients
Laura and Cole Eicher, Dakota Fisher-Vance, Shauna Monagan
and Suzanne Pilon
ALL Webinars will be available
The “Voices of the De Novo - A Q/A-Based Panel Discussion with FAP Patients” webinar will present patient advocates responding to a pre-set Q&A including questions such as:
What challenges did you face in being diagnosed with FAP?
What were your first thoughts when you found out you had FAP?
How did you integrate your diagnosis into your life planning?
How has your diagnosis affected…
- your education and career goals?
- your personal relationships?
- your family planning decisions?
What would have made your diagnosis easier to accept?
To incorporate patient perspectives/insights into their clinical practice
To communicate tips/tools to their patients to help navigate the landscape of their adenomatous polyposis condition
To identify common psychosocial effects of being diagnosed with an adenomatous polyposis condition.
8 Part Webinar Series: $70* by February 23rd
8 Part Webinar Series: $80* after February 23rd
According to the criteria of the American Board of Certification for Gastroenterology Nurses (ABCGN), 8 hour(s) earned in this activity are considered GI Specific for the purpose of recertification by contact hours through the ABCGN.
The Hereditary Colon Cancer Foundation is collaborating with University of Pittsburgh School of Nursing to provide these learning activities. Registered nurses participating in the entire series of webinars and completing the evaluation tools may receive a maximum of eight (8) continuing nursing education contact hours for the entire series. (One contact hour per webinar.) The University of Pittsburgh School of Nursing is an accredited provider of continuing nursing education from the American Nurses Credentialing Center’s Commission on Accreditation.
This conference has been approved by the Canadian Association of Genetic Counsellors (CAGC) for 7.33 CECs.
The Genetic Counsellor Registration Board (UK) will award one hour of CPD credit for each hourly webinar.
The National Society of Genetic Counselors (NSGC) has authorized the Hereditary Colon Cancer Foundation to offer up to 0.80 CEUs or 8.00 Category 1 contact hours for the event: Recognizing and Treating Polyposis Conditions. The American Board of Genetic Counseling (ABGC) will accept CEUs earned at this program for the purposes of genetic counselor certification and recertification.
*At the time of registration, a one time $25 fee will be added for individuals desiring CEUs through the NSGC.
Sessions may be attended LIVE or viewed On-Demand.
Registration fees cover the cost of CEUs, and production and promotion of the webinar series. Proceeds benefit the Hereditary Colon Cancer Foundation. If you would like to receive a refund, please email 24 hours prior to the first webinar's start time. Refunds will exclude a 10% processing fee.