🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Updated #SickleCell research priorities are live! For the next 5 years, we encourage researchers to study unaddressed questions and specific research topics aimed to help #ConquerSCD. Read the announcement here: ow.ly/MIjA50TvoAV

🩸OFFICIAL TRAILER🩸 SICKLE - The Docufilm For information on where to view the full film, you have to subscribe to The Red Cell Network Website! uclh.nhs.uk/theredcellnetw… #SickleCellAwarenessMonth #SickleCellDisorder

📣​We are pleased to announce the launch of the second version of the anonymous survey by ERN EuroBloodNet , The Lancet Haematology, & Academy for Sickle Cell & Thalassaemia (ASCAT) to gather the perspectives of people affected by sickle cell disease. Survey: lnkd.in/df5CcGwP #ERNeu #ERNs #HealthUnion

Our new @MarmotIHE review concludes racism damages health & wellbeing & drives avoidable inequalities between ethnic groups across London Sadiq Khan Dr Habib Naqvi MBE London Gov London Assembly @UCL theguardian.com/world/2024/oct…

Social justice requires we take urgent action on the evils of racism Dr Habib Naqvi MBE @profkevinfenton Sadiq Khan @mayorofLDN London Gov London Assembly @UCL bmj.com/content/387/bm…

🔔 Excited to share our latest blog post which focused on #sicklecell awareness month and more! Fred Piel 💙🖤🌍 NHS Race & Health Observatory Sickle Cell Society Click the link below 👇🏾 blogs.imperial.ac.uk/uk-sickle/2024…

“For more than 20 years, The Global Fund to Fight AIDS, Tuberculosis and Malaria has been at the forefront of efforts… with remarkable success... We urge [them] to make hydroxyurea universally accessible for #sicklecell disease… in LMICs” New Comment thelancet.com/journals/lanha…

Our Editorial in HemaSphere Journal (IF = 14.6) is published today. doi.org/10.1002/hem3.7…. Lots happening on #sicklecell in #India at the moment. ICMR-NIIH ICMR

Sickle cell disease is a lifelong blood disorder, with many patients needing regular blood transfusions. To help treat thousands of people living with sickle cell disease, Give Blood NHS 🩸🩹 urgently needs more people of Black heritage to donate blood. blood.co.uk

🩸 We need more people of Black heritage to #GiveBlood this #BlackHistoryMonth to grow the number of blood donors with well-matched blood to help those with sickle cell disorder. Become a donor or book your next appointment ➡️ orlo.uk/0mdD1 #SaveLives #GivingType

New #EHAUnplugged episode available now: Screening for Sickle Cell Disease In this engaging episode, Prof. David Rees discusses the present challenges of sickle cell disease screening in Europe and beyond. The conversation explores antenatal and neonatal screening practices and

🔔 Delighted to share our latest blog post on our #sicklecell comparative research with NHS Race & Health Observatory in which we focus on our patient engagement survey Fred Piel 💙🖤🌍 blogs.imperial.ac.uk/uk-sickle/

Our survey aims to gather insights on inequalities in sickle cell and is open to adults with sickle cell or caregivers of people living with sickle cell. Please share our survey to those who may be eligible. Sickle Cell Society Ethnicity & Health Unit Fred Piel 💙🖤🌍 imperial.eu.qualtrics.com/jfe/form/SV_bH…

🚨 Dear #SickleCellDisease Community 🚨 We invite patients, caregivers, & families to join a 🌍 global survey on improving #SCD care. 💬 Share your insights! 🔗EUSurvey - Survey 🌐 Available in 8 languages. Your voice matters—let’s shape the future of #SickleCell healthcare! ❤️

Experiences of people with sickle cell are key to our comparative research programme with Imperial College London. We encourage you to participate in this short survey, or to share the survey with others who may be eligible: imperial.eu.qualtrics.com/jfe/form/SV_bH…

📣 Help Shape the Future of Sickle Cell Research! Patients, caregivers & professionals—share your top research priorities through our survey. Together, we can focus on what matters most. 🌟 Have your say: buff.ly/41rgyax #PSP #SickleCell #PatientVoice #ResearchMatters

(1/6) Cities bring particular challenges and opportunities for the health of those who live, work and study in them. This CMO annual report explores what we can do to improve health in cities: gov.uk/government/pub…

🩸 What is the PSP? The Priority Setting Partnership unites patients, carers & professionals to identify key unanswered questions in Sickle Cell research, focusing on genomics to improve care.📢 Share your insights: buff.ly/41rgyax #SickleCell #PSP #Genomics #PatientVoice

📣The 5th Global Congress on Sickle Cell Disease is now accepting abstract submissions! 🗓️The deadline for submission is: Wednesday, January 15, 2025, at 11:59 p.m. Pacific time. More information↪️ tinyurl.com/2h28h4j2

🔔Sharing our last blog post of 2024! Our deepest thanks and appreciation for your incredible response and effort in participating and disseminating our #sicklecell survey NHS Race & Health Observatory Fred Piel 💙🖤🌍 Sickle Cell Society blogs.imperial.ac.uk/uk-sickle/2024…