Patients with haemophilia have the drive to live to their full potential. Let's encourage them to be amazing every day. To know more: changinghaemophilia.com.

#WHD2021 #WorldHemophiliaDay #InternalBleeding #BloodDisorder #ReinventLife #AlwaysMovingForward #ChangingHaemophilia

#SickleCell Disease #SickleCell Awareness #SickleCell , #19JuneWorldSickleCellDay #blooddisorder , #DonateBlood , Prabhat Sinha ,TIF,@thalassemic , Thalassemics India ,@NTWS1 , Thalassemia Patients Advocacy Group, World Health Organization (WHO), ORDIndia,PatientsEngage

#ITPAware #immunethrombocytopenia #lowplatelets #blooddisorder #raredisease

#Rotaract Club of #SmartCity #NaviMumbai

presents,

THALASSEMIA : A BRIEF OVERVIEW

BUT WHAT EXACTLY IS “THALASSEMIA MINOR' & “THALASSEMIA MAJOR'? 🤔

Read on to find out & let’s all be #smart in time.

#RCSmartCity #Thalassemia FreeIndia #Thalassemia #Blood Disorder #Blood

Sickle Cell Disease marjiesimpleword.com/sickle-cell-di…
#sicklecell#blooddisorder#pain#geneticdisease

#GrandRound today is #Heamatology delivered by Dr Amin Islam, Dr Shiraz Bashir & Dr Francesca Reeder
#MedEd #BloodDisorder #BloodDisease
Medical Education - Mid & South Essex NHSFT

#SCD is a rare, inherited #blooddisorder affecting approx. 100,000 in the U.S. & can occur in people of ANY background. SCD is characterized by low red blood cells, #Pain , Anemia, Infections, Fatigue.
I have a #RareDisease , I have #SickleCellDisease .

#RDDNIH
#RareDisease Day2022

Join us and help us spread the word..
#Thalassemia is a #Preventable #BloodDisorder

Waiting to do lab work trying to get a decent selfie I probably should find a decent face 🙄 to work with 🤪 #highWBC #blooddisorder #Warrior

Have you ever heard of the Yoruba word 'Agbana'? Okay let's explain it. When some one is called that, it means they make you squander money and drain your pocket.

#sickletember #sicklecell #sicklecell awarenessmonth #Togetherwecan #Blooddisorder #Health

On #InternationalThalassemiaDay let’s spread awareness about this #blooddisorder !

Full video link: youtube.com/watch?v=sqTOUj…
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This video addresses being a vulnerable person in the UK during this pandemic @tif_thalassaemia Sickle Cell Society NHS London
NHS Blood+Transplant Professional Patient
#sicklecellawareness #covid19 #vulnerableperson #Sicklecell #haemoglobin #blooddisorder

#OneCountryOneTreatment #HFI #Hemophilia #BloodDisorder #Hemophilia @HemophiliaHfi

Friday is #WorldThalassemiaDay – Test your Knowledge of Hemoglobin Variants – Check out our Library of Variants #BloodDisorder #8May2020 #SickleCell #ThalassemiaAwareness bit.ly/LOV_2020

With a strong 29.7% compound annual growth rate (CAGR) from 2017 through 2025, #ASEAN and #China #biosimilars Market will be a $5,506.2 Million market by end of the forecast period, Read More: bit.ly/2W9cdqU #pharmaceuticals #BloodDisorder #oncology #Chronic #autoimmune

A million people around the world have #sicklecell making it the most common #genetic #blooddisorder . 🌍🧬

Learn more for #WorldSickleCell Day via Nationwide Children's Hospital: nationwidechildrens.org/family-resourc….

Our very own: Julia Warren, MD, PhD, (top right) a fellow in pediatric hematology/oncology, is a recipient of the 2020 ASH Scholar Awards that provide funds for #BloodDisorder research. bit.ly/2SUVZyr

'Can Cord Blood be used for #RettSyndrome ?' Dr. Moshe Israeli answers your questions in the #WorldCordBloodDay post-conference Q&As. Read: buff.ly/3rNJTqL
#RareDisease #BloodDisorder #Disability #BioPharma #LifeSciences #WisdomWednesday #RareInsights #MedEd #Research

“ #Crohns Disease was a contributing factor to the #bloodclots , as well as the #blooddisorder I have”: buff.ly/2Cv1gFz The Spoonie Mummy #spoonie #chronicillness

Multiple #Emmy Awatd winning actress (and voice of Lois Griffin on Family Guy) Alex Borstein talks about the rare #BloodDisorder #hemophilia