Multiple
Sclerosis (MS) is a painful disease that needs better treatment than
what is conventionally available (just one of many such diseases). In
the United States (US), The National Multiple Sclerosis Society says
that development of more treatments for symptoms of the disease is
one of its priorities. The Society goes on to say that despite the
uncertainties of cannabis
benefits, it supports MS patients' rights to work with care providers
to access medical cannabis in US states where it is approved. The
Society also supports further research to learn more about the
benefits and any potential risks.
In
Australia, in their recent submission
to
the Senate Legal and Constitutional Affairs Legislation Committee
Inquiry into the Regulator of Medicinal Cannabis Bill 2014, MS
Australia (MSA)
and MS Research Australia stated they were committed to supporting
the provision of proven therapies for improving the lives of people
with MS, and that they would continue to monitor the debate regarding
cannabis use for medical purposes and their potential impact on
people affected by MS;
"...
our policy on these issues is guided by a scientific, evidence-based
approach and we would advocate for a regulatory framework that will
facilitate further clinical trials to determine the components,
dosage and frequency of cannabis-based products and their
effectiveness in managing a range of symptoms for people living with
chronic conditions like MS. MSA and MS Research Australia would
welcome products such as Sativex® being made available for people
with MS in Australia, if regulations regarding access to clinically
proven cannabis-derived products were to change."
In
late 2012
the medicinal cannabis based mouth spray Sativex®
was
listed for use for people with Multiple Sclerosis (MS) with muscle
spasticity by the Therapeutic Goods Administration (TGA) in
Australia. MSA says of Sativex®;
"... it
is important to note however that Sativex® does have side effects
that will vary with each case. These can include dizziness,
tiredness, depression, memory loss and nausea."
In
July 2013 both MSA and MS Research Australia wrote to
the Pharmaceutical
Benefit Advisory Committee (PBAC)
secretariat in support of the inclusion of Sativex® on the
Pharmaceutical Benefits Scheme (PBS), although this application was
not approved.
In
an article earlier this year in The Medical Journal of Australia, by
David G Penington (University of Melbourne, Victoria) he points out
that the debate about the medical use of cannabis in Australia has
become confused with the proposal for a formal clinical trial instead
of proceeding to legislation in New South Wales (NSW), the Australian
Capital Territory (ACT) and Victoria. Debates about prohibition
of cannabis have
a long history, as has the proposal
for medical cannabis in Australia.
Politicians are nervous about being 'soft on drugs' but the clinical
trial proposed, if successful, presumes that cannabis would then be
approved and regulated as a pharmaceutical substance. Cannabis can
never be a pharmaceutical agent in the usual sense for medical
prescription, as it contains a variety of components of variable
potency and actions, depending on its origin, preparation and route
of administration. Consequently, cannabis has variable effects in
individuals. It will not be possible to determine universally safe
dosage of cannabis for individuals based on a clinical trial.
While
there is a plethora of anecdotal claims to draw from to suggest that
cannabis in general eases pain, a clinical study
at
the University of California (UC San Diego) backed up the claim in
2012. The study of adults with MS showed that smoked cannabis may be
an effective treatment for spasticity, a common and disabling symptom
of this neurological disease. The placebo-controlled trial also
resulted in reduced perception of pain, although participants
reported short-term, adverse cognitive effects and increased fatigue.
They found that smoked cannabis was superior to placebo in reducing
symptoms and pain in patients with treatment-resistant spasticity, or
excessive muscle contractions. Earlier reports suggested that the
active compounds of medical cannabis were potentially effective in
treating neurologic conditions, but most studies focused on orally
administered cannabinoids. There were anecdotal reports of MS
patients that endorsed smoking cannabis to relieve symptoms of
spasticity.
However,
this trial used a more objective measurement which graded the
intensity of muscle tone by measuring such things as resistance in
range of motion and rigidity. The secondary outcome, pain, was
measured using a visual analogue scale. The researchers also looked
at physical performance, cognitive function and asked patients to
assess their feeling of 'highness'. Although generally well
tolerated, smoking cannabis did have mild effects on attention and
concentration. The researchers noted larger, long-term studies are
needed to confirm the findings and determine whether lower doses can
result in beneficial effects with less cognitive impact. Four other
human studies on control of neuropathic pain also reported positive
results and added to the growing body of evidence that cannabis has
therapeutic value for selected indications and may be an adjunct or
alternative for patients whose spasticity or pain is not optimally
managed.
