Monday, January 14, 2008

Fibromyalgia: Is disease real?

Finally, recognition. Turns out to be bad, though Fibro made the front page of the NY Times but appparently it's a fake disease. I sure wish my symptoms were fake too.
I am furious about this article (see below) and have been writing about it for hours, but because of "nebulous conditions" like cognitive impairment, I lost the post. I will vent nonetheless.
This article is insulting, irresponsible, ill-researched and biased.
Fibromites are presented as a group of overweight, stressed, over-anxious middle-aged women, obsessing about illness.
Worse, it is based on an misleading and improbable TV commercial for a drug that targets limited and specific symptoms. Fibromyalgia is a syndrome; there are many symptoms and different manifestations of those symptoms in different people. None of that is described in the article. It's very difficult to make generalized statements about Fibromyalgia, yet many are quoted (and unsubstantiated) in the article. Dr Hadler: “These people live under a cloud,” he said. “And the more they seem to be around the medical establishment, the sicker they get.” The doctor implies that avoiding medical professional will render us less sick.
Most people “manage to get through life with some vicissitudes, but we adapt,” said Dr. George Ehrlich, a rheumatologist and an adjunct professor at the University of Pennsylvania. “People with fibromyalgia do not adapt.” One wonders if the same standards apply to people with cancer or other diseases.
Poor research aside, certainly the NYT could try to be more open-minded. The headline itself biased: "is it real?" Guilty till proven innocent? The caption on the picture is also biased: "Lynne Matallano, who SAYS she has fibromyalgia". The implication is that she diagnosed herself. The "experts" interviewed are biased and /or work for drug companies.
Fibromyalgia is often associated with other auto-immune diseases such as Lupus, Sjogren's Syndrome and Rheumatoid Arthritis.
A little more research and a lot more respect please.


January 14, 2008 Drug Approved. Is Disease Real?

Fibromyalgia is a real disease. Or so says Pfizer in a new television advertising campaign for Lyrica, the first medicine approved to treat the pain condition, whose very existence is questioned by some doctors.

For patient advocacy groups and doctors who specialize in fibromyalgia, the Lyrica approval is a milestone. They say they hope Lyrica and two other drugs that may be approved this year will legitimize fibromyalgia, just as Prozac brought depression into the mainstream.

But other doctors — including the one who wrote the 1990 paper that defined fibromyalgia but who has since changed his mind — say that the disease does not exist and that Lyrica and the other drugs will be taken by millions of people who do not need them.

As diagnosed, fibromyalgia primarily affects middle-aged women and is characterized by chronic, widespread pain of unknown origin. Many of its sufferers are afflicted by other similarly nebulous conditions, like irritable bowel syndrome.

Because fibromyalgia patients typically do not respond to conventional painkillers like aspirin, drug makers are focusing on medicines like Lyrica that affect the brain and the perception of pain.

Advocacy groups and doctors who treat fibromyalgia estimate that 2 to 4 percent of adult Americans, as many as 10 million people, suffer from the disorder.

Those figures are sharply disputed by those doctors who do not consider fibromyalgia a medically recognizable illness and who say that diagnosing the condition actually worsens suffering by causing patients to obsess over aches that other people simply tolerate. Further, they warn that Lyrica’s side effects, which include severe weight gain, dizziness and edema, are very real, even if fibromyalgia is not.

Despite the controversy, the American College of Rheumatology, the Food and Drug Administration and insurers recognize fibromyalgia as a diagnosable disease. And drug companies are aggressively pursuing fibromyalgia treatments, seeing the potential for a major new market.

Hoping to follow Pfizer’s lead, two other big drug companies, Eli Lilly and Forest Laboratories, have asked the F.D.A. to let them market drugs for fibromyalgia. Approval for both is likely later this year, analysts say.

Worldwide sales of Lyrica, which is also used to treat diabetic nerve pain and seizures and which received F.D.A. approval in June for fibromyalgia, reached $1.8 billion in 2007, up 50 percent from 2006. Analysts predict sales will rise an additional 30 percent this year, helped by consumer advertising.

In November, Pfizer began a television ad campaign for Lyrica that features a middle-aged woman who appears to be reading from her diary. “Today I struggled with my fibromyalgia; I had pain all over,” she says, before turning to the camera and adding, “Fibromyalgia is a real, widespread pain condition.”

Doctors who specialize in treating fibromyalgia say that the disorder is undertreated and that its sufferers have been stigmatized as chronic complainers. The new drugs will encourage doctors to treat fibromyalgia patients, said Dr. Dan Clauw, a professor of medicine at the University of Michigan who has consulted with Pfizer, Lilly and Forest.

“What’s going to happen with fibromyalgia is going to be the exact thing that happened to depression with Prozac,” Dr. Clauw said. “These are legitimate problems that need treatments.”

Dr. Clauw said that brain scans of people who have fibromyalgia reveal differences in the way they process pain, although the doctors acknowledge that they cannot determine who will report having fibromyalgia by looking at a scan.

