HT>Non-profit Organization Marches on Canadian Capital To Fight for Therapeutic Mushrooms

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Over the course of the past two years, TheraPsil has assisted over 130 patients, but it calls the country’s current limitations a “cruel approach” on the part of Health Canada. The organization has attempted to set up a formal meeting with parliament members, but so far has been denied, so it’s taking the conversation straight to the capital to protest between Nov. 28-30.

According to TheraPsil CEO Spencer Hawkswell, there needs to be a proper channel for patients to be able to legally access psilocybin and psilocin. “There is ample evidence of both the safety and efficacy of psilocybin in the treatment of various mental health conditions,” said Hawkswell in a press release. “The previous Minister recognized this and started approving exemptions. Unfortunately, this Minister has stopped and refused to consider reasonable regulations to ensure vulnerable Canadians don’t have to go to Court to access treatment that can improve their quality of life and death.”

Currently, psilocybin and psilocin are listed as a Schedule III substance under the Controlled Drugs and Substances Act. However, some patients gain legal access with an improved exemption called the Special Access Program. 

TheraPsil uses the example of Thomas Hartle, who was diagnosed with cancer in 2016, to demonstrate the problems that patients are encountering. Hartle was one of the first to receive approval from former Health Minister Patty Hajdu to use psilocybin to treat “end-of-life anxiety” in 2020, which was valid for one year. His treatments were successful, and he reapplied for continued access in October 2021, but was denied by current Health Minister Jean-Yves Duclos.

“We hope to meet with the Minister to find out why he and his officials are being so cruel to us,” said Hartle in a press statement. “Instead of a compassionate response, Health Canada is referring dying and vulnerable patients to a special access program that results in lots of red tape but no access for most. Many, like me have gone over a year without a response to their urgent requests.”

TheraPsil will be arranging media interviews over the next few days to raise awareness both for the medical benefits that psilocybin offers, as well as the need for improved access. “Mental health is a non-partisan issue,” said palliative care physician Dr. Valorie Masuda. “Reasonable treatment options should be available to Canadians who have the right to MAiD [Medical Assistance in Dying]. It is cruel to withhold medicine from vulnerable patients, especially when those medicines have worked for them.”

TheraPsil also sent a joint letter earlier this month signed by medical practitioners and social workers calling for the need for psilocybin regulations. “We believe that our patients have a right to Medical Psilocybin and this open letter is to demand this right on their behalf. We need a compassionate and immediate response and solution to the Section 56 applications for psilocybin access and seek your response to our proposed request for ‘Access to Psilocybin for Medical Purposes Regulations,’” the letter stated.

Meanwhile in Canada, Apex Labs received a “no objection” letter from Health Canada, which effectively greenlit the first North American study on psilocybin as a treatment for military veterans who suffer from conditions such as depression and post-traumatic stress disorder. “Veterans are already self-medicating with micro-doses of unregulated psilocybin products without knowing the potency and safety of the product they are consuming,” said Apex Labs CEO Tyler Powell. “Our goal is to expand access to pharmaceutical grade drug products through regulated systems, providing transparency and support for patients in need.”

A new study published in The New England Journal of Medicine on Nov. 3 also provided evidence of the benefits of psilocybin in a double-blind trial. “In this phase 2 trial involving participants with treatment-resistant depression, psilocybin at a single dose of 25 mg, but not 10 mg, reduced depression scores significantly more than a 1-mg dose over a period of 3 weeks but was associated with adverse effects,” the researchers wrote. Those adverse effects included headaches, nausea, dizziness, and suicidal ideation.

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