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23andMe Sarcoma Community Event!

Tuesday, June 28 from 6:15 - 9:00 PM
23andMe Headquarters at 1390 Shorebird Way, Mountain View, California.

Please RSVP to sarcoma-help@23andme.com. Space is limited.

Mix and mingle with fellow sarcoma patients while learning about patient and caregiver support opportunities and 23andMe's Sarcoma Research Initiative. Engage in informational talks by top sarcoma physicians from Stanford and UCSF as well as patient advocacy leaders.
Drinks and hors d'oeuvres will be served.

Event Speakers
Dr. Kristen Ganjoo, Stanford Medical Oncologist
Dr. Eric K. Nakakura, UCSF Cancer Surgeon
Nathalie Criou, Survivor and Beat Sarcoma Founder
Arthur Beckert, Sarcoma Alliance Executive Director


This is the research on sarcoma genomes. If you have not participated, go here www.23andme.com/sarcoma
Participants in this study are genotyped (for free) and asked to complete online surveys about their experiences with the disease and their treatments. They need 1000 sarcoma participants, they have 500 so far. If you come to their patient education event, you will learn more about it - and be able to sign up.



Last Edited - 13 June 2011 01:02 am
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