A little child needs very rare blood for cancer. The world helps him find it



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The biopsies and blood tests were completed, and Zenaab Mughal's blood pressure explained that her parents had a sudden impact on the problem in their daughter's cancer fighting. So if the two years of age were alive, it would take something that had no control over it: Rejoice strangers.

Zainab, who lives in Florida in the US, has been confirmed in October with neuroblastoma, aggressive cancer that will usually happen in children. The doctors said the tumor had been growing inside her; inside Zainab for almost half of her life. He had to attend two bone marrow remodeling and a series of robots to complete her blood supply again because cemotherapy has been carried out; avoiding the disease, doctors said.

"The results came in and the results were really bad," said her father, Raheel Mughal, in a video. "We were all shouting. This was the worst thing we expected."

There was another big problem: Mughal and his wife were tested to see if they were supporting blood. No. A procession of family and friends went into the hospital to be picked up with threads. Not fortunate.

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"And that's when it came to be a warning warning," said Mughal.

Toddler Zainab needs to move blood as chemotherapy to & # 39; flowing into a tumor.

PARLIAMENT / POST WASHINGTON

Toddler Zainab needs to move blood as chemotherapy to & # 39; flowing into a tumor.

Now, two-year-olds are at the heart of world-wide research to find out as rare as possible their blood, a battle that is the responsibility of statistics and their parents seem to have grown know him.

The most susceptible blood of a Pakistani, Indian or Iranian descendant, according to OneBlood, is the unprofitable blood center that is the research guide. But even in these numbers, less than 4 per cent of people suffer blood from Zainab's body.

Most people do not have to go to; Strive to the world that is often hiding of rare blood movements.

There are about 360 different antigons on the surface of red blood cells, but most people do not react directly to these features, said FriedBill Bright, an OneBlood advocacy manager. For most people, it's a & # 39; Getting the right blood type is what matters.

But a small number of people – including Zainab – a & # 39; make antibodies in attendance or not doing special antigan, asking for a & # 39; body to refuse blood. But these people still get into accidents or to # 39; come down with diseases like everyone else, so there is a network of blood centers that rarely specialize in blood, maintains a database of tight combinations of antibodies and moving across the country to patients who need it.

That's a great deal in Bright work. It is part of a team that works around a clock, 365 days a year, to identify rare and uninstalling blood units and, where possible, to achieve applications. Despite this, the Zainab case is so rare that Bright needs to work in the & # 39; business for 20 years – go to textbook to learn more about it.

Now, OneBlood is working with its American Affordable Program, an organization that is The link of patient donors with worldwide use. For Zainab, three matching donors were found – one living in London, and the other two in the United States.

That is a promising sign, but it is not enough. Rules constrain the frequency of blood donors. Zainab doctors have to settle up to 10 donors to make sure she gets it when Zainab needs blood.

The remedy of a remedy that doctors are saying is that Zainab's tumor is already in decline.

More than 1000 people of Iran, India or Pacastani have given blood in an effort to see if they are consistent with Zainab.

But her parents and team of experts understand that it is not until Zainab gets out of hospital, cancer is free. So they have launched a sensory campaign to use the best weapons; : the story of Zainab, and an unfinished stream of delightful – sometimes without tooth – a child's pictures. One of them shows a & # 39; a castle with a birthday cat and a pig-dotag cloth, another guys show her; Apply for a picture with superficial dress and flowers and ribbons. A third, post-diagnosis, which shows large eyes of brown under a bald head.

It is still too young to understand how often & # 39; she has exhausted her or her great ventures. But her father hopes to explain her one day as she helped a group of people who were unaware of their life.

"It's a humiliating demand, and I want it from my heart," said Mughal in a video made by OneBlood. "My daughter's life is heavily dependent on the blood …

"What you are doing to save human life, to save my daughter's life, it's amazing. When my daughter's appearance, I remember to have tried to save your life. "

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