OUCH Volume 5 Issue 1 Spring Summer 2014

OUCH
Optimism and Understanding Creates Hope
ACTION Ontario Patient Advocacy Newsletter
Volume 5 Issue 1
ACTION’S Advocacy Pays Off
ACTION Ontario has been advocating for the need to
better address the diagnosis and management of
chronic pain through the implementation of a comprehensive pain strategy. As part of such a strategy, ACTION Ontario’s professional and patient members have
been sharing their experience and evidence in order to
seek system improvements.
On April 8, 2014, with ACTION
Ontario in attendance,
Ontario Minister of Health and
Long-Term Care Deb Matthews, announced a number
of steps in order to address
chronic pain in the province’s
health care system. She specifically thanked Dr. Angela
Mailis-Gagnon and ACTION
Ontario for their part in
making this happen.
Spring/Summer 2014
Inside this issue:
now there are often long wait times for diagnostic tests
due to inappropriate use.
Additionally, the government reaffirmed its steps to
assist in reducing the inappropriate use of prescription
narcotics. As part of the announcement, Janice
Frampton spoke on behalf of
the millions of Ontarians living
with chronic pain.
Project ECHO
Dr. Ruth Dubin, an ACTION
Ontario board member, first
heard of the Extensions of
Community Healthcare Outcomes (ECHO) project in
New Mexico while at an
American Academy of Pain
Medicine conference in 2012.
Minister of Health and Long-Term Care Deb
Dr.
Dubin
connected with Dr. AnMatthews and representatives of ACTION
drea
Furlan
from Toronto Rehab,
Ontario, UHN and Project ECHO
The first was the announcement of
and ACTION Ontario, about bringECHO Ontario demonstration proing this model to address patient and physician needs
ject that will connect primary care providers from
in Ontario.
around the province with experts in managing chronic
“I’m really excited that we were able to bring to Onpain. The model uses videoconferencing and casebased learning to connect physicians in the community tario – in relatively short time – a model that has worked
so well in New Mexico,” said Dr. Dubin.
with the experts to problem solve on how to manage
chronic pain through the development of care plans
“Patients will benefit from reduced wait times because
and the safe use of treatments like opioids.
capacity to treat pain will be built at the community
level. Currently, patients can wait for months to be able
The second announcement was funding for the develto access a clinician with expertise in treating pain,” Dr.
opment of provincial referral guidelines for magnetic
Dubin said. “The primary care physicians benefit from
resonance imaging (MRIs), computerized tomography
connecting with experts in pain, mental health and
scans (CTs) and other diagnostic imaging in chronic
addiction, receiving continuing
pain. These guidelines will help ensure appropriate use
education and being able to pracof diagnostic imaging equipment so that these tests
tice at the highest level of scope.”
are available to patients who need them, whereas
Dear Readers
2
Physical Therapy
the Brain and
Chronic Pain
2
3
Profile—Dr. Jackie 4
Gardner-Nix:
Mindful Meditation
Soars
Nutrition for
Neuropathic Pain
5
Pain Free Quinoa
Recipe
6
Profile—Jim Smith:
My Journey After
Shingles
6
The Last Word—
POT for PAIN:
Myths and Truths
7
As part of ACTION Ontario’s dedication to the needs of the pain community, several members of
ACTION PNP have completed the Stanford Chronic Pain Self-Management Leader course and are
now qualified to facilitate the Stanford Chronic Pain Self-Management program. The Stanford
program was developed by Canadian Dr. Sandra LeForte and her colleague Dr. Kate Lorig at
Stanford University and is recognized as one of the best and most comprehensive chronic pain
self-management programs available. The six-week workshop consisting of 2.5 hours once
weekly over a six-week period.
If you or anyone in your community would like further information regarding bringing the program
to a community group please email: [email protected] or [email protected] .
&
Leaders Julie Feldman, Alissa Von Bargen,
Glen Hutzul, Nikki Vernon, Lisa Hooper,
Janice Frampton & Nancy Becker-Halford
&
8
Page 2
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Editor’s Message
Dear Readers,
“Pain nourishes courage. You can’t be brave if you’ve only had
wonderful things happen to you.” - Mary Tyler Moore
Over the past year I have watched with amazement and a bit of
envy as our two beautiful granddaughters have struggled with sheer
determination and grit to do what we all did as human beings: sit
up, fall over, do it again, stand up, fall down, do it again, walk, fall
down, do it again. What happens to us as adults I often wonder? Do
we just forget what it is to try? Or are we too afraid to fall down? Or
are we just too embarrassed when we do?
Thankfully I have always been a child at heart, some may even say
childish and extremely determined, even stubborn— I don’t mind.
My greatest successes have always come when I’ve put my heart
on the line and been fearless. Have I gotten hurt? You bet. Have I
been told my dreams and ideas were foolish? Absolutely! Still do.
