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“It was like a miracle” – MS sufferer who supplied hundreds of patients with medical cannabis

Diagnosed with MS aged 21, Lezley Gibson supplied medical cannabis to patients across the country.



Lezley Gibson (right) was diagnosed with MS at the age of 21

Over the past 25 years, Lezley and Mark Gibson have supplied £500,000 worth of cannabis-infused chocolate free of charge to MS patients across the country. Having faced prosecution five times, they are now both benefitting from a legal medical cannabis prescription. 

In 1985, at the age of 21, Lezley Gibson was diagnosed with multiple sclerosis.

Her doctors told her that within five years she would be incontinent and in a wheelchair. Thirty six years later, Lezley is neither – and she believes she has cannabis to thank.

“Everything that I’d ever seen about MS was very gloomy”, Lezley said.

“I was destroyed when I was told about the diagnosis.”

At the time, Lezley was in the midst of starting a business, having just opened her own hair salon.

“I had big plans for myself, but then halfway through opening my own salon, I was diagnosed with MS and that was my career over. It’s very difficult to cut hair when you’re shaky and you can’t walk properly,” she said.

“It was a very hard time for me; I found it very difficult. I was your typical 21-year-old. I was into clothes and makeup, I was a hairdresser and I loved people and dancing. But that was the end of that.”


A year after her diagnosis, Lezley met her now-husband, Mark. As a recreational user at the time, Mark introduced Lezley to cannabis and she said the effect it had on her condition was “miraculous”.

“I had never really come across cannabis before, but I noticed when I was with Mark and his friends that I felt an awful lot better, not just because of the relationship but because I was consuming cannabis,” Lezley recalled.

Lezley and Mark Gibson

Prior to taking cannabis, Lezley’s body felt tense and was prone to spasms.

“I never felt very comfortable,” she said.

“My body never really worked properly. But I noticed with the cannabis in my system, my body was calmer, my spasms disappeared and all the other little things faded into insignificance.”

The pain and nausea that she experienced on a daily basis began to fade as well. Meanwhile, her eyesight and speech, which she had begun to lose over the past few years, improved.

At the time, in the mid-1980s there was very little information about cannabis as a therapeutic drug, but Lezley was finding that consuming the plant was having a much more positive effect on her condition than the medications prescribed by her doctors.

“I’m not a fan of drugs of any description… they’re far too strong,” Lezley said.

“They put me on steroids, which made me double in weight and grow a beard, which was fantastic at 21. After that, it absolutely terrified me.

“With everything they offered me, they said ‘it might make you worse’, which wasn’t very appealing. But with cannabis, there weren’t any of the side effects. It was nothing like what the doctors were offering me.”

She added: “The only side effect I found with cannabis was it made me feel quite nice and there are not many things that do. I have MS so I don’t get to feel nice very often.”

As Lezley continued to benefit from taking cannabis, she decided not to keep it to herself. She wanted to make other people with MS aware of its benefits and how it had improved her condition.

Lezley (right) produced cannabis-infused chocolate for other MS patients

In 1995, she was a guest on the popular BBC One chat show, Kilroy. On the show, she met other people like her, including Claire Hodges, an influential activist who campaigned for the therapeutic benefits of cannabis and later played an important role in GW Pharmaceuticals earning its licence to produce Sativex.

Lezley became good friends with Hodges and soon found herself in a circle of fellow MS-sufferers campaigning for the benefits of cannabis. One of these campaigners was Elizabeth Ivol, who was producing cannabis-infused chocolate from her home in Orkney.

Unfortunately, Ivol was raided by the police and soon lost the ability to continue producing the chocolate as her condition worsened. She asked Lezley and her husband, Mark to take over the operation.

The couple found themselves making cannabis chocolate for hundreds of people with MS. The very real possibility of them being raided by the police rarely left their mind, but they were determined to continue helping patients.

“There was success with the people who used our chocolate and this is why we kept going,” Lezley said.

“In one instance a lady from a nearby village wrote me a letter. She’d been bedridden for four years so her husband came knocking on my door to get some chocolate. Within a week of her using the chocolate, she was taking her grandchildren to the park and sewing curtains. It was like a miracle.”

Over a two year period, Mark and Lezley supplied 33,000 bars of THC chocolate, free of charge to MS patients across the country.

Lezley and Mark continued the operation for over two decades

But such a large operation was difficult to conceal from the local police and the couple were raided three times between 1995 and 2003.

“I have a daughter and my poor daughter has witnessed all of this since it began,” Lezley said.

