Mission

PCOS Network is dedicated to increasing public and professional awareness of resources for the treatment and prevention of polycystic ovarian syndrome.

Vision

PCOS Network will strive to develop a forum for clinical and scientific professionals working in the field of PCOS in order to build a collaborative, informed and engaged network. By providing an environment which encourages growth and new initiatives, PCOS Network will promote excellence in the care of women with polycystic ovarian syndrome.

The subspecialty of PCOS is a growing field and there are currently limited pcos specialists across disciplines. Levels of insulin resistance and diabetes are continuing to rise and more women are being diagnosed with PCOS. Therefore referrals to specialists will continue to rise and as a profession we need to be developing and advancing. I am committed to driving this forward by developing a network for professionals with an interest in PCOS to share information and resources.

To achieve its mission and vision PCOS Network will:

  • Serve as a forum for the interchange of ideas and resources between disciplines
  • Encourage and promote the advancement and exchange of information about the treatment and prevention of polycystic ovarian syndrome
  • Recruit new practitioners and researchers into the subspecialty by promoting the Student Member Program
  • Encourage evidence based knowledge, systematic reviews of lectures and ethical approaches to standards of care to maintain a reputable presence
  • Include professional development resources such as business enhancement ideas, online marketing strategies and career opportunities
  • Provide and publish thought leadership surveys
  • Encourage advocacy initiatives around strategic agendas
  • Provide a forum for peer networking events
  • Provide a knowledge bank and content archive
  • Publish a periodical e-newsletter and special e-bulletins
  • Provide a directory to the public searching for PCOS resources
  • Provide a bookstore and virtual library
  • Provide relevant association and resource links
  • Interview and report on professionals in the field
  • Post upcoming and recent events and conferences
  • Create a Speakers Bureau for members to access thought leaders
  • Provide an forum for regional interest groups to develop
  • Establish partnerships with other organizations
  • Provide online dialogue

Designed to Benefit:

physicians, dietitians, scientists, school health professionals, nurses, patients, exercise physiologists, psychologists, alternative/holistic professionals, the public, spiritual practitioners, aesthetics, health educators, eating disorder organizations

About The Founder

Stacy was the Founding Program Director of Center for Discovery Eating Disorder Program and has directed/consulted for five other eating disorder programs. She was lead therapist at Del Amo Hospital’s Trauma Recovery Program. Stacy has presented at many conferences on the subject of trauma, recovery and eating disorders.

Stacy’s current objective is to assist with professional development of practitioners and resources for the treatment of PCOS. As the organizational culture of chronic disease management changes, improved outcomes are made with an informed, activated patient and a prepared, proactive practice team. Her belief is that when patients receive effective treatments, self-management support, and regular follow-up, they do better. She believes that an organized multidisciplinary team is essential in producing positive outcomes.

Stacy is from Phoenix, Arizona and currently resides in Southern California with her two children.

Stacy is a member of the following affiliations:

AES – Androgen Excess and PCOS Society
IAEDP – International Association for Eating Disorder Professionals
CAMFT – California Association for Marriage and Family Therapists
The Endocrine Society
ASRM – American Society for Reproductive Medicine
WAAT – Women’s Association of Addiction Treatment


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