How do you then see a company recovering the massive research and development costs of the drug, Gary?
I claim that, if such a regulatory scheme were to be implemented, we’ll see the generation of new drugs, devices, and treatment regimens drop sharply in the US, becoming similar to the dearth of innovation found in these price-controlled countries. If not, why would it be different here?
I am no less outraged over this situation than anyone else here. The main difference is, I’m not willing to kill the goose that lays the golden egg. I want more golden eggs. I hope for a “cure” egg some day.
Until someone comes up with a way to make the economics of these medical advances globally fair, I’d rather live with being on the unfair end of things and have to figure out some way to pay for it than not be able to have it at all at any price.
Of course, the only truly fair solution is for everyone, worldwide, to pay the fair market value, which includes a reasonable profit return for the company. This would require that non-US payers cough up about US$60-70 per 10ml bottle of insulin, instead of $20-25. And then US diabetics could also pay the same, instead of more than US$200 a bottle.
It will never happen, though. Ever. So, I’m actually rather pessimistic and depressed about future innovations in diabetes. The scales are tipping in the US toward publicly financed, universal healthcare, and increased regulation of the pharmaceutical and medical devices industry. We need not speculate on the effect this will have – it’s happening already. Denial of advanced treatment is already being denied diabetics that previously had access.
I’m being told by our small-company insurance agent that my blessed days as a T2 with the Omnipod and Dexcom G4 are over starting in 2016. Next year, the exemption we had (we’re still not on an ACA-compliant plan yet, thanks to the President’s Executive Order delays).
Starting with the new plan next year, I will no longer be approved for these devices as a T2. In fact, I’ve done such a good job controlling my D with these tools (a1c now 5.8, down from 11.3 two years ago) that I may not even be able to continue taking insulin. No, for a T2 with my numbers, it’s metformin and sulfonylureas for me.
T1s… You think you’re going to get MORE test strips with socialized medicine? What are you smoking? Can I have some? Keep in mind that in many (if not most) nations with socialized medicine, PWD can’t get CGMs covered health insurance. They simply are not a part of the treatment universe. Why is that?
And CGMs have been available for how long, and have clearly proven their efficacy, no?
These are not easy problems to solve. However, I’ll offer this prophetic warning: Seeking to increase what you have others pay for, particular through the force of government an law, is generally a way to get LESS, overall, rather than more. People who don’t have diabetes, don’t understand it, etc., will listen to whoever gives them the cheapest “solution” to a problem they really don’t care about because they don’t have any skin in the game.
Sadly, I believe our D future will be getting worse, not better, given current social and political trends. Its depressing, so I try not to ponder it too much.