“It was a difficult time. When I did the school run you had all the women standing in little groups and it was definitely them and me. A lot of people thought I was just a ‘druggie’ which I can assure you I am not.

She added: “Even members of my own family had an opinion, but I had to do what I had to do – I had to be well and that was how I was well. If people didn’t believe me then that was their fault, not mine.”

In 2003, a police raid resulted in them being charged with conspiracy to supply £500,000 worth of the illicit chocolate.

It wasn’t their first run-in with the law. In 1999, Lezley had been charged with possession for carrying a small amount of cannabis flower. She successfully pleaded not guilty, arguing that using cannabis prevented an MS attack, with the jury accepting her argument.

This time, they weren’t so lucky.

The judge agreed that what they were running was an ‘altruistic enterprise’ with little to no money made during their time supplying cannabis to MS patients.

But unfortunately, the jury found them guilty and the couple along with a collaborator, Marcus Davies, were sentenced to 18 months in prison which was then suspended for two years due to Lezley’s condition and Mark’s responsibility as her primary carer.

Lezley and Mark kept their heads down for the next 15 years, but after the police were informed of the couple’s cannabis consumption, their home was raided once more in 2019.

Lezley and Mark (left) were found not guilty in 2020.

The police only found three bars of cannabis chocolate for Lezley’s own personal use, but a discovery of Mark’s modest-sized grow room set off another court case.

In between being charged and appearing in court, Lezley became one of the first patients in the UK to receive a medical cannabis prescription, which Mark believes prompted the Crown Prosecution Service (CPS) to rethink their position.

Although Lezley and Mark both freely admitted possession and production of cannabis, the CPS decided not to offer any evidence and the couple were found not guilty in January 2020, a year after being arrested.

“To be found not guilty when you’re not denying any of the facts and you clearly are guilty in the eyes of the law, that’s a real seismic shift,” Mark added.

“We were both prepared to go to court, run it to the jury and stick to our principles and our staunch refusal to plead guilty. However tiring it is, sometimes you just have to stick to your guns and say you’re not going to bend.

“We did absolutely nothing wrong but treat our illnesses with an herbal remedy.”

Mark and Lezley both have a legal medical prescription now and although they believe things are headed in the right direction, they remain critical of a system that shuts many people out.

Mark continued: “What we’ve got now is what I would call economic legislation. Those who can afford it can have it, and those that can’t afford it can’t have it and that’s wrong.

“How is it fair to prosecute somebody around the corner who is medicating for an ailment and bought the cannabis illegally because they can’t afford the consultancy fee and prescription?”


“I could be a better father with cannabis as my medicine”

Dad-to-be can only afford to fund his prescription for two more months.



Leigh Hardwick lives with chronic pain and mental health issues.

Dad-to-be, Leigh Hardwick believes his medical cannabis prescription will allow him to be a better father when the time comes, but unable to work to sustain the crippling costs, he faces a future reliant on opioids.

Fifteen years ago, Leigh Hardwick, was the victim of a violent attack.

In the early hours of the morning at the front door of his flat, he was hit on the head 20 to 30 times with a brick at the hands of a stranger. 

At the hospital he was cleaned up and X-Rayed, but was never given a brain scan or offered any psychological support. He was sent home a few hours later with four stitches and a prescription for a packet of painkillers.

No one was ever changed with the attack, but the incident changed the course of Leigh’s life.

He experienced horrendous night terrors and turned to drink and drugs to self-medicate for symptoms which he now knows to be a result of PTSD.

The “impulsive behaviour” and a “lack of self control” he describes at the time, led to him getting in trouble with the police and serving two years in prison for drug-related offences.

“The mental health issues all started at the attack. The anxiety, depression, PTSD, addiction and recreational drug use was accelerated massively by my self-medicating to cope with the PTSD symptoms that I didn’t understand at the time,” says Leigh, now 36. 

After experiencing pain since birth, Leigh had been diagnosed with idiopathic scoliosis at the age of 23. He used his time in prison to focus on his health, exercising and attending counselling where he was then diagnosed with PTSD.

But after injuring his back through training he was prescribed codeine, which he pinpoints as the beginning of his problem with pharmaceuticals. 

Upon release I worked hard but I had struggled mentally to adjust,” he recalls.

“After losing some very close relatives I had trouble sleeping again and started to abuse sleeping tablets and benzodiazepines for anxiety.

“My work was being affected and I had a six month absence due to panic attacks and stress, including suicidal thoughts. I was put onto anti-depressants, but nothing improved.”

