With high quality care, women with #SickleCell disease can have safe and healthy pregnancies and births. They need: 👨🏿‍⚕️ Access to skilled health workers to help them manage their condition 🩺 Additional health checks 🤰🏾 Individualized and respectful care 🔬 More research to

🩸La #TerapiaGénica se aplica por primera vez en España para tratar la #HemofiliaB: menos infusiones, menor riesgo de hemorragias y una mejor calidad de vida. 👩‍⚕️ Mayte Álvarez Román, presidenta de la #SETH, analiza su impacto clínico y organizativo👉seth.es/espana-aplica-… #SETH

Reversal of Glomerular Hyperfiltration Following Hematopoietic Stem Cell Transplantation in Children With Sickle-Cell Anemia AmericanJournalofHematology onlinelibrary.wiley.com/doi/10.1002/aj…

📌 Approach to Hyperferritinemia 🧪 #Ferritin >200 ng/mL (♀) or >300 ng/mL (♂)? 🔍 Check transferrin saturation ➡️ >45% ➡️ HFE testing for 🧬 #hemochromatosis ➡️ ≤45% ➡️ Rule out: 🔥 Inflammation 🍷 Alcohol 🩸 Hematologic & liver diseases 🧲 MRI T2* if unclear #Hematology

1/3 INDIRECT HYPERBILIRUBINEMIA Saw a 50M in clinic for isolated indirect hyperbilirubinemia. Known thalassemia trait. His bilirubin has chronically hovered around 3 mg/dL, but 6 months ago jumped to 5–6 and stayed there. Got me thinking about causes of elevated indirect bili.

HFE genotypes must be modified, C282T homozygous only as HFE Hemochromatosis

CASE CHALLENGE Patient’s hemoglobin plummeted within hours. Labs scream hemolysis (↑LDH, ↑indirect bilirubin, dark plasma, elevated K+), but haptoglobin is normal?! What’s going on here? #MedTwitter #HemeTwitter #MedEd

Hoy en #ColoniasASAFE2025, taller teórico-práctico de reanimación cardiopulmonar y atragantamiento, impartido por la Dra. Áurea Cervera, gracias a la financiación de Vertex Pharmaceuticals

Another major milestone for our C3G patients & community!! C3 inhibitor, Pegcetacoplan approved for C3G and IC-MPGN 🧬💊 investors.apellis.com/news-releases/… #C3G #Nephrology #RareDisease #FDAApproval #ComplementTherapy

L'U.S. FDA concedeix la designació de medicament orfe a una teràpia gènica per a l'#ELA desenvolupada per la UAB amb el #VHIR que, en models animals, ha retardat l'inici de la malaltia, preservat la funció neuromuscular i allargat la supervivència. Més: vhir.vallhebron.com/ca/societat/no…

🩺 Als anys 70, Vall d’Hebron va començar a desplegar les especialitats mèdiques: Cardiologia, Digestiu, Hematologia... Fins a convertir-se en l’únic hospital català amb totes les especialitats. #70anysVH Descobreix més👇 vhc.cat/anys70fita1

#destacadoSEHH | “A la sangre no le damos la importancia que merece” #JornadaHematoAvanza25 noticiasdealava.eus/salud/2025/07/… a través de @noticiasdealava

Not all red blood cells are created equal. 🩸Why have  #Fcells have attracted considerable interest? Read about in this impactful papar👉bit.ly/44pMdJj

Viajar con #hemofilia es posible con buena planificación: 🕛 Duración del viaje 💉 Dosis extra 🎒 Medicación en equipaje de mano 📋 Informe médico 👩‍⚕️ Consulta siempre con tu médico 🩸 La Dra. Olga Benítez te lo cuenta todo en el pódcast #HemofiliaOutLoud liberatelife.es/podcast-hemofi…

L'U.S. FDA concedeix la designació de medicament orfe a una teràpia gènica per a l'#ELA desenvolupada per la UAB amb #VallHebron, la qual cosa reconeix el potencial del tractament per a aquesta malaltia rara i greument discapacitant. Més: vallhebron.com/actualitat/not…

Inhibition of the complement pathway might prevent acute chest syndrome, one of the severe complications of sickle cell disease, according to new US research published in Science Translational Medicine. Read the latest #BSHNews story here: b-s-h.org.uk/about-us/news/…

Breakthrough hemolysis in paroxysmal nocturnal hemoglobinuria throughout clinical trials: from definition to clinical practice ow.ly/qSNu50WuY8U #redcellsironanderythropoiesis

Ayer, en #ColoniasASAFE2025, nuestros chicos recibieron una visita muy especial, la de Antonio Arenas, nuestro presidente, que les habló de ASAFE pero también como persona con #drepanocitosis que es mucho mayor que ellos, transmitiéndoles muchos consejos y resolviendo sus dudas.

💊#Iron #Chelators in #Thalassemia 1️⃣DFO:💉SC/IV, best for liver iron (+++), 💔(++), ⏱️5–7x/week 2️⃣DFP:💊Oral, 💔iron removal(+++), ⏱️2–3x/day, watch⚠️ neutropenia 3️⃣DFX: 💊Once daily, 💩fecal excretion, best for liver (+++), 💔 (++) 👀Monitor: GI upset, ALT, Cr, agranulocytosis

1/3 CHRONIC NON-ANEMIC IRON DEFICIENCY I have seen quite a few patients with chronically depleted iron stores (ferritin < 10 x several years) who never develop anemia. How is that possible? ✅ The body needs ~20–25 mg of iron/day to support new RBC production