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About LACNETS

MISSION STATEMENT

The mission of the Learn Advocate Connect Neuroendocrine Tumor Society (LACNETS) is to provide a community of support and education for patients (those with neuroendocrine cancer) and to advocate for all people impacted by this rare disease by expanding awareness and by voicing the patient’s perspective in collaborative dialogue with healthcare professionals. 

We aim to improve the quality of life of those with neuroendocrine cancer by offering support and expanded access to information on diagnosis, treatment options, research, and resources. LACNETS makes it possible for patients to share experiences, encouragement, and hope.

We work to improve outcomes for patients through early diagnosis by raising awareness among healthcare professionals and with the public about neuroendocrine and carcinoid cancers. 

HISTORY

Giovanna Joyce Imbesi, a NET patient and patient advocate, founded a non-profit organization named GeneratePossibility in 2012. She launched Los Angeles Carcinoid Neuroendocrine Tumor Society (LACNETS) to offer Patient Education Speaker Series.

Since 2012, LACNETS has presented leading NET experts in oncology, gastroenterology, radiology, nuclear medicine, clinical trials, pain management, surgery, and psychiatry and has addressed patient concerns about insurance coverage and nutrition. Starting in 2014, the patient educational programs are recorded for a global audience and posted on the LACNETS YouTube Channel.

In November 2022, LACNETS changed its name to Learn Advocate Connect Neuroendocrine Tumor Society.

Contact: info@LACNETS.org

LACNETS is a 501(c)(3) California non-profit corporation.

All or part of your donation may be tax deductible as a charitable contribution.

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