Leigh sought help through his GP, but despite his scoliosis, doctors decided to detox him from all of his pain medication.

“Because of the addiction and part-substance dependence on the diazepam, it was treated as though every substance I was using I was addicted to unnecessarily. When actually, some of them were needed,” he says.

Leigh was prescribed the opioid substitute, Buprenorphine, leaving him with no pain relief.

Leigh Hardwick has had a legal prescription since January.

“It was horrendous, I was in agony, but received no counselling or support and was continually disbelieved about the pain I was in,” he says.

“I was treated like an addict when really I needed a pain clinic.

“It’s very difficult once you are involved in a drug detox service you’re then tarred with that brush.”

Due to his pain, Leigh was unable to work and over the next few years his mental and physical health deteriorated.

After two years trying to get a referral he detoxed himself from Buprenorphine and a few months later re-presented to the doctor, clean but suffering debilitating pain.

He was referred to rheumatology for tests and a neurophysiological scan and his pain was treated with a cocktail of drugs including, dihydracodeine, gabbapentin and diazepam.

“I was back in front of him in agony, needing scans and painkillers, and so I started back on the carousel,” says Leigh.

“All together, I was prescribed 22 tablets per day at one time and I stuck to my prescriptions but I felt like a zombie. My symptoms were barely under control and I was unable to attend work most of the time. 

“Over the four years I was taking these medications I lost touch with myself.

“The combination left me ‘existing’ but with no quality of life. I’d decided the world was better off without me and had zero interest in living.”

Then last year, Leigh’s wife and partner of 11 years, shocked him with the news that she was expecting their first child. 

He aimed to get completely clean, using Rick Simpson Oil and THC flower illicitly to cope with the withdrawal symptoms, while he reduced his other medication. 

Cannabis helps with pain, but also with sleep, the muscle twitching and the IBS symptoms. It definitely helped me through the process,” he admits.

“I had no idea medical cannabis was legal at that point, until someone mentioned Project Twenty21 in a group chat, but I put off looking into it for fear of disappointment.”

In January of this year, Leigh had his first consultation with a leading pain specialist at The Medical Cannabis Clinics.

“In my initial consultation I was understood, I was listened to and treated like an adult. It was a really refreshing experience,” he says.

“It is not a cure. I’m not jumping around, by any means. I do still suffer pain most days and struggle with mobility, but it’s more about the lack of side effects from the other drugs that I was taking.”

But unable to work and relying on disability benefits, funding the monthly £680 private prescription long-term, is unsustainable for Leigh, even with the support of Project Twenty21.

His wife currently supports him with her income, but he only has enough savings for around two more months and has already had to go back on some of his prescription drugs to help reduce the costs.

Leigh also has to fund private mental health support and counselling, as he is no longer able to access NHS services due to his previous drug use.

“It’s just a matter of time until we’re unable to afford it anymore,” he says.

“If money wasn’t an issue and I could access as much cannabis as I need for my conditions, I believe I could probably function as a normal human being in society, albeit with pain issues.

“I could probably go back to work, if it was a part time job where I sitting down.”

He fears that if he has to go back to relying solely on opioids and depressants, he won’t be able to be the father he hopes to be to his soon-to-be-born daughter.

“My main focus and priority now is being the best father that I can be,” says Leigh.

“The best way that I can do that is with cannabis as my medicine. It’s definitely the way I am most in charge of my thoughts and the most competent.

“Previously, I was totally disinterested in life. I had a consistent mantra in my mind, that was, if anything goes wrong, at least I can kill myself. I was on the verge of that for years, but that option is gone now, because I’ve got a child and that’s also not what I want for myself or for my family.”

He adds: “The worry is, if I reduce the cannabis and take on other medications I may become disconnected again and that will emotionally close me off.”

During lockdown this year, Leigh connected with other medical cannabis patients and helped set up an online support group. 

Along with his co-founders, Sylv, Ryan Holmwood  and Dominic Stenning, he guides others through the process of approaching healthcare professionals and accessing a prescription, as well as campaigning for ‘fair access’ to cannabis-based medicines on the NHS and to change societal and cultural views.

But supporting other patients has had benefits for Leigh too, giving him something positive to focus on. 

“I’ve contributed to negativity to society and I suppose this is my way of trying to make reparations for that, to try and swing the karma balance back a bit,” he adds.

“I’m really thankful to everyone we’ve supported, for their feedback and ongoing help that’s given me so much over the last four months. 

