‘Please let me have my medicine’

Abi Longfellow and her parents Andy and Jo.

Abi Longfellow and her parents Andy and Jo.

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A 12-year-old girl has been denied potentially life saving drug treatment - despite it being locked in a cupboard in the hospital where she is treated.

Abi Longfellow suffers from a one-in-a-million kidney disease called Dense Deposit Disease (DDD), which stops the kidneys from filtering waste from the blood.

A petition set up by her parents, Andy and Jo Longfellow, to get her the drugs she needs has been signed by more than 160,000 people.

And Abi wrote a heartfelt letter to Prime Minister David Cameron asking for his help.

But health bosses will not pay for the Eculizumab drug, which costs £393,000 a year, because her condition is too rare to be covered by the national funding policy, but not rare enough to qualify as an exceptional case.

Mr Longfellow, 45, said the family want the NHS to fund five dosages to see if it works.

He said: “It could mean Abi could be a normal teenager again. She would be able go back to school and hang out with her friends.

“It could totally transform her life.

He added: “We are not asking the NHS for a miracle but to reconsider and give our daughter the medication she needs.”

Abi, of Robin Hood, was diagnosed with the disease aged 10 when a trip to A&E for a throat infection revealed she was suffering from the kidney disease.

She now spends 10 hours a day at home on a dialysis machine and it means she cannot return to school full time.

And the drugs which could help change her life are kept under lock and key in Leeds General Infirmary where Abi is treated.

A spokesperson for NHS England North said: “These are incredibly difficult situations, but in this case doctors and medical experts decided that it would not be right to fund a treatment that hasn’t been proven to work for patients in these circumstances.”

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