I take CBD oil to help with chronic pain caused by Ehlers Danlos Syndrome and it They give relief from aches, pains, sore muscles and the capsules help me. Manage Your Medications · Pill Identifier · Check for Interactions Pain Management · News MONDAY, May 7, (HealthDay News) -- Cannabidiol (CBD) oil has become the hot new product in There also are concerns about both the quality of CBD oil being produced and its potential side effects, the experts added. Full spectrum and isolate-based oils; Tinctures, capsules.
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Other synthetic cannabinoids, such as ajulemic acid, are in development. Crude herbal cannabis remains illegal in most jurisdictions but is also under investigation.
Numerous randomized clinical trials have demonstrated safety and efficacy for Sativex in central and peripheral neuropathic pain, rheumatoid arthritis and cancer pain.
Cannabinoid analgesics have generally been well tolerated in clinical trials with acceptable adverse event profiles. Their adjunctive addition to the pharmacological armamentarium for treatment of pain shows great promise. Chronic pain represents an emerging public health issue of massive proportions, particularly in view of aging populations in industrialized nations. Associated facts and figures are daunting: Particular difficulties face the clinician managing intractable patients afflicted with cancer-associated pain, neuropathic pain, and central pain states eg, pain associated with multiple sclerosis that are often inadequately treated with available opiates, antidepressants and anticonvulsant drugs.
Physicians are seeking new approaches to treatment of these conditions but many remain concerned about increasing governmental scrutiny of their prescribing practices Fishman , prescription drug abuse or diversion.
The entry of cannabinoid medicines to the pharmacopoeia offers a novel approach to the issue of chronic pain management, offering new hope to many, but also stoking the flames of controversy among politicians and the public alike.
An effort will be made to place the issues in context and suggest rational approaches that may mitigate concerns and indicate how standardized pharmaceutical cannabinoids may offer a welcome addition to the pharmacotherapeutic armamentarium in chronic pain treatment. Cannabinoids are divided into three groups.
The first are naturally occurring carbon terpenophenolic compounds found to date solely in plants of the Cannabis genus, currently termed phytocannabinoids Pate In , the first cannabinoid receptor was identified CB 1 Howlett et al and in , a second was described CB 2 Munro et al Both are 7-domain G-protein coupled receptors affecting cyclic-AMP, but CB 1 is more pervasive throughout the body, with particular predilection to nociceptive areas of the central nervous system and spinal cord Herkenham et al ; Hohmann et al , as well as the peripheral nervous system Fox et al ; Dogrul et al wherein synergy of activity between peripheral and central cannabinoid receptor function has been demonstrated Dogrul et al CB 2 , while commonly reported as confined to lymphoid and immune tissues, is also proving to be an important mediator for suppressing both pain and inflammatory processes Mackie Following the description of cannabinoid receptors, endogenous ligands for these were discovered: These endocannabinoids both act as retrograde messengers on G-protein coupled receptors, are synthesized on demand, and are especially active on glutamatergic and GABA-ergic synapses.
The endocannabinoid system parallels and interacts at many points with the other major endogenous pain control systems: Interestingly, our first knowledge of each pain system has derived from investigation of natural origin analgesic plants, respectively: Notably, no endocannabinoid has ever been administered to humans, possibly due to issues of patentability and lack of commercial feasibility Raphael Mechoulam, pers comm For an excellent comprehensive review of the endocannabinoid system, see Pacher et al , while Walker and Huang have provided a key review of antinociceptive effects of cannabinoids in models of acute and persistent pain Walker and Huang A clinical endocannabinoid deficiency has been postulated to be operative in certain treatment-resistant conditions Russo , and has received recent support in findings that anandamide levels are reduced over controls in migraineurs Sarchielli et al , that a subset of fibromyalgia patients reported significant decreased pain after THC treatment Schley et al , and the active role of the ECS in intestinal pain and motility in irritable bowel syndrome Massa and Monory wherein anecdotal efficacy of cannabinoid treatments have also been claimed.
