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Sickle Cell Foundation of Minnesota
Home
About Us
Sickle Cell Disease & Trait
Treatments, Therapies & Clinical Trials
History & Timeline of SCD
Warrior Stories
Education & Awareness
Advocacy & Leadership
Patient Empowerment
SCDC Program Overview
SCDC Program Data
More Projects
Self-Advocacy Resources
Patient Assistance
Public Health Resources
Social Security Information
Ways to Support Us
Community Advocacy
Join Our Team
Contact Us
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Filtering by: “Provider”

2022 RARE Patient Advocacy Summit
Sep
12
to Sep 13
Virtual, In-Person, Conference, Warriors, Caregivers, Family, Rare Disease, Provider, Stakeholders

2022 RARE Patient Advocacy Summit

  • Mon, Sep 12, 2022 8:00 AM Tue, Sep 13, 2022 5:00 PM
  • Virtual Meeting (map)
  • Google Calendar ICS

Each year, Global Genes convenes one of the world’s largest gatherings of rare disease patients, caregivers, advocates, healthcare professionals, researchers, partners, and allies at the RARE Patient Advocacy Summit.

This year, the Summit will be a hybrid event so all can attend – in person at the Town & Country Hotel in San Diego, California and live streamed online in our virtual event platform.

View Event →
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P.O. Box 22306 Minneapolis, MN 55422

Contact us: (612) 444-1727