DrMagborAkanni

[RC of Pathologists @RCPath]

The transition to registrar can often be challenging – this change is particularly stark in #haematology. Discover how simulation training can provide beneficial experience to new haematology trainees in our April Bulletin article. ⬇️ @OUHospitals https://t.co/SI9Son9lZR

[Sickle Cell Society @SickleCellUK]

We’re continuing to support reviews of sickle cell hospital care. A review visit to Cambridge University Hospital NHS Trust is taking place on 10th March 2025.

Attendance is free, by Microsoft Teams. Register now: https://t.co/1hBt7b718b

#SickleCellUK #LondonHospital

[Sickle Cell Society @SickleCellUK]

We’re continuing to support reviews of sickle cell hospital care. A review visit to London North West University Hospital NHS Trust is taking place on 3rd March 2025.

Attendance is free, by Microsoft Teams. Register now: https://t.co/wqqYfA6m5G

#SickleCellUK #LondonNorthWest

[Carly Flanagan @CarlyFlanagan11]

We welcomed Dr Akanni to Medsoc this afternoon. Dr Akanni shared her experiences of working in Haematology and her journey to becoming a Consultant. Such an excellent session for our aspiring medics! @TheRoyalLatin @RLSMedSoc

[DrMagborAkanni @MagborAkanni]

@CarlyFlanagan11 @TheRoyalLatin @RLSMedSoc Thank you for having me!

[The Red Cell Network @TRCNHCC]

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:

https://t.co/Yk2Mjh1laI

[The Red Cell Network @TRCNHCC]

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.

https://t.co/wIYtH4S4Fg

[DrMagborAkanni @MagborAkanni]

@LouiseMew @BoneJointOpen @MKHospital @Wrenly_74 @antoanela09 Congratulations to you 🎉

[REDRESS Study @redress_study]

Our team captains @vicpotter123 @DrRachelKesse
share info on the #redresstrial looking at new treatment for #sicklecell. If you are interested, please get in touch!
@KingsCollegeNHS @KingsCollegeLon @GSTTnhs @KHPHaematology @SickleCellUK

[Sickle Cell Society @SickleCellUK]

Sickle Cell: Fact or Fiction? How much do you really know about Sickle Cell? We've put together some common myths and facts to share with our community. Got any insights or questions about Sickle Cell? Share them in the comments, and let’s clear up the facts together! #SickleCell

[British Journal of Haematology @BrJHaem]

Guideline for the management of conception and pregnancy in thalassaemia syndromes: A British Society for Haematology Guideline
https://t.co/a39kVCZAuG
@farrukh1707 @DocCSarah @Shivan_TT @BritSocHaem

[The Red Cell Network @TRCNHCC]

We are thrilled to announce that we have now published our Guide to Living with Sickle Cell

Compiled with help from our SCD patients, this guide is filled with vital information for all those affected by the condition

Retweet & help us spread the word!
https://t.co/1074KshgFU

[Aaron Logan, MD, PhD, MPhil @hemedoc]

#HSMtg2023 Kumar: not everything meeting HLH-2004 criteria is HLH. Think about other possibilities (viral infxn, lymphoma) @HistiocyteSoc

[Sickle Cell Society @SickleCellUK]

Monday is #WorldSickleCellDay. This year we are “Celebrating Progress” to highlight recent progress made in medical advances for #sicklecell, improved standards of care (via our No One’s Listening campaign) and awareness to talk about topics like Priapism. https://t.co/UEbHpLcsn2

[Sickle Cell Society @SickleCellUK]

Did you know that most males with sickle cell anaemia (HbSS) will likely experience a #priapism in their lifetime?

Check out our guide to Priapism, including our new educational animation. Pls share.

https://t.co/UEbHpLcsn2

#sicklecell #sicklecellawareness #wscd23

[DrMagborAkanni @MagborAkanni]

@modeldoc @emory_heart @ABCardio1 @GradyHealth @EmoryatGrady @EmoryDOMRyse @EmoryDeptofMed @EmoryMedicine @SharonneHayes @DrJMieres @gradydoctor @CarlosdelRio7 Congratulations my friend. So proud of you 👏🏾👏🏾👏🏾🎉🎉🎉

[DrMagborAkanni @MagborAkanni]

@tobyeyre82 Congratulations Toby 🎉

[BSH - Haematology @BritSocHaem]

The NHS must redesign the operating model of sickle cell services, according to a new report into the experiences of people living with the disease.

Read the latest #BSHNews story: https://t.co/TA3gh5xagG

[Ayesha Zia @AyeshaNZia]

I'll shout from the rooftops if I have to:

Do NOT refer to individuals or persons or patients with #SickleCell disease as "sicklers."

It's offensive!

Overheard this in the hallway while rounding. I addressed it immediately, but I am still annoyed.

CC: @DrJessGarcia

[NHS England @NHSEngland]

If you're of Black African or Black Caribbean heritage, you're more likely to have a blood type used to treat sickle cell, the fastest growing genetic condition in the UK.

Start your year by doing something amazing — visit https://t.co/yP8Qu0rS1q and sign up to #GiveBlood. 🩸