Some
of the side effects that occur from taking pharmaceutical drugs for
treating MS can include stress,
depression
and
fever,
any of which can last for months. But medical cannabis can be used to
reduce these factors as well as giving patients an overall sense of
well-being. Thanks to medical cannabis, MS symptoms such as muscle
spasms, tremors and effects on speech and vision can also be
relieved. Other common side effects which cannabis can relieve
include dizziness, headaches and fatigue.
Some
patients who appear to be bound for wheelchairs have claimed that
cannabis helps them walk. A study in the US and UK in the late 1990's
of 112 MS patients published by the European Journal of Neurology
found that 70% of respondents who used cannabis claimed improvement
in several symptoms. Weakness in legs was one of the symptoms, along
with pain in legs and spasticity when walking. A study in 2009 by the
Global Neuroscience Initiative Foundation suggested that cannabis
helps improve mobility among MS patients. Whole
plant cannabis extracts in the treatment of spasticity in multiple
sclerosis: a
systematic review,
reached
the conclusion;
"We
found evidence that combined THC and CBD extracts may provide
therapeutic benefit for MS spasticity symptoms. Although some
objective measures of spasticity noted improvement trends, there were
no changes found to be significant in post-treatment assessments.
However, subjective assessment of symptom relief did often show
significant improvement post-treatment. Differences in assessment
measures, reports of adverse events, and dosage levels are
discussed."
Numerous
studies have also shown the efficacy of medical cannabis in treating
neuropathic
pain,
which is the most
common pain
type experienced by patients with MS. For example; Low-dose vaporised
cannabis significantly improves neuropathic pain; a double-blind,
placebo-controlled, crossover study
was
conducted evaluating the analgesic efficacy of vaporised cannabis in
subjects, the majority of whom were experiencing neuropathic pain
despite traditional treatment. Patients with central and peripheral
neuropathic pain underwent a standardised procedure for inhaling
medium-dose (3.53%), low-dose (1.29%) or placebo cannabis.
Psychoactive side effects and neuropsychological performance were
also evaluated. Mixed-effects regression models demonstrated an
analgesic response to vaporised cannabis. There was no significant
difference between the 2 active dose groups' results. The results
were comparable to those of traditional neuropathic pain medications;
cannabis has analgesic efficacy with the low dose being as effective
a pain reliever as the medium dose. Psychoactive effects were minimal
and well tolerated, and neuropsychological effects were of limited
duration and readily reversible within 1 to 2 hours. Vaporised
cannabis, even at low doses, may present an effective option for
patients with treatment-resistant neuropathic pain. The analgesia
obtained from a low dose of delta-9-tetrahydrocannabinol (THC
[1.29%]) in patients, most of whom were experiencing neuropathic pain
despite conventional treatments, is a clinically significant outcome.
As a result, one might not anticipate a significant impact on daily
functioning.
In
the past few years, studies into MS and cannabis have exploded.
Granny
Storm Crow's List has
hundreds of links to everything cannabis from scientific papers
through to blog posts and anecdotal articles. PubMed
comprises
more than 23 million citations for biomedical literature from
MEDLINE, life science journals and online books as part of the
US National Library of Medicine. Google
Scholar is
another resource for finding scientific, medical research and
information, online. One
thing that MS and cannabis have in common is the medical community, in general, doesn't seem to have many answers to their mysteries. Some
scientists, for example, seem to be in the dark about the side
effects of medical cannabis, MS cures and how to speed up the
research on both. What many patients already know is cannabis
relieves pain, often with fewer side effects than conventional
medicine.
adapted
from an article by the Medicinal
Marijuana Association
further
information from The Medical Journal of Australia, Safe
Access Now,
Granny
Storm Crows List 2015 and
MS
Australia
Synthetic replication of a nontoxic plant, so pharmaceutical companies can profit. The plant, the whole plant, and nothing but the plant.
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