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MAGICAL BUTTER TINCTURE



Welcome

    personal-photo
    Hello and welcome to Pediatric Cannabis Therapy! My name is Rebecca Brown and I am the founder of Pediatric Cannabis Therapy. My journey began almost two years ago when I started treating my then 14 year old son who has Dravet syndrome with a high cbd low thc ratio medical cannabis. I reached out to other parents in the Dravet community who were also treating their children with cannabis and the Pediatric Cannabis Therapy facebook group was born. We started with 6 parents but have grown to a staggering 2500 members and are growing daily. The need for the website became very clear as more and more people were looking for information regarding the therapeutic application of cannabis in the pediatric community.

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What is clinical endocannabinoid deficiency?


Clinical endocannabinoid deficiency (CEDC) is a proposed spectrum disorder that has been implicated in a range of illnesses, including fibromyalgia, migraine and irritable bowel syndrome. So far, very little research has been conducted on this speculative disorder, but if it is found to exist, it could be responsible for these very common conditions as well as many related ones.
Clinical endocannabinoid deficiency (CEDC) is a proposed spectrum disorder that has been implicated in a range of illnesses, including fibromyalgia, migraine and irritable bowel syndrome. So far, very little research has been conducted on this speculative disorder, but if it is found to exist, it could be responsible for these very common conditions as well as many related ones.

The three conditions feature common clinical and biochemical patterns that may point to underlying CEDC. Migraine is thought to be influenced by endocannabinoid function, as areas suspected to be involved with generation of migraines are also affected by cannabinoid activity; furthermore, the endocannabinoid anandamide, with its role in pain modulation and serotonin transmission, is believed to positively affect sufferers of the condition.
The biochemistry of migraine is highly complex and poorly understood, but it known that high levels of serotonin are present during attacks. THC and its endogenous ligand, anandamide, have been shown to inhibit serotonin in high doses (although low doses may increase its production), particularly in the platelets of the blood plasma. The platelets contain the body’s highest reserves of serotonin, which is also present in the ENS as well as throughout the brain. Serotonin release from the platelets is thought to be crucial to generation of migraines, and migraine is often thought to be a disease of the blood on this basis.

Fibromyalgia, a pain disorder which is widely considered to be neuropsychiatric in nature, is treated with cannabis in approximately 10% of patients in the USA (either through self-medication or prescription), and has been shown to respond favourably to the synthetic THC-mimic nabilone. In a study which documented the effect of nabilone on fibromyalgia sufferers, subjects experienced significant improvement of symptoms when administered the cannabinoid. Another study demonstrated that quality of life was markedly improved in fibromyalgia sufferers that self-administered oral or smoked cannabis.

Serotonin levels in the platelets are also known to be affected in fibromyalgia, although it is thought that deficiency of serotonin, rather than over-abundance, is responsible for the sufferer’s aberrant perception of pain. This disparity is not fully understood, and is somewhat surprising given the high degree of comorbidity between the diseases: in one study, up to 63% of primary fibromyalgia sufferers also reported symptoms of migraine, in another, 22.2% of primary migraine sufferers were also found to have fibromyalgia. This disparity may be partly explained by gender differences, as none of the male migraine sufferers reported symptoms of fibromyalgia, and the latter disease is overwhelmingly experienced by women, who comprise 90% of sufferers.

Irritable bowel syndrome (IBS) is a common gastroenteric condition that presents as bloating, abdominal cramps and diarrhoea. It is long been suspected that there is a link between IBS and neuropsychiatric dysfunction, as the condition is often comorbid with psychiatric conditions such as anxiety, depression and PTSD; acute symptoms often arise in times of mental distress. However, as endocannabinoids are expressed in the enteric nervous system (ENS), as well as the areas of the brain affected by such psychiatric disorders, their effect may be independent.
Serotonin also plays a part in IBS, influencing gut motility (the peristaltic actions of the colon, which become “spastic” or uncontrolled during bouts of IBS), sensitivity and secretion of fluid. Interestingly, IBS-D (characterised by diarrhoea) sufferers have been shown to have increased blood serotonin levels, while sufferers of IBS-C (characterised by constipation) experience reduced levels of serotonin.

It has been demonstrated that activation of the cannabinoid receptors in the ENS decreases hypersensitivity of the gut, as well as reducing gut motility and inflammation. Many sufferers of IBS use cannabis to alleviate their symptoms, although some report that symptoms worsened subsequent to commencing use; some even postulate cannabis as a trigger for IBS in certain individuals.

The overlap between instances of these conditions has led to the hypothesis that they are all expressions of the same underlying somatic disorder. Many sufferers of IBS also report symptoms of migraine, and up to 70% of fibromyalgia sufferers also present IBS symptoms. Many have all three, but it is not strictly necessary for all three to be present for an underlying condition to be the cause, as many spectrum disorders manifest markedly different symptoms from patient to patient, and other related conditions may be involved.

The idea that a dysfunctional endocannabinoid system is responsible for this postulated somatic disorder first arose within the last few years. In 2004, the condition CECD was first proposed; researchers suggested that the high degree of comorbidity, along with the common feature of unusual cannabinoid receptor activity, pointed to an underlying disorder of the endocannabinoid system. Many known conditions can be attributed to dysfunction of a specific neurotransmitter system: Alzheimer’s is caused by deficiency of the acetylcholine neurotransmitter, and Parkinson’s by age-related dopamine deficiency. It is therefore logical to assume that deficiency of the cannabinoid neurotransmitters would also cause a specific disorder, or set of related disorders.

The relationship with the serotonin signalling system cannot be ignored when researching the possibility of CECD’s existence. Behavioural studies suggest that the effects of endocannabinoid signalling are mediated by regulation of the serotonin system: THC has been shown to inhibit serotonin release from the platelets in migraine sufferers, as well as increasing synthesis of serotonin in the brain; 2-AG and cannabidiol have demonstrated similar effects. However, the independent effects of cannabinoids on the cannabinoid receptors are thought to be the underlying cause of CECD, despite this possibly fundamental relationship with serotonin signalling.

If the existence of CECD is proven, targeted therapies can be investigated, which would pinpoint the precise nature of the deficiency and determine the appropriate ration and dosage of supplemental exogenous cannabinoids. At present, treatment of these conditions is usually through ingestion of crude cannabis extract, or through smoking, which may involve wildly different cannabinoid ratios between cannabis strains. Due to the dose-dependent effect of many cannabinoids, relief of symptoms may not be adequate with some varieties.

Written by Seshata is a freelance cannabis writer currently based in Amsterdam, Netherlands for
http://sensiseeds.co...oid-deficiency/


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