Relief As Doctors Now Have Permanent Cure for Sickle Cell Anaemia

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Doctors at the University of Ibadan in partnership with the University of Illinois, Chicago, USA and University of Loyola, Chicago have discovered a permanent cure for Sickle Cell Anaemia.

 

Over five million Nigerians suffer from Sickle Cell Anaemia, a severe hereditary form of anaemia in which a mutated form of haemoglobin distorts the red blood cells into a crescent shape at low oxygen levels.

 

Professor of Medicine, Victor Gordeuk, who is the Director, Sickle Cell Centre, University of Illinois, Chicago, USA and his colleagues, Prof. Damiano Rondelli and Prof. Bamidele Tayo, University of Loyola, Chicago claim the cure is bone marrow transplant.

 

The experts accompanied by the Chief Medical Director, UCH, Prof. Temitope Alonge, Dr Titilola Akingbola, a haematologist and Dr Foluke Fasola explained that the stem cell transplant is a standard procedure for the treatment of many blood cancers in both adult and children.

 

He said “With this chemotherapy-free transplant, we are curing adults with sickle cell disease, and we see that their quality of life improves fast within just one month of the transplant.

 

“About 90 per cent of the approximately 450 patients who have received stem cell transplants for sickle cell disease have been children. Chemotherapy has been considered too risky for adult patients, who are often more weakened than children by the disease.

 

“Adults with sickle cell disease can now be cured without chemotherapy — the main barrier that has stood in the way for them for so long. Our data provide more support that this therapy is safe and effective and prevents patients from living shortened lives, condemned to pain and progressive complications.”

 

“In the new procedure, patients receive immunosuppressive drugs just before the transplant, along with a very low dose of total body irradiation, a treatment much less harsh and with fewer potentially serious side effects than chemotherapy.

 

“ Donor cells from a healthy and tissue-matched sibling are transfused into the patient. Stem cells from the donor produce healthy new blood cells in the patient, eventually in sufficient quantity to eliminate symptoms. In many cases, sickle cells can no longer be detected. Patients must continue to take immunosuppressant drugs for at least a year.”

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9 Comments
  1. Stephany Lmte True Africana says

    How can 1 get in touch with d doctors in charge?

    1. Taiwo Ajani says

      Get their names. Search the internet for their emails at their respective institutions. Write them!

      1. Warren says

        My son is 22 years old he has one brother,different mother two sisters different mother can any of them help him with the stem cell operations. to get cured

    2. Taiwo Ajani says

      You can also google their names for their email addresses.

  2. Gloria says

    I have two brothers with the disease, how can we get in touch with the doctors? I see in the comments below that i should google their names. which site? more information please

  3. Jessica LadyJay says

    This procedure typically requires that the sibling be same mother and father, unfortunately, my Lil warrior doesn’t have that sibling.

  4. Almeda MszKitty Waldron says

    We live in a technology world but people still don’t know what sickle cell is my last 3 girlfriends didn’t have a clue what it was till they met me alot of ppl will still say what is that or is it contagious no dummy it isn’t and it’s not taught in all schools cuz it was never taught in any school I went to

  5. Ja-Quanda Boston says

    My uncle died on Mother’s Day 2014 the doctors said that he was pose to die at age 19 or 20 but he was 41 if this would’ve been 2years ago he would still be here LIP UNCLE ????❤️?? no more pain

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