Due to growing up with an undiagnosed Tethered Spinal Cord I was
never an “athlete” but prior to my five spinal surgeries I had been
fairly fit and active as a flight attendant, wife to Phil and the mother
of four girls. After illness, diagnosis and surgeries that all changed, I
struggled to find a vehicle that I could do, was safe and inspired me
personally to exercise consistently. The treadmill was out because
the constant pounding motion is very hard on my back and legs.
In the Fall/Winter issue, I shared with you that I was disgusted with
myself and could not cope with another sedentary winter. I also
mentioned my discovery of the “Gazelle” as the vehicle for my
transformation. So, now it is with great pleasure that I share with you
the results of consistent exercise. Not only did I lose weight and
inches but a funny thing happened during my last physical examination; my bad cholesterol had decreased and the good cholesterol
had gone up. Also, my creatinine
level, kidney function, had improved – all without the use of
medication.
Did I hurt myself while exercising? Yup;
my own fault, I pushed too hard and
paid the price, a month laid up in bed
in agony. Was it a quick fix? Nope;
slowly but surely the weight came off
and my self-esteem increased. As an
absolute marvelous consequence and
bonus of my new found fitness I am
also now in the process of slowly minimizing a couple of my more toxic pain
medications, something I didn’t think
would ever happen.
Nov. 19, 2013
May 15, 2014
Change can happen – when and if
you are prepared to do the work. This process was 10 years in the
making. Without failure none of us would have success, it’s all part of
learning. We’re not all the same, I know that, but maybe this might
inspire one person to try and take that first little baby step, fall down
and get back up again. It can change your mindset and your life.
Thank you to Dr. Angela Mailis-Gagnon, the life blood of this organization. She demands a lot, but gives ten times as much in return.
Thank you as well to all our contributors on this journey. Your stories
continue to teach, inspire and make a difference.
Have a safe and magical summer
Best, as always
Janice Frampton
[email protected]
www.actionontario.ca
Physical Therapy, the Brain and Chronic Pain
By: Judith Hunter, PhD
Movement is a basic function of the human body. People in pain
move differently. One reason may be the residual effects of the initial injury on a body part itself. However, another reason is the longterm effect of the physiological stress of having a painful condition.
Overtime, the nervous system has “learned” that you are in a stressful situation and it mounts a protective response. Although these protective responses
were useful in an acute pain situation, they
are not useful when the pain is no longer
acute. Muscles fatigue, movement patterns
change, and movement can be more uncomfortable than it should.
These protective responses are not conscious.
They include the normal physiological responses to protect you from a threat. For example, blood supply is
diverted from core muscles to leg muscles that are used to help a
body can run away from a threat. This response is designed to protect you for short periods. However, the persistence of the protective responses is connected to many of the issues that you may be
experiencing, including fatigue, appetite changes, sleep disturbance, and posture issues. Even worse, they make exercise difficult.
There is very good evidence that exercise can impact pain by improving general health, mood, circulation, and tissue healing. Exercise is a core component of managing your chronic pain. But movement has to be efficient before you can benefit, and not do more
harm, from exercise. There is a two-way relationship between movement and pain; each impacts the other. The good news is that there
is an explanation for this response and a
supervised plan of movement rehabilitation
can help the nervous system “unlearn” this
protective responses, move more naturally,
allowing you to participate in the healthful
effects of exercise.
Training the brain
The brain constantly “learns” and “unlearns”
movement patterns. Muscle and joint pain can change how the
brain controls movement (motor control strategies). The nervous
system is wired so that the muscles will respond to an acute stimulus
by moving you away from the stimulus and protecting you from receiving additional painful stimuli from the same source. So we are
wired to learn how to avoid pain. The brain learns quickly to avoid
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Volume 5 Issue 1
(Continued from page 2)
pain. This can persist after the pain is gone so that even though you
may be having a great day, and you may not consciously fear certain movements, the brain may have already re-wired to avoid certain aspects of that movement.
The evidence shows people with chronic pain, can lack “movement
variability”. Normally, we have a number of ways we can perform
even the simplest of movements. For example, you may not realize it,
but there are a number of very slight variations in the way you can
reach up and pick up a book from a bookshelf. But because of the
persisting protective responses, people with chronic pain have much
more stereotypical movements. This makes you less adaptable to
normal changes in posture and movement that occur as you move
across different types of surfaces and through different postures.
This lack of variability in movement patterns becomes a limitation to
recovery of normal function in people with pain. When your movement patterns are limited, muscles can fatigue more rapidly, and
connective tissue can be more easily stressed. This makes movement less rewarding for you and then you will want to move even
less. Thus, pain impacts movement and lack of movement impacts
pain, and so on.
How do physical therapists use movement and exercise therapies to
train the brain?
Physical therapists, also called physiotherapists, are licensed health
care professionals. They are concerned with your physical function
and movement to maximize your physical potential and maintain or
improve your quality of life. Movement is the fundamental tool for
physical therapists. They will help you move better so you can manage your pain and how it affects your day-to-day function including
your ability to exercise. You will be actively involved in your physiotherapy. You may learn how to look after your own injuries, illnesses,
or disabilities.
