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Sickle Cell Foundation of Minnesota
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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
Login Account
Donate
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Filtering by: “In-Person”

14th Annual SCD Educational Summit
Sep
15
to Sep 17
Virtual, In-Person, Conference, Warriors, Caregivers, Providers, Family, Stakeholders

14th Annual SCD Educational Summit

  • Thu, Sep 15, 2022 10:00 AM Sat, Sep 17, 2022 6:00 PM
  • Virtual Meeting (map)
  • Google Calendar ICS

14th Annual Sickle Cell Disease Educational Seminar, hosted by Cayenne Wellness Center

The theme is Embracing Possibilities! This year’s event is virtual AND in-person! Registration is now open.

View Event →
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