Actively lobbying against his proposal? The Colorado Department of
Public Health and Environment, which has been providing legislators with
a fact sheet, on view below. Among the document's arguments: "There is
no evidence of efficacy of marijuana for treatment of PTSD in the
medical literature. In fact, the published literature suggests that such
use leads to addiction and abuse of other substances."
This stand frustrates Steve Fox, director of state campaigns for the
Washington, D.C.-based Marijuana
Policy Project, who not only refutes this statement but points out
that New Mexico has approved medical marijuana for PTSD treatment.
"In New Mexico, there's a medical
advisory board that examined PTSD as a condition for medical marijuana
patients and recommended that it be added as a qualifying condition,"
Fox says. "The secretary of the health department there looked at the
evidence and agreed that it should be available for patients. But in
Colorado, there doesn't seem to be any desire to examine the evidence.
"The standards the health department has set up is almost like an
FDA-approval standard, where they're not going to approve any condition
unless there are rigorous studies demonstrating its usefulness," he
continues. "And while that would be nice, it's well known that the
federal government has stood in the way of effective trials for decades.
That's why we have medical marijuana approved on the state level --
because the federal government has blocked trials."
In Fox's opinion, this policy means the Colorado health department
will continue to oppose the use of medical marijuana in PTSD treatment
despite information available from the state directly to the south.
"If they would simply speak to people in New Mexico, where PTSD is
the most common qualifying condition for medical marijuana treatment at
this point, they would know it's helpful," he argues. "It's being
recommended by psychiatrists" -- as Pace's amendment would require --
"and patients are truly benefiting from it. But they seem to have a
callous disregard for this evidence."
"It's a legitimate treatment, and it's been found to be incredibly
helpful," he says. "So it's ridiculous that our state health department
is proactively fighting to keep our nation's veterans from getting
access to a medicine that could very well benefit them."
Tvert's heard that health department personnel have suggested that
giving medical marijuana to PTSD patients is the equivalent of giving
alcohol to an alcoholic -- "which is incredibly ironic, because many
people who suffer from PTSD also suffer from serious alcohol problems,
which worsens their state of health. Whereas using marijuana can reduce
their alcohol intake and dramatically improve their quality of life.
"We're talking about veterans who've served their country, and as a
result have developed serious problems related to PTSD -- and they're
being denied effective treatment," he adds. "And the worst part of this
is, our bureaucrats at the department of health want that denial to
continue. They clearly don't have the best interests of our veterans in
mind."
Rather than directly address such assertions, the health department
provided the aforementioned release. Read it in its entirety below,
followed by a report and minutes from the New Mexico medical advisory
committee meeting in January 2009 at which medical marijuana was
approved for treating PTSD. The latter were provided by MPP's Fox:
Colorado Department of Public Health and Environment release about
medical marijuana and post-traumatic stress disorder:
Committee Report
Medical Advisory Committee to the New Mexico Medical Cannabis Program
Public Meeting, Thursday, January 15, 2009
Prepared by Steve Jenison, M.D., Medical Director, New Mexico Medical
Cannabis Program
The Medical Advisory Committee to the New Mexico Medical Cannabis
Program held a public meeting on Thursday, January 15, 2009 at the Los
Griegos Community Center in Albuquerque to consider petitions for the
addition of new conditions to those eligible for enrollment in the
Program.
The following is a summary of the recommendations of the Committee:
I. Conditions that are recommended for addition to the list of
eligible conditions:
A. Painful peripheral neuropathy
B. Intractable nausea / vomiting
C. Severe anorexia / cachexia
D. Hepatitis C infection currently receiving antiviral treatment
E. Crohn's Disease
F. Post-Traumatic Stress Disorder (PTSD)
G. Amyotrophic Lateral Sclerosis (ALS; Lou Gehrig's Disease)
H. Fibromyalgia
II. Conditions that are not recommended for addition to the list of
eligible conditions:
A. Depression
B. Environmental Illness
C. Brain Dysfunction
D. Estrogen Replacement Therapy
E. Chronic Hepatitis C Infection (except for those currently
receiving antiviral treatment)
III. Conditions that require further evaluation
A. Chronic pain
B. Arthritis
C. Asthma / Chronic Obstructive Pulmonary Disease (COPD)
D. Chronic Fatigue Syndrome
E. Chronic sinus congestions from blunt facial trauma
For each of the conditions that are being considered for addition to
the list of medical conditions eligible for enrollment in the New Mexico
Medical Cannabis Program, the following factors are discussed:
1. The biologic plausibility that medical cannabis would be helpful
in the management of the condition based upon what is understood about
the biology of cannabinoid receptors and their actions.
