Colon Cancer Alliance for Research and Education for Lynch Syndrome

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The non-profit dedicated to Lynch Syndrome education & awareness, the # 1 hereditary cause of uterine & colon cancers. Leading the fight against Lynch Syndrome - the most common hereditary cause of colon & uterine cancers, through education, advocacy and research. Visit www.fightlynch.org to learn more.

ICO

271839697

Facebook

2700

X (Twitter)

953

Address

Chicago

Address: 127 W Oak St Apt C, ChicagoWeb: Sign in to see organisation websiteFacebook: lynchsyndromeX (Twitter): CCAREfightlynchICO: 271839697

Fight Lynch Syndrome Colon Cancer Alliance for Research and Education for Lynch Syndrome Our Mission Educate the public and healthcare professionals about Lynch Syndrome and to help fund research for a cure for this disease. What is Lynch Syndrome. Lynch Syndrome is a hereditary disorder that affects up to 1. 2 million people in the United States.

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News about from their social media (Facebook and X).

Sharon

Thank you for shedding light on Lynch Syndrome and the importance of early education and awareness! Together, we can make a difference in the fight against hereditary cancers. 💙 #FightLynch

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Colon Cancer Alliance for Research and Education for Lynch Syndrome

Honored to represent CCARE Lynch Syndrome at the CGAIGC International Conference and American Cancer Society National Colorectal Cancer Meeting.

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Jane

This is such crucial work! I had no idea Lynch Syndrome impacted so many lives. I’ll definitely be sharing this with my family and friends to spread awareness! 🌟 #LynchSyndromeAwareness

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Diana

2. How can healthcare professionals be better trained to recognize and address Lynch Syndrome in their patients, especially in families with a history of multiple cancers?

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Lucy

1. What are some effective strategies for increasing public awareness and understanding of Lynch Syndrome among younger generations who may be at risk?

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