National Society of Genetic Counselors explained

National Society of Genetic Counselors
Type:Professional society
Headquarters:Chicago, IL
Location:United States
Membership:3,600+
Leader Title:President
Leader Name:Sara Riordon, MS, CGC
Abbreviation:NSGC

The National Society of Genetic Counselors (NSGC), founded and incorporated in 1979, is the largest association of genetic counselors with over 3,600 members. Its membership includes genetic counselors and other healthcare professionals working in the field of medical genetics from the United States, Canada, and around the world.[1]

NSCG has a Code of Ethics which provides guidance to the members on the ethical responsibilities of a genetic counselor. This code is reviewed periodically to best represent the current needs of the public and of genetic counselors.[2] There is also a Conflict of Interest policy, which addresses possible conflicts of interest of members when they are acting on behalf of NSGC.

There are similar associations, such as the Canadian Association of Genetic Counselors, the Association of Genetic Nurses and Counsellors, the Professional Society of Genetic Counselors in Asia, and the Australasian Society of Genetic Counsellors for those genetic counselors who are currently practicing in Canada, the UK and Ireland, Asia, Australia, and New Zealand, respectively.[3] [4] [5] [6]

NSGC Leadership

The NSGC Board of Directors consists of the President, President-Elect, Secretary/Treasurer, Secretary/Treasurer-Elect, Immediate Past President, Executive Director, and 7 Directors At Large.[7]

Other leadership roles, including the Chair, Vice-Chair, and NSGC Board Liaison positions, can exist within the following committees:

Other groups within the NSGC include the Ethics Advisory Group, the Jane Engelberg Memorial Fellowship (JEMF) Advisory Group, and the Audrey Heimler Special Projects Award Committee.

NSGC leadership positions are volunteer roles obtained through member voting, appointment, or self-nomination, depending on the position.

There are several Special Interest Groups (SIG) that provide a smaller group setting for education, consultation, and activity within a specific clinical subspecialty such as Cancer, Cardiovascular, Prenatal, and Public Health.

Policy and Publications

NSGC advocates on a number of issues related to genetic counseling including support and strategic guidance for state licensure, federal efforts on improving services and professional standing, awareness on cultural competency, as well as various workforce initiatives.[8]

NSGC also maintains a variety of publications regarding the profession and practice of genetic counseling:[9]

NSGC provides an online resource for patients and the lay community to learn more about genetic disease and genetic counselors through a Patient Resource Site and the NSGC Blog.

Continuing Education

Continuing education enables genetic counselors to remain current about new technologies and testing modalities, and about relevant psychosocial, ethical, and legal implications.[13] Typically, genetic counselors require a certain number of Continuing Education Units (CEUs) to keep their certification/licensure active.

NSGC has numerous continuing education programs for genetic counselors through the provision of Continuing Education Units (CEUs) in courses and conferences. CEUs earned through NSGC-approved educational opportunities are accepted by the American Board of Genetic Counseling for purposes of Genetic Counselor recertification.[14]

The NSGC Annual Conference, usually held in the fall in a U.S. city, typically offers a certain number of CEUs each year. The conference covers a variety of topics applicable to genetic counselors in a variety of specialties, as well as other healthcare providers. The conference is open to NSGC members, as well as non-members. The 2021 Annual Conference will be held in New Orleans, LA, on September 22–26.[15]

NSGC also offers an Online Education Center with professional courses on topics including Business of Healthcare, Clinical Skills, ELSI and Policy Issues, Professional Development, Technology, and past Conference Recordings.[16]

See also

References

  1. Web site: National Society of Genetic Counselors : NSGC Membership Bylaws. www.nsgc.org. 2018-09-17.
  2. Senter. L. February 2018. National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions. Journal of Genetic Counseling. 27. 1. 9–15. 10.1007/s10897-017-0165-9. 29075947. 9845513.
  3. Web site: Canadian Association of Genetic Counselors.
  4. Web site: Association of Genetic Nurses and Counsellors.
  5. Web site: Australasian Society of Genetic Counselors.
  6. Web site: Chinese Board of Genetic Counseling.
  7. Web site: NSGC Leadership.
  8. Web site: Policy and Publications.
  9. Web site: NSGC publications.
  10. Web site: NSGC Practice Guidelines.
  11. Berliner. Janice L.. Cummings. Shelly A.. Burnett. Brittany Boldt. Ricker. Charité N.. Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors. Journal of Genetic Counseling. 2021. 30. 2. 342–360. en. 10.1002/jgc4.1374. 33410258. 230821996. 1573-3599. free.
  12. Web site: Perspectives in Genetic Counseling.
  13. Book: Uhlmann, W. A Guide to Genetic Counseling. John Wiley & Sons. 1998. 331–340.
  14. Web site: Recertification for ABGC.
  15. Web site: National Society of Genetic Counselors : NSGC 40th Annual Conference : Conference Home. 2020-04-05. www.nsgc.org.
  16. Web site: Online education.

External links