“I don’t think there’s anything better you could do, than to help disabled people live a better life.”

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Jane West – The mum who was fired for using cannabis built her own empire

The entrepreneur and founder of Women Grow is determined to change the narrative around cannabis



Jane West was fired from her job in 2014 after hosting cannabis-friendly events

Made famous by her high-end cannabis-friendly events, Jane West was fired from her corporate job for consuming on TV. Now at the helm of her own cannabis empire, she is determined to change the industry narrative.

Jane West’s ideal Friday night is putting on a cocktail dress, going to a fancy restaurant or event and “getting high”.

“I’m an avid cannabis consumer,” she tells me from her home in Colorado, where cannabis has been legal for recreational use since 2012.

“I see it as part of a wellness routine.

“If I’m going to get a babysitter and go out on a Friday night and spend $100 at an event, I want to get dressed up and be fancy and also be high.”

In 2014, alongside her corporate job, West launched her own cannabis-friendly events, where adults could get together to consume socially.

The events took place in private art galleries, with live music and even hosted a fundraiser for the Colorado Symphony Orchestra held at the famed Red Rocks amphitheatre with 5,000 guests.

They also attracted international media coverage. A reporter from the UK Telegraph attended the first one, with the Daily Mail later describing them as ‘sophisticated cannabis soirees’ with ‘foodies for munchies’. 

At her second event, a clip of West unashamedly telling the camera; ‘I’m a mum and I use marijuana, and that’s okay’ was so newsworthy it made the five o’clock evening news. 

West was fired from her job when her bosses saw the clip.

“I’ve never been fired from everything in my life and I have had a job since I turned 15, so to have a career where you have a salary end like that was dramatic,” she recalls.

“I definitely did not intend that to happen, at the time was that people thought I was trying to get fired.

“The fact that the woman hosting the weed events got fired from her job became a whole new story.”

West founded networking group Women Grow to promote diversity in the industry

Even though cannabis is legal and easily accessible for many in Colorado, residents are not permitted to consume it publicly.

As West puts it: “Even though everyone has access to it, there’s very few places where you can go to consume it.”

Eventually one of West’s events was raided by police and she received criminal charges.

“They had me on probation and made it clear that if I did anything else they would put me straight in jail, so I had to figure out what I was going to do,” she says.

“My event company wasn’t going to work until we passed social legalisation.”

Even now, six years on there is little sign of this, with several bills which would permit social consumption businesses failing to get through in recent years. 

West is hopeful though, that the need to restart the economy and hospitality sectors following the coronavirus pandemic may spur things on.

“Social use is going to be the last domino,” she says. 

“I hope that this might come from the pandemic, in the next year or two as these, as we start to get back to normalcy and we have all these empty storefronts and restaurants and hotels.”

West adds: “One of the biggest issues, is that we don’t see people consuming cannabis like you see people drinking alcohol. 

“A significant element of cannabis culture is those scenes of a dude sitting on a couch with a bong at his crotch, but that doesn’t reflect my cannabis experience. I want images of a woman, dressed up with a joint in a high-end setting, then people will start to think differently.

“With social use, that’s when people will actually be able to see people using cannabis and realise that it’s for everyone.”

Edible Events was over – at least for the time being – but West’s cannabis career was just starting to take seed.

“Women from all over the world were reaching out to me and asking how to get into the cannabis industry,” she says.

“I was like, ‘I don’t have a job anymore, I don’t grow weed and the events that I planned are completely illegal, I am not the person you should be asking’ – but no one else was paying attention to women.

“All of the legalisation groups and companies launching were led by men – mainly generationally wealthy white men, who had the money to get started.”

Under her new alias – Jane West – she founded the networking organisation Women Grow, to connect women with others in the industry and with the premise to create more female-owned cannabis companies.

“I realised that women need to change the way they think about cannabis, or uneducated stereotypes about it would to prevent them from entering the industry at exactly the time they should,” she says.

Over a quarter million people have attended Women Grow’s networking events and national conferences in Colorado since its inception, with members launching their own branches in 40 cities across the US.

By 2016, West was ready to dabble in cannabis entrepreneurialism herself, and having recruited the next generation of Women Grow leaders, she divested the vast majority of her interest in the company and it is now majority black female-owned, she tells me.

After testing the water with a limited edition range of glassware and smoking paraphernalia, West went on to raise $1.3 million in seed funding from 22 accredited investors, 80 percent of which is held by women and people of colour. 

