A World without Sickle Cell Anemia

A World without Sickle Cell Anemia This page support Sickle Cell Awareness, educates and brings hope to families affected by this devastating disease.

Sickle cell disease and thalassemia are genetic disorders caused by errors in the genes for hemoglobin, a substance composed of a protein ("globin") plus an iron molecule ("heme") that is responsible for carrying oxygen within the red blood cell. These disorders can cause fatigue, jaundice, and episodes of pain ranging from mild to very severe. They are inherited, and usually both parents must pass on an abnormal gene in order for a child to have the disease. When this happens, the resulting diseases are serious and, at times, fatal.

Tommy's is proud to support Black Maternal Mental Health Week 2025, led by The Motherhood Group.This year’s theme is Mak...
01/10/2025

Tommy's is proud to support Black Maternal Mental Health Week 2025, led by The Motherhood Group.

This year’s theme is Make Black Mothers Visible.

Data has shown Black women are more likely to experience perinatal mental health problems, yet less likely to receive support. And, only 13% of Black women with mental health issues during pregnancy or after birth seek help, compared to 25% of White women.

Together, we want to change this:
https://www.justgiving.com/page/peace-adetoro

24/09/2025

A powerful new story about a London schoolgirl’s journey of living with sickle cell has been brought to life in My Blood, Your Blood — a children’s book commissioned by NHS Blood and Transplant (NHSBT).

Inspired by the real-life experiences of 10-year-old Angel Salami from Sydenham, the book will be gifted to all Brixton primary schools this September during Sickle Cell Awareness Month 2025.

Angel says:
💬 “I feel really good that the book is based on me, as people can learn what it is like to live with sickle cell and maybe be inspired by me. I hope the book makes more people want to give blood donations and learn more about sickle cell from a young age.”

🩸 This book is more than a story — it’s a step towards recognition, awareness, and inspiring future generations to support those living with sickle cell.

Read full update online.

In aid of Sickle Cell Awareness, I did an interview with the BBC last Thursday and it also aired on the BBC 3 Counties R...
15/09/2025

In aid of Sickle Cell Awareness, I did an interview with the BBC last Thursday and it also aired on the BBC 3 Counties Radio.
https://www.bbc.co.uk/news/articles/ce9r82xjglgo

Luton and Dunstable University Hospital is seeking about 12,000 new blood donors.

Please watch and share this devastating documentary about Sickle Cell Disease. My heart goes out to Sam and I am using t...
10/09/2025

Please watch and share this devastating documentary about Sickle Cell Disease. My heart goes out to Sam and I am using this platform to send my condolences. 🙏

What is Sickle Cell? Well Sickle cell is one of the most common inherited blood conditions in the world yet so many people still don’t know what it really is...

19/05/2024

I gifted the Duchess of Sussex 6 yards of the A*o Ebi we were wearing and my book, A World Without Sickle Cell.
Two very important causes for me. The A*o Ebi we are wearing is the Invictus Games colours and a very brief conversation about Sickles Cell Awareness with the Duchess. ❤️

From today, thousands of people with sickle cell disorder and thalassaemia in England will have access to a world-first ...
22/01/2024

From today, thousands of people with sickle cell disorder and thalassaemia in England will have access to a world-first ‘blood matching’ genetic test on the NHS to better match their future blood transfusions, reducing the risk of side effects and offering more personalised care.

The NHS is the first healthcare system in the world to provide a new blood group genotyping test which is set to transform care for patients living with sickle cell disorder and thalassaemia, with almost 18,000 people in England now being eligible.

The tests will be carried out at NHS Blood and Transplant’s (NHSBT) Diagnostics department in Bristol.

Live-saving transfusions are commonly used to treat rare inherited blood disorders, but around a fifth of patients develop antibodies against certain blood groups following transfusion. They can then experience delays to treatment due to the difficulty in finding enough matching blood and sometimes blood transfusion reactions.

To help improve blood-matching and reduce the risk of antibodies developing, NHS England, in partnership with NHSBT, is encouraging patients with sickle cell, thalassaemia and transfusion-dependent rare inherited anaemias to have this test taken alongside their routine hospital blood tests.

In England, there are around 17,000 people living with sickle cell disorder, with 250 new cases a year. The disorder can result in severe organ damage and intense pain if damaged red blood cells block vessels and restrict oxygen supply – it is more common in people of Black African and Caribbean heritage.

People with thalassaemia cannot produce enough haemoglobin, which is used by red blood cells to carry oxygen around the body, causing severe anaemia, which can be fatal if not treated. Thalassaemia is mainly seen in those with an Asian, Middle Eastern, or Southern Mediterranean heritage.

The blood group genotyping test will also help patients living with transfusion-dependent rare inherited anaemias, such as Diamond Blackfan Anaemia, a disorder that affects people’s production of red blood cells.
To learn more about this testing, please visit our website. If you have any questions, please contact our team at PublicAffairs@nhsbt.nhs.uk.

My 15th Blood Donation of my special RO blood. If you can donate blood, please do so. RO blood subtype is used to treat ...
24/11/2023

My 15th Blood Donation of my special RO blood. If you can donate blood, please do so. RO blood subtype is used to treat all chronic diseases like Sickle Cell.
Giving Blood Saves Lives.

I attended ASCAT 2023: 18th Annual Sickle Cell & Thalassaemia Conference in collaboration with EHA & BSH. It was a 3 day...
30/10/2023

I attended ASCAT 2023: 18th Annual Sickle Cell & Thalassaemia Conference in collaboration with EHA & BSH. It was a 3 days conference, I was at the Corporate day and the Gala. I am so looking forward to the next one, I met so many inspirational people.

June the 19th is World Sickle Cell Day. Today I went to donate my special Ro blood. Ro blood is used to help cure all ch...
18/06/2023

June the 19th is World Sickle Cell Day. Today I went to donate my special Ro blood. Ro blood is used to help cure all chronic diseases like Sickle Cell Disease. I have done my good deed for today and its now time to put my feet up and relax. You can also do a good deed, blood donation, Saves Lives.
NHS Blood Donation

My mission is accomplished for today. I have donated my special Ro Blood and someone with Sickle Cell Disease will be th...
09/10/2022

My mission is accomplished for today. I have donated my special Ro Blood and someone with Sickle Cell Disease will be the recipient.


September is Sickle Cell Awareness Month. Let's get Sickle Cell Aware. There is an urgent plea for black blood donors, h...
01/09/2022

September is Sickle Cell Awareness Month. Let's get Sickle Cell Aware. There is an urgent plea for black blood donors, help the Sussex Squad to spread the word.

Checkout my new Website, I have partnered with the NHSBT to encourage black and brown people to donate blood. Book your appointment through my website. Giving blood saves lives.

aworldwithoutsicklecell.org

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21/06/2022

All in aid of World Sickle Cell Day.

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