2. Published clinical evidence of the effectiveness of medical
cannabis in the management of the condition.
3. The seriousness of the medical condition and whether alternative
medications for its management are available.
4. Whether there are well defined and verifiable clinical criteria
for making the diagnosis of that condition.
5. Specific considerations for including the condition as an eligible
medical condition
I. Conditions that are recommended for addition to the list of
eligible conditions:
A. Post-Traumatic Stress Disorder (PTSD)
1. Biological plausibility:
The two main cannabinoids present in smoked cannabis,
delta9-tetrahydrocannabinol (delta9-THC) and cannabidiol (CBD) appear to
differ in their effects upon induction of anxiety and relief of
anxiety, and they appear to mediate this effect by acting on different
areas of the central nervous system. The endocannabionoid system is
also required for the extinction of conditioned fear responses which are
characteristic of PTSD:
a. Fusar-Poli P et al., "Distinct effects of
delta9-tetrahydrocannabinol and cannabidiol on neural activation during
emotional processing", Archives of General Psychiatry 66: 95-105, 2009.
b. Chhatwal JP et al., "Functional interactions between
endocannabinoid and CCK neurotransmitter systems may be critical for
extinction learning", Neuropsychopharmacology 34:509-521, 2009.
c. Chhatwal JP et al., "Enhancing cannabinoid neurotransmission
augments the extinction of conditioned fear", Neuropsychopharmacology
30:516-524, 2005.
d. Lin HC et al., "Effects of intra-amygdala infusion of CB1 receptor
agonists on the reconsolidation of fear-potentiated startle", Learning
& Memory 13:316-321, 2006.
e. Pamplona FA et al., "The cannabinoid receptor agonist WIN 55,212-2
facilitates the extinction of contextual fear memory and spatial memory
in rats", Psychopharmacology (Berlin) 188:641-649, 2006.
f. Resstel LB et al., "5-HT receptors are involved in the
cannabidiol-induced attenuation of behavioural and cardiovascular
responses to acute restraint stress in rats" British Journal of
Pharmacology 156:181-189, 2009.
2. Clinical data
There are no specific clinical trials data regarding the use of
cannabinoids for the treatment of PTSD. However, there are some
preclinical data related to the treatment of anxiety disorders with
cannabidiol and cannabidiol cogeners. There is also a published survey
study of Vietnam combat veterans in which participants reported that
marijuana use made their PTSD symptoms better.
a. Roser P et al., "Potential antipsychotic properties of central
cannabinoid (CB1) receptor antagonists", World Journal of Biological
Psychiatry 7:1-12, 2008.
b. Bremner JD et al., "Chronic PTSD in Vietnam combat veterans:
course of illness and substance abuse", American Journal of Psychiatry
153:369-375, 1996.\
3. Seriousness of the condition
PTSD is a very serious condition that significantly affects social
functioning and quality of life. It can be difficult to treat with
existing modalities. The lack of documented effective treatment
modalities for PTSD is discussed at length in the Institute of Medicine
Report titled "Treatment of Posttraumatic Stress Disorder: An Assessment
of the Evidence" (IOM, October 17, 2007). In this study, the Institute
of Medicine reviewed 90 randomized clinical trials, 37 pharmacotherapy
studies and 53 psychotherapy studies. The panel concluded that, with the
exception of exposure therapies, there was inadequate evidence to
support the effectiveness of standard interventions for the management
of PTSD. The panel recommended implementation of a rigorous PTSD
treatment research program.
4. Verification of the condition
There are DSM-IV criteria for making the diagnosis of PTSD.
5. Special considerations for the inclusion of the condition
The Medical Cannabis Program should require medical records that
document an assessment by a licensed psychiatrist and a DSM-IV diagnosis
of PTSD. In addition, the psychiatrist should attest that other
treatment modalities have failed to provide adequate relief of symptoms
and that medical cannabis might be of benefit to the patient.
