New paper: Inability of ME patients to reproduce VO2 max indicates functional impairment
- Thread starter Countrygirl
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Nothing was done to treat H pylori induced gastric ulcers either. Doctors largely ignored the finding. They were even stopped from talking about it at medical conferences, as most conferences were funded by companies that produced antacids. This is a matter of public record, its not conspiracy.
Yet when patients demanded treatment, became active to make it happen, things changed.
Nothing may happen with CPET only if we let nothing happen. This is hard evidence, not quite as good as it could be but darn close. Its irrefutable when a patient is tested, and any of us who can afford it and are not too sick to prevent it can get tested. People are winning legal challenges based on this.
Our researchers are now using CPET. Most are aware of it. Its not going away.
Currently CPET, from my understanding of cost, is about 20% of the cost of a PET scan that can show detailed brain inflammation (the Japanese research). Its also direct evidence of disabling pathophysiology.
Let me reassert the main point: nothing will happen only if we let nothing happen. We may have to fight for this, but the evidence backs us.
Yet when patients demanded treatment, became active to make it happen, things changed.
Nothing may happen with CPET only if we let nothing happen. This is hard evidence, not quite as good as it could be but darn close. Its irrefutable when a patient is tested, and any of us who can afford it and are not too sick to prevent it can get tested. People are winning legal challenges based on this.
Our researchers are now using CPET. Most are aware of it. Its not going away.
Currently CPET, from my understanding of cost, is about 20% of the cost of a PET scan that can show detailed brain inflammation (the Japanese research). Its also direct evidence of disabling pathophysiology.
Let me reassert the main point: nothing will happen only if we let nothing happen. We may have to fight for this, but the evidence backs us.
@alex3619 Dr. Barry Marshall (an amazing Australian doctor
) proved that the bacterium Helicobacter Pylori is the cause of most peptic ulcers, by infecting himself with H. Pylori and subsequently developing peptic ulcer.
For this important "discovery", or shall we say reversal of the medical doctrine, which previously supported stress, spicy foods and stomach hyperacidity as causes of ulcers, he was awarded the Nobel Prize in Physiology.
Makes you wish we had a similar scenario with ME, but I think the situation is a tiny bit more complicated ... ;(
As far as CPET's cost goes, here in the US, specifically in California the Workwell Foundation charges at least $ 2000, a sum of money that for most of us is out of reach.
I don't think that any insurance policy, at this time, covers or reimburses it and that is why we need to be advocating studies done by our ME/CFS doctors' clinics, funded by the CDC, but with the 2 Days CPET.
) proved that the bacterium Helicobacter Pylori is the cause of most peptic ulcers, by infecting himself with H. Pylori and subsequently developing peptic ulcer.For this important "discovery", or shall we say reversal of the medical doctrine, which previously supported stress, spicy foods and stomach hyperacidity as causes of ulcers, he was awarded the Nobel Prize in Physiology.
Makes you wish we had a similar scenario with ME, but I think the situation is a tiny bit more complicated ... ;(
As far as CPET's cost goes, here in the US, specifically in California the Workwell Foundation charges at least $ 2000, a sum of money that for most of us is out of reach.
I don't think that any insurance policy, at this time, covers or reimburses it and that is why we need to be advocating studies done by our ME/CFS doctors' clinics, funded by the CDC, but with the 2 Days CPET.
How can they justify charging $2000? Have they got a closed-shop union like lawyers do?
It's not expensive to do.
To many folk nowadays know the price of everything and the value of absolutely nothing.
(wearing my grumpy old wumman head today)
It's not expensive to do.
To many folk nowadays know the price of everything and the value of absolutely nothing.
(wearing my grumpy old wumman head today)
@peggy-sue the equipment is not inexpensive. You need gas exchange reading machinery, ECG machinery, a bike, and manpower. These machines need to be serviced. Then there is software costs, including the xognitive testing software which is not particularily free. Then these people have to earn a living, on top of covering the cost of the location.
And while these services are expensive, oftentime they are priceless in validating illness and for proof of disability.
And while these services are expensive, oftentime they are priceless in validating illness and for proof of disability.
How can they justify charging $2000? Have they got a closed-shop union like lawyers do?
It's not expensive to do.
To many folk nowadays know the price of everything and the value of absolutely nothing.
(wearing my grumpy old wumman head today)
It's not expensive to do.