The endocannabinoid system is tonically active in control of pain, as demonstrated by the ability of SRA rimonabant , a CB 1 antagonist, to produce hyperalgesia upon administration to mice Richardson et al As mentioned above, the ECS is active throughout the neuraxis, including integrative functions in the periacqueductal gray Walker et al a ; Walker et al b , and in the ventroposterolateral nucleus of the thalamus, in which cannabinoids proved to be fold more potent than morphine in wide dynamic range neurons mediating pain Martin et al The ECS also mediates central stress-induced analgesia Hohmann et al , and is active in nociceptive spinal areas Hohmann et al ; Richardson et al a including mechanisms of wind-up Strangman and Walker and N-methyl-D-aspartate NMDA receptors Richardson et al b.
It was recently demonstrated that cannabinoid agonists suppress the maintenance of vincristine-induced allodynia through activation of CB 1 and CB 2 receptors in the spinal cord Rahn et al The ECS is also active peripherally Richardson et al c where CB 1 stimulation reduces pain, inflammation and hyperalgesia.
These mechanisms were also proven to include mediation of contact dermatitis via CB 1 and CB 2 with benefits of THC noted systemically and locally on inflammation and itch Karsak et al Recent experiments in mice have even suggested the paramount importance of peripheral over central CB 1 receptors in nociception of pain Agarwal et al Cannabinoid agonists produce many effects beyond those mediated directly on receptors, including anti-inflammatory effects and interactions with various other neurotransmitter systems previously reviewed Russo a.
Briefly stated, THC effects in serotonergic systems are widespread, including its ability to decrease 5-hydroxytryptamine 5-HT release from platelets Volfe et al , increase its cerebral production and decrease synaptosomal uptake Spadone THC may affect many mechanisms of the trigeminovascular system in migraine Akerman et al ; Akerman et al ; Akerman et al ; Russo ; Russo 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 Additionally, cannabinoids reduce hyperalgesia via inhibition of calcitonin gene-related peptide Richardson et al a.
As for Substance P mechanisms, cannabinoids block capsaicin-induced hyperalgesia Li et al , and THC will do so at sub-psychoactive doses in experimental animals Ko and Woods These are all promising attributes for an adjunctive agent in treatment of clinical chronic pain states. The anti-inflammatory contributions of THC are also extensive, including inhibition of PGE-2 synthesis Burstein et al , decreased platelet aggregation Schaefer et al , and stimulation of lipooxygenase Fimiani et al THC has twenty times the anti-inflammatory potency of aspirin and twice that of hydrocortisone Evans , but in contrast to all nonsteroidal anti-inflammatory drugs NSAIDs , demonstrates no cyclo-oxygenase COX inhibition at physiological concentrations Stott et al a.
Cannabidiol, a non-euphoriant phytocannabinoid common in certain strains, shares neuroprotective effects with THC, inhibits glutamate neurotoxicity, and displays antioxidant activity greater than ascorbic acid vitamin C or tocopherol vitamin E Hampson et al These activities reinforce the conception of CBD as an endocannabinoid modulator, the first clinically available Russo and Guy CBD additionally affects THC function by inhibiting first pass hepatic metabolism to the possibly more psychoactive hydroxy-THC, prolonging its half-life, and reducing associated intoxication, panic, anxiety and tachycardia Russo and Guy A new explanation of inflammatory and analgesic effects of CBD has recently come to light with the discovery that it is able to promote signaling of the adenosine receptor A2A by inhibiting the adenosine transporter Carrier et al Cannabichromene CBC is the third most prevalent cannabinoid in cannabis, and is also anti-inflammatory Wirth et al , and analgesic, if weaker than THC Davis and Hatoum Furthermore, CBG has more potent analgesic, anti-erythema and lipooxygenase blocking activity than THC Evans , mechanisms that merit further investigation.
It requires emphasis that drug stains of North American ElSohly et al ; Mehmedic et al , and European King et al cannabis display relatively high concentrations of THC, but are virtually lacking in CBD or other phytocannabinoid content.
Cannabis terpenoids also display numerous attributes that may be germane to pain treatment McPartland and Russo Myrcene is analgesic, and such activity, in contrast to cannabinoids, is blocked by naloxone Rao et al , suggesting an opioid-like mechanism.
