Thank you Sis Laure NGANLAY

We’re thrilled to unveil our new social media handles. We're a unifying force across Africa—championing SCD awareness, care, and research. Join us to reshape the SCD narrative across Africa, one story at a time. UNITY and ONENESS for SCD in Africa. #OneAfrica #OneVoice #OneFight

Nous sommes heureux de dévoiler nos nouveaux comptes. Nous unissons l’Afrique pour sensibiliser, soigner et rechercher sur la drépanocytose. Rejoignez-nous pour changer l’histoire de la drépanocytose. UNIS pour la drépanocytose en Afrique. #UneAfrique #UneVoix #UnCombat

Since our inception,UMASCCO has grown into a vibrant network of members from over 31 countries. Meet the passionate individuals behind this movement across Africa #OneAfrica #OneVoice #OneFight. UNITÉ et UNITÉ pour la drépanocytose en Afrique. #UneAfrique #UneVoix #UnSeulCombat

Love seeing good communication in action, especially for #SickleCellDisease! Thrilled to see the World Health Organization (WHO)'s June newsletter featuring their first-ever global guidelines for managing pregnancy with #SCD. This is huge! 👏 Check it out 👉linkedin.com/pulse/all-sick…

This September, #SickleCellAwarenessMonth, I will be looking at the powerful journey of patients who have become role models for their peers. By sharing their experiences, I hope to empower others & inspire a new way of thinking about #SCD. Stay tuned!👉bit.ly/4oR2UH7ord

🗓️It is #SickleCellAwarenessMonth. 💡 Are you #SickleCellDisease aware? Do you know what your genotype is? This month of #September, take a moment to find out where you stand. 🔬 Consider getting tested for sickle cell disease. #SickleCellAwarenessMonth

We look forward to seeing you all join us for this upcoming webinar. Save the date!

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!👇 open.spotify.com/episode/71Bqc3… Like, comment and share!

Very necessary

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.

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 🙏🏾

Important because doing so helps you to make informed decisions.

Tommorrow, in #NewYork, #SickleCellDsiease will enter into the discussion table at #UNGA80. Calling all the warriors in NewYork to attend. Register here: bit.ly/46jYXSV. Let through you, the voice of every #warrior be heard. #SickleCellAwarenessMonth #SCDAwareness

#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

The end of September doesn't end the work. Advocacy has no timeline so let's keep advocating.

🚩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📷youtube.com/post/UgkxvSyFb… #SickleCellDiseaseAwareness #SDG3 #podcast

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: youtu.be/qjOSa_ANt7M🎧 Spotify: open.spotify.com/episode/0juRSq… #SCD

Stigmatisation in #SickleCellDisease remains a significant barrier to equitable #PatientCare. In the latest #podcast, LoisTwiz -Palmer offered a powerful, practical tip on tackling this critical issue. 👉Spotify: lnkd.in/ek5_MiUz 👉YouTube: lnkd.in/ezVPX79a