Physiotherapists assess your pain and movement in detail. They work
toward your mutually agreed upon functional goals so you learn to
control your pain while maximizing your physical function. Movement activities and exercises may be directed to include stretching
or strengthening or endurance activities to help counteract the effects of longstanding protective muscle responses. But, in addition,
the important overall approach is to restore normal movement patterns, with functional movement activities. They help you “Retrain the
Brain”.
A therapist will tailor exercises so they do not cause unwanted protective responses. Strengthening exercises help to desensitize the
nervous system so it is less sensitive to the forces of muscle contractions. Motor stability exercises focus on the deep stability muscles.
These muscles may be inhibited in people with chronic pain. Motor
stability exercises also require you to concentrate. They force the
nervous system to focus on the exercise and away from the pain. In
the beginning, motor control exercises are gentle. This way, the sensitized nervous system does not
interpret the exercises as dangerous for the affected muscles. This type of exercise plan is
called “Graded Motor Activity”.
Some people have such a sensitive nervous system from these
protective responses, that any
movement is uncomfortable.
The physical therapist will use
imagery. Studies show that
imagined movements can start
to retrain the brain as well as
A therapist will
tailor exercises
so they do not
cause unwanted
protective
responses.
the movement itself. This type of
exercise plan is called “Graded
Motor Imagery”.
Physical modalities versus physical therapy
There are many physical modalities that help relieve short-term
pain: ice or heat, (TENS), acupuncture, manual therapies including mobilization and manipulation, massage. Many professions and patients themselves
use these modalities. These modalities in themselves do NOT
constitute physical therapy. Just
like medications, these modalities are “passive”. They are
Judith Hunter PhD
meant to be used so that you
can actively move and function.
The problem is that they can also promote a comforting, “fix-me”
belief. In isolation, they are not considered “physical therapy” for
chronic pain. Your physical therapist should be working with you to
teach you how to manage your pain and movement.
Why is regular exercise important when you have chronic pain?
General exercise: Movement and exercise can help your brain
‘unlearn’ the protective responses to movement. This will help you
move more normally and decrease muscle fatigue and general fatigue. You learn to recognize and distinguish “hurt” vs “harm” and
learn the role of pacing. This helps you increase your activity so you
can do the physical activities you want to do in day-to-day life. The
physical therapist may use a “Quota- system of activity management”, also called “Pacing-up” to help you safely increase movement while retraining the brain to accept that the activity is not
threatening.
Aerobic exercise: You don’t need to run marathons or climb mountains. Aerobic exercise refers to exercise that aims to get your heart
rate up and blood pumping through your body, such as brisk walking, yoga, biking, or swimming. In people with fibromyalgia, researchers have shown that aerobic exercise is beneficial. First, it can flush
out the stress chemicals (like cortisol) out of your blood. The effect of
this is to calm your sensitive nervous system and improve sleep, concentration, and mood. In addition, the blood circulation helps tired,
sore, sensitive and deconditioned muscles get a boost of blood and
oxygen.
Studies have shown that there is a definite time and intensity needed
in aerobic exercise to ease pain. The results are surprising. Stated
simply, the average person with fibromyalgia will need to do aerobic
exercise for just over 10 minutes and their heart rate up to 95-100
beats per minute to get some benefit. Just think – a 10 minute walk
can improve your life, and help you control your pain! In general,
the evidence shows that individuals who have decreased function
due to pain should learn about the benefits and realistic expectations of exercise, including the potential for slight initial increases in
pain. This highlights the importance of professional supervision in retraining movement and determining exercise prescription and as
part of a pain management program.
There are two excellent books available on Amazon to help patients
understand the link between protective responses and pain. One is
called “Why do I hurt?” by Adrian Louw; the other is “Explain
Pain” (2nd edition) by David Butler and Lorimer Moseley. This is also
available as an audio book at http://www.noigroup.com/en/
Product/EPA
Dr. Judith Hunter PhD
Department of Physical Therapy, University of Toronto
Faculty of Rehabilitation Medicine, University of Alberta
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Profile—Dr. Jackie Gardner-Nix
Mindfulness Meditation Soars
Shortly after emigrating from the UK to Canada to start a Terry Fox
Cancer Research Fellowship in 1982, Dr. Jackie Gardner-Nix came
to a realization that eventually led her to create the MindfulnessBased Chronic Pain Management (MBCPM) program in Ontario.
As a medical student, she saw many physicians stepping away
from patients with chronic pain whose treatment
had failed them, and concluded that chronic pain
was an undermanaged practice that needed
attention.
to restore the balance between their mind
chronic stress with mindfulness and meditation
evaluating the effectiveness of these courses
reductions in pain, increased self-esteem, and
mood in chronic pain and other patients.
and body from
practice. Studies
found significant
improvements in
“The psychosocial aspect of pain is very important,” says Dr. Gardner-Nix. “The MBCPM program
basically aims to harness the mind’s power to
quiet the patient’s pain, see pain as an appropriate message that requires compassionate attention, and put patients in control of their pain.”
