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TRCN recently ran a series of 4 lectures which focused on the role of Nutrition in Thalassaemia. If you attended any / all of the sessions, please take 5 mins to complete this survey forms.office.com/e/c98LKPEdL4 If you missed it, you can catch up on our website! Thank you 😊

Here is the link to the sessions on our website. uclh.nhs.uk/theredcellnetw… Don't forget to subscribe!

Subscribe to our website to get first notice of upcoming training, focus groups, engagement events, and all sorts of useful information for red cell! It takes 30 seconds, and we don't spam. What's not to like? uclh.nhs.uk/theredcellnetw…

We are thrilled to see this position out for advert 👏🏾 If you consider yourself, or someone you know to be a strong candidate, we strongly encourage you to apply. Good luck! 🤞🏾

Great to see Amanda Pritchard spreading the wore on #WorldSickleCellDay. Here is a link to the nationally approved Sickle Cell training: uclh.nhs.uk/theredcellnetw… Soon to be a lovely eLearning package. 6 CPD points and RCN accredited!!

Nurses can now offer extended blood group testing to anyone with #sicklecell and thalassaemia. Bernadette is UCLH’s lead haemoglobinopathy clinical nurse specialist and just one of many nurses being encouraged by @nhsbt to offer the test to their patients. buff.ly/4c5pSDx

The subscribers know... we are going to London Zoo. We'll be posting links on our website soon so people can request tickets!

Great team work and example of persistence! UK Thalassaemia Society Sickle Cell Society TIF The Red Cell Network

Do you have a child aged 4-17 with SCD, transfusion dependent Thalassaemia, or a rare inherited anaemia? Do you live in North Central or West London, East Anglia, or Southwest England? Then you're invited to London Zoo on Oct 19th! Request tickets now! buytickets.at/theredcellnetw…

Limited tickets still available but hurry! 🐘🐯 Christopher Dean Bernadette Emma Drašar Sara Trompeter Sickle Cell Society

Amazing work highlighting #SCD proud of all the staff and patients and activists who contributed to this ❤️❤️❤️🩸🩸🩸

It is #BlackHistoryMonth and The Red Cell Network are excited to announce we will be doing another screening of SICKLE Docufilm to mark it. Be first to know details by signing up to our website. The last event sold out in only 36 hours - so don't be slow! uclh.nhs.uk/theredcellnetw…

UCLH @RedCellsrus Emma Drašar UK Thalassaemia Society

Who is ready for another screening of ‘SICKLE’ ? We’re ready!!! Stay tuned and keep your eyes on the listings page right here 👉🏾 uclh.nhs.uk/theredcellnetw…

A pleasure hosting Aerosoul Limited ™ on a visit to see the Junglist Movement plaque on an Apheresis machine UCLH which honoured its founder, Leke. Leke's monthly blood transfusions using Apheresis machines significantly reduced the amount of time he spent in hospital. 🎧💜🤎🌟😎

New National Education Course for Sickle Cell Disorder now Launched!!!! This innovative programme has been commissioned by NHS England as part of its ongoing efforts to enhance healthcare equity. e-lfh.org.uk/sickle-cell-di…

Open to all NHS staff who support people during a sickle cell crisis, book your webinar place to learn more about the ACT NOW approach and how it supports rapid help for patients. Book now via this link: events.england.nhs.uk/events/act-now

Anyone wanting to learn more about sickle cell disorder have a look at the NHS England commissioned e-learning I authored below 👇🏻

SICKLE CELL NUTRITION . Join in on this 4 part course, curated by Dr Claudine Matthews, to educate and empower Sickle Cell Patients through nutrition education and training to improve quality of life outcomes as well as knowledge on nutrition. Book here : tickettailor.com/events/theredc…

ACT NOW Webinar recording now available If you missed the ACT NOW Webinar on the 30th Jan, you can watch and listen to the recording of the webinar, via this link: youtu.be/lnbYyhq9xRs?si… #actnow #webinar #healtheducation #nhs #sicklecellawareness #sickle #theredcellnetwork