Walsall siblings' stomachs removed over cancer risk


Sophia Ahmed, Omar Khan and Tahir KhanImage copyright
Sophia Ahmed

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Sophia, Omar and Tahir all opted to have their stomachs removed after finding out they had a cancer gene

Three siblings have had their stomachs removed after testing positive for a cancer gene following the deaths of their mother and sister from stomach cancer.

Tahir Khan, 44, Sophia Ahmed, 39, and Omar Khan, 27, from Walsall, underwent the surgery after a series of tests at Addenbrooke’s Hospital in Cambridge.

They said the operation had saved their lives and “eliminated” the risk.

However, Tahir’s daughter has now been found to have the same gene.

The siblings’ mother, Pearl Khan, was 49 when she died 16 years ago, six months after she was diagnosed.

Their 32-year-old sister Yasmin Khan died about six years ago.

Tahir said: “We didn’t even think about genetic testing at that time but Sophia was very tenacious and worked with Cancer Research UK to get us all tested.”

The screening and tests for all four of the remaining siblings, including their other sister Tracy Ismail, 49, took from about 12 months to three years.

‘Totally devastated’

They identified three of them were carriers and each decided to undergo the operation as a preventative measure. Sophia had the operation first, followed by Tahir and Omar.

Tracy, who was the only sibling to find out she did not have the gene, said: “They told me my results first, so I just thought we would all be the same.

“It was very bittersweet. I was totally devastated.

“At one point we were told that if we hadn’t had the testing done, I’d be the only sibling left.

“Knowing what my mom and sister had gone through and so quickly, I encouraged them to have the procedure done, and they’re all still here.”

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Sophia Ahmed

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The siblings’ mum Pearl Khan and sister Yasmin Khan both died from cancer

Sophia said: “I read in my sister Yasmin’s notes in hospital that they thought it may be genetic so I did some research and found out the hospital in Cambridge was doing a study with Cancer Research so I contacted them and went from there.

“Everyone thought I was mad until we had the results come back and when we saw it was three of us out of the four, I knew it was worth it.

“I have nothing but positive things to say about it, I can still eat and do everything, the only issue is maintaining my weight and my vitamin deficiencies but in comparison to having stomach cancer and a few years to live, I can’t complain.

“I even had a baby after the operation, they thought I might be malnourished or the baby would be tiny, but everything was absolutely fine.”

Now, the food the siblings eat goes into a “small pouch” that was made by connecting the oesophagus to the intestine.

“I used to be 15st but now I’m only just over 10,” Tahir said.

“I have to graze constantly because my body just can’t get the nutrients it needs otherwise.

“My brother, on the other hand, he still eats like a horse!”

‘Best decision’

Omar has a different view of the procedure.

He said: “At first after everything with my mom and sister I didn’t want anything to do with hospitals or doctors or anything like that.

“But seeing my Sophia go through the procedure and have a baby afterwards, I thought ‘I’ve got no excuse’.

“It was a really hard decision for me but it was the best one I’ve ever made.

“I still can eat whatever I like – burgers, steaks – the only thing I get is exhaustion and cold sweats but I’m still breathing and I’m so thankful for that.”

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The screening and tests for all of the siblings took from about 12 months to three years

However, Tahir’s daughter, Farah, who is 21, has since tested positive for the gene too.

He said: “I am worried about my daughter’s future, but I say to her we have all gone through it and are fine now, so whatever happens she’ll be OK.”

Tahir underwent his surgery five-and-a-half years ago after his test found he had clusters of cancerous cells in his stomach lining.

“They said I effectively had cancer but because it was contained in my stomach lining and I had all that removed, it eliminated it. I could have had only days, weeks, maybe a year maximum left before I would have been diagnosed with terminal cancer.

“There’s no doubt in my mind that having the tests and the procedure done saved my life.”

Dr Marc Tischkowitz, consultant physician in medical genetics at the University of Cambridge, said: “This is a very rare, specific type of stomach cancer.

“It’s a gene that carriers can have for their lifetime and means that they are at risk of developing cancer any time.

“We do offer total removal of the stomach as a preventative measure.

“It is a dramatic life-changing procedure and of course there is no way of knowing in all cases that the person who carries the gene will 100% have developed cancer in their lifetime.”

Georgina Hill, from Cancer Research UK, said: “It’s estimated only 3-10% of cancer cases are linked to an inherited faulty gene.

“Anyone worried about their genetic cancer risk should talk to their doctor, who can refer those with a strong family history of certain cancers to a genetic counselling clinic if appropriate.”

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