Are you concerned with the Healthcare industry becoming socialized in the US?
I have a degree in economics and I have lived in Europe under a socialized healthcare system and frankly I am quite concerned about healthcare in the US and where it will be going.
If it is up to the government to determine if I need Pulmozyme or VX 770 Kalydeco, particularly given their expense I wonder if I will be receiving these meds or all the others I routinely use. I remember a thread here on Cysticfibrosis.com a couple of years ago in which a person living in Britain didn't have access to Pulmozyme. He lived in a smaller town or at least not London and he communicated that due to rationing Pulmozyme was only accessable if you lived in London. This may square with all of those living in a large metropolitian area, but not all of us do. As it is now with healthcare as it is I can get my meds anywhere and at any time I need them. Subsequently, not once in my 40 years of having CF have I been denied a perscribed medicine due to accessability or cost or anything.
Additionally, all these drugs have been developed in a competitive and financially motivated capitalistic markets. What happens when the drug companies incentives to develope meds is diminished or removed by some new social policy where the expensive chronic or critical patient care is compromised so that everyone has healthcare? I anticipate a more challenging and frustrating life as a CF patient living under a socialized healthcare system.
Are you concerned?
Thanks.
I have a degree in economics and I have lived in Europe under a socialized healthcare system and frankly I am quite concerned about healthcare in the US and where it will be going.
If it is up to the government to determine if I need Pulmozyme or VX 770 Kalydeco, particularly given their expense I wonder if I will be receiving these meds or all the others I routinely use. I remember a thread here on Cysticfibrosis.com a couple of years ago in which a person living in Britain didn't have access to Pulmozyme. He lived in a smaller town or at least not London and he communicated that due to rationing Pulmozyme was only accessable if you lived in London. This may square with all of those living in a large metropolitian area, but not all of us do. As it is now with healthcare as it is I can get my meds anywhere and at any time I need them. Subsequently, not once in my 40 years of having CF have I been denied a perscribed medicine due to accessability or cost or anything.
Additionally, all these drugs have been developed in a competitive and financially motivated capitalistic markets. What happens when the drug companies incentives to develope meds is diminished or removed by some new social policy where the expensive chronic or critical patient care is compromised so that everyone has healthcare? I anticipate a more challenging and frustrating life as a CF patient living under a socialized healthcare system.
Are you concerned?
Thanks.