Join voices across Africa on 30th May 2026 as we unite to address the burden of SCD through African-led advocacy, research, innovation, policy, and implementation. Together, lets break barriers, amplify patient voices & build a future where no warrior is left behind.
Stigmatisation in #SickleCellDisease remains a significant barrier to equitable #PatientCare.
In the latest #podcast, @LaurelBrumant -Palmer offered a powerful, practical tip on tackling this critical issue.
👉Spotify: https://t.co/1mYBCyTfHr
👉YouTube: https://t.co/ou2C0Z5P9w
NEW SCD PODCAST! The 3rd edition of Sickle Cell Role Models and Mentors is ON AIR, focusing on women's resilience:
Facing Stigma.
Faith as a key coping tool.
Don't miss this powerful conversation. 👇
📺 YouTube: https://t.co/A8N3zX7GJt🎧 Spotify: https://t.co/LNzXLrEiL6
#SCD
🚩Soon on air!
Edition 2 of Sickle Cell Role Models and Mentors is out this Friday on @YouTube & @Spotify!
We talk to an SCD Coach who gives empowering, practical advice on thriving with #SCD.
More📷https://t.co/OGzWH2cRRZ
#SickleCellDiseaseAwareness#SDG3#podcast
The curtain may be closing on #SickleCellDiseaseAwarenessMonth, but our work is far from over.
SCD advocacy must be a year-round commitment.
We need a September-to-September cycle of continuous action. Join us! Many drops make an ocean. 🌊
#SCD#ContinuousAdvocacy#HealthForAll
#DidYouKnow? Many kids don't know about #SickleCellDisease?
The school is the FIRST place to promote #SCD awareness.
Let's educate pupils/students to create a stigma-free future & support classmates with SCD.
This is urgent!
#SCDEducation#SCDAwarenessMonth
Saviez-vous que le #dépistagegénétique avant le mariage peut aider à enrayer la transmission de la #drépanocytose ?
En le rendant obligatoire, les nations peuvent s'assurer que les couples sont informés pour faire des choix éclairés pour leur avenir et celui de leurs enfants.
When we voice it out, know that we have already reached our tolerance threshold. Because you don't see it doesn't mean it is not there.
Believe Us when we say we are in pain and show a little empathy 🙏🏾
A painful reality for many with #SickleCellDisease:
"I'm in pain, I need help." "Are you sure? You don't look like it."
The mildest #SCD pain can be an 8/10. When a patient arrives at the ER, they are likely at a 10/10.
Treat every case as a near-emergency.
#PatientAdvocacy
Plus de 500 000 bébés dans le 🌎naissent avec la #drépanocytose chaque année, surtout en #Afrique. Sans dépistage néonatal, beaucoup ne survivent pas à l'âge de 5 ans. Il est temps de militer pour un dépistage national obligatoire. Luttons pour le droit de chaque enfant à la vie.
It's still #SickleCellDiseaseAwarenessMonth!
What better way to raise awareness than through the power of #storytelling?
Listen to my podcast, "Sickle Cell Role Models and Mentors," now on @Spotify!👇
https://t.co/g0S77RrvER
Like, comment and share!
📢Save the date!
This #SickleCellAwarenessMonth, join our webinar focused on improving sickle cell disease outcomes in Africa.
We will take a deeper look at how uniting our voices can create a powerful impact.
Stay tuned for registration details!
#SickleCellAwareness