Dr. Gardner-Nix began her work in pain management in the mid-1980s when she helped set up an
at-home palliative team for cancer patients, while
The MBCPM program features four levels of
doing her cancer research. The team was so succourses, conducted in a similar environment at
cessful that her colleagues convinced Dr. Gardner
various hospitals and health facilities in Ontario.
-Nix to start another at-home palliative program
Patients from Toronto can attend MBCPM classes
when, after finishing her fellowship, she relocated
at a Toronto location including St. Michael’s Hospito Scarborough, Ont., and went into family pracDr. Jackie Gardner-Nix
tal. Patients from outside Toronto and within Ontice. Although her experience was with cancer
tario can join via telemedicine; although courses
pain patients, Dr. Gardner-Nix was referred many
are now being run at some of these locations on-site by newly
chronic pain patients suffering from pain associated with the back
trained MBCPM facilitators. The average number of patients varies
and other parts of the body, in addition to cancer patients. In
per course (between 10 to 70 people), and classes typically run
1998, after 15 years in cancer pain work, Dr. Gardner-Nix decided
for two hours and 50 minutes with a break in between. Small
to dedicate her efforts entirely to finding solutions for chronic, nongroup work also makes up a part of class time to help build trust
cancer pain patients.
and community within each site.
“I was already interested in chronic pain while studying medicine
The MBCPM program is covered by OHIP if led by an MD, with a
in the UK. It was through my work with cancer patients that I realsmall materials and enrollment fee. Facilitators
ized more needed to be done to understand
are usually certified at a Masters or MD level with
and properly treat patients suffering from nonprior experience with mindfulness before training
cancer chronic pain,” says Dr. Gardner-Nix.
to become a MBCPM facilitator. Many have or
From her work with chronic pain sufferers, Dr.
had chronic pain themselves. There is a mentorGardner-Nix came across a common pattern.
ing and certification process, which facilitators
More than 90 per cent had suffered adversity in
undertake after their initial training on the curchildhood, including exposure to parent diriculum and auditing of a course.
vorce, parent alcoholism, death of a loved one,
“Training patients to be mindful of their pain redepression in a parent, and sexual, emotional or
quires an attitude of acceptance and collabophysical abuse. This discovery was one of the
ration, and is not easy. However, we have seen
motivating factors that led Dr. Gardner-Nix to
fantastic, life-changing results from the MBCPM program, with a
establish the MBCPM program.
70 per cent reporting increase in productivity and an up to 25 per
“A lot of chronic pain patients that suffered from childhood ad- cent reporting reduction in medication intake. In addition, a few
versity were highly sensitive individuals that responded strongly to patients are able to return to work after years out of the workit. But many do not realize they have been chronically stressed as force. The Mindfulness Solution to Pain course book has been
result of these challenging experiences. Chronic stress impairs translated and acquired by publishers in Korea and Germany as
healing, especially as we enter middle age when the immune we look into introducing our courses into more countries,” says Dr.
system is less robust compared to when young. To really manage Gardner-Nix.
chronic pain, it is important to get to its source and go below the
Currently, the MBCPM course is offered by trained facilitators in
surface in order to heal,” says Dr. Gardner-Nix.
several regions of Ontario as well as in Melbourne and Las Vegas.
The idea that the mind can affect a person’s health is not new. An additional course is just about to launch in Hong Kong. For
Mindfulness meditation began in 1979 when Jon Kabat-Zinn more information on the MBCPM program, visit http://
opened the first Stress Reduction Clinic at the University of Massa- www.neuronovacentre.com/.
chusetts. His practice helped heal patients by teaching them how
The idea that
the mind can
affect a
person’s health
is not new.
Volume 5 Issue 1
Page 5
Nutrition for Neuropathic Pain
Neuropathic pain is unimaginable. It compares to no other pain. I
learned this after a car accident 25 years ago. The collective pain of
breaking my back, shattering my wrists, smashing my skull, puncturing
my lungs and lacerating my internal organs didn’t rival the agony of
the neuropathic pain I experienced from damaging the nerves in my
spinal cord. My neuropathic pain is best described as an ice pick being stabbed into my bones every 30-to-60 seconds. In the months following my accident, as my orthopedic and visceral injuries healed, the
daily wrath of excruciating neuropathic pain emotionally, mentally
and physically consumed, exhausted and debilitated me. Making
matters worse, there wasn’t as much knowledge about neuropathic
pain then as there is today. So during my four months in acute care
hospital I was told that due to my paralysis it was impossible for me to
feel anything below my level of spinal cord injury and refused any kind
of pain medication.
