Advocating for Awareness and Research
CALL TO ACTION: Help Us Make September 21st Official!International Situs Inversus Awareness Day is approaching, and the SITUS Foundation is […]
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Building a Supportive Community
Recognizing the emotional and psychological aspects of living with a rare condition, we offer a peer-led support group. This group
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Educating and Inspiring Through Storytelling
Understanding the importance of medical education, we are in the process of creating a children’s book that highlights the significance
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Global Impact Through Medical ID Bracelets
We have proudly distributed medical ID bracelets worldwide to toddlers, children, and adults with Situs Inversus and other rare conditions.
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Celebrating Uniqueness: A Message from Our Hearts
At our charity, we believe that every individual is extraordinary, and those with Situs Inversus and rare conditions are especially
Medical Research
We actively support scientific studies and creation of a database for research focused on Situs Inversus and related rare conditions
Family Counseling
We offer a Situs Support Group for Patients and Families these meetings are virtual and are offered bimonthly and sometimes
Awareness Campaigns
Upcoming Events Light Up for Rare 2026! Join the global chain of lights this Rare Disease Day (Feb 28, 2026)
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