Committee Report
Medical Advisory Committee to the New Mexico Medical Cannabis Program
Public Meeting, Thursday, January 15, 2009
Prepared by Steve Jenison, M.D., Medical Director, New Mexico Medical
Cannabis Program
The Medical Advisory Committee to the New Mexico Medical Cannabis
Program held a public meeting on Thursday, January 15, 2009 at the Los
Griegos Community Center in Albuquerque to consider petitions for the
addition of new conditions to those eligible for enrollment in the
Program.
The following is a summary of the recommendations of the Committee:
I. Conditions that are recommended for addition to the list of
eligible conditions:
A. Painful peripheral neuropathy
B. Intractable nausea / vomiting
C. Severe anorexia / cachexia
D. Hepatitis C infection currently receiving antiviral treatment
E. Crohn's Disease
F. Post-Traumatic Stress Disorder (PTSD)
G. Amyotrophic Lateral Sclerosis (ALS; Lou Gehrig's Disease)
H. Fibromyalgia
II. Conditions that are not recommended for addition to the list of
eligible conditions:
A. Depression
B. Environmental Illness
C. Brain Dysfunction
D. Estrogen Replacement Therapy
E. Chronic Hepatitis C Infection (except for those currently
receiving antiviral treatment)
III. Conditions that require further evaluation
A. Chronic pain
B. Arthritis
C. Asthma / Chronic Obstructive Pulmonary Disease (COPD)
D. Chronic Fatigue Syndrome
E. Chronic sinus congestions from blunt facial trauma
For each of the conditions that are being considered for addition to
the list of medical conditions eligible for enrollment in the New Mexico
Medical Cannabis Program, the following factors are discussed:
1. The biologic plausibility that medical cannabis would be helpful
in the management of the condition based upon what is understood about
the biology of cannabinoid receptors and their actions.
2. Published clinical evidence of the effectiveness of medical
cannabis in the management of the condition.
3. The seriousness of the medical condition and whether alternative
medications for its management are available.
4. Whether there are well defined and verifiable clinical criteria
for making the diagnosis of that condition.
5. Specific considerations for including the condition as an eligible
medical condition
The conditions reviewed by the Medical Advisory Board to the Medical
Cannabis Program will be discussed in the following order:
1. Conditions that are recommended for inclusion in the list of
conditions eligible for enrollment in the New Mexico Medical Cannabis
Program.
2. Conditions that are not recommended for inclusion in the list of
conditions eligible for enrollment in the New Mexico Medical Cannabis
Program.
3. Conditions that the Medical Advisory Board believes need further
examination before making a recommendation.
I. Conditions that are recommended for addition to the list of
eligible conditions:
A. Painful peripheral neuropathy
1. Biological plausibility:
CB1 receptors present in peripheral nerves mediate the major activity
of endogenous and exogenous cannabinoids. There may be a minor role of
CB2 receptors in decreasing inflammatory processes in some forms of
peripheral neuropathy. (Martín Fontelles et al., "Role of Cannabinoids
in the Management of Neuropathic Pain", CNS Drugs 22:645-653, 2008).
2. Clinical data:
Two recently published clinical trials of neuropathic pain associated
with HIV disease and its treatment support the effectiveness of smoked
cannabis in the relief of neuropathic pain. A study of pain related to
brachial plexus avulsion showed a benefit in terms of pain relief and
sleep for two cannabis based medicinal extracts not currently available
in the U.S.
a. Abrams DI et al., "Cannabis in painful HIV-associated sensory
neuropathy; a randomized placebo-controlled trial", Neurology
68:515-521, 2007.
b. Ellis RJ et al. ,"Smoked medical cannabis for neuropathic pain in
HIV: a randomized, crossover clinical trial", Neuropsychopharmacology
34:672-680, 2009.
c. Berman JS et al., "Efficacy of two cannabis based medicinal
extracts for relief of central neuropathic pain from brachial plexus
avulsion: results of a randomized controlled trial", Pain 112: 299-306.
3. Seriousness of the medical condition:
Painful peripheral neuropathy is a serious medical condition that can
have a significant impact upon the mobility, daily functioning and
quality of life of an individual. It is pain condition that is very
difficult to manage in many cases with existing medications.
4. Verification of the medical condition
The diagnosis of peripheral neuropathy can be confirmed by diagnostic
tests and by the evaluation of a qualified medical practitioner.
5. Specific conditions for inclusion of the condition:
All cases of peripheral neuropathy should be verified by objective
diagnostic testing and should be confirmed by a qualified medical
practitioner. Application to the Medical Cannabis Program should be
accompanied by medical records that confirm the presence of intractable
nausea and vomiting that has been refractory to other treatments.