When I was transferred to a rehabilitation hospital my pain was finally
addressed with narcotic medication. While the meds certainly didn’t
eliminate my pain, it controlled it allowing me to start participating in
my rehabilitation program and rebuilding my life. However, I worried
about the long-term effects of taking anywhere from two to eight pain
killers a day on my stomach lining, liver and overall health. I knew
there had to be a healthier way to address my pain and after 10 years
of suffering I found it. I changed my diet.
Good nutrition can help reduce pain impulses within the nerves, limit
the brains perception of pain, and decrease tissue inflammation and
damage without the negative side effects associated with pain medications. Here are some recommendations how you can help address
your neuropathic pain.
1. Reduce Inflammation
Inflammation of tissues can contribute to the onset and intensity of
pain. A diet high in processed foods, such as refined sugar (pop,
candy, pastries, cakes, cookies etc.), white breads/pasta/rice and
dairy will over time lead to chronic inflammation in the body. Eliminating these kinds of food from your diet will help decrease inflammation.
Additionally, there are certain foods that actively help reduce inflammation such as turmeric (contains a compound called curcumin,
which reduces inflammation) and essential fatty acids (natural oils
from plants and fish), so start introducing and/or increasing these in
your daily diet. If you don’t like fish or don’t eat it three-four times a
week, consider taking daily fish oil supplement (two-four, 1000 mg capsules a day). See side bar for other anti-inflammatory foods.
Anti-inflammatory Foods
·
Turmeric
·
Omega 3 essential fatty acids –salmon, sardines,
mackerel
·
Olive oil
·
Green leafy vegetables
·
Berries
·
Beets
·
Almonds/walnuts
·
Ginger
·
Garlic
*If you are on blood thinning medications – talk to your
physician first before taking Omega-3 supplements
2. Avoid Food Allergens and Food Additives
It is important to identify and eliminate
any food allergies and/or food intolerances from your diet because they can
cause inflammation and contribute to
pain. Some of the most common food
allergens/intolerances are milk, dairy,
wheat, gluten, citrus, corn, eggs, sugar,
soy, peanuts, pork and yeast.
Food additives such as MSG, artificial
sweeteners, colours and flavours can
also be toxic to your nerve cells and
increase sensitivity to pain. Read food
labels carefully and avoid these as
much as possible.
3. Six-Eight Cups of Fluid a Day
Joanne Smith BA, BRT Dip; CNT
When the body has a build-up of toxins
it can irritate the nerves leading to pain. Certified Nutritional Practitioner
Drinking six-eight cups of water, diluted
juice and/or herbal tea can help flush out excess toxins from your
body.
4. Increase B-vitamins
There are eight B-vitamins and many promote healthy nerves and can
provide nerve pain relief. For example, biotin can help in the prevention and management of neuropathy and vitamin B6 plays a critical
role in pain management by making pain-inhibiting neurotransmitters.
Many people are deficient in B-vitamins, so include plenty of vitamin Brich foods in your diet such as avocados, carrots, legumes, lentils, quinoa and whole grains. These foods are also high in fibre so they will
assist in removing toxins from your body. If you don’t eat these foods
on a regular basis consider taking a B-complex supplement.
5. Eat Tryptophan Rich Foods
Eating foods containing the amino acid tryptophan (found in turkey,
eggs and salmon) helps to manufacture a natural pain killer called
serotonin. Serotonin can help increase a person’s pain threshold.
6. Boost Your Immune System
Maintaining a strong immune system is important because bacterial,
yeast and viral infections can cause pain and inflammation. For example, fungal and bacterial infections can produce myotoxins that can
cause inflammation and irritate the nerves resulting in pain.
Consume a diet high in fruits/vegetables and nuts/seeds, which are
high in immune boosting nutrients. Daily probiotic supplements
(minimum 8 billion micro-organisms) also helps support the immune
system.
7. Eat Chili Peppers
When tissues become injured they send a pain message to the brain.
Nerves use a chemical called substance P to transmit pain signals. Hot
chili peppers and cayenne pepper contain a substance called capsaicin, which helps reduce substance P.
By following all of the recommendations I’ve made here I was able to
reduce my daily debilitating bouts of neuropathic pain to just one-two
short episodes a month. I also experienced many other benefits such
as weight loss, increased energy and reduced headaches. While my
neuropathic pain isn’t completely gone there is no doubt that my
quality of life has improved has immensely.
www.actionontario.ca
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(Continued from Nutrition for Neuropathic Pain on page 5)
Try this delicious recipe that combines many pain-relieving ingredients!
Pain Free Quinoa
2 tbsp
olive oil
1 stalk
celery, chopped
2
carrots, sliced
1 small
onion, minced
1 clove
garlic, minced
1 cup
vegetable stock
½ cup
uncooked quinoa
1 tsp
turmeric
¼ cup
fresh parsley
Sea salt & pepper to taste
Instructions
Heat the olive oil in a saucepan over medium heat. Stir in the celery,
carrots, onion, and garlic. Cook and stir until the onion has softened
and turned translucent, about five minutes.
