The Maryland Sickle Cell Disease Association, Inc. (MSCDA) seeking to improve the lives of persons affected by Sickle Cell Disease in Maryland
Joined August 2013
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- Following189
- Followers433
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MSCDA retweeted
🌟 In loving memory of Dr. Rashid, a remarkable hematologist/oncologist and Nevada's champion for sickle cell healthcare. Her tireless dedication improved lives and inspired us all. Rest in peace, dear doctor. Your legacy lives on. 🙏❤️ #RememberingDrRashid #SickleCellAdvocate
MSCDA retweeted
This is David Dandridge Jr.‘s story. ▶️ When he was 18, sickle cell disease disrupted his dreams of joining the military & law enforcement. Thanks to a lifesaving blood transfusion, he persevered — he completed college, married his high school sweetheart and became a father. ❤️
MSCDA retweeted
Set your calendars from now. This is going to be a groundbreaking one of a kind event.
MSCDA retweeted
If you had a choice between an LLC and a nonprofit, which would you choose?
43%LLC
43%Nonprofit
14%Other
7 votes • Final results MSCDA retweeted
DYK that #sicklecell patients benefit most from blood transfusions from people of similar ethnicity, but only 5% of donors are Black? You can make an impact. Find out how to donate: buff.ly/3q1058b #NationalBloodDonorMonth
MSCDA retweeted
Government House is lit red tonight in recognition of Sickle Cell Disease Awareness Month and in support of the approximately 100,000 people in the United States affected by this inherited blood disorder.
MSCDA retweeted
Spending the day attending the 4th annual @mscdaorg conference so that I can better serve kids & teens with #SickleCell, their families, their school teams, and their health care teams through our Hospital Education Liaison Program (HELP) @KennedyKrieger
The 4th Annual Sickle Cell Education Conference is underway. We are virtual again this year. You could still join us. Register via 👉🏽 whova.com/portal/registratio…
MSCDA retweeted
Today was a day! Stepped away from science for a sec to talk science w/my mentor Dr. Ludmila Prokunina-Olsson @prokuninaolsson during @theNCI Live event “Ask a Researcher: Working in a Cancer Research Lab”. It was an honor & pleasure to share this moment w/her #NothingWillStopUs
MSCDA retweeted
Murder Mystery Night is back and we are so excited! Trust us, you DO NOT WANT TO MISS this event at the 8th Annual Warrior Convention. Register at sicklecellconvention.org!
#WarriorsConvention21
#SC3WC21
#StrongerTogether2021
MSCDA retweeted
Are you ready to #BeASickleCellAdvocate? Learn how during our National Advocacy Day events on April 20 -21 from 4-5 p.m. Join us to find out about key SCD legislative issues and how to make change. Learn more and register: buff.ly/3eNdzRm
MSCDA retweeted
Plz Retweet.
Town Hall: Gene Therapy & Sickle Cell Disease
Feb 23 & 24: Drs. Sharma & Walters
Register: ow.ly/CODS50DG2cV
@SickCells @SickleCellUK @SCDFoundation @ConquerSCD @ASHCollab @drzsicklecell @thecuresci
#sicklecellwarriors
#sicklecell
#genetherapy
MSCDA retweeted
World leaders and local governments have made progress to improve access to #SickleCellDisease screening and care where SCD is endemic, but there is more to do. Read the State of Sickle Cell Disease 2020 Report Card: bit.ly/3huPrk4 #ConquerSCD #SickleCellAwareness
MSCDA retweeted
September is National Sickle Cell Awareness Month. SCD affects an estimated 100,000 Americans, but more research is needed to find effective treatment options. Learn more and join us to bring attention to SCD: bit.ly/SCDAAAwareness #SickleCellMatters
MSCDA retweeted
Sickle cell disease affects about 100k people in the U.S., most of whom are of African or Latino descent. Right now, @RedCross critically needs African American blood donors to give to ensure sickle cell patients receive treatments. Make an appt at rcblood.org/2w7EUXi.
MSCDA retweeted
All Aboard!!! For Orlando @ASHCollab #sicklecell Workshop we have charted a bus from So. Florida to provide free round trip transportation 2 stops: Miami and Ft. Lauderdale/Hollywood areas. Register at bit.ly/2ZlYPhh by July 1 for chance to win an additional $50!
MSCDA retweeted
Should you wear compression stockings on long flights to prevent blood clots? Visit the link and click on #VTE Clinical Practice Guidelines Snapshot for more takeaways from our guidelines buff.ly/2EOffaU #ASHGuidelines
MSCDA retweeted
On #WorldSickleCellDay, @SecAzar and @HHS_ASH reflect on the work being done at the Department, across the country, and worldwide to cure Sickle Cell disease within 10 years. hhs.gov/blog/2019/06/19/comi…
MSCDA retweeted
Excellent comments made by Derek Robinson of the @mscdaorg that models such as designated Hemophilia Treatment Centers and the need for #SickleCell Warriors on the @theNASEM Committee on Addressing #SickleCell Disease
MSCDA retweeted
Today on #WorldSickleCellDay the @ASHCollab joined Twitter! Please follow us and share the word with others in the #sicklecell community
MSCDA retweeted
The SickleGenAfrica Network: made up of African scientists and international collaborators who will study 7,000 children & adults with SCD in Africa to identify genetic markers associated with the development of organ damage bit.ly/2Kiyy0b #WorldSickleCellDay