West recently completed another successful seed funding round

She spent the money developing her signature travel collection – a range of sleek, stylish and discreet vaporisers and pipes and now partners with minority and family-owned businesses across the US to supply Jane West-branded CBD products and whole-plant cannabis, which comes in two simple formulations; day and night. 

“Cannabis is confusing and intimidating, which is unfortunate because it is a safer alternative to prescription medications and alcohol, which are the primary substances that people are consuming. We want to take that confusion away.” West explains.

“Our customers know that I vet and find great growers, so it makes them more confident and it simplifies the buying process.”

In 2020, the number of cannabis retailers carrying the Jane West brand tripled from the previous year and it has now secured licensed cannabis partners in 13 US states, and Canada.

West doubled her revenues last year and recently closed another round of seed funding, with thousands of investors from 42 countries.

But despite its success on paper, she insists the company is still in “start-up mode” – and that she really “didn’t know what she was doing”.

“I did my best to leverage the fact that my name was out there, but I definitely wasn’t trying to front anything,” she says.

“I was like ‘I think we should have this networking group, and I don’t know what I’m doing but I think we should make bongs.’

“The more candid you are about what you don’t know, the more transparent conversations end up being and the further you get. I think that’s important in cannabis now more than ever, we need more transparency.”

This might not have been the plan, but having built her own cannabis empire – and a space which empowers women to do the same – I can’t imagine West would change anything now?

“I don’t have any regrets… I helped women make the critical connections they needed to manage an extremely hostile unwelcoming business environment, but I wish I could point to more female-owned businesses and say that’s because of Women Grow,” she admits.

“In Illinois only 21 licenses to grow have been issued, in Colorado there’s 2,500. In most of the states in the US, women and minorities were not granted licences – why that occurred is up for question.”

West adds: “I wish I’d spoken up earlier about the inequality.

“The most important reason to keep talking about being a woman or a minority is to keep pointing out that you’re the only person in the room. This [industry] just started, it shouldn’t be so inequitable already.”


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Epilepsy Awareness Week: “To see your child have a seizure is devastating”

Epilepsy affects over 600,000 people in the UK – including 60,000 children and young people under 18.



Amy and her daughter Abbie both have epilepsy

On National Epilepsy Awareness Week two families share how the condition has affected them and how they’ve found support from others on the journey to accessing medical cannabis.

Epilepsy is one of the most common neurological disorders in the world, affecting over 600,000 people in the UK – including 60,000 children and young people under 18 – and tragically causing 21 deaths every week. 

Most people with epilepsy are treated with anti-epileptic drugs, but what if these fail to keep the condition under control, as with one third of patients whose epilepsy is deemed to be drug-resistant or ‘intractable’?

Many families have turned to medical cannabis and seen huge improvements in their loved ones quality of life.

An audit of the impact of medical cannabis in 10 patients with severe epilepsy, published by Drug Science in December 2020, found that there was on average a 97 percent reduction in monthly seizures.

Authors concluded that the impact of cannabis medicines on these patients was ‘remarkable’ and often ‘life-changing’.

But many are still paying thousands of pounds a month for private prescriptions of these treatments and some are unable to access them at all. 

With access restricted on the NHS and the use of cannabis medicines still “controversial” among the medical community, many doctors are unwilling to even engage in a conversation about it – meaning it can be hard to know where to turn for advice. 

Last year Matt Hughes, dad to Charlie, three, who has West syndrome, and Hannah Deacon, co-founded Medcan Support, an education platform to provide families with the guidance that was lacking when he began fighting for access to medical cannabis for his son.

As well as bringing together scientific research, advice for caregivers and hosting webinars with experts from across the globe, the Medcan Support Facebook group provides a space for members to ask questions and connect with others as they navigate this new field. 

Gus has been diagnosed with West syndrome

Amanda Birch, 41, would never have had the confidence to try her son on CBD oil if it wasn’t for the group, she tells Cannabis Health. 

“Our paediatrician and neurologist are both great, but they don’t want to talk about cannabis.

“They just don’t want to get involved in any conversations about it, so where else do you go for support?”

Amanda’s two-year-old Gus also has West syndrome, and suffers around 100 seizures every day. 

He has only been taking CBD oil for two weeks, after trying eight different anti-epileptic drugs and being turned down for brain surgery. 

“I’ve been asking our doctors about CBD oil for a while and they’ve always said no, but we need help, we have literally run out of options,” says Amanda.

“It’s been constantly on my mind. You need somebody to give you that confidence to try it and the reassurance.