Stir in the vegetable stock, quinoa and turmeric. Bring to a simmer,
then reduce heat to low, cover, and simmer 25 to 30 minutes until the
quinoa is tender and has absorbed the liquid.
Once done, fold in parsley and season to taste with salt to serve.
Joanne Smith BA, BRT Dip., CNP
Certified Nutritionist
Co-author of: Eat Well Live Well With SCI and Other Neurological Conditions
For more information on neurological injuries go to
www.eatwelllivewellwithsci.com
Profile—Jim Smith: My Journey After Shingles
As an individual that suffers from chronic pain, I am going to start this
piece on a positive note. I was recently very pleased to see the recent commercials on the shingles vaccine. As someone who didn’t
originally even know what shingles was, I thought, at last, the info is
out. However, I feel the commercial doesn’t go far enough.
Up to one in two people will develop shingles sometime
in their lifetime and the pain that the commercial demonstrates is absolutely true; however it doesn’t show that
a percentage of those people will have long-term
chronic pain that can fundamentally change their lives
for a very long time. I am one of those percents.
It took a lot of documentation on my part and my specialists’ parts to
be accepted for disability. I was very clear in describing the pain —
deep sharp stabs that would bring tears to one’s eyes and even
worse surface pain, which is best described as a bad burn and then
rubbing sandpaper on it. Even today, I am on a very high dose of
the narcotic fentanyl which does a good job in controlling the deep
pain, but not the surface pain which quickly moves from
a level four to an eight pain scale with 10 being a level
you would wish for death as the day and the clothing
wears on.
My only hope was a specialist I saw a few years ago, a
doctor in his 80’s, that actually hugged me and said I am
so so sorry, but I have had patients that have gotten
some relief after five years. He was right in that the number of pain hours per day has gone down, but still I am
unable to know if I will have a good day or a bad day.
And every evening is bad regardless.
I first experienced the pain in January 2007 and my family doctor urged me to go to the hospital thinking it was
possibly a kidney stone or a heart problem. A day later
the rash started on my torso and back and shingles was
confirmed. I received the recommended antivirals and
then had to wait for the virus to take its course. UnfortuJim Smith
nately, it is now 2014 and I am still suffering. The impact
The impact on my family was huge. For my wife and
was life altering — for the first few years I could not bear the touch of teenage daughter the condition took an enormous toll on our family
clothing or even a gentle breeze on my skin. Today I still cannot
life, social outings and ability to just enjoy what we used to do on a
have bed sheets touch me.
day-to-day basis. The financial impact to my family was significant
even though I did get disability income. The cost to my employer
The lasting pain from shingles has impacted every part of my life. I
was very significant given the payment of disability benefits. I did
held a senior position in government with a staff of over 300 people
find that CPP Disability was supportive and didn’t challenge me the
— a career I had worked hard at and was rewarded by a number of
way my employer’s disability provider did. Seven years of struggle
promotions. That all came to an end as I was no longer able to perwith so many impacts. After seeing the impact on my life, all of my
form at work due to the agonizing pain I suffered after contracting
friends have run to get the shingles vaccine. Today, I have hope
shingles. Fortunately my employer was supportive and I was put on
that the impact of neuropathic pain from shingles can be reduced
special assignments, including a teaching position at an Ontario
through vaccination. I personally would recommend vaccination at
university, that would let me better control my hours. Ultimately I had
age 50, as I was 52 when my life was changed forever.
to go on disability. This resulted in a huge psychological conflict for
me, as I want to work and have committed my life to a career. The
The Ontario government needs to make this vaccine available for
situation was compounded as I was dealing with chronic pain that
free to the public and the public needs to be educated about the
was invisible to those around me.
potential long-term impacts of this illness. From a cost benefit analysis, one month of full CPP disability income is just over $1000. A vacI had gone to a number of pain clinics and had tried a range of
cine that costs less than $200 per dose could prevent the payments
drugs, all with major psychological impacts and no real pain relief. I
of hundreds of thousands if not millions of dollars in
also had a neurostimulator implant that would send signals through
disability income to individuals that are impacted by
my spinal cord to try to out compete the pain signals to the brain.
shingles.
The process involving neurosurgery was significant and unfortunately
The Shingles Virus
only provided limited relief.
Volume 5 Issue 1
Page 7
The Last Word:
POT for PAIN; Myths and Truths
By: Dr. Angela Mailis-Gagnon
This is a topic I have avoided in past articles for OUCH as I considered it truly too hot and messy. However, the issue has reached a
boiling point and cannot be avoided: Is pot useful in the treatment of chronic pain? And if so, how does one get a prescription
for medical marijuana?
actions of cannabinoids have been conducted in Great Britain,
Australia, and the United States, and all have concluded that
smoking pot should be permitted under special circumstances,
such as when patients are terminally ill, or in other cases for a limited time only. All however, suggest research into alternative methods of administration of the active ingredients in marijuana for
rapid action without the risks associated with smoke inhalation.
