Wednesday, 31 October 2012

Obamacare vs. RomneyCare - Poll Results

The 2012 U.S. Presidential Election is coming down to the wire... less than one week to go... and it's finally time for me to weigh in on the Obamacare vs. Romneycare debate. More specifically, which man, as president, would be better for people with fibromyalgia?

Before I spout my opinion, let me tell you what YOU said.


In a nutshell, roughly half of all respondents felt that Obama would be better, one in four felt Romney would be better; and the remaining one in four either didn't know or felt there was no difference between the two men. To be honest, I find these results not at all surprising... and here's why.

To begin with, Romney himself, during this campaign, claimed that he was writing off anyone relying on government financial support... he was conceding them to Obama. What this means is that any of you who are receiving government assistance for disability or for unemployment, Romney doesn't really really value. He is already convinced you won't vote for him, and doesn't see this as a problem. How does that feel?

Second, although Obama's health care reform is not perfect, it is skewed towards helping those who cannot afford private insurance or who are otherwise ineligible for it. In my years working with many patients with fibromyalgia, I found that many were dropped by their private insurance carrier once fibro was diagnosed. Some individuals who continued to work, lost their insurance when their company switched from one insurance carrier to another, because each employee had to be approved before being covered. Others retained their insurance, but only for non-pre-existing conditions... so, if you had fibromyalgia before your company switched insurers, you were out of luck. Returning to a system that relies predominantly on private insurers, as Romney and Ryan intend (as a priority), will open all these cans of worms again for Americans with fibro, and many will lose their insurance one way or the other. Obama has fought to make sure those who can't afford or are otherwise ineligible for insurance still can get the health care they need (and, in his and my opinion both) deserve.

Also, as someone who has lived and worked as a physician in both countries, let me tell you a little bit about how insurers pay emergency rooms or clinics (as an example) for services, if you happen to go there. Hospitals and clinics generally have negotiated arrangements with insurers, so they pay only a percentage of the actual bill. For example, if you go to the ER and have an X-ray done, the charge might be $350 for the X-ray itself, but also $250 to cover the fee of the doctor who ordered it, and $250 for the radiologist who reads it. The final bill for that one X-ray, therefore, will be $350 + $250 + $250 = $850.  Wow, right?  BUT, if you have private insurance and they are billed, the hospitalmight only be paid $200, and yet the bill is considered paid. But what happens if you DON'T have private insurance and, hence, DON'T have a pre-negotiated  arrangement for the hospital? Answer: You are on the hook for the full $850. It is for this reason that, despite Romney's and Ryan's assertions that the U.S. can't AFFORD universal health care, in fact, universal health care is less expensive... because hospitals and emergency rooms, and clinics and private physicians all have pre-negotiated arrangements with the universal insurance provider, so NO ONE has to pay $850 for an X-ray that the hospital is actually happy to accept $250 for. Evidence of this fact is that health care costs in Canada are much lower, per person, than in the U.S.... the two countries aren't even close. In fact, health care services in the U.S. are among the most expensive in the world. And does that make U.S. health care better? The answer is a resounding no. In a just published study, the U.S. was found to have the worst health care delivery system of any of the world's economic superpowers. Again, I truly believe that Obama's health care plan is intended to change this.

Another issue I'll discuss thaty favors Obama over Romney is their stance on women's issues, since fibromyalgia is predominantly a disease of women, with 80% or more of diagnosed cases being female. According to Romney and Ryan, women's disease screening procedures like mammography (for early detection of breast cancer) are 'non-essential' and should not be covered by insurers. Though long considered an 'invisible disease', the truth is that we now have the technology (via specialized imaging scans like SPECT and functional MRI) to SEE pain, and considerable research is being conducted at several centres around the world to refine such tests, as well as to develop blood tests to facilitate in the diagnosis of fibromyalgia. This is a critical issue because one in four doctors in North America still believes that all fibromyalgia patients are faking. Once an objective test is available to diagnose this disorder, many if not the vast majority of these naysayers will become believers. But if Romneycare won't even cover a long-standing, routine and relatively inexpensive screening test for breast cancer, what chance is there it will spring for ANY of these new tests for fibro? Answer: virtually none.

I pride myself on being a fairly balanced and even-minded person; so I would like to say a few nice things about Romney here; but frankly, in terms of the fibromyalgia and chronic pain issue, I just can't see them. Each person who reads this must make their own decision. But I've made mine as a dual citizen who is eligible to vote in both Canada and the U.S., and as a physician, researcher and staunch fibromyalgia patient advocate.

I'm sorry, Mitt. But Obama and Obamacare have my vote.



Kevin White, MD, PhD, multiple award-winning researcher, author, teacher & speaker

Tuesday, 16 October 2012

Breaking Thru Hits #3 on Amazon

Thanks to everyone who has bought my fibromyalgia book or has recommended it to someone else... just today, it climbed to #3, as the third most popular book on fibromyalgia at Amazon.