It also blocks inflammation via PGE-2 Lorenzetti et al It is anti-inflammatory comparable to phenylbutazone via PGE-1 Basile et al , but simultaneously acts as a gastric cytoprotective Tambe et al Cannabis flavonoids in whole cannabis extracts may also contribute useful activity McPartland and Russo Cannflavin A, a flavone unique to cannabis, inhibits PGE-2 thirty times more potently than aspirin Barrett et al , but has not been subsequently investigated. Very few randomized controlled trials RCTs have been conducted using smoked cannabis Campbell et al despite many anecdotal claims Grinspoon and Bakalar A recent brief trial of smoked cannabis 3.
This short clinical trial also demonstrated prominent adverse events associated with intoxication. In Canada, 21 subjects with chronic pain sequentially smoked single inhalations of 25 mg of cannabis 0, 2.
Even after political and legal considerations, it remains extremely unlikely that crude cannabis could ever be approved by the FDA as a prescription medicine as outlined in the FDA Botanical Guidance document Food and Drug Administration ; Russo b , due to a lack of rigorous standardization of the drug, an absence of Phase III clinical trials, and pulmonary sequelae bronchial irritation and cough associated with smoking Tashkin Although cannabis vaporizers reduce potentially carcinogenic polyaromatic hydrocarbons, they have not been totally eliminated by this technology Gieringer et al ; Hazekamp et al Two open label studies in France of oral dronabinol for chronic neuropathic pain in 7 subjects Clermont-Gnamien et al and 8 subjects Attal et al , respectively, failed to show significant benefit on pain or other parameters, and showed adverse event frequently requiring discontinuation with doses averaging 15— Dronabinol did demonstrate positive results in a clinical trial of multiple sclerosis pain in two measures Svendsen et al , but negative results in post-operative pain Buggy et al Table 1.
Another uncontrolled case report in three subjects noted relief of intractable pruritus associated with cholestatic jaundice employing oral dronabinol Neff et al Some authors have noted patient preference for whole cannabis preparations over oral THC Joy et al , and the contribution of other components beyond THC to therapeutic benefits McPartland and Russo THC absorption orally is slow and erratic with peak serum levels in 45— minutes or longer. Systemic bioavailability is also quite low due to rapid hepatic metabolism on first pass to hydroxy-THC.
A rectal suppository of THC-hemisuccinate is under investigation Broom et al , as are transdermal delivery techniques Challapalli and Stinchcomb The terminal half-life of THC is quite prolonged due to storage in body lipids Grotenhermen Nabilone Cesamet Figure 1 , is a synthetic dimethylheptyl analogue of THC British Medical Association that displays greater potency and prolonged half-life.
Serum levels peak in 1—4 hours Lemberger et al It was also primarily developed as an anti-emetic in chemotherapy, and was recently re-approved for this indication in the USA. Prior case reports have noted analgesic effects in case reports in neuropathic pain Notcutt et al and other pain disorders Berlach et al Sedation and dysphoria were prominent sequelae. An RCT of nabilone in 41 post-operative subjects actually documented exacerbation of pain scores after thrice daily dosing Beaulieu Table 1.
An abstract of a study of 82 cancer patients on nabilone claimed improvement in pain levels after varying periods of follow-up compared to patients treated without this agent Maida However, 17 subjects dropped out, and the study was neither randomized nor controlled, and therefore is not included in Table 1.
Part of its analgesic activity may relate to binding to intracellular peroxisome proliferator-activator receptor gamma Liu et al Peak plasma concentrations have generally been attained in 1—2 hours, but with delays up to 4—5 hours is some subjects Karst et al Debate surrounds the degree of psychoactivity associated with the drug Dyson et al Current research is confined to the indication of interstitial cystitis.