Lynne Matallana, president of the National Fibromyalgia Association, a patients’ advocacy group that receives some of its financing from drug companies, said the new drugs would help people accept the existence of fibromyalgia. “The day that the F.D.A. approved a drug and we had a public service announcement, my pain became real to people,” Ms. Matallana said.

Ms. Matallana said she had suffered from fibromyalgia since 1993. At one point, the pain kept her bedridden for two years, she said. Today she still has pain, but a mix of drug and nondrug treatments — as well as support from her family and her desire to run the National Fibromyalgia Association — has enabled her to improve her health, she said. She declined to say whether she takes Lyrica.

“I just got to a point where I felt, I have pain but I’m going to have to figure out how to live with it,” she said. “I absolutely still have fibromyalgia.”

But doctors who are skeptical of fibromyalgia say vague complaints of chronic pain do not add up to a disease. No biological tests exist to diagnose fibromyalgia, and the condition cannot be linked to any environmental or biological causes.

The diagnosis of fibromyalgia itself worsens the condition by encouraging people to think of themselves as sick and catalog their pain, said Dr. Nortin Hadler, a rheumatologist and professor of medicine at the University of North Carolina who has written extensively about fibromyalgia.

“These people live under a cloud,” he said. “And the more they seem to be around the medical establishment, the sicker they get.”

Dr. Frederick Wolfe, the director of the National Databank for Rheumatic Diseases and the lead author of the 1990 paper that first defined the diagnostic guidelines for fibromyalgia, says he has become cynical and discouraged about the diagnosis. He now considers the condition a physical response to stress, depression, and economic and social anxiety.

“Some of us in those days thought that we had actually identified a disease, which this clearly is not,” Dr. Wolfe said. “To make people ill, to give them an illness, was the wrong thing.”

In general, fibromyalgia patients complain not just of chronic pain but of many other symptoms, Dr. Wolfe said. A survey of 2,500 fibromyalgia patients published in 2007 by the National Fibromyalgia Association indicated that 63 percent reported suffering from back pain, 40 percent from chronic fatigue syndrome, and 30 percent from ringing in the ears, among other conditions. Many also reported that fibromyalgia interfered with their daily lives, with activities like walking or climbing stairs.

Most people “manage to get through life with some vicissitudes, but we adapt,” said Dr. George Ehrlich, a rheumatologist and an adjunct professor at the University of Pennsylvania. “People with fibromyalgia do not adapt.”

Both sides agree that people who are identified as having fibromyalgia do not get much relief from traditional pain medicines, whether anti-inflammatory drugs like ibuprofen — sold as Advil, among other brands — or prescription opiates like Vicodin. So drug companies have sought other ways to reduce pain.

Pfizer’s Lyrica, known generically as pregabalin, binds to receptors in the brain and spinal cord and seems to reduce activity in the central nervous system.

Exactly why and how Lyrica reduces pain is unclear. In clinical trials, patients taking the drug reported that their pain — whether from fibromyalgia, shingles or diabetic nerve damage — fell on average about 2 points on a 10-point scale, compared with 1 point for patients taking a placebo. About 30 percent of patients said their pain fell by at least half, compared with 15 percent taking placebos.

The F.D.A. reviewers who initially examined Pfizer’s application for Lyrica in 2004 for diabetic nerve pain found those results unimpressive, especially in comparison to Lyrica’s side effects. The reviewers recommended against approving the drug, citing its side effects.

In many patients, Lyrica causes weight gain and edema, or swelling, as well as dizziness and sleepiness. In 12-week trials, 9 percent of patients saw their weight rise more than 7 percent, and the weight gain appeared to continue over time. The potential for weight gain is a special concern because many fibromyalgia patients are already overweight: the average fibromyalgia patient in the 2007 survey reported weighing 180 pounds and standing 5 feet 4 inches.

But senior F.D.A. officials overruled the initial reviewers, noting that severe pain can be incapacitating. “While pregabalin does present a number of concerns related to its potential for toxicity, the overall risk-to-benefit ratio supports the approval of this product,” Dr. Bob Rappaport, the director of the F.D.A. division reviewing the drug, wrote in June 2004.

Pfizer began selling Lyrica in the United States in 2005. The next year the company asked for F.D.A. approval to market the drug as a fibromyalgia treatment. The F.D.A. granted that request in June 2007.

Pfizer has steadily ramped up consumer advertising of Lyrica. During the first nine months of 2007, it spent $46 million on ads, compared with $33 million in 2006, according to TNS Media Intelligence.

Dr. Steve Romano, a psychiatrist and a Pfizer vice president who oversees Lyrica, says the company expects that Lyrica will be prescribed for fibromyalgia both by specialists like neurologists and by primary care doctors. As doctors see that the drug helps control pain, they will be more willing to use it, he said.

