
HOPE IN FOCUS INC
Transforming the lives of those affected by blindness from inherited retinal disease. Hope in Focus is a 501c(3) nonprofit patient advocacy organization dedicated to transforming the lives of those affected by blindness caused by rare inherited retinal diseases. Our mission is to generate awareness, raise funds for research, and provide outreach, support and education to those affected by LCA and other rare retinal diseases.

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2014
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Ledyard
Leber Congenital Amaurosis Non-Profit | Hope in Focus Supporting the LCA community Supporting the LCA community We see a cure for blindness We see a cure for blindness Join us for the LCA Family Conference. Join us for the LCA Family Conference. June 2021 2025 Embassy Suites Minneapolis MNThis conference will provide information about advances in research deepen your understanding of various stakeholders roles in developing treatments and provide an opportunity for those living with rare inherited retinal disease and those involved in developing treatments to learn from each other. What is Leber Congenital Amaurosis LCA.
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Check out our latest newsletter. In this issue, we’re recapping highlights from our recent LCA Family Conference—perfect for those who couldn’t attend. You'll also find important updates on gene therapy research, along with a personal story from one of our LCA community members.
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Exciting news for the LGBTQ+ community! 🌈 The most banned book in America, Maia Kobabe's "Gender Queer," is getting an expanded edition next year! 🥳 "Gender Queer: The Annotated Edition" will be available in May. Let's celebrate diverse stories and promote inclusivity! 📚✨ #LGBTQ #Diversity #GoodNews
The most banned book in America (about growing up LGBTQ+) is getting a new expanded edition
Los Angeles Times
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