Smith-Lemli-Opitz Foundation

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The Smith-Lemli-Opitz Foundation is a non-profit organization dedicated to supporting families, individuals and professionals dealing with Smith-Lemli-Opitz. The Smith-Lemli-Opitz Foundation works worldwide to improve the quality of life for people with Smith-Lemli-Opitz Syndrome through educating and supporting families, spreading SLO awareness, and funding research into the disorder.

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232635206

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Fargo

Address: PO Box 10598, FargoWeb: Sign in to see organisation websiteX (Twitter): slosfEmployees: 2Volunteers: 30Revenue: 205034ICO: 232635206

Home β€’ Smith-Lemli-Opitz Foundation - Smith-Lemli-Opitz Foundation Who We Are Our Mission Contact Us Living with SLOS Support Resources Education Resources Research Studies We came home from the NIH study empowered with knowledge tests and research which essentially saved our daughters vision. SLOS RESEARCH Ways to Give Fundraise Volunteer Advocate Who We Are Our Mission Contact Us Living with SLOS Support Resources Education Resources Research Studies We came home from the NIH study empowered with knowledge tests and research which essentially saved our daughters vision. SLOS RESEARCH Ways to Give Fundraise Volunteer Advocate Supportresources hope for lives affected by SmithLemliOpitz syndrome. learn the basics and the latest find support in a caring network increase your confidence and hope A network of professionals supporters and more than 1000 families from around the world who share experiences and information about SmithLemliOpitz syndrome 2025 SLOS CONFERENCE BOSTON Massachusetts USA Family Medical ConferenceJune 20th 21st 2025 Register for the conference today.

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Louise

Such an inspiring community! Grateful for the support and resources the Smith-Lemli-Opitz Foundation provides to families navigating SLOS. πŸ’™

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Jennifer

1. How can we improve awareness and understanding of Smith-Lemli-Opitz syndrome within the medical community and among the general public?

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Terry

2. What strategies can the Smith-Lemli-Opitz Foundation implement to enhance support for families navigating the challenges associated with SLOS?

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Janet

Can't wait for the 2025 SLOS Conference in Boston! It's amazing to connect with other families and share experiences. Let's raise awareness together! 🌟

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