- Hannah says Alfie is being put at risk because of bureaucracy
- She teamed up with Professor David Nutt for a recent BMJ article
- He urges medical community to embrace cannabis like it did penicillin
Alfie Dingley, who has severe epilepsy, was one of several high profile cases that helped bring about the legalisation of medicinal cannabis.
After the boy became the first person in the country to be granted a licence for the drug last June – as a special case before the law change – his mother revealed how he was living seizure-free and learning to ride a bike.
But now the eight-year-old has grown used to the strain of the treatment and has begun to have fits again. Hannah Deacon says her son needs a new strain to be able to cycle between two products to overcome his tolerance – but because of the UK’s strict rules importing it into the country could take months.
It has lead her to post a tearful video to Twitter to beg for change in the system.
“The receptors get dulled by the same strain of THC and CBD,” she told i. “It’s a well-known thing to happen. Alfie has an NHS prescription but the red tape to get a new product into the country will take time and meanwhile I have to watch my son suffer.
“My little boy is being put at risk because of bureaucracy. Cannabis is now legal but access to it really needs to improve.”
Please RT we need some help! pic.twitter.com/eQfxeJRvoA
— Alfie’s Hope – Hannah Deacon (@Hanseizuremum) May 16, 2019
New licence needed
Alfie, who had his first fit when he was just eight months old, has a rare form of epilepsy which affects just nine children in the world. It can cause up to 30 seizures a day or ‘catastrophic clusters’ of’ fits which are unresponsive to anti-epilepsy drugs.
Before he tried cannabis, the youngster had been pumped with steroids his whole life that were making him aggressive. His family feared his fits could cause him lasting brain damage.
But when taking the Bedrocan strain of cannabis oil his seizures dropped to zero, or sometimes one a month.
“We know cannabis works, and is the only thing that works,” said Hannah. “Alfie is still doing so much better than he was. Since March he’d had three cluster attacks of around eight seizures each time, so nowhere near as many or as severe as before. But it could get worse.
“Cannabis gave my son 11 months of an amazing life and with his products mixed up that will continue.”
Hannah, from Kenilworth in Warwickshire, says changes to her son’s medication will all have to be approved through a new licence.
“The importer will have to apply to the Home Office for approval, and then order it from the supplier. I will keep on fighting for my son to have what he needs but I shouldn’t have to. It’s very frustrating.”
Attitudes slow to change
In a paper published in the British Medical Journal (BMJ) earlier this month, Professor David Nutt warned that despite the law change last year, access to medical cannabis in the UK has been much slower than patients and their families had hoped.
The neuropsychopharmacology expert from Imperial College London argued that still only a small number of children with severe juvenile epilepsy are being treated with it.
In the paper, which is linked to an article written by Hannah, Professor Nutt argues that cannabis is the oldest medicine in the world Cannabis and its prohibition was relatively recent. It was believed Queen Victoria used cannabis medicines, particularly for period and childbirth pains, he said.
Although it was first made illegal in the UK in 1928, it was still allowed to be prescribed by doctors until 1971 when the when the Misuse of Drugs Act prevented its use medicinally.
Following Hanna’s high profile campaign, in June the Home Office announced a U-turn and a few months later, on 1 November 2018, the law was changed and cannabis products were allowed to be prescribed by specialist doctor, or a GP acting under the instructions of one.
Yet many children with severe, uncontrolled epilepsy continue to suffer because neurologists won’t prescribe, argues Nutt. He cites lack of training, fear of prescribing off licence, refusal by some to pay, and difficulties obtaining supplies from foreign producers as potential reasons.
Regarding the argument the long-term effects of cannabis on conditions like severe epilepsy in children have not been fully ascertained, Nutt points to penicillin, which he says is another natural medicine that was welcomed by UK doctors even though there had been no trials of its effectiveness.
“We must hope the situation will improve,” he wrote. “If today’s medical profession could embrace cannabis in the same way as it did penicillin then the true value of this plant medicine should rapidly be realised.”
Patients still forced to break the law
Hannah works with the campaign group End Our Pain, which is currently supporting 16 families in desperate need of medical cannabis prescriptions.
She is also involved with the Medical Cannabis Clinicians Society which has been set up by neurologist Professor Mike Barnes to educate doctors about cannabis medicine. It aims to provide quality, balanced educational programmes in order to inform clinicians about the current state of evidence with regard to the efficacy of cannabis, its side effects and dosages.
Hannah says many other children in similar situations have not been able to access these medicines, even though they are now legal.
“The Home Secretary acted quickly to change the law which was great, but it was done without any planning, education or understanding of patient needs,” she said.
Read more: Epileptic girl, 2, who has been prescribed medicinal cannabis still can’t get it on the NHS – leaving her father paying £1,000 a month for a private supply
“Patients thought they’d be able to get the prescriptions they need. I feel sorry too for the clinicians being bombarded by desperate patients because they’re not educated enough about cannabis to feel they can safely prescribe it.
“I know people who are paying £500 for a bottle privately when it costs €178 (£155) in Holland.
“They are either having to break the law and import it from Holland or follow the law but pay thousands for a prescription from a private doctor. It’s a disgrace.
“I acknowledge that the NHS is underfunded, but the costs of long term care for children damaged by epilepsy far outweighs those of a product that could give them a life worth living.”
i has approached the Department of Health and NHS England for comment on these issues.
Full story is available here.