Before we begin I will provide a brief, historical overview of marijuana, or hemp plant, from my book BEYOND PAIN, published in
2003 with David Israelson. The cannabis sativa L or hemp plant was
one of the first plants to be used by man all over the world to create fibers for the manufacturing of clothes and ropes, food and
medicines and, in social and religious rituals. When it comes to
pain, the extracts of the cannabis plant called cannabinoids were
used by ancient populations thousands of years ago, as well as by
Asian populations in the Middle Ages and for different pains in the
West during the 1800s, with commercial preparations supplied at
the time by the pharmaceutical company Lilly and Squibb.
On July 30, 2001, following a highly publicized Supreme Court of
Canada case, the federal government hastily established a set of
Marijuana Medical Access Regulations. These regulations spelled
out three categories of people who can apply to possess marijuana for medical reasons:
1.
People who suffer from a terminal illness and are doomed
to die within 12 months;
2.
Those who suffer from multiple sclerosis, spinal cord diseases, AIDS etc, provided that all other available treatments have
been tried or found not to be appropriate;
3.
An all-inclusive “non-of-the-above” category, consisting
of those suffering from conditions other than those mentioned
above, provided again that all
Health Canada announced other treatments have failed.
Cannabinoids were however
discontinued as medical As of March 31, 2014,
agents in the 1930s. It was
only in 1964 that the sole psybig changes to the country’s medical marijuana Patients once prescribed
choactive ingredient of canmedical marijuana by their
rules. In a capsule, a) the option for patients to
n a bi s ,
D el ta
9
- TH C ,
physician via a lengthy proc(tetrahydrocannabinol), was
grow their
own pot was ess could either grow their
isolated in pure form. The disown pot or find someone to
covery of morphine receptors
grow it for them. Nevertheless,
revoked,
and they
in the brain and the spinal
from 2001 to now, about
must now
acquire their 37,000 patients had been record in the 1970s led to the
discovery of endorphins, the
ceiving medical marijuana
marijuana
from a
body’s own pain killers. Simiacross the country.
larly the discovery of cannabi- designated provider, and b) the requirement that
noid receptors in the brain
As of March 31, 2014, Health
Health Canada approves the use of medical
(CB1) made scientists quesCanada announced big
tion whether the brain prochanges to the country’s
marijuana was lifted
duces marijuana-like submedical marijuana rules. In a
stances as well. Indeed, two
capsule, a) the option for pasuch
internally
produced
compounds,
c a l l e d tients to grow their own pot was revoked, and they must now ac“endocannabinoids”, were discovered.
quire their marijuana from a designated provider, and b) the requirement that Health Canada approves the use of medical mariAfter that discovery, synthetic cannabinoids were created, some juana was lifted.
of which have other than psychoactive functions. Today synthetic
cannabinoids are in use to increase the appetite of patients with Two kinds of patients visit me in my clinic asking for marijuana preAIDS and for prevention of vomiting and nausea in cancer pa- scriptions. One of my latest cases happened just a couple of
tients who are undergoing chemotherapy.
months ago. This 26-year-old man was a labourer, working for a
large company and handling heavy equipment. He recently apCannabinoids seem to have protective effects on nervous tissues, peared in his place of employment with a license for medical
and may work on inflammation, anxiety and several other condi- marijuana and asked to have a 10-minute break “every 90-120
tions. Numerous animal experiments to date also demonstrate minutes” to smoke a joint. The employer put him on medical leave
that cannabinoids can block many different kinds of pains. A very and asked for an assessment regarding the validity of his claim.
interesting aspect of cannabinoids is their potential to help other
drugs work better. For example, L-DOPA, a drug used in Parkin- While taking a proper history from this healthy looking young man,
son’s disease, works much better in people when combined with I discovered that he lived in the GTA, drives to work in Toronto daily
apomorphine, a cannabinoid. Some cannabinoids are commer- and had been smoking pot for many years before obtaining a
cially available in Canada in the form of pill such as nabilone medical marijuana prescription. Also, for the past three years his
(known as Cesamet) as well as an oral spray (Sativex).
family physician saw him once a year only when renewing his pot
license. When I asked on what medical grounds he was granted a
The current major debate in medical and political circles relates to medical marijuana license, I was presented with a single specialist
the question of whether smoking marijuana for medical reasons
should be permitted. Major reviews of the possible therapeutic
(Continued on page 8)
Page 8
OUCH
The Last Word
(Continued from page 7)
consultation page from 2005, eight whole years ago, saying
“maybe he has fibromyalgia.”
My detailed examination failed to find a single spot of tenderness
to confirm the diagnosis. Naturally, I concluded that I saw no
medical reason for this man to justify his pot smoking, that I did not
agree with the physician who granted him the license, and I expressed serious concerns about him driving under the influence of
cannabis or operating heavy equipment.