CBD ratios reviewed in Russo and Guy , generally approximately 2: Two pharmacokinetic studies on possibly related material have been reported Nadulski et al a ; Nadulski et al b. Both Marinol and Cannador produced reductions in pain scores in long-term follow-up Zajicek et al Cannador was assayed in postherpetic neuralgia in 65 subjects with no observed benefit Ernst et al Table 1 , and in 30 post-operative pain subjects CANPOP without opiates, with slight benefits, but prominent psychoactive sequelae Holdcroft et al Table 1.
It was approved by Health Canada in June for prescription for central neuropathic pain in multiple sclerosis, and in August , it was additionally approved for treatment of cancer pain unresponsive to optimized opioid therapy.
Sativex effects commence in 15—40 minutes, an interval that permits symptomatic dose titration. A very favorable adverse event profile has been observed in over patient years of exposure in over experimental subjects.
Patients most often ascertain an individual stable dosage within 7—10 days that provides therapeutic relief without unwanted psychotropic effects often in the range of 8—10 sprays per day. In a Phase II double-blind crossover study of intractable chronic pain Notcutt et al in 24 subjects, visual analogue scales VAS were 5. During that time, there was no escalation of dose indicating an absence of tolerance to the preparation.
Similarly, no withdrawal effects were noted in a subset of patients who voluntarily stopped the medicine abruptly. Upon resumption, benefits resumed at the prior established dosages. In a Phase II double-blind, randomized, placebo-controlled, 5-week study of 56 rheumatoid arthritis patients with Sativex Blake et al , employed nocturnal treatment only to a maximum of 6 sprays per evening In a study of spinal injury pain, NRS of pain were not statistically different from placebo, probably due to the short duration of the trial, but secondary endpoints were clearly positive Table 1.
Finally, in an RCT of intractable lower urinary tract symptoms in MS, accompanying pain in affected patients was prominently alleviated Table 1.
Common adverse events AE of Sativex acutely in RCTs have included complaints of bad taste, oral stinging, dry mouth, dizziness, nausea or fatigue, but do not generally necessitate discontinuation, and prove less common over time. While there have been no head-to-head comparative RCTs of Sativex with other cannabinoid agents, certain contrasts can be drawn.
Sativex Rog et al and Marinol Svendsen et al have both been examined in treatment of central neuropathic pain in MS, with comparable results Table 1.
However, adverse events were comparable or greater with Marinol than with Sativex employing THC dosages some 2. Similarly, while Sativex and smoked cannabis have not been employed in the same clinical trial, comparisons of side effect profiles can be made on the basis of SAFEX studies of Sativex for over a year and up to several years in MS and other types of neuropathic pain Russo b ; Wade et al , and government-approved research programs employing standardized herbal cannabis from Canada for chronic pain Lynch et al and the Netherlands for general conditions Janse et al ; Gorter et al over a period of several months or more.
As is evident in Figure 2 Figure 2 , all adverse events are more frequently reported with herbal cannabis, except for nausea and dizziness, both early and usually transiently reported with Sativex see Russo b for additional discussion. Comparison of adverse events AE encountered with long term therapeutic use of herbal cannabis in the Netherlands Janse et al ; Gorter et al and Canada Lynch et al , vs that observed in safety-extension SAFEX studies of Sativex oromucosal spray Russo ; Wade et al Phytocannabinoids are lipid soluble with slow and erratic oral absorption.
While cannabis users claim that the smoking of cannabis allows easy dose titration as a function of rapid onset, high serum levels in a short interval inevitably result. This quick onset is desirable for recreational purposes, wherein intoxication is the ultimate goal, but aside from paroxysmal disorders eg, episodic trigeminal neuralgia or cluster headache attack , such rapid onset of activity is not usually necessary for therapeutic purposes in chronic pain states.
The vast majority of subjects in Sativex clinical trials do not experience psychotropic effects outside of initial dose titration intervals Figure 2 and most often report subjective intoxication levels on visual analogue scales that are indistinguishable from placebo, in the single digits out of Wade et al Thus, it is now longer tenable to claim that psychoactive effects are a necessary prerequisite to symptom relief in the therapeutic setting with a standardized intermediate onset cannabis-based preparation.
