Event

28 Feb 2020
When:
Fri 28 February, 2020
Location
275 Mt. Carmel Ave, Hamden, CT 06518
North Haven, CT
USA
2020 events in United States
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RareDisease Day Speaker Series
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Rare Disease Day Virtual Race
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Perthes Kids Rare Art Contest
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Rare Disease Family Night at
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15 Feb 2020 - 29 Feb 2020 Nationwide
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Rare Disease Day Educational
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Empowered #patientchat – Driving
You’re invited! Join us
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Second Annual World Rare Disease
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22 Feb 2020 Charlotte, NC
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Alabama Rare Disease Symposium
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SEE RARE RUN Virtual Race
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23 Feb 2020 - 29 Feb 2020
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Rare Disease Research at Yale
Stop by the Yale New Haven
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NYPD Rare Disease Day
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27 Feb 2020 New York City, NY
KY Rare Disease Day 2020
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UPMC Children's Rare Disease
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Soft Bones Southwest Patient
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Rare Disease Day at Metropolitan
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Focus on Rare Disease: Putting
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Rare Disease Day Symposium
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Rare Disease Day at NIH
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Rare Disease Day 2020
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Rare Disease Day Symposium 2020
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On line Kallmann Syndrome patient
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Rare Disease Day San Jose
Please join us as we come
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Rock Your Rare Disease
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Leap for a Cure
Join RSDSA for a mini-winter
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LA Clippers NBA Game Event for
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Topgolf Tournament for Myotonic
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California Rare Disease Day Virtual
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Ohio Rare Disease Day Event
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West Virginia Rare Disease Day
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Colorado Rare Disease Day Virtual
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New Hampshire Rare Disease Day
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Virginia Rare Disease Day Virtual
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Massachusetts Rare Disease Day
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Kansas Rare Disease Day Virtual
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Florida Rare Disease Day Virtual
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Illinois Rare Disease Day Virtual
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Texas Rare Disease Day Virtual
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Rare Disease Day At SkyView Atlanta
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Promoting Life Skills Through
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A Rare Disease and Mental Health
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Raise Awareness for KLS in Times
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Move2Advocate Pledge2Move
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Research for the CURE
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Maine Rare Disease Day Virtual
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Utah Rare Disease Day Virtual
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New Jersey Rare Disease Day Virtual
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Hello, all! Come join the
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United States

Rare Disease Day Symposium 28 February 2020 275 Mt. Carmel Ave, Hamden, CT 06518, North Haven, CT, USA
2035827844
Hosted by Quinnipiac University

Since 2015, the Frank H. Netter MD School of Medicine at Quinnipiac University has hosted Rare Disease Day, providing an opportunity for patients, family members and researchers to share their stories and promote education, awareness, and advocacy. The event has also become a powerful learning opportunity for students and professionals regarding the unique needs of individuals affected by rare disorders.

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