B. Intractable nausea / vomiting
1. Biological plausibility:
CB1 receptors are present both in the dorsal vagus complex of the
brainstem and in the myenteric plexus of the stomach and duodenum. The
role of central CB1 receptors probably mediates the effect of
cannabinoids on "anticipatory" nausea and vomiting. (Croxford JL et
al., "Therapeutic potential of cannabinoids in CNS disease", CNS Drugs
17: 179-202, 2003.
2. Clinical data:
There is an extensive medical literature on the effectiveness of
cannabinoids in the treatment of intractable nausea and vomiting, much
related to cancer chemotherapy-induced nausea and vomiting. This
experience is reviewed in:
Machado Rocha FC et al., "Therapeutic use of Cannabis sativa on
chemotherapy-induced nausea and vomiting among cancer patients:
systematic review and meta-analysis", European Journal of Cancer Care
17: 413-443, 2008.
3. Seriousness of the condition:
Intractable nausea and vomiting has a significant impact upon
functionality and quality of life. It can have an impact as well upon
nutrition and can lead to damage of the upper gastrointestinal tract.
4. Verification of the medical condition
The condition can be verified by medical history and the evaluation
of a qualified clinician.
5. Specific conditions for inclusion of the condition:
Application to the Medical Cannabis Program should be accompanied by
medical records that confirm the presence of intractable nausea and
vomiting that has been refractory to other treatments.
C. Severe Anorexia / Cachexia
1. Biological plausibility:
The appetite stimulatory effects of the cannabinoids are well
described and are mediated by CB1 receptors in the central nervous
system. (Croxford, ibid.)
2. Clinical data:
A randomized placebo-controlled trial of smoked cannabis in patients
with HIV demonstrated benefits in terms of calorie intake and weight
gain:
Abrams DI et al., "Short-term effects of cannabinoids in patients
with HIV-1 infection: a randomized, placebo-controlled clinical trial",
Annals of Internal Medicine 139:258-266, 2003.
3. Seriousness of the condition:
Severe anorexia related to medical conditions can have a significant
effect upon nutritional status and quality of life.
4. Verification of the medical condition
The condition can be verified by medical history, by a nutritional
evaluation and physical examination by a qualified clinician.
5. Specific conditions for inclusion of the condition:
Application to the Medical Cannabis Program should be accompanied by
medical records and the evaluation of a qualified clinician that confirm
the presence of severe anorexia that has been refractory to other
treatments.
D. Hepatitis C infection under current antiviral treatment
1. Biological plausibility:
Treatment of hepatitis C with exogenous interferons in particular is
associated with frequent and significant adverse events including severe
nausea, vomiting and anorexia. The biological role of cannabinoids in
treating nausea, vomiting and anorexia are described above.
2. Clinical data:
There is one clinical trial of the use of oral cannabinoids in the
management of HCV therapy related symptoms. That study showed
significant relief of symptoms, with a higher proportion of oral
cannabinoid users being able to complete a full course of HCV treatment:
Costiniuk CT et al., "Evaluation of oral cannabinoid-containing
medications for the management of interferon and ribavirin-induced
anorexia, nausea and weight loss in patients treated for chronic
hepatitis C virus", Canadian Journal of Gastroenterology 22:376-380,
2008.
One cautionary study is worth noting. Recent studies have found an
association between daily cannabis smoking, hepatic steatosis and
progression of fibrosis in chronic hepatitis C.
Therefore, cannabis could not be recommended at this time for people
with chronic hepatitis C except for those individuals currently
undergoing treatment with interferon:
a. Hézode C et al., "Daily cannabis smoking as a risk factor for
progression of fibrosis in chronic hepatitis C", Hepatology 42: 63-71,
2005.
b. Hézode C et al., "Daily cannabis use: a novel risk factor of
steatosis severity in patients with chronic hepatitis C.
Gastroenterology 134: 432-439, 2008.
3. Seriousness of the condition:
Severe side effects related to exogenous interferon therapy can
significantly affect the ability of the patient to complete a course of
treatment.
4. Verification of the medical condition
The presence of hepatitis C infection and its current treatment are
readily verified with medical records.