Intoxication has remained a persistent issue in Marinol usage Calhoun et al , in contrast. Recent controversies have arisen in relation to non-steroidal anti-inflammatory drugs NSAID , with concerns that COX-1 agents may provoke gastrointestinal ulceration and bleeding, and COX-2 drugs may increase incidents of myocardial infarction and cerebrovascular accidents Fitzgerald ; Topol Frequent questions have been raised as to whether psychoactive drugs may be adequately blinded masked in randomized clinical trials.
Internal review and outside analysis have confirmed that blinding in Sativex spasticity studies has been effective Clark and Altman ; Wright Sativex and its placebo are prepared to appear identical in taste and color.
Great public concern attends recreational cannabis usage and risks of dependency. The addictive potential of a drug is assessed on the basis of five elements: Drug abuse liability DAL is also assessed by examining a drug's rates of abuse and diversion. US Congress placed cannabis in Schedule I of the Controlled Substances Act in , with drugs categorized as addictive, dangerous, possessing severe abuse potential and no recognized medical value.
Marinol was placed in Schedule II, the category for drugs with high abuse potential and liability to produce dependency, but certain recognized medical uses, after its FDA approval in Marinol was reassigned to Schedule III in , a category denoting a lesser potential for abuse or lower dependency risk after documentation that little abuse or diversion Calhoun et al had occurred. Nabilone was placed and has remained in Schedule II since The degree to which a drug is reinforcing is determined partly by the by the rate of its delivery to the brain Samaha and Robinson Sativex has effect onset in 15—40 minutes, peaking in a few hours, quite a bit slower than drugs of high abuse potential.
It has been claimed that inclusion of CBD diminishes psychoactive effects of THC, and may lower potential drug abuse liability of the preparation see Russo b for discussion. These easy-to-swallow capsules still enable you to get your daily dose of CBD but are arguably more convenient than their oil counterpart.
Keep reading to learn more about the best CBD capsules online. CBD Capsules are a fast and easy way to digest cannabidiol. Manufacturers created these capsules so that they are as simple to consume as any other pill. You may be surprised to learn that there are different types of CBD capsule. CBD oil isolate based capsules are also an option, but they are currently not mainstream.
These products are typically mixed with inert powders to increase the volume of the capsule. This process is necessary since isolate is extremely pure and only a small amount is required to get a very high dosage.
At the time of writing, these capsules are quite impossible to find, but they are becoming more popular as the price of isolate continues to fall.
There are also water soluble CBD oil capsules. Again, these are new products with outstanding bioavailability, but you will pay a pretty penny for them at present. The most obvious difference is the method of consumption. You can swallow a capsule with water whereas oil users can place it beneath their tongue or add it to food or drink.
CBD oil is more versatile as users can consume it in a manner of ways and change the dose as they see fit. However, capsules allow for convenience since it only takes a second to pop one in your mouth.
Once again, convenience is the word of the day. Some users may dislike the taste of oil and prefer to consume their CBD quickly and effectively. CBD capsules also have the following advantages:. With CBD Capsules, what you see is what you get. If each one contains 25mg of CBD and you need 50mg a day, simply take two capsules. There is no second-guessing and no chance of an overdose. Once you have decided how much CBD you want to consume per day, it is easy to find a capsule with the exact amount.
It also makes budgeting easier. You can take your capsules with you no matter where you go. Keep some in your desk at work, in your gym locker or the medicine cabinet at home. There are dozens of companies selling CBD capsules, but we feel that the following organizations are five of the best. Each capsule contains certified organic CBD; they are non-GMO and contain no solvents, chemical fertilizers, herbicides or pesticides. You won't get the psych high from it.
Helps my friend with PArkinsons tremors. She takes 50mg of tincture and uses the rub morning and night. It is a miracle for arthritis. Tammy M October 9, I have cervical dystonia with head tremors. Been receiving Botox injections with really no good results. I want to try CBD oil to calm tremor down but unsure of which one or how much to take.
