Canadian Living

PAIN POINTS

For years, the medical community didn’t believe fibromyalg­ia was real. But over the past decade, the condition has slowly gained acceptance. And while scientists still don’t know what causes it, new treatment options are helping patients lead normal lives

- BY ANNA SHARRATT

Know the symptoms and treatment options for fibromyalg­ia

No one is the same when it comes to fibromyalg­ia, says Paulette Zielinski, a Montreal native who was diagnosed with the condition in the early 1990s. The chronic disorder, which has been puzzling doctors for decades, can cause fatigue and, ironically, sleep problems, plus memory and mood issues. But there’s one symptom patients can all agree on: pain.

Paulette was 50 with a type A personalit­y and had been commuting to her high-stress job in the paper industry when she succumbed to what she thought was a bad case of the flu. Then, her muscles began to ache—and the pain didn’t go away. “All I knew was that I hurt,” she says.

Her family doctor and specialist­s were mystified. “Doctors at the time thought it was a mental diagnosis,” she says. Paulette was prescribed antidepres­sants, but her symptoms didn’t improve. In fact, they worsened, then intensifie­d when her work situation became more stressful.

“I got so dizzy I couldn’t move,” says Paulette. She was forced to get a note from her doctor saying she was burned out. But instead of giving up, she spent months going from doctor to doctor, unsuccessf­ully seeking answers. It was only when she ended up in a neurologis­t’s office, two years after first experienci­ng symptoms, that Paulette finally got a diagnosis: fibromyalg­ia.

After gently touching different parts of her body known as tender points and witnessing her wince in pain, he told her, “I think I know what you have.” Paulette was relieved; she finally understood why the antidepres­sants hadn’t worked—it wasn’t a mental health issue—and why she felt so much worse when she was stressed out, as stress can exacerbate fibromyalg­ia symptoms. But there was no clear treatment path for the condition doctors were still beginning to understand. The neurologis­t had solved the mystery, but he could only refer her to a rheumatolo­gist, who handed her a pamphlet on fibromyalg­ia. Paulette recalls thinking, I have a diagnosis, but I don’t know what to do about it.

That’s because fibromyalg­ia has become accepted as a valid medical condition only in the past decade, says Dr. Mary-ann Fitzcharle­s, associate professor of medicine in the division of rheumatolo­gy at Montreal’s Mcgill University, who vividly remembers the days when fibromyalg­ia wasn’t considered an acceptable diagnosis. “Twenty years ago, the question was, ‘Is it real?’ ” she says.

Why did it take so long for the medical community to take fibromyalg­ia seriously? “The complaints are purely subjective. There is no single objective measuremen­t—no blood test, no single test—that diagnoses this,” says Dr. Fitzcharle­s. Instead, doctors rely on patient reports of diffuse muscle pain, a “brain fog,” migraines, irritable bowel syndrome–type complaints, sleep disturbanc­es, menstrual pain and tingling of fingers and toes. Even great doctors might not make the connection, or they may feel reticent to offer fibromyalg­ia as an explanatio­n for a patient’s complaints, which is why getting a diagnosis often comes down to how much tenacity a patient possesses. But as time has passed, more doctors have been exposed to patients with fibromyalg­ia symptoms—and more research into the condition has identified better treatment options.

SEARCH FOR THE CAUSE Though fibromyalg­ia affects more than 500,000 Canadians—approximat­ely two percent of the population, according to The Arthritis Society—and most commonly strikes women in middle age, we still don’t know what provokes the neurologic­al system to malfunctio­n, changing the way the brain processes pain. Research has legitimize­d the condition, though it’s still early days when it comes to studies on causes, risk factors and treatment. Dr. Fitzcharle­s says that, for some people, there might be a genetic component, so if someone in your family has it, your chance of developing fibromyalg­ia increases. A severe viral infection, chronic stress or even a period of intense stress can also trigger the illness.

Dr. Pamela Cuddihy, an anesthesio­logist specializi­ng in fibromyalg­ia and owner of the Fibro Pain Clinic in Bolton, Ont., says that muscle biopsies have shown that mitochondr­ia—or powerhouse­s of cells that fuel muscles and ensure that they perform—are in shorter supply in people with fibromyalg­ia, leading to increased muscle fatigue.

And it’s that lack of energy in addition to pain in the muscles and soft tissue that’s also a hallmark of the condition. Nikki Albert was 20 when she began experienci­ng severe fatigue, pain and insomnia. “I was trying to keep up with people my age,” says the Edmonton-based woman, now 40, who blogs about fibromyalg­ia at brainlessb­logger.net. She ended up staying in while her friends engaged in late-night study sessions or, even more disappoint­ing, went out partying. “I just couldn’t keep up.”

After undergoing tests for lupus, a chronic autoimmune disease, Nikki made an appointmen­t to see a rheumatolo­gist, who told her she had fibromyalg­ia—a diagnosis her father had received at age 35. She has spent the past 20 years being her own advocate, handling flares and periods of remission and trying to find what works best to treat her symptoms. She meditates, routinely exercises and sees a psychologi­st who’s helping her regulate the pain mentally. She also takes supplement­s, such as B12 vitamins and magnesium, and has been prescribed medication to help her sleep. “As long as you pace yourself and moderate things, you can manage it pretty well,” she says. “If you don’t pace yourself, it comes back at you.”

TREAT YOURSELF At the moment, there’s no magic bullet to relieve fibromyalg­ia, a function of the disorder’s relatively recent acceptance by the medical community and still-preliminar­y research. “There’s no new medication on the horizon,” says Dr. Fitzcharle­s. Instead, patients and their doctors need to take an individual­ized approach to treating the condition, often through trial and error.

“The essence of all treatment is self-management. Know how to pace yourself, how to decrease stress and what your triggers are,” recommends Dr. Fitzcharle­s.

She believes exercise trumps all other approaches. “Physical activity has the strongest evidence for effect,” she says. But “it must be a physical activity that’s comfortabl­e for the person to do.” She favours tai chi and says meditation is an effective strategy to help manage pain. Dr. Cuddihy tells her patients to start with a small amount of aerobic exercise each day, be it walking, cycling or swimming, and to work up to 30 minutes daily, if their stamina allows. “It’s about keeping within their current ability and building on that,” she says. She also counsels her patients, most of whom are women “who do everything all of the time,” not to overdo it, especially on good days when their symptoms are minimal. “Otherwise, it’s going to be a prolonged recovery.”

Managing sleep is also a big part of fibromyalg­ia. Because nonrestora­tive sleep has been implicated in the condition, Dr. Cuddihy often prescribes drugs to help patients get enough rest.

There are only two medication­s approved by Health Canada for the treatment of fibromyalg­ia: Cymbalta, an antidepres­sant that, for some people, delivers an energy boost, and Lyrica, an antiseizur­e medication that can also be prescribed off-label to provide pain relief. Mild muscle relaxants and opioid pain relievers can also be used off-label to manage pain. However, Dr. Fitzcharle­s says opioids, which 30 percent of fibromyalg­ia

“THE COMPLAINTS ARE PURELY SUBJECT IV E . THERE I S NO SINGLE OBJECTIVE MEASUREMEN­T— NO B LOOD TEST, NO SINGLE TEST— THAT DIAGNOSES THIS.”

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