Of course, my goal is to have it hit #1 in this list and the top 100 overall at Amazon. Why? Because the top 100 books at Amazon make other best-seller lists, like the NY Times best seller list... and then the book can really take off. Note that 15% of GROSS proceeds are being donated to charity to fund fibromyalgia research. It'd be really great to see my book start making serious money for research purposes to help find a cure for fibro, with other proceeds going towards supporting other charities like the Kid's Help Phone and Big Brothers, Big Sisters.

So PLEASE let others know about my book, which you can check out at
http://thefibrofog.com

Thanks


Kevin White, MD, PhD, multiple award-winning researcher, author, teacher & speaker

Tuesday, 25 September 2012

Six Secrets to Living Better with Fibromyalgia



Yesterday at around 4:30 p.m., I received a phone call from Harry Douglas, the host of a nationally-syndicated radio show.   The first thing he said was: “This may seem like a strange request, but stick with me, Doc.  I want you to be on my radio show, Car Concerns Radio U.S.A.”  I laughed. Really?  “I know it sounds strange, Doc,” he said. “But I talk all the time about car’s engines and tires and so on... but the most important piece of any car is the nut behind the wheel.”  It turns out he also does shows on things that affect drivers, and wanted to do one on fibromyalgia.

“When do you want me on the show?” I asked.

“How about tomorrow morning at nine?” he answered.

So now it’s 8:43, and I’m quickly finishing up this blog, because I just KNOW someone is going to call in (it’s a call-in show) and ask me how to treat fibromyalgia.  So here are my Six Secrets to Living Better with Fibro.

Before I get into them, may I say that, although no one has ever proven the ability to CURE fibro, fibromyalgia CAN be treated. Again, not cured… but certainly treated to the point that people feel better than they did. 
 
There are six secrets, because there is no ONE THING that reverses fibro. You can’t just shove a couple of cinnamon sticks up your nose, wait 5 minutes, and expect to feel 98.2% better.  And all those books that claim that all you need to do is start this or stop that and everything will melt away... well, go back to my cinnamon stick example. Sure, SOME people DO respond beautifully to a given drug or therapy or dietary change (especially the small percentage who are gluten sensitive). But MOST DO NOT. For the  vast majority, feeling better with fibro requires several things. Here are the six I think are MOST IMPORTANT.
The SIX SECRETS to doing better with fibromyalgia are these:
(1)    Learn as much as you can about what fibromyalgia, including what it is and what it isn’t (do you remember all those myths I told you about at the start?); no one likes to fight in the dark; truly knowing what you are up against and climbing out from all the lies, misconceptions and misunderstandings is a HUGE first step.

(2)    Educate important people around you, so they can be more supportive (some doctors are even open to being educated, if the source is legitimate. True stories: one patient gave her disbelieving doctor a copy of my book and received a letter of apology from him a week later; and a lawyer in England was gifted with one from a woman fighting for disability payments, won the case, and now gives FREE copies to ALL his clients).

(3)    Recognize that the management of fibromyalgia is not usually a single, simple thing, like a little pink pill you take twice a day, or avoiding sugar, or bathing in coconut oil. Long-term results with fibromyalgia usually require a combination of approaches that include things your doctor or other health care professionals can do for you, AND things you must do for yourself, like lifestyle, dietary, and attitudinal changes, as well as carefully increased activity and exercise

(4)    Here I’m largely going to repeat what I just said, that doing better with fibro requires things that YOU must do. Don’t rely totally on your doctor or your therapist or anyone else. In fact, the more you can do for yourself, the more control you have over your own health.

(5)    Don’t overlook or let others other treatable conditions that often co-exist with fibromyalgia, like tendonitis of the heel causing foot pain, which might result in you being unable to walk but can often be treated with a custom shoe insert +/- occupational therapy +/- a short course of an anti-inflammatory drug; this is where having a conscientious and fibro-educated doctor or therapist is a HUGE plus.

And finally…
(6)    Keep a sense of humour - this might seem silly, but the fibro patients I’ve seen do best are those who still can laugh, even when they hurt. Perhaps my favorite patient of all time was a man who had terrible fibro but loved to laugh.  Every time I saw him, he’d tell me about how the last thing I’d tried with him hadn’t worked, and then would start telling me a couple of good jokes he’d just heard.  One day after about a year of trying one thing after another, he came back and something HAD worked. He was feeling better than he had in years. The last time I saw him he was volunteering at a local railway museum 20-30 hours per week and “loving it”.  This time, he was doing so well we hardly had to talk about his pain or fatigue at all. But he STILL had a long list of new jokes to tell me.

Dr. Kevin White

IMPORTANT NOTICE: Note that, in recognition of National Pain Awareness Month, all through September, my book is selling for $18 off the cover price through the publisher, Wortley Road Books. Get your copy now before the price goes up again.

Buy my book


Kevin White, MD, PhD is a world expert in fibromyalgia research and treatment, a staunch fibromyalgia patient advocate who tours Canada, the U.S. and Europe educating people about the realities of fibromyalgia, and the multiple award-winning author of Breaking Thru the Fibro Fog: Scientific Proof Fibromyalgia Is Real. Visit him at http://thefibrofog.com. His award-winning, best-selling book is available as both a printed soft-cover and eBook at http://amazon.com and bookstores.