Can you help me? Laura Richards October 8, After fighting the effects of thyroid cancerfor 12 years I wanted to die. Now, please understand that these were thoughts with no actions, I was just miserable in pain. After 1 week on the CBD oil, 5 drops under the toungue 2x per day I am a different woman. I now have hope. Cindy September 6, I suffer fr migraines. Currently having Botox injections every three months for the last three years. This has helped went fr 24 to 30 migraines a month to 6 to 8 , now I'm back up to 14 to 20 a month.
My doctor thought CBD oil might help. I have also started having anxiety attacks for a year now. I'm really confused with the dosages. Any thoughts would b helpful. Pat keener September 3, I'm a type 2 diabetic, have degenerative dics, osteoarthritis, skin alergies,finger and feet neuropathy.
What dosage and product is good for these issues. Ebony November 3, I have the same thing. I was told cbd oil mg. Larry August 19, I have crohns dibeates 2 stage kidney failure I take mg of chemicals a day when I get a flair l might lose a lot of blood I've had fistula surgery once darn mean killed me 2 more just gut surgerys little bit of gut removed I tease my gut doctor he schoold just put in a zipper any way I'm looking for something natural to try for pain also where I live if you get caught automatic life so the delima begins how much would any one suggest starting out with thanks for your time also compared to most of the folks mine seems like a minor problem on this site but I would appreciate some advice I hope all you folks have good lives and remember god always loves you even though sometimes you think he may have forgotten you.
Heidi April 9, Hello I have crohns disease severe also. I also have ulcerative colitis I have had part of my upper and lower bowel removed. I am now trying cbd oil the euphoria one I just started taking it so still learning it seems to be helping a lot I take it 4 times a day about a dropper full. If you have any other insight it would be much appreciated Heidi. Pat Irwin August 13, What product should I try and at what dose? I need a high dose. Casey June 3, Hi, I was also diagnosed with MS has anyone given you the correct dosage yet?
Glenda Bishop August 10, I have severe neuropathy in both feet and legs. I just got the CBD oil and I am interested in learning if anyone out there has had any success with this.
I know each case and pain levels are different. Just would like to see some positive remarks from people who suffer with it. I am not looking for a cure just need an update on someone who took and it helped. I already know there is no cure.
I need help with the pain. I had a client using CBD from whole hemp for neuropathy with great success! The most important thing is taking it apart from other medications esp for heart, and giving yourself enough of a dose.
If I were you, I would just go slow for the first few days then go up. Meyers March 21, I also have severe neuropathy, pain in both knees, hips and lower back. I just bought a bottle of Hemp Oil and an unmarked dropper. I need to know how many drops do I start with. Thank you for any help. Diane March 24, I suffer from severe neuropathy in both feet. I bought some CBD oil today and started with 3 drops at 2 pm and 3 drops at 9: I am praying it works. Miss Lyn Nichols July 19, Hi Diane, how did you go on with the CBD oil please.
If it worked how long before you saw any results. I'm scared of flaring everything. Nerve damage across buttocks from a surgeon who found the nerve stuck to the bulge during a laminectomy operation and prised it off. I haven't sat for 5 years and getting worse.
A muscle in my buttock is now throbbing constantly and causing pain to the muscle above. I've only started taking it today but the muscle pain is still as painful. Does it take a while for it to work. Only started on low dose to see what happens. Karen August 13, I have idiopathic peripheral neuropathy I picked up some CBD oil yesterday morning.
I am prescribed to take 75 mg of lyrica 3x per day. I took one yesterday morning and have only used the CBD oil since. I bought the Koi brand, flavored, MG. I used a full dropper yesterday late morning and a full dropper yesterday late afternoon. I used it once today one full dropper and I am amazingly pain free. Lauren June 5, I have severe neuropathy from mid torso down. I started reducing the gabipitin every two weeks because of the success with CBD.
This is my second attempt to get away from the synthetic drugs with CBD oil. The first time was not taking enough, now I take three dropper full everyday. Hi Lauren I've just started today with mg cbd oil. I'm starting low to see what happens.
I've nerve damage across buttocks from a laminectomy. I've not been able to sit for 5 years. I've recently started with a muscle spasm in my left buttock and the muscle above is painful. It is only the first day, also tried a cbd night time tea as well. Do change in muscle pain so tight on my left hand side. How long before felt it starting to work please.