To many folk nowadays know the price of everything and the value of absolutely nothing.
(wearing my grumpy old wumman head today)
I also think they justify the high price by the fact that they are the ones who have been putting out solid clinical data on this specific test and the peculiar results in PWME.
My ME dr. told me to wait until his clinic will have the capacity and proper technician to interpret it, but so far they seem busy with other important clinical trials, none of which involves a 2 days CPET. Eventually they'll run it but if it's with the CDC's money it seems it will be done only on one day only, so we're basically back to square one!
Eventually if we push for it, more of our drs.' clinics will start to offer it, but for the time being I think our specialists are all overloaded with clinical and research work and have to prioritize and strategize ...
Also here in the US there is no universal social medicine and prices are inflated by the insurance companies greediness and by doctors who have to buy very expensive malpractice policies to cover their backs. The situation is simply CRAZY!!!
In sweet old Europe you have cuts to health services and if you have ME/CFS, you're certainly not in a better position, except maybe lucky enough to have the chance to get a CPET done, only not to have it recognized for disability purposes.
That's why we have to organize an international movement, backed by our doctors, to have this test done properly, by knowledgeable people, over 2 days and in clinical trials settings.
I hear the cost of a cognitive test is close to 5000$-
You pay for a service. The Workwell foundation are very much the best around. My test was not performed there and their CO2 sensor was de-calibrated, invalidating all of the results and there was no way to fly again across the country to get it done again and I got a 2mo ths relapse from that. i didn't know this ( the problems with the sensor) until after the fact.
You pay for the equipment, the time, qualifications and ta detail report that will describe abnormalities and typical pathology to all of your physicians including your GP.
You pay for a service. The Workwell foundation are very much the best around. My test was not performed there and their CO2 sensor was de-calibrated, invalidating all of the results and there was no way to fly again across the country to get it done again and I got a 2mo ths relapse from that. i didn't know this ( the problems with the sensor) until after the fact.
You pay for the equipment, the time, qualifications and ta detail report that will describe abnormalities and typical pathology to all of your physicians including your GP.
Darn, much cheaper than what I heard some time back about the USA, which is about $2000 for two day testing.
I spent $500 recently for basic cognitive testing which told me nothing. I was told that I really needed testing that costs thousands, cash please. Cost is relative to what you get.
I spent $500 recently for basic cognitive testing which told me nothing. I was told that I really needed testing that costs thousands, cash please. Cost is relative to what you get.
@alex3619 Dr. Barry Marshall (an amazing Australian doctor) proved that the bacterium Helicobacter Pylori is the cause of most peptic ulcers, by infecting himself with H. Pylori and subsequently developing peptic ulcer.
For this important "discovery", or shall we say reversal of the medical doctrine, which previously supported stress, spicy foods and stomach hyperacidity as causes of ulcers, he was awarded the Nobel Prize in Physiology.
Makes you wish we had a similar scenario with ME, but I think the situation is a tiny bit more complicated ... ;(
As far as CPET's cost goes, here in the US, specifically in California the Workwell Foundation charges at least $ 2000, a sum of money that for most of us is out of reach.
I don't think that any insurance policy, at this time, covers or reimburses it and that is why we need to be advocating studies done by our ME/CFS doctors' clinics, funded by the CDC, but with the 2 Days CPET.
) proved that the bacterium Helicobacter Pylori is the cause of most peptic ulcers, by infecting himself with H. Pylori and subsequently developing peptic ulcer.For this important "discovery", or shall we say reversal of the medical doctrine, which previously supported stress, spicy foods and stomach hyperacidity as causes of ulcers, he was awarded the Nobel Prize in Physiology.
Makes you wish we had a similar scenario with ME, but I think the situation is a tiny bit more complicated ... ;(
As far as CPET's cost goes, here in the US, specifically in California the Workwell Foundation charges at least $ 2000, a sum of money that for most of us is out of reach.
I don't think that any insurance policy, at this time, covers or reimburses it and that is why we need to be advocating studies done by our ME/CFS doctors' clinics, funded by the CDC, but with the 2 Days CPET.
