A Mississippi woman's life has been transformed by a treatment for sickle cell disease with the gene-editing technique CRISPR. All her symptoms from a disease once thought incurable have disappeared. https://t.co/1bQpa98O4J
I’m delighted to have been accepted unto the UN Women UK delegation for this years Commission on the Status of Women. In the process of my application, my aim was to show that having sickle cell is not a barrier to doing & aiming for the best. Happy IWD to all my women!! 💜💜💜
Very very proud of this project! @BlackGirlFest teamed up with @GiveBloodNHS and invited ten amazing women and their mothers to discuss blood donation and the need for more black donors. https://t.co/SSInLa68el 💉❤️
We’re excited to be teaming up with @GiveBloodNHS for the release of Black Panther: #WakandaForever, working together to inspire more people to give blood, bringing to life the power of community that Wakanda represents.
Learn more ➡️ https://t.co/i6LxbtwuxG
#InOurBlood
*WE NEED MORE BLACK BLOOD DONORS*
Sickle cell disease is the fastest-growing genetic disorder in the UK, affecting Black communities in greater numbers. There is a shortage of Black donors, the NHS need 16,000 new Black donors in order to provide better care to those w/ SC.
If someone is having a sickle cell crisis, acting fast saves lives.
Complete the new e-learning module for NHS staff to help you spot the signs of a sickle cell crisis and learn how it should be treated. https://t.co/AD5LNjW1zW
Just booked an appointment to donate!!
Reminder that you CAN donate blood if you have sickle cell trait (I was incorrectly told for years that I couldn't)
Today is one year since the government announced the removal of a discriminatory blood donation rule affecting Black people of African heritage.
Our EDI Director Glenda Bonde reflects on the change and how we can encourage more Black donors to come forward. #BlackHistoryMonth
Women of colour who have had a mastectomy are for the first time to be offered soft prosthetics (“softies”) in their skin tone. @nubianskin, a #BlackOwned lingerie and hosiery brand, has partnered with The Royal Marsden hospital to develop the product 🤎 https://t.co/7xIVDztf6b
A Voices piece from me to end Sickle Cell awareness about navigating dating with my now wife who’s a sickle cell carrier.
As I write in the piece it’s not the sexiest dating chat but it was an eye opener for me and discussing early on really helped.
https://t.co/pFXmkd47s5
Eva Barnard fought through fatigue and pain, but now she has a name for her condition and wants others to understand the symptoms. #sicklecell https://t.co/5M44UXIY3f
September is Sickle Cell Awareness Month & as I sat for my latest donation I remember when I first found out I'm a R0 Subtype Donor (my donations go to people with Sickle Cell Disease).Pls consider blood donation 💉🩸 @NHSBT@acltcharity@SickleCellUK#SickleCellAwarenessMonth
If someone is having a sickle cell crisis, acting fast saves lives.
Complete the new e-learning module for NHS staff to help you spot the signs of a sickle cell crisis and learn how it should be treated. https://t.co/AD5LNkdCYw
The Queen died peacefully at Balmoral this afternoon.
The King and The Queen Consort will remain at Balmoral this evening and will return to London tomorrow.
'If it was any other illness affecting white people, we would not be getting this treatment.'
Thank you Stephanie for sharing what it feels like to have a sickle cell crisis and your experience of seeking help. #SickleCellAwarenessMonth