I'm trying not to expect changes straightaway. I also take mg gabapentin and 30mg amitriptyline and I hate both of them - they both can cause muscle tightness affecting the nerve.
Jacki August 12, Acupuncture helped my painful feet. They are or never will be perfect but so much better. Just bought some cbd drops trying tobfigure out how much to take. Denise August 6, I also have a daughter on the Autism spectrum with anxiety. She weighs about - Does anyone else give CBD to someone with autism, and if so, at what dose?
Brenda March 23, I have a friend that gives it to her son whom is severely autistic. It calms him down and helps him to sleep well. Suzanne Arthurs July 22, Keum Chough July 20, Does it mean to say that no more treatment needed and it would cure it?? Indeed mg a day is enormous amount not to mention the cost to be realistic as a treatment.
Your response is appreciated. Eddy December 22, Pardon me, I looked at a clinical trial and they are testing mg twice a day with addition to regular medication one would take for schizophrenia. My dad has severe advanced stage Dementia. Will CBD oil help him at this point? He is now refusing to eat any solid food, but will accept most drinks. In addition, he has lost a great deal of weight even though they're giving him Mega Shakes containing a full meals worth of proteins, etc.
He gets at least 4 of these a day.. Is his Dementia too far gone for CBD oils to help him? Kent Autrey July 8, Emily April 1, Kent, My mother has suffered from severe migraines since she was a child. Six weeks ago, she received the hemp oil tincture I do not know what dosage. She does not take it daily. She rubs a drop or two on her temples at the start of a migraine. The drops worked more effectively for her than her medication did, and now that is all she uses. Mike June 27, Morher-inlaw 78 just diagnosed with lymph node breast cancer.
Due to her age wondered of CBD would be useful and her situation. Chemotherapy would just kill her I believe. Just looking for Alternatives any information would be great thank you. Mike, what kind of breast cancer invasive ductal, I presume? How many of her lymph nodes were positive?
How big was the primary tumor? That type of breast cancer mentioned above, which I had as Stage IA, is treated in postmenopausal women with anti-estrogen drugs called aromatase inhibitors aka AIs: CBD oil is effective for this joint pain it is not, I repeat, NOT a substitute for chemo, radiation or these anti-estrogen drugs.
If she lives in a state where medical marijuana is legal, there are doctors who sub-specialize in certifying applications for a medical marijuana card, and in the interim before the card is issued can advise as to the appropriate dose of CBD oil legal and over-the-counter in all 50 states. Eve Klatt June 12, I have lower back pain with some arthritis and arthritis in my hands. It really does work. I have the drops and ointment. Because of the back pain I never would have been able to go on a hike with my family.
We had a lot of fun. And "No Pain", all day. I'm also Type 2 diabetic. Anxious to see what my A1C is next month. Melanie April 20, Angela Torrance May 1, Hi Candy I also have lower back pain and arthritis in fingers can you tell me what type of oil you take and the dose please I am anxious to see if it will do me any good although Im not sure I can get it in Scotland!?
Rosita June 9, Hi, I had ovarian cancer stage 2 and went to do chemotherapy for 16 times in It came back last year but I did not do chemotherapy or radiation therapy as suggested by the doctor. I am taking hormone therapy at the moment. Can anyone give some idea?. Thank you very much. Lewi May 23, Hi, My dad has severe Neuropathy in both his feet and Parkinsons disease.
There are several kinds of CBD oils out there, what kind would be the best to use brand and what might be the dosage. Thank you very much,Gordon. Customer Care May 25, Unfortunately due to strict FDA regulations I am unable to make claims on our products based on your specific needs, I can however say that CBD is a natural anti-inflammatory and could assist.
I can also share our top selling products in each category. Please view the links below: Doug May 14, What is the right product strength for a 75 yr old female with stage IV lung cancer metastic to her bones. Both for pain and hopefully to slow down and kill cancer cells? Please help me, I am her husband and desperate. Customer Care May 29, Thanks for your interest in our products.
