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Saturday, August 4 • 10:30am - 12:00pm
Parent to Parent Initiative and Roundtable

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The Sickle Cell Community Consortium has begun a national parent to parent initiative with the goal to connect parents from diagnosis through adult living. Join us to learn more about how this initiative is designed, what we have accomplished thus far, and how you as a parent can join us and provide your valuable input!

avatar for Rosemary Britts

Rosemary Britts

Executive Director, Sickle Cell Association
Rosemary Britts enjoys helping others and takes every opportunity in life to do just that. She is a happily married mother of five children, ages 8 to 28. Her oldest daughter lives with sickle cell disease (SS) which gives her a natural passion for bringing awareness of the disease... Read More →
avatar for Lisa Rose

Lisa Rose

Instructional Designer, HOPE for SCD
Lisa Rose is the Executive Director for HOPE for SCD, an organization focused solely on providing research based medical education around Sickle Cell Disease and areas of complimentary interest. She has a Master's Degree in Education and has been developing curricula and trainings... Read More →

Saturday August 4, 2018 10:30am - 12:00pm CDT