A woman, aged 39, has been recommended for Sativex by her neurologist as an add-on remedy to decrease the pain generated by overbearing spasticity in her legs, which makes walking very nearly impossible. She has to use crutches about her home, and a wheelchair when outdoors, as she is at risk of falling.

She is now in high levels of oral morphine to try to tackle the pain, however, is keen to wean herself off the extremely addictive medication as soon as possible, especially if there is another option accessible. Nevertheless, the Worcestershire Area Prescribing Committee, answerable for commissioning medications, has declined her the treatment, stating that they require more proof that it is value for money.

Her caliber of life alters day-to-day. However, the pain that she experiences is continually there, 24 hours a day. Her neurologist believes that Sativex might help as it’s a medication which tackles spasm pain.

There are sections of the country that are capable of getting it, and it has helped quite a few people.

This is not right at all, and it frustrates me that research has ascertained about 48 percent of people who use it display good significant improvement, nevertheless, individually local NHS trusts can currently determine whether they want to provide patients with it or not.

In addition, with anecdotal data hinting high levels of people with MS turn to unlawful cannabis to help tackle the pain, campaigners are at this time crying out on the health service to make it more extensively accessible.

Cannabis itself has served as a curative remedy for hundreds of years, nevertheless, however, it is forbidden in the United Kingdom in its natural arrangement.

There are a lot of people who self-medicate with cannabis, through different support organizations and networks online. It shouldn’t be about where you live, it’s off balance, and entirely wrong. How can you pinpoint who should get medical care merely based on where they live?

It’s a situation which has acquired the assistance of the MS Society, which set in motion its Treat Me Right campaign previously this year to call on health bosses to evaluate prescribing levels for people diagnosed with MS. For years, the government has said that they will bring to justice people who handle cannabis medicinally, that people should wait for the pharmaceutical product to be accessible and that it will then be prescribed.

Well, the product is presently accessible, and it’s not being designated to those who require it most, therefore, that leaves people between a rock and a hard place. People should be given access to it so they’re not compelled to look for what is still an illicit drug.

On reflection, the Area Prescribing Committee did not consider it suitable for NHS funding owing to constraints in clinical trial data and the nonexistence of proof on account of, they did not think it was value for money, especially when then NHS were funding it.

Consequently, Sativex is not sanctioned for usability within Worcestershire Clinical Commissioning Groups. If new evidence becomes attainable, local clinicians may make a resubmission for consideration to the Worcestershire Area Prescribing Committee reciting details of the new details attainable.

MS is not the only condition for which cannabis-derived medication is thought to have a positive effect, and Cancer Research UK is among those charitable institutions which have started to finance comprehensive investigation into how it could be handled to manage various types of cancer.

It is perceived that cannabinoids, the functioning substances found in cannabis, can have a scope of distinct influences on cancer cells grown in the research facility and animal tumours. However, at the moment there isn’t suitable proof from clinical tests to substantiate that they can safely and efficiently treat cancer in patients.

In spite of this, there is knowledge that a few cancer patients do decide to treat themselves with cannabis extracts. These stories can help researchers build a picture of whether these remedies are helping or not, though this is deficient evidence in contrast to properly-run clinical tests.

Cancer Research UK is supporting clinical trials for treating cancer with cannabis derivatives and a synthetic cannabinoid by means of the national network of Experimental Cancer Medicine Centres, in order to assemble reliable data on how suitable these drugs can be managed to help people with cancer.

When I viewed the internet, and looked up Sativex, it visibly pointed out that Nabiximols, trade name Sativex is a trademarked cannabinoid oromucosal mouth spray developed by the UK company GW Pharmaceuticals for multiple sclerosis (MS) patients, who can use it to ease neuropathic pain, spasticity, overactive bladder, and other symptoms.

Nabiximols is distinct from all other pharmaceutically produced cannabinoids currently accessible on account of, it is a blend of composites acquired from Cannabis plants, rather than a mono-molecular artificial commodity. The drug is a pharmaceutical commodity regulated in composition, formulation, and dosage, even though it is still effectively a tincture of the cannabis plant.

Its leading functioning cannabinoid elements are the cannabinoids: Tetrahydrocannabinol (THC) and cannabidiol (CBD). The product is formulated as an oromucosal spray which is administered by spraying into the mouth.

Each spray delivers a near 1:1 ratio of CBD to THC, with a predesigned dosage of 2.7mg THC and 2.5mg CBD. Nabiximols is also being developed in Phase III trials as a possible remedy to relieve pain due to cancer. It has also been examined in various models of peripheral and central neuropathic pain.

If Nabiximols, trade name Sativex is a trademarked cannabinoid oromucosal mouth spray developed by the UK company GW Pharmaceuticals for multiple sclerosis (MS) patients, then for what reason are people being turn down for treatment, and why is it being said that there needs to be more evidence, when the medication is already on the market with Pharmaceutical companies.

Each new drug and treatments has to be thoroughly examined before they are authorized and accessible for patients. It takes ages for a new drug to go from beginning to end to the various degrees of testing. This method is usually termed the bench to the bedside. A new drug is chiefly analyzed in a research facility. If the drug appears to be encouraging, it is conscientiously examined in people. Research that involves people are called clinical experiments.

It is only then that new drugs are appointed and put to use, up till that time they cannot be used on everyone that requires that particular medicine. Therefore, why are people being rejected for treatment with Sativex, it’s easy, it’s called the ‘Postcode lottery’ of the NHS.

If you live in the wrong area, then you won’t get the treatment that you need, if you do live in the correct area, then you will get the treatment that you require. Which means that the NHS is failing to furnish us with universally high caliber care across the country and shows that all care is nothing but a postcode lottery.

If you are not looked upon as ‘sustainable’, then you simply will be unable to obtain the medical care that you require, even if you are in excessive need of it. If it is going to cost the NHS excessive sums of money, and they do not look upon you as sustainable, then you will be sacrificed like a ritual slaughter, you will be eradicated on account of, you will be looked upon as a waste by-product and nothing more than that.

We are being treated like animals. In fact, we are being treated worse than animals because animals simply sense pain or anguish in the moment, and perceive no tangible emotion. Human beings have a tactile sense, emotion and an impulse to fight back, however we are still treated like we are nothing more than beasts of burden.

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