🩸 Behind every blood donation is a family like this.
For many living with #SickleCellDisease, every #transfusion represents hope and more family moments.
To the donors who help make those moments possible: thank you. ❤️
#DonateBlood #SickleCellMN
✨ Join us for a #ChildrensMN #SickleCell #FamilyFunDay 🦕 at the #ScienceMuseum of MN!
🎁 REGISTER & CHECK-IN to receive a 💳 gift card!
⚠️ Must be an active SCD patient/family at #ChildrensMN
🔗 loom.ly/wkdDwhY
💙 #SickleCellMN #ScienceIsCool
UNITED BY BLOOD, CONNECTED BY PURPOSE
Worldwide #warriors & #advocates rise w/one voice on #WorldSickleCellDay 2025❤️🌏
🎉 Register for this FREE global event on #June19 and meet #sicklecell #warriors from around the world!
🔗 tinyurl.com/register2025wscd
#GASCDO #SickleCellMN
🏆 Today, @RaeBlaylark, Founder & Executive Director at @sicklecellmn, received the #DrCharlesDrew Achievement Award 👏🏾
🎉 Join us in congratulating Rae on 20+ years of #bloodbanking advocacy!
#advocacy#education#partnership#SickleCellMN#BloodDonorsMatter#DonorDiversity
Sickle cell disease: time to act on the most neglected global health problem - The Lancet Haematology thelancet.com/journals/lanha…
We have 3 new followers from Kenya 🇰🇪, and more last week. See fedica.com/!SickleCellMN
We're a small #communitybased #patientadvocacy org
❤️ We depend on YOU our family friends neighbors & co- workers, to help us
🙏🏾 #GTMD is a perfect opportunity to help us fulfill our mission
🤲🏾 Give today and support tomorrow's future! #SickleCellMN
💰 givemn.org/organization/Sick…
We're a small #communitybased #patientadvocacy org
❤️ We depend on YOU our family friends neighbors & co- workers, to help us
🙏🏾 #GTMD is a perfect opportunity to help us fulfill our mission
🤲🏾 Give today and support tomorrow's future! #SickleCellMN
💰 givemn.org/organization/Sick…
Join #DrRashidaDavis for OUR FINAL 2024 Smart Wellness Workshop!
✅ November 13
📆 6 PM CST, via Zoom ✨
🔗 bit.ly/smartwellness 🌿
#SmartWellness #MentalHealthAwareness #Wellbeing #Resilience #SickleCell
#WellnessWorkshop #smartwellness #sicklecellmn
#healtohear
Sharing Our Voice: Representing United States in the Middle East 🇴🇲
SickleCellMN is honored to be in Muscat, Oman sharing our voice and representing America from a global stage in the Middle East.
Sharing Our Voice: America's Representation in the Middle East 🇴🇲
We are honored to be in Muscat, Oman sharing our voice and representing America from a global stage in the Middle East.
Join #DrRashidaDavis for our FINAL #SmartWellnessWorkshop
☑️📆 May 8 - Support Systems
☑️🗓️ July 10 - Healthy Coping
☑️🗓️ Sept 11 - Medical Gaslighting
✅🗓️ Nov 13 - Emotional Intelligence
Register:
🔗 bit.ly/smartwellness
#sicklecell
#sicklecellmn
#healtohear
We have 10 new followers from India, Kenya, and more last week. See fedica.com/!SickleCellMN
Interview study about your experience of fatigue in #sicklecelldisease #pyruvatekinasedeficiency #alphaorbetathalassemia
For more info please contact the Clarivate study team at [email protected]
#sicklecell #pkd #thalassemia #agiospharmaceuticals
@agiospharma @agiosmedical
📢 Calling All Immigrant Professionals!
Looking to take your career to the next level? Join #AfricanBridgeNetwork for a Fireside Chat
🗓️ Date: Mon Oct 28, 2024
🕒 Time: 4:00 PM - 5:30 PM CDT
🔗 Register: eventbrite.com/o/african-bri…
#ImmigrantProfessionals#CareerGrowth#Networking
We're just going to leave this right here... 😆😜
📹: @healthwithscotty (IG)
❤️ Today is #WorldMentalHealthDay and a reminder that #mentalhealth is just as important as #physicalhealth.
🗣 Let’s advocate for #holisticcare that addresses better physical, mental, and emotional health for our #SickleCellWarriors.
#BreakTheStigma
#SickleCellAwareness
SickleCellMN retweeted
Food Deserts, Limited Access to Transportation Linked to More Complications Among Preschool Children with Sickle Cell Disease.
Read more about this new study, published today in @BloodAdvances: ow.ly/VkCC50TFJy8 #SickleCell #SCD #SDOH
SickleCellMN retweeted
Join us at SCDAA’s 52nd Annual National Convention from Oct. 23-26 for an essential conversation on LGBTQIA+ issues. The Lonzie Lee Patient Advocacy Symposium will bring together advocates from across the country to share their unique sickle cell stories!


























