For some chronic pain sufferers, a simple hug can turn into a horrible event. What is usually a comforting, therapeutic, loving gesture has layers of complexity. It hurts to be hugged, but you don’t want to say anything because it hurts the “hugger’s” feelings. Plus, you’re not sure if they’ll believe you — I mean, it sounds pretty dramatic to say you’re in so much pain you can’t tolerate a hug. Calming pain, anxiety, and the PTSD trigger response all help very much in these tough situations. Maybe with a nervous system nourished via the endocannabinoid system with CBD, you’ll be able to gently express that hugs aren’t for you.
While there are more unknowns than knowns at this point, Grant says he doesn’t discount all the anecdotal CBD reports. “You hear somebody say, ‘Hey, I gave this to myself and my kid and we feel a lot better,’ and we should never dismiss that kind of information,” he says. He points out that many modern medicines were discovered when researchers followed up on exactly this sort of human trial-and-error evidence. “But we still need to do the studies that confirm whether all the good things are true, and how much to give, and how to give it,” he says. “These are all questions that need to be answered.”
CBD is a safe, long-term aid which is why it has gained such momentum and why our customers are turning to it for relief. CBD, scientifically known as cannabidiol, is a non-psychoactive, natural compound found in the hemp plant. When it interacts with the body’s endocannabinoid system, CBD provides powerful health benefits without the side effects of conventional drugs. The CBD utilized in our tinctures is extracted from industrial hemp cultivated in the United States. To further ensure quality and purity, our industrial hemp goes through a supercritical CO2 extraction process to obtain the best possible CBD solution. This solution is then formulated by our board-certified pharmacists into finished products and sent out for third-party testing. Our CBD oil is made with high-quality CBD extracted from natural hemp that is abundant in naturally produced terpenes, oils, vitamins, omega fatty acids, and other components.
That leaves those touting CBD’s effectiveness pointing primarily to research in mice and petri dishes. There, CBD (sometimes combined with small amounts of THC) has shown promise for helping pain, neurological conditions like anxiety and PTSD, and the immune system—and therefore potentially arthritis, diabetes, multiple sclerosis, cancer, and more.
I am 81 years old next month. I have been in serious pain from Fibromyalgia since I was in my 50s. Also for the last 5 or 6 years, I have suffered from painful arthritis in my shoulders, back, neck and knees. I walk with a walker and have to sit down after doing any chores that take standing for more then 8 or 10 minutes. My care-giver told me about Hemp oil for pain so I decided to try it. It took about 2 weeks before I began to realize that I wasn't using my BioFreeze and my muscle pain lotion nearly as often. Before, I had needed it every night just to sooth my pain enough to sleep at night. Also, it has taken a month and half for me to feel much of my arthritis pain is gone now. I have been using it now for almost two months and I have almost no fibromyalgia pain and very little arthritis pain. I haven't used my lotions and pain pills for weeks now in order to get to sleep. I am so excited, since doctors have not been able to help my Fibromyalgia at all in the past with all the pills and exercise they had me try. God bless my care-giver for turning me on to this stuff. I can only say it has been a total MIRACLE for me. I now move about with very little pain. I am stocking up on this product. By all means, those of you out there who suffer from Fibromyalgia give this product a try. Give it enough time and I am sure you will feel your pain go away. Yes, the taste is unpleasant, but I just gulp it down and then fill my mouth with my breakfast fruit and cereal and it only takes seconds for the taste to go away. I recommend this product and this Brand to anyone who has pain.
Information from adverse event reports regarding marijuana use is extremely limited; the FDA primarily receives adverse event reports for approved products. General information on the potential adverse effects of using marijuana and its constituents can come from clinical trials using marijuana that have been published, as well as from spontaneously reported adverse events sent to the FDA. Additional information about the safety and effectiveness of marijuana and its constituents is needed. Clinical trials of marijuana conducted under an IND application could collect this important information as a part of the drug development process.
4) context is really important to your brain with psychoactive drugs, and this is as true for CBD as it is for prescription drugs that affect the serotonin cycle like stimulants and SSRIs. If you’re using CBD to target serotonin in order to have a productive workday, for example, make sure you use the CBD vape right before you sit down to work, and don’t hit it when you’re going out or watching TV.
As always, every Green Roads product is infused with hemp-derived CBD, extracted from the hemp plant via supercritical CO2 extraction, then winterized to purify the concentrated CBD and purge all unwanted plant products/cannabinoids from the final product. In addition, our Relief Cream is infused with menthol, chamomile extract, and lavender oil to bring you the relief you need and the pleasant aroma you desire, without leaving a greasy residue behind.
"It's important to know that the research in this area is in its infancy, partly because we haven't really understood much about CBD until relatively recently," said Marcel Bonn-Miller, an adjunct assistant professor at the University of Pennsylvania Perelman School of Medicine. He pointed out that the classification of marijuana as a Schedule 1 drug by the DEA makes it difficult to get material to use in laboratory studies. Schedule 1 drugs have a high potential for abuse, according to the DEA, and are illegal under federal law.
Reality: Hemp oil is an increasingly popular product, used for an expanding variety of purposes. The washed hemp seed contains no THC at all. The tiny amounts of THC contained in industrial hemp are in the glands of the plant itself. Sometimes, in the manufacturing process, some THC- and CBD-containing resin sticks to the seed, resulting in traces of THC in the oil that is produced. The concentration of these cannabinoids in the oil is infinitesimal. No one can get high from using hemp oil.
Until 2017, products containing cannabidiol marketed for medical purposes were classed as medicines by the UK regulatory body, the Medicines and Healthcare products Regulatory Agency (MHRA) and could not be marketed without regulatory approval for the medical claims. As of 2018, cannabis oil is legal to possess, buy, and sell in the UK, providing the product does not contain more than 0.2% THC and is not advertised as providing a medicinal benefit.
Hemp oil is an abundant source of alpha-linolenic acid. Alpha-linolenic acid is an omega-3 fatty acid that is essential to proper organ function. It is similar to the omega-3 fatty acids found in fish oil, and can help prevent heart disease, arthritis and depression, according to the University of Maryland Medical Center. It can also help reduce low density lipoprotein cholesterol, the "bad" cholesterol that clogs arteries.
The glutamatergic system is integral to development and maintenance of neuropathic pain, and is responsible for generating secondary and tertiary hyperalgesia in migraine and fibromyalgia via NMDA mechanisms (Nicolodi et al 1998). Thus, it is important to note that cannabinoids presynaptically inhibit glutamate release (Shen et al 1996), THC produces 30%–40% reduction in NMDA responses, and THC is a neuroprotective antioxidant (Hampson et al 1998). Additionally, cannabinoids reduce hyperalgesia via inhibition of calcitonin gene-related peptide (Richardson et al 1998a). As for Substance P mechanisms, cannabinoids block capsaicin-induced hyperalgesia (Li et al 1999), and THC will do so at sub-psychoactive doses in experimental animals (Ko and Woods 1999). Among the noteworthy interactions with opiates and the endorphin/enkephalin system, THC has been shown to stimulate beta-endorphin production (Manzanares et al 1998), may allow opiate sparing in clinical application (Cichewicz et al 1999), prevents development of tolerance to and withdrawal from opiates (Cichewicz and Welch 2003), and rekindles opiate analgesia after a prior dosage has worn off (Cichewicz and McCarthy 2003). These are all promising attributes for an adjunctive agent in treatment of clinical chronic pain states.