It’s International Thalassaemia Day!
We value the amazing individuals that live with this condition every day & the wonderful healthcare workers/specialists supporting them.
As always, think; ‘How can I make a difference?’
#internationalthalassaemiaday#ITD2026#Hiddennomore
It's #WorldThalassaemiaDay
Thalassaemia is a blood disorder causing severe anaemia. Most people need regular transfusions from closely ethnicity-matched donors.
Your donation could save a life �It's #WorldThalassaemiaDay
Thalassaemia is a blood disorder causing severe anaemia. Most people need regular transfusions from closely ethnicity-matched donors.
Your donation could save a life �It's #WorldThalassaemiaDay
Thalassaemia is a blood disorder causing severe anaemia. Most people need regular transfusions from closely ethnicity-matched donors.
Your donation could save a life �It's #WorldThalassaemiaDay
Thalassaemia is a blood disorder causing severe anaemia. Most people need regular transfusions from closely ethnicity-matched donors.
Your donation could save a life �It's #WorldThalassaemiaDay
Thalassaemia is a blood disorder causing severe anaemia. Most people need regular transfusions from closely ethnicity-matched donors.
Your donation could save a life �It's #WorldThalassaemiaDay
Thalassaemia is a blood disorder causing severe anaemia. Most people need regular transfusions from closely ethnicity-matched donors.
Your donation could save a life 🩸
It's only 1 week to go until #COMy2026 – the 12th World Congress on Controversies in #MultipleMyeloma! 🇫🇷
From 14-17 May in Paris, France, we will be interviewing top experts to gain insights into the latest in #Myeloma.
Stay tuned on https://t.co/Vqyt4af67F! 👀
#MMSM#HemOnc@COMyCongress
Happy #ITD2026 to all our patients, families and friends!
We are promoting diagnosis, awareness and understanding today across our network
#hiddennomore#VisabilityVoiceValue
Today is International Thalassaemia Day. How are you raising awareness today? We have lots of activities happening within our network. Photos to follow.
https://t.co/wa4HWilGPx
It’s International Thalassaemia Day!
We value the amazing individuals that live with this condition every day & the wonderful healthcare workers/specialists supporting them.
As always, think; ‘How can I make a difference?’
#internationalthalassaemiaday#ITD2026#Hiddennomore
For every patient.
For every family.
For every caregiver, healthcare professional, and advocate.
This #ITD2026, we raise our voices in hope, solidarity, and purpose — making the unseen visible and the unheard heard.
Together, we are #HiddenNoMore.
#8May#VisibilityVoiceValue
🎉Don't forget to join us for Milestones: Life Journeys with Sickle Cell this Saturday – a powerful event celebrating the journeys of those living with sickle cell into older adulthood 🩸💪.
Register now: https://t.co/oBj22QFxyY #SickleCell#Milestones#PatientVoices
If you’re thinking more about dating and relationships, or love life and family planning, we’ve got you covered with two podcast episodes on these topics.
Check them out on our website or YouTube Channel or wherever you listen.
https://t.co/0P0Sc8N8Um
To the public & all Sickle Cell Disorder (SCD) stakeholders (patients, family, friends, carers, clinical staff); please sign this Parliamentary petition to list SCD drugs for NHS prescription charge exemption. Reduce the health inequalities. Change lives. https://t.co/LLHAPPqt01
It's #WorldSickleCellDay This year’s theme ‘Tell it Loud’ reminds us to raise vital awareness. Many #SickleCellWarriors depend on regular blood transfusions so why not do something special and #GiveBlood. A good deed plus you get free tea & biscuits! Info: https://t.co/fIjVdZlEXS