5. Special considerations for inclusion of the condition:
Application to the Medical Cannabis Program should be accompanied by
medical records and the evaluation of a qualified clinician that confirm
that the patient has hepatitis C infection and is currently undergoing
antiviral treatment for the hepatitis C infection.
E. Crohn's Disease
1. Biological plausibility:
CB2 receptors within the gastrointestinal tract appear to modulate
intestinal inflammation and limit visceral sensitivity and pain.
Gastrointestinal CB2 receptors are being actively investigated as
targets for treating inflammatory bowel diseases:
Wright KL et al., "Cannabinoid CB2 receptors in the gastrointestinal
tract: a regulatory system in states of inflammation", British Journal
of Pharmacology 153: 263-270, 2008.
2. Clinical data:
A Medline search reveals no published clinical data on the use of
medical cannabis for the treatment of inflammatory bowel disease.
3. Seriousness of the condition:
Crohn's disease can be manifested by severe inflammatory disease and
associated abdominal pain and GI dysmotility.
4. Verification of the medical condition
The presence of Crohn's disease is readily verified by medical
records and by the evaluation of a qualified medical practitioner.
5. Special considerations for the inclusion of the condition:
Application to the Medical Cannabis Program should be accompanied by
medical records and the evaluation of a qualified clinician that confirm
that the patient has Chrohn's disease and that it is refractory to
treatment with other modalities.
F. Post-Traumatic Stress Disorder (PTSD)
1. Biological plausibility:
The two main cannabinoids present in smoked cannabis,
delta9-tetrahydrocannabinol (delta9-THC) and cannabidiol (CBD) appear to
differ in their effects upon induction of anxiety and relief of
anxiety, and they appear to mediate this effect by acting on different
areas of the central nervous system. The endocannabionoid system is
also required for the extinction of conditioned fear responses which are
characteristic of PTSD:
a. Fusar-Poli P et al., "Distinct effects of
delta9-tetrahydrocannabinol and cannabidiol on neural activation during
emotional processing", Archives of General Psychiatry 66: 95-105, 2009.
b. Chhatwal JP et al., "Functional interactions between
endocannabinoid and CCK neurotransmitter systems may be critical for
extinction learning", Neuropsychopharmacology 34:509-521, 2009.
c. Chhatwal JP et al., "Enhancing cannabinoid neurotransmission
augments the extinction of conditioned fear", Neuropsychopharmacology
30:516-524, 2005.
d. Lin HC et al., "Effects of intra-amygdala infusion of CB1 receptor
agonists on the reconsolidation of fear-potentiated startle", Learning
& Memory 13:316-321, 2006.
e. Pamplona FA et al., "The cannabinoid receptor agonist WIN 55,212-2
facilitates the extinction of contextual fear memory and spatial memory
in rats", Psychopharmacology (Berlin) 188:641-649, 2006.
f. Resstel LB et al., "5-HT receptors are involved in the
cannabidiol-induced attenuation of behavioural and cardiovascular
responses to acute restraint stress in rats" British Journal of
Pharmacology 156:181-189, 2009.
2. Clinical data
There are no specific clinical trials data regarding the use of
cannabinoids for the treatment of PTSD. However, there are some
preclinical data related to the treatment of anxiety disorders with
cannabidiol and cannabidiol cogeners. There is also a published survey
study of Vietnam combat veterans in which participants reported that
marijuana use made their PTSD symptoms better.
a. Roser P et al., "Potential antipsychotic properties of central
cannabinoid (CB1) receptor antagonists", World Journal of Biological
Psychiatry 7:1-12, 2008.
b. Bremner JD et al., "Chronic PTSD in Vietnam combat veterans:
course of illness and substance abuse", American Journal of Psychiatry
153:369-375, 1996.
3. Seriousness of the condition
PTSD is a very serious condition that significantly affects social
functioning and quality of life. It can be difficult to treat with
existing modalities. The lack of documented effective treatment
modalities for PTSD is discussed at length in the Institute of Medicine
Report titled "Treatment of Posttraumatic Stress Disorder: An Assessment
of the Evidence" (IOM, October 17, 2007). In this study, the Institute
of Medicine reviewed 90 randomized clinical trials, 37 pharmacotherapy
studies and 53 psychotherapy studies. The panel concluded that, with
the exception of exposure therapies, there was inadequate evidence to
support the effectiveness of standard interventions for the management
of PTSD. The panel recommended implementation of a rigorous PTSD
treatment research program.
