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Alberta woman 1st adult in Canada to be ‘cured’ of sickle cell anemia through stem cell transplant

CBC | Revée Agyepong of Edmonton underwent the procedure at Calgary cancer centre with donor cells from sister

An Alberta woman is the first adult in Canada to be cured of sickle cell anemia with the help of a sister’s love — and a stem cell transplant.

Revée Agyepong
Revée Agyepong, 26, of Edmonton was diagnosed with the disease as a toddler and has never known life without it.

“I remember as far back as elementary feeling sickle cell complications and not knowing what it was,” she said.

“I thought that everyone would go out for recess and play, then come back with a terrible headache and body pain, couldn’t breathe … eventually I realized it was just me.”

Sickle cell anemia is a genetic disease in which red blood cells change into a semi-circular shape and block blood vessels. Symptoms vary from patient to patient but it puts every organ in the body at risk.

Agyepong’s disease manifested as chronic bone and joint pain, irregular heartbeat, kidney stones and shortness of breath.

Successfully treated in kids
Two years ago, the Alberta Children’s Hospital announced it was successfully treating sickle cell disease in pediatric patients using stem cell transplants.

Agyepong said when she found out about the success of the treatment in pediatric patients, she was at a point where her health was declining and she was running out of treatment options, but doctors told her she was too old to undergo the procedure.

She was devastated.

According to Alberta Health Services, the older the patient and donor in bone marrow transplants, the greater the risk of graft versus host disease, which is a type of immune rejection that can have serious health repercussions and can even result in death.

But Stephanie Amoah, Agyepong’s older sister, said she could no longer watch her sister struggle in constant pain and started to research which other centres were testing the treatment on adult patients.

“My sister has always been my protector, my guardian, she found a way,” Agyepong said.

Sister was a 100% match

The sisters approached Agyepong’s doctors and told them of the treatment going on in the east coast of the United States. Dr. Andrew Daly, who leads Alberta’s bone marrow transplant program and oversaw Agyepong’s stem cell transplant, said they had coincidentally been thinking about conducting adult stem cell transplants for sickle cell disease.

Stephanie Amoah, Revée Agyepong’s older sister
“My persistence, my sister’s persistence, and they said my dedication to wanting a cure, was enough for them to just say, you know what, she’s going to be the person, let’s do this,” Agyepong said.

Amoah was tested and was found to be a 100 per cent match for her sister. Daly said the odds of siblings being a perfect match is one in four.

The transplant, which took place at Calgary’s Tom Baker Cancer Centre, involved Agyepong taking drugs to suppress her immune system and doing a course of low-dose radiation. Amoah underwent a process called apheresis that collected her sickle-cell-free stem cells, which were then given to Agyepong.

‘Do the things she’s always wanted’

“Over the past few months, what we’ve seen is that Revée’s sister’s bone marrow has taken over the production of Revée’s red blood cells,” Daly said. “The amount of sickle cell hemoglobin in her bloodstream has decreased almost to zero.”

Today, Agyepong’s blood tests don’t show any signs of the disease, which makes her essentially cured. Amoah said the change she sees in her sister is amazing.

“It’s phenomenal. I’m just so happy to have been part of a process that will give her a new life, a new hope and be able to do the things she’s always wanted to do,” Amoah said.

Agyepong said she is still recovering from the transplant but when she is one year out, she plans to dedicate her time to advocating for the disease, and just live her life like a normal person.

“I want to travel somewhere exotic and somewhere warm and feel dehydration like anyone else would, because I couldn’t with sickle cell, I would be dehydrated and end up in the hospital,” she said.

“It sounds so insignificant but it’s really exciting just to be able to be more spontaneous.”

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  1. And God said: `Let there be light`, and so it happened.
    Let your success, be the start to a new beginning. LUCK.

  2. Fantastic! You got a second chance in life, use it well.
    Thanks to science, research, and luck too..
    Blood is really thicker than wather.

  3. congratulation and Thank you for accepting to be the first to pave the way and Give hope to the Millions praying for a solution.

  4. What could be more patriotic than using some of the nation’s billions to build and equip a center at home and attracting world-class talents to come and perform?

    • Politics of hatred, marginalization, high taxation to see it fail, bottlenecks,
      slander etc etc, will kill the idea and make it look a bad thing.
      You can know, `why black man di sofar today`.

  5. knowledge is power

  6. Epée Dipanda

    Such news is impossible to be had in Larepublique… Increasingly cursed Larepublique du Cameroun

    • Pal,
      Sickle cell anemia is a global problem with a particularly high incidence among the black race, especially those with ancestry in malaria-endemic regions of Africa. It is one of those ironies of nature that what the body developed as a resistance to malaria turned out to be even more problematic than the malaria itself!
      The blood cells containing HbS ( the defective sickle cell hemoglobin) are not attacked by malaria parasites; but by their very distorted nature, they impede blood flow and lead to oxygen starvation in vital organs like the brain. Stem cell extraction and transfer to affected individuals is a wonderful break through because the donor can now manufacture healthy red blood cells containing normal HbA.
      Technology transfer will bring this nearer home to Cameroon.

      • Would’nt it be wonderful if you come here one day and inform us that you have find a vaccin/ cure against malaria?
        Like someone said before: ” If our education is not about gaining real power, we are being miseducated and misled and we will die “educated ” and misled “.
        That is what I call a wasted life.

      • John Dinga @ thankyou for your clear explanation of how this is a very relevent joyous breakthough ,as you say its interesting for cameroon and other countries with the technology transfer ,indeed stories like this make you realise how wonderful breaking health barriers is ,when it happens ( and if it wasnt for the deep belief of these sisters it may of taken many more years to happen)