Lynch Syndrome International

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Lynch Syndrome International (LSI) stands as a beacon of hope and support for those grappling with Lynch syndrome, a genetic disorder that increases the risk of many types of cancer. Established as the premier organization focusing on this hereditary condition, LSI plays a pivotal role in raising awareness, offering support, and facilitating research in the realm of Lynch syndrome.

Historical Background and Establishment[edit | edit source]

Established with a clear vision and mission, Lynch Syndrome International was conceived to fill a significant gap in the medical community's understanding and support structures for Lynch syndrome. Recognizing the unique challenges and needs of individuals diagnosed with this condition, LSI emerged as the first organization singularly dedicated to those affected by Lynch syndrome.

Organizational Status and Structure[edit | edit source]

  • Lynch Syndrome International is registered as a 501(c)(3) not-for-profit charitable organization, as acknowledged by the Internal Revenue Service1.
  • Adhering to the tenets of transparency and dedication, LSI operates with an all-volunteer staff, ensuring that maximum resources are directed towards its core mission.
  • Contributions made to LSI are tax-deductible, in line with federal and state regulations, fostering a culture of philanthropy and community support.

Mission and Activities[edit | edit source]

At the heart of LSI's operations lies its commitment to:

  • Support: Offering unwavering support to both survivors and previvors diagnosed with Lynch syndrome. These individuals, often termed 'previvors,' are those who carry the genetic mutation but have not yet developed the disease.
  • Education: Spearheading awareness campaigns and educational initiatives to ensure that the wider public, as well as the medical community, is well-informed about Lynch syndrome.
  • Research Facilitation: Collaborating with medical professionals, researchers, and institutions to foster research on Lynch syndrome, its implications, and potential treatments.
  • Community Building: Creating a platform for those affected by Lynch syndrome to share their experiences, seek advice, and build a community of shared understanding and empathy.

Location and Reach[edit | edit source]

The international headquarters of Lynch Syndrome International is strategically located in Vacaville, California, allowing it to effectively coordinate its global initiatives. However, the organization's influence transcends geographical boundaries, as it operates on an international scale, connecting survivors, previvors, medical professionals, and researchers from around the world.

Conclusion[edit | edit source]

Lynch Syndrome International stands as a testament to the power of community-driven initiatives. Through its dedication, outreach, and relentless advocacy, LSI has carved out a niche as the leading voice in the realm of Lynch syndrome, offering hope, support, and a brighter future for those affected by this hereditary condition.

References[edit | edit source]

  • Internal Revenue Service. (20XX). Exempt Organizations Select Check. U.S. Department of the Treasury. ↩
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Contributors: Prab R. Tumpati, MD