Unfortunately due to strict FDA regulations I am unable to make claims on our products based on your specific needs, I can however share our top selling products in each category. There are so many uses for CBD and it's great to see that you have included the fact that many conditions such as schizophrenia require larger doses of up to 1,mg per dose day JT April 4, Victoria Hebner April 4, The dosage recommendations come from the manufacturers themselves.
I hope this helps. I just started taking CBD oil , I am on my 2nd Hip replacement surgery due to device failures looking at a 3rd surgery.
Has you can imagine the pain, stress and anxiety levels are off the charts. Especially at an otherwise healthy 54 yr women. So i understand from reading posts its best to take it under the tongue. I am taking ml a day. I can tell some difference,is your recommended dosage. I am using for pain , stress and sleep. I appreciate your feedback. Dawn Theilgaard March 23, I was wondering if anyone has has used cbd oil to aid with skitzophrenia. I have read that it helps one to focus and silences the voices one may hear.
I am trying to help my son as he has been on many meds and none have really worked. I have asked his dr about this treatment and he did tell me I could try it. Sandra March 17, My daughter is on the spectrum for Autism and has anxiety. She is 12 years old and weighs about lbs. I'm wondering what dosage to give her for her anxiety? Madelen Poston March 13, My husband has stage 4 liver cancer. He has no appetite, and can't sleep. What strength and how much should he take for relief? Victoria Hebner March 23, Unfortunately, due to strict FDA laws, I am not legally able to say that CBD will help with your husbands specific condition, however I can direct you to some literature to help you better understand what CBD may offer.
I have attached links below. As far as strength and dosage goes, tinctures and concentrates are absorbed the fastest since it goes directly into your blood stream; the dosage on these can be measured and controlled.
Capsules take a little longer to enter your body since it goes through your digestive tract, these are also measured and controlled. I would recommend reading through our page on dosing as well to get a better understanding. Nik Oakley June 14, Customer Care June 15, Douglas Murphy February 2, Have arthritis severe pain in hands started CBD last week almost pain free and makes me feel better.
Debbie ganote December 21, LE November 26, I wanted to tell people here that CBD has been very effective for my anxiety, and helps with insomnia. For me, it was a cumulative effect, after a week of one dropper of oil, I can sleep very well at night. I feel like I am not polluting my body with commercial pharmaceuticals.
I wish everyone here the best, and hope it works for you as well as it has for me. Sfelts February 25, I have it really bad on top of Sciatica. Jerry September 18, I have benign essential tremor, primarily of my hands. I'm 75 years old. I've heard of CBD oil and wonder if it would be beneficial for me.
If so, what would be the suggested amount and dosage? Raquel Torres June 13, I want to give my mom CBD oil she is 97 and not sure how much to give her, she has dementia and has lost her ability to speak, and often cries when I leave the house she is in, my son sent me some oil that is labeled as anxiety relief tincture LadyLady November 17, Did you figure out how much to give her?
Bronson August 14, Use coconut oil or MCT oil to treat dementia. The spice turmeric could help too. My mom is late stage dementia. Gives only tine bit of help, and is not something that reverses dementia. Maybe in someone who can score better than a 14 on the mme it could be of help. But cannabinoid is a different story. Cannabinoids produce better results in less time. Can't say yet that they will reverse anything though. Carolyn September 20, Ted spring May 26, I have severe arthist in my lower spin end hips.
Pain all the time. How much cbd should I start vapeing? Rita Grier October 29, Barb March 31, I am new to using cbd oil. I take 1 tablespoon daily and have had great result from doing this. My issues are arthritis, bulging disc and periferal neuropathy I look forward to my days now with the relief I have achieved with Cbd. Woody May 7, Woody, i also suffer from arthritis and neuropathy in my feet so far. How has cbd oil helped you.
I have severe neuropathy in my feet and legs. I just bought the CBD oil and need to know how many drops to take and has it helped you. Jeannie December 20, I just started vaping CBD for life long anxiety. I will tell you it is a miracle thing. Hardly think of my meds.
I know I have to get off of Klonopin slowly, but I don't need it. Zac February 17, Toni L Tucker March 3,
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