“When you help physicians to recognize the condition and you give them treatments that are well tolerated, you overcome their reluctance,” he said.

Both the Lilly and Forest drugs being proposed for fibromyalgia were originally developed as antidepressants, and both work by increasing levels of serotonin and norepinephrine, brain transmitters that affect mood. The Lilly drug, Cymbalta, is already available in the United States, while the Forest drug, milnacipran, is sold in many countries, though not the United States.

Dr. Amy Chappell, a medical fellow at Lilly, said that even though Cymbalta is an antidepressant, its effects on fibromyalgia pain are independent of its antidepressant effects. In clinical trials, she said, even fibromyalgia patients who are not depressed report relief from their pain on Cymbalta.

The overall efficacy of Cymbalta and milnacipran is similar to that of Lyrica. Analysts and the companies expect that the drugs will probably be used together.

“There’s definitely room for several drugs,” Dr. Chappell said.

But physicians who are opposed to the fibromyalgia diagnosis say the new drugs will probably do little for patients. Over time, fibromyalgia patients tend to cycle among many different painkillers, sleep medicines and antidepressants, using each for a while until its benefit fades, Dr. Wolfe said.

“The fundamental problem is that the improvement that you see, which is not really great in clinical trials, is not maintained,” Dr. Wolfe said.

Still, Dr. Wolfe expects the drugs will be widely used. The companies, he said, are “going to make a fortune.”



7 comments:

HEATHER said...

Thanks for sharing this. I got mad at the Times, about a month ago when they came to my hometown and wrote about how everyone in Appalachia did not take care of their teeth and made us sound like a bunch of tobacco spitting, meth-taking hillbilly rednecks who would rather chew tobaccy than take care of our dental needs. What kind idiots are running things over there now? The CDC recognized Fibro about 3 years ago or so, my fog is creeping in! AARRGGHHH!!!!

Anonymous said...

When I saw the title of the story, it made me wonder if the person was real or fake? I like many fibromites know, that what we have is for real. Who would want to manage with all this pain and medication every day, I know I would rather have more important things to do in life then counting the med's for the week. Pain is a part of me and my life, it's part of the family I can't get rid of like an odd-ball relative. Fibro brings many of it's friends besides pain, and they over stay there welcome. Medication that I take doesn't scare any of them away, it just soothes them at times, so I can get some peace. So is Fibro fake? It isn't in my life. It's very much alive and kicking here and causing a lot of trouble in my body.
Jacki K
North Carolina

Anonymous said...

I only got diagnosed a month ago. I was furious as well. I wrote to the NY Times author, wrote to the aol webmaster for voting on the condition as if people really could, sent the article to my doctor in Boston. OMG it turns out I am fat, middled aged no nester, want to stop working to collect disability. Does that cover all the critics' comments? ....Moreover looking for drugs on a daily basis at least legally ha ha. Nothing could be further from the thruth! Thank God I never share my condition with others than my husband and kids cause apparently I live under a cloud.
PS: I tried Lyrica for 2 weeks and I was blinded one eye. Read below yesterday's posting.
ON DR. WOLFE
He graduated from Medical School in 1966, wrote the Paper in 1990 and now in 2007 he is making statements to the NY times. Obviously he is well past his prime and maybe he wanted to make $ off the Lyrica. Is he now saying that all his world colleagues and followers are wrong? I will be sure to let my doctor/insurance company know that I have been diagnosed me with a fake disease cause I have no interest of taking medicine, being in pain, and I would hate to stop working, something I really enjoy.

Thanks Dr. Wolfe!!!!!!!!! Are you trying to make world news again?

pami said...

It was great to meet you yesterday! Hope you got a chance to discuss this topic after I left. I know it was really getting you down. It has done the same to me and although I have been quite righteous in my expressions of disregard, I've definitely had a few moments pause. I resent the author and the sources quoted within the article for making me second guess myself for even a second.All we can hope for is that the NYT will indeed post one op-ed piece or another on the topic. My hope for all of us is that we can take our various actions of protest and move on as the strong and resilient people we are. This author could never have the capacity to understand what we truly endure and the depth of soul it takes to find even a little joy in life despite this very real disease.

Anonymous said...

Western Witch Says: Sounds like they treat this disease just like they treat everything that is concerned mainly with women...with disdain and disregard and of course the ever familiar "It's all in your head!" Yuck!

Anonymous said...

“You know what Fibromyalgia really is, don’t you? It a few doctors getting together and deciding that if you hurt in these 18 places they’d just all tell you that you have fibromyalgia. Not to say that you aren’t really in pain, but…”

Translation: It’s all in your head and it’s a fake disease because doctors don’t know what’s wrong with you or there’s nothing wrong with you.

3 Words to all of you

SNAP OUT OF IT

Anonymous said...

real or fake? we will never know...there's no way to prove this, so why not medicate these people? if you will never know if its real, why not ease the pain? Seems simple and non-debatable to me...but this world is a cruel place.