CPET is the first test we have that is soundly backed by independently replicated published controlled studies. We need to push this. Other tests will come along though, this is only the first. I also have high hopes for PET scans, cytokine testing etc.
http://forums.phoenixrising.me/index.php?entries/here-we-go-round-the-merry-go-round-part-one.1229/
http://forums.phoenixrising.me/index.php?entries/here-we-go-round-the-merry-go-round-part-two.1230/
The story of H. pylori and what it might teach us.
http://forums.phoenixrising.me/index.php?entries/here-we-go-round-the-merry-go-round-part-two.1230/
The story of H. pylori and what it might teach us.
@NK17- Some private insurance policies will reimburse for the 2 day test. Mine did partially- last year at least. Medicare won't.
In addition to Kati's excellent analysis for why it costs so much, Workwell also justifies the cost of their testing by saying that the fees are used to support them in doing more research. Since they are no longer affiliated with a university they have to find ways to pay for the research studies they are doing. They say doing the disability evals (2 day CPET tests) are how they are getting money to continue their research- which is what they're primarily interested in doing.
In addition to Kati's excellent analysis for why it costs so much, Workwell also justifies the cost of their testing by saying that the fees are used to support them in doing more research. Since they are no longer affiliated with a university they have to find ways to pay for the research studies they are doing. They say doing the disability evals (2 day CPET tests) are how they are getting money to continue their research- which is what they're primarily interested in doing.
@alex3619 Dr. Barry Marshall (an amazing Australian doctor) proved that the bacterium Helicobacter Pylori is the cause of most peptic ulcers, by infecting himself with H. Pylori and subsequently developing peptic ulcer.
For this important "discovery", or shall we say reversal of the medical doctrine, which previously supported stress, spicy foods and stomach hyperacidity as causes of ulcers, he was awarded the Nobel Prize in Physiology.
) proved that the bacterium Helicobacter Pylori is the cause of most peptic ulcers, by infecting himself with H. Pylori and subsequently developing peptic ulcer.For this important "discovery", or shall we say reversal of the medical doctrine, which previously supported stress, spicy foods and stomach hyperacidity as causes of ulcers, he was awarded the Nobel Prize in Physiology.
I'm weary about the risk of relapse with this test and the cost of it, but in the end I would be OK with saving up $1000 and risking prolonged relapse in a one-off (2 day) CPET test, if it meant we would finally no longer be subjected to psychobabble in the future and unrealistic expectations about mind over body recovery, and would never have to redo the test on a periodic basis, unless feeling much better and testing the objective reality of my own self-perceived recovery.
The CPET equipment at KDM's clinic wasn't even remotely brand-new looking, but all functional. About what you'd expect to see in a well-used clinic or university setting.
However, the blood-pressure monitor kept trying to over-inflate and popping off, so they'd probably benefit from having one which isn't as picky about getting a strong consistent reading. A lot of us tend to have low pulse pressure, which results in weak readings that often get missed or ignored by BP monitors. But BP isn't a primary concern in the CPET, so meh
My big batch of results from the clinic included a half-page summary of the CPET results - KDM is a cardiologist, so he knows his stuff! Highlights are an usual ECG wave with a merged T and U wave, VO2max at 52% of expected predicted value, and RQ of 1.23 indicating definite maximal effort from me. Also a page of results with all of the raw data.
So I think most of the expense from other locations is coming from the equipment used, and probably the software, and possibly to fund research costs as someone else suggested. Basically it's the difference between a clinical setting and a research setting - the clinical setting is much cheaper! A clinical setting doesn't require the absolute perfection needed in a research setting.
However, the blood-pressure monitor kept trying to over-inflate and popping off, so they'd probably benefit from having one which isn't as picky about getting a strong consistent reading. A lot of us tend to have low pulse pressure, which results in weak readings that often get missed or ignored by BP monitors. But BP isn't a primary concern in the CPET, so meh
My big batch of results from the clinic included a half-page summary of the CPET results - KDM is a cardiologist, so he knows his stuff! Highlights are an usual ECG wave with a merged T and U wave, VO2max at 52% of expected predicted value, and RQ of 1.23 indicating definite maximal effort from me. Also a page of results with all of the raw data.
So I think most of the expense from other locations is coming from the equipment used, and probably the software, and possibly to fund research costs as someone else suggested. Basically it's the difference between a clinical setting and a research setting - the clinical setting is much cheaper! A clinical setting doesn't require the absolute perfection needed in a research setting.
That is scandalous, especially since the research by Barry Marshall was right here and he shared a Nobel prize!