Parents Fight for Access to Safe, Quality Medicine

Dispensary Tour - Cannabis Education - Kansas City, MO

Oftentimes we learn about patients in the media who are struggling from having legal access to safe medicine.  While every patient story is heart-wrenching, it’s the ones about children that seem to stick with us and sometimes serve up the impetus for policy change.  Charlie Hughes is one such patient story that both touches and infuriates readers who learn of the battle his family is waging for access to medicine.

 

In the UK, parents of toddler Charlie Hughes are fighting the National Health Service (NHS) and seeking a policy change that could radically alter his quality of life.  Charlies, 3, has a rare form of epilepsy called West Syndrome, known best for its frequent seizures – up to 120 per day – and historically treated with benzodiazepines which have side effects ranging from lethargic to dazed and not effective at reducing either the seizures nor their impact. 

 

Under the NHS protocols, he has been prescribed seven different prescriptions for anti-epilepsy medication, yet he was still experiencing up to 100 seizures a day.  Charlie’s parents, Allison and Matt claim that with full extract cannabis oil, the number of seizures he experiences in the course of a day is dramatically decreased.  The family pays hundreds of pounds per month to source full extract cannabis oil privately because clinicians at NHS have refused to prescribe Dutch-made oils (which meet the European Medicines Agency guidelines for Good Manufacturing Practice).  

 

Matt said of his son’s improvement since taking cannabis: “Charlie is happier, more alert, far more vocal, constantly babbling and takes an interest in his toys. He can feed himself and loves nothing more than some rough and tumble with me. He’s come alive again.

“No one knows definitively what effect all those anti-epileptic drugs in combination with each other have on the development of the brain. If he wasn’t asleep or completely zonked out, he was just seizing. Cannabis has massively improved his general wellbeing.”

The decision in the Hughes’ case against the NHS could have profound impact on cannabis oil as medicine and the ability for parents like the Hughes to have access to what is clearly making a difference in their son’s quality of life.

Visit the link below to learn more about the Realm of Caring. Not only are they actively involved in making cannabis accessible to all who could benefit, but they provide a financial assistance program as well. 

The Hochstein’s Find Hope

Cannabis & Epilepsy | The Cannabis Care Team of Kansas City, MO

A Nebraska family advocates for the use of cannabis.

Medical marijuana has been making a sweep across our nation as legalization efforts bring the medicine that shows remarkable results to patients in need. While some have been using marijuana as medicine for decades, in recent years, we’ve heard about families with small children who feel as if their children with epilepsy have run out of options without medical marijuana.


The Hochsteins of Nebraska, are one of these families. Son Jayen, aged 10, has intractable epilepsy and suffered from his first seizure at just 4 months old. Jayen had brain surgery in 2014 and has a VNS which is like a pacemaker installed in 2019 and now his family contemplates another brain surgery to stop his seizures.


They have tried every treatment offered to them, but few have been fully successful. Many treatments carry side effects or have not been approved yet for minors. Balancing risk and reward is a balancing act for the family. After a year of steroids, another seemingly viable option at the time, the couple said the seizures returned. Other medications have only worked for a short time.


Nicole Hochstein said she isn’t sure her son can endure many more procedures or unsuccessful treatments. However, she said she also fears he could succumb to sudden unexpected death in epilepsy (SUDEP).


The youngest Hochstein’s use of cannabis treatment could lead to other benefits, according to his father.


“If he had alternatives such as medical marijuana, it could be possible to take him off some of his current medications that have side effects,” he said. The Hochsteins have become some of the largest and most active voices in Nebraska in terms of legalization efforts and like in many other states, parents of children who have debilitating diseases have found themselves in the role of advocates for an industry they never considered relevant for themselves.


Read more about this family by visiting mom Nichole’s blog. http://nicolehochstein.blogspot.com/