On the other hand, this 32-year-old woman, mother of four young
kids, has been my patient for four to five years. She was the victim
of a bad accident when her leg was crushed by her car door
after a truck drove into her. She ended up with a very painful and
twisted foot, which is permanently contracted and deformed as
she walks on the outside of the foot. She is a very good mom, a
very active woman, has taken every prescribed drug properly
and followed every recommendation I’ve made. Unfortunately,
the effect from painkillers is moderate and not effective enough
for her needs.
Lately she started using two-to-three cups of marijuana tea to
enhance the effects of the painkillers and sleep. She is a very
compliant patient who has not done well with all appropriate
drugs I have prescribed for her condition and does not use any
illicit drugs (except pot that she told me about). I have tested her
with urine drug screens and I know she is indeed clear from other
substances, and does not use smoked pot (that means she minimizes the risk to her lungs from other inhaled substances that exist
in a pot cigarette). In other words, she is an ideal patient for medical marijuana, and I had no problems signing the appropriate
papers.
I hope these examples give you an idea of the two types of people that approach me for medical marijuana. The first group is
characterized by many or all of the following: young age, previous pot use, possible other illicit drug and/or alcohol abuse, questionable indication for pain with no evidence of substantial physical pathology, unemployed and/or on disability payments, while
their complaints are vague at best (diffuse body pain, mechanical back pain, insomnia, anxiety, etc.). This is the group I have no
good reason to prescribe pot. The second group includes patients
of all ages or social status, with serious pathology who have
followed medical recommendations faithfully for long periods,
have failed medical management and have serious conditions
affecting the nervous system (such as nerve injury, multiple sclerosis, spinal cord injury, neuropathy associated with AIDS, etc).
Unfortunately, the vast majority of those who approach me seeking medical marijuana prescriptions
belong to the first group
and this is exactly the
population that frightened
family doctors tell me will
overwhelm their offices
once the floodgates of
Medical Marijuana’s new
rules open.
I have reviewed numerous scientific studies (my reviews are in the
e-CARP advocacy newsletter where I write monthly). To summa-
rize for the reader, this is what science
says so far regarding the effectiveness
of pot:
·
Cannabis products in general
and smoked cannabis in particular
work for certain kinds of pain specifically due to injury of the nervous system (AIDS neuropathy, Multiple Sclerosis, Spinal Cord Injury, etc);
·
The effect is no better than
that of weak (but not strong) opioids
or non-opioid drugs for neuropathic
pain;
·
Very low dose of smoked
cannabis three times a day (a single
Dr. Angela Mailis-Gagnon
puff actually each time) may work for
pain and sleep problems in neuropathic pain patients;
·
Higher doses of cannabis have an adverse effect on
memory and attention and can actually increase instead of decreasing pain;
·
When smoked cannabis is compared to cannabis in the
form of a legally prescribed pill on experimental pain, the pill
seems to have longer lasting effects.
So what do the doctors say? The Canadian Medical Association,
the College of Family Physicians of Canada and the Federation of
Medical Regulatory Authorities of Canada and other professional
medical associations, are against the new regulations of Health
Canada, because the effectiveness and safety of smoked cannabis has not been established.
While smoked cannabis can offer some reprieve from pain in
some specific conditions for neuropathic pain, smoked cannabis
is NOT innocuous. A recently published Swedish study on 50,000
Swedish males over a 40-year period showed definite evidence
that smoked cannabis is a risk factor for lung cancer.
Studies also show that users of medical cannabis are at higher risk
than the general pain population for addiction to cannabis and
other drugs, because they a) are mostly young and male, and b)
they have higher rates of mental illness and opioid and illicit drug
misuse. Recreational cannabis use is a well-established risk for psychosis and for the development of schizophrenia. Cannabis use is
associated with mood and anxiety disorders, and an increased
risk of suicide in both psychotic and non-psychotic samples. Preliminary evidence as well links cannabis use during pregnancy to
neuro-developmental abnormalities in infants. Finally, adolescent
users in general appear to be at risk for long-term cognitive impairment, social dysfunction, impaired work and school performance, anxiety and depression, and psychotic disorders.
Health Canada has created a nightmare for both physicians and
patients with these new regulations, so that both physicians and
patients are quite unhappy. As I said over 10 years ago in my
book BEYOND PAIN, when the first medical marijuana regulations
were imposed on doctors by the federal government in 2001, politicians then put “the cart before the horse”. History now repeats
itself only this time, unfortunately, it is a much bigger cart.
Angela Mailis Gagnon, MD, MSc, FRCPC(PhysMed)
Director, Comprehensive Pain Program,
Senior Investigator, Krembil Neuroscience Centre
Toronto Western Hospital,
www.drangelamailis.com
Chair ACTION Ontario www.actionontario.ca
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