4. Verification of the condition
There are DSM-IV criteria for making the diagnosis of PTSD.
5. Special considerations for the inclusion of the condition
The Medical Cannabis Program should require medical records that
document an assessment by a licensed psychiatrist and a DSM-IV diagnosis
of PTSD. In addition, the psychiatrist should attest that other
treatment modalities have failed to provide adequate relief of symptoms
and that medical cannabis might be of benefit to the patient.
G. Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
1. Biological plausibility
Cannabinoids appear to have a neuroprotective effect in certain
neurodegenerative diseases through activity upon CB2 receptors:
a. Weydt P et al., "Cannabinol delays symptom onset in SOD1 (G93A)
transgenic mice without affecting survival" Amyotrophic Lateral
Sclerosis & Other Motor Neuron Disorders 6: 182-184.
b. Shoemaker JL et al., "The CB2 cannabinoid agonist AM-1241 prolongs
survival in a transgenic mouse model of amyotrophic lateral sclerosis
when initiated at symptom onset", Journal of Neurochemistry 101:87-98,
2007.
c. Kim K et al., "AM1241, a cannabinoid CB2 receptor selective
compound, delays disease progression in a mouse model of amyotrophic
lateral sclerosis", European Journal of Pharmacology 542:100-105, 2006.
2. Clinical data
There are no clinical data that are directly relevant to the
evaluation of medical cannabis in ALS. There is one published survey
of the use of medical cannabis by ALS patients that indicates that
patients received benefit in terms of reducing symptoms of appetite
loss, depression, pain, spasticity and drooling, but no relief in terms
of speech and swallowing or sexual dysfunction:
Amtmann D et al., "Survey of cannabis use in patients with
amyotrophic lateral sclerosis", American Journal of Hospice and
Palliative Care 21:95-104, 2004.
3. Seriousness of the condition
ALS is a very serious condition with significant morbidity and a poor
prognosis. Therapeutic options, both in terms of slowing disease
progression and managing clinical manifestions, are available.
4. Verification of the condition
The diagnosis of ALS is verifiable by clinical criteria and
diagnostic tests.
5. Special considerations for inclusion of the condition
The Medical Cannabis Program should require medical records that
document the diagnosis of ALS, and a written statement from the
patient's attending physician that medical cannabis is likely to be of
benefit.
H. Fibromyalgia
1. Biological plausibility
Fibromyalgia is a pain syndrome with a poorly defined
pathophysiology:
Bradley LA. "Pathophysiologic mechanisms of fibromyalgia and its
related disorders" Journal of Clinical Psychiatry 69 Suppl 2: 6-13,
2008.
It is conceivable that the action of cannabinoids of CB1 receptors
might have a beneficial effect upon the pain that is characteristic of
fibromyalgia:
a. McPartland JM. "Expression of the endocannabinoid system in
fibroblasts and myofascial tissues", Journal of Bodywork & Movement
Therapies 12:169-182, 2008.
b. Russo EB. "Clinical endocannabinoid deficiency (CECD): can this
concept explain therapeutic benefits of cannabis in migraine,
fibromyalgia, irritable bowel syndrome and other treatment-resistant
conditions?" Neuroendocrinology Letters 29:192-200, 2008.
2. Clinical data
There are no published clinical data regarding the effectiveness of
medical cannabis in the management of fibromyalgia.
3. Seriousness of the condition
Fibromyalgia can have a significant impact upon social functioning
and quality of life.
4. Verification of the condition
The American College of Rheumatology "1990 Criteria for the
Classification of Fibromyalgia" (Wolfe F et al., "The American College
of Rheumatology 1990 Criteria for the Classification of Fibromyalgia:
Report of the Multicenter Criteria Committee", Arthritis &
Rheumatism 33:160-172, 1990) include:
a. History of widespread pain present for at least 3 months, on both
sides of the body and above and below the waist.
b. Pain in 11 of 18 tender point sites on digital palpation ("trigger
points")
c. In addition to muscular pain, frequent association of the
following signs and symptoms: fatigue, insomnia, joint pains, headaches,
restless legs, numbness and tingling, impaired memory, leg cramps,
impaired concentration, nervousness, major depression
5. Special considerations for inclusion of the condition
For the purposes of the Medical Cannabis Program, the clinical
diagnosis of fibromyalgia would be problematic to verify.