• P.O. Box 10598
  • Fargo, North Dakota 58106-0598
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Our Members are family

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Our Member Families are united by their shared love for their children and hope for now and the future with SLOS.

Some of our families sharing their lives with you.
 You are not alone!

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We work worldwide to improve the quality of life for people with Smith-Lemli-Opitz syndrome through educating and supporting families, spreading SLOS awareness, and funding research into the disorder.

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The Smith-Lemli-Opitz Foundation does not provide medical advice.  Any content provided on the Smith-Lemli-Opitz Foundation website is for informational purposes only and is not a substitute for professional medical advice. Please consult your personal medical professional for any questions you may have about any medical condition. Smith-Lemli-Opitz Foundation does not endorse or recommend any particular provider, testing, product, procedures, opinion or other information which may be mentioned on this website.

The Smith-Lemli-Opitz Foundation is a registered charitable organization. Donations are tax-exempt under IRS 501(c)(3), ID #23-2635206.

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