I don't really know what to call our system.
But i know that everyone here has private insurance. You can choose wich one you want, and can see what they cover and each insurance has a few different ones. It's how much you want to pay per month, the more you pay the more you get. They also pay for IVF/ICSI and things like that, although they would maybe do one round.
Every company has a basic insurance and then you can get extra. I have extra, the most you can get i think, and pay 120 euro's per month. With the basic you can get a specific number of physio visits and with the extra like i have i can go as much as needed.
With that i can get about everything. The only things they don't pay are vitamins (i think that's because lots of people take them as supplements while they don't need them, while us CFers need them for real but because it is taken so much we have to pay for it). Though the vitamins don't cost much, i would think about 30 euro per 3 months.
There are other things like my feeds, traveling to the hospital, saline flushes and such that they don't pay for as a standard but i need to get a letter from my doctor and then then the insurance does pay for it. They do that for a year and after a year i have to apply again.
I can choose which doctor i want. Although the insurance companies do have 'contracts' with everything. They have contracts with about every hospital. And with a lot of gp (our home doctors, the doctor we go to that is in our village, for a cold or with a sprained(?) ankle or anything. Everything that's not serious really...) and with physiotherapists. And when they don't have a contract they can 'make' one.. So as long as i can remember everything has always worked out.
I think our system is really good. You can choose where you want to go. Don't have to pay for the expensive meds. I will never have to worry about having to pay for my transplant, or for meds after my transplant, or for iv's... anything...
When you don't have insurance i think hospitals can't 'not treat you'. I think they have to treat you.
Waiting lists for surgery can go up to a few months... When i had to have an MRI for my back i called a few hospitals and had to wait 4 weeks i think. When i had to go the the orthopedic doc for my back my gp called for an appt. First the hospital said i could have an appt in a month, but my gp said that wasn't good enough. That i couldn't walk at all, that i was post tx, that i needed to exercise. And that way i could come the same week! So everything is possible <img src="i/expressions/face-icon-small-wink.gif" border="0">
When i needed to see my CF doc i could come right away. And when i need to see my tx doctor i can too.
When i have to be admitted the ward is sometimes full.. Last time i slept in the 'family waiting room' for 2 nights. My doctor wanted me on his ward.. The ER said they could find a place another ward but my doc didn't want that. He said he was going to find a place, and he did hehe.
This is a long story i think, i don't know if it makes much sense.
But i think i should finish with this.. When i read some stories on these boards.. I glad i live here!
But i know that everyone here has private insurance. You can choose wich one you want, and can see what they cover and each insurance has a few different ones. It's how much you want to pay per month, the more you pay the more you get. They also pay for IVF/ICSI and things like that, although they would maybe do one round.
Every company has a basic insurance and then you can get extra. I have extra, the most you can get i think, and pay 120 euro's per month. With the basic you can get a specific number of physio visits and with the extra like i have i can go as much as needed.
With that i can get about everything. The only things they don't pay are vitamins (i think that's because lots of people take them as supplements while they don't need them, while us CFers need them for real but because it is taken so much we have to pay for it). Though the vitamins don't cost much, i would think about 30 euro per 3 months.
There are other things like my feeds, traveling to the hospital, saline flushes and such that they don't pay for as a standard but i need to get a letter from my doctor and then then the insurance does pay for it. They do that for a year and after a year i have to apply again.
I can choose which doctor i want. Although the insurance companies do have 'contracts' with everything. They have contracts with about every hospital. And with a lot of gp (our home doctors, the doctor we go to that is in our village, for a cold or with a sprained(?) ankle or anything. Everything that's not serious really...) and with physiotherapists. And when they don't have a contract they can 'make' one.. So as long as i can remember everything has always worked out.
I think our system is really good. You can choose where you want to go. Don't have to pay for the expensive meds. I will never have to worry about having to pay for my transplant, or for meds after my transplant, or for iv's... anything...
When you don't have insurance i think hospitals can't 'not treat you'. I think they have to treat you.
Waiting lists for surgery can go up to a few months... When i had to have an MRI for my back i called a few hospitals and had to wait 4 weeks i think. When i had to go the the orthopedic doc for my back my gp called for an appt. First the hospital said i could have an appt in a month, but my gp said that wasn't good enough. That i couldn't walk at all, that i was post tx, that i needed to exercise. And that way i could come the same week! So everything is possible <img src="i/expressions/face-icon-small-wink.gif" border="0">
When i needed to see my CF doc i could come right away. And when i need to see my tx doctor i can too.
When i have to be admitted the ward is sometimes full.. Last time i slept in the 'family waiting room' for 2 nights. My doctor wanted me on his ward.. The ER said they could find a place another ward but my doc didn't want that. He said he was going to find a place, and he did hehe.
This is a long story i think, i don't know if it makes much sense.
But i think i should finish with this.. When i read some stories on these boards.. I glad i live here!