HOPE for SCD (@HOPEforSCD) header
HOPE for SCD (@HOPEforSCD) profile picture

Non-Profit Educational Org dedicated to creating patient education tools related to Sickle Cell Disease using research based best practices for Adult Learners

Raleigh, NC
Joined March 2014
Photo by HOPE for SCD (@HOPEforSCD)Photo by HOPE for SCD (@HOPEforSCD)Photo by HOPE for SCD (@HOPEforSCD)Photo by HOPE for SCD (@HOPEforSCD)Photo by HOPE for SCD (@HOPEforSCD)Photo by HOPE for SCD (@HOPEforSCD)Photo by HOPE for SCD (@HOPEforSCD)Photo by HOPE for SCD (@HOPEforSCD)
Replying to @HOPEforSCD
@HOPEforSCD “Mobile Health Technology App Development Survey for Sickle Cell Disease Adolescents and Young Adults.” surveymonkey.com/r/YHKHS8L
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HOPE for SCD retweeted
September is #SickleCellAwarenessMonth. We’re proud to partner with the #SickleCell community and amplify their voices. Learn more about our commitment to #SickleCellDisease through the inspiring video and song created by #SickleCell warrior, DeMitrious. ow.ly/QlTS50G6s8Y
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Our last Talking Tuesday read aloud is tomorrow at 2:00pm EST! Our ED Lisa Rose will be reading her book, “Sickle What?” The focus will Be on Chapter 2- genetics and “gene shopping”! This book was medically reviewed… instagram.com/p/CAWtpZpDle9/…
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Our last Talking Tuesday read aloud is tomorrow at 2:00pm EST! Our ED Lisa Rose will be reading her book, “Sickle What?” The focus will Be on Chapter 2- genetics and “gene shopping”! This book was medically reviewed… instagram.com/p/CAWthAKjYAH/…
HOPE for SCD retweeted
Replying to @KingsCollegeLon
@KingsCollegeLon @lifecourse_KCL @KingsGHP new lancet paper on transition from paediatrics to adults in @HOPEforSCD
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HOPE for SCD retweeted
Random thought...the only thing more agonizing than watching someone in a #SickleCell crisis is being the patient who is experiencing it. Truthfully, there is nothing like it.
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"We now have a therapy that significantly improves hemoglobin levels, has a favorable safety profile and reduces the anemia and hemolysis," states Elliott Vichinsky, M.D. Oxbryta will be available to patients in the U.S. ⁠⁠ #oxbryta #FDA #sicklecell #sicklecell101 ⁠
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It's #GivingTuesday Eve! Tomorrow's the day and we are so excited to officially join the movement. Give a little, save a life! Donate here to help our #TraitWarriors asonefoundation.org/giving-t…
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… and stronger than most. Don’t forget it. Tag someone who needs this. #teamsicklecell #sicklecellanemia #sicklecell #sicklecell101
Learn more about #ClinicalTrials. We can't expect a cure without our own participation! #sicklecell #educationiskey facebook.com/hopeforscd/post…
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Calling all caregivers. Simple online research study for $50! your child must be 6 or older. Patients 16 and older can also participate! Contact- Elisa at (469) 422-8174 (text is easier for her) or you can email her at elisa@murrayhillnational.com
HOPE for SCD retweeted
There have been a lot of questions about genetics and the punnet square. Here is a video we made to help you understand! youtube.com/watch?v=4KD8N2ha… youtube.com/watch?v=4KD8N2ha…
grant funding opportunity through @gbtpharma for CBOs. Deadline 5/1/2019, check it out! gbt.com/patients/accel-grant… gbt.com/patients/accel-grant…
This is a fantastic idea. Blood saves a person living with #sicklecell more often than we know. Thank you donors! facebook.com/story.php?story…
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