“It’s a really big thing to know that there’s a space where you can ask questions, and hearing actual experiences from other parents is worth so much more. Even just being able to ask for tips, such as how to get the oil into him, because it doesn’t taste very nice – that support is important.”

Although Gus has only been taking the oil for a short amount of time and is yet to see any significant changes, she is cautiously optimistic.

“It’s really hard to feel hopeful, over the last couple of years I’ve learned that hope is actually a really dangerous thing – with each drug and each new treatment method, you hope it will work and when it doesn’t that is just so painful,” she says. 

“I’m not naive enough to think that it’s going to stop his seizures, but when you’re dealing with such a complex condition any improvement can make a big difference to yours and their life.

Gus can have hundreds of seizures in one day

“If it makes his quality of life 10 percent better, then it will be 100 percent worth it.”

Although Amanda would like Gus to have the opportunity to try a full spectrum cannabis oil, she fears the crippling costs that come with the prescription.

“It sounds really back to front, but what puts me off is the fear that if it does work, we’re faced with this huge bill each month,” she admits.

“How could we afford it? The fact that it looks like it is so far from being available to us on the NHS is a big factor.”

The cost is also preventing Amy Errico’s daughter Abbie, 16, from being able to access the cannabis medicines she needs. 

Abbie, who was diagnosed with epilepsy at 10 months old, is currently prescribed a broad spectrum oil which costs around £350 a month. 

Amy would like her daughter to have a full extract oil, but at her age she is ineligible for Project Twenty21 and would have to pay the full price, at around £1,500 a month. 

“I’m frustrated at the moment,” Amy says, speaking to Cannabis Health.

“Things have definitely improved since she has been on the oil but we’re nowhere near at the therapeutic level for her… and £350 a month is a lot of money if you’re on a low income.”

Abbie’s seizures have reduced as she’s gotten older, as a baby she would have hundreds a month, whereas now it’s closer to one a week. But they can last for up to half an hour every time. 

“It worries me that she’s in that state for quite a prolonged time, to see your child go through that is just so devastating,” says Amy.

Abbie was diagnosed with epilepsy at 10 months old

“I will keep pushing, in my opinion, it should be available for everyone, at any age. I’m upset and shocked that they would consider surgery for Abbie, before trying cannabis oil.”

At the age of 43, Amy is also undergoing tests for epilepsy, having suffered seizures throughout her life but never getting a definitive diagnosis. 

She recently got a prescription for medical cannabis, but struggles with the fact her daughter still doesn’t have access. 

“I feel guilty that I’ve managed to get the oil and at the moment I can’t get it for Abbie,” she says.

“I have had seizures at night, my whole life. My mum took me to the doctors when I was younger and they were quite dismissive, but it’s happening more now, I think because of my age.

“I cannot tolerate artificial lighting, it just shuts my body down and makes me so ill, so I can’t be in the workplace, I can’t even walk into a shop.”

She adds: “There’s a tendency for people to think of epilepsy as someone having a tonic clonic seizure, but there’s aspects that people are not aware of, you can’t necessarily just live your life as everyone else does.”

Amy found Medcan after researching cannabis on her own for around 10 years, it’s been reassuring for her to have support from other parents.

Her mum Amy, also has suspected epilepsy.

“I don’t personally know anyone else who has a child with epilepsy, so it’s been fantastic to have that support,” she says.

“It’s so reassuring to have someone that is just at the end of the text, who knows what you’re going through.”

Medcan has recently had confirmation of its status as a community interest company and hopes to raise enough this year to begin supporting families with grants and mental health support. 

“We will be taking applications for grants for general things like respite, holidays, specialist equipment, the things that families have to go without because they are funding private prescriptions,” comments Matt.

“We also want to support parents with mental health. It’s an area that is often overlooked, with the focus on the children, but so many parents suffer with anxiety, depression and PTSD, yet continue to care and fight for their children. We’ll be linking parents with mental health services and they can also apply for funding to cover costs.”

Its expert committee, which includes cannabis scientist Dr Callie Seaman, paediatric consultant Dr Bonnie Goldstein, neurologist Dr Evan Lewis and CBD expert Jade Proudman, are also working with Drug Science on a new study examining which cannabis chemovar profiles are most effective for childhood epilepsy.

“This will be a more focussed study which we hope will lead to further research, but also allow families and clinicians to make better informed decisions,” added Matt.

“I’d like to thank Hannah, Callie, Jade for their support, they contribute so much, along with Dr Evan Lewis, Dr Bonnie Goldstein.”

For support and information visit 

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