I can never get over how expensive meds are in the USA and the awful Health insurance system it has. We know of people who got fired when they got ill and they lost their insurance. My Pramipexole ER costs me $5 for 30 and Levodaopa combo $5 for 100 on NO health insurance. Neurologist is free too. GP Dr visits free. Govt pays for it. I feel sorry for US PD peeps. From Australia
USA Expensive Meds: I can never get over... - Cure Parkinson's
USA Expensive Meds
NvaGivUp, You obviously have a kind heart. Thank you for the sympathy. With our current federal adminisitration here in the U.S., there is imminent danger of our healthcare system becoming much worse than it is already. But this is no place to go into the rage-inducing topic of politics. In our role as Parkies, we are urged to focus as much as possible on the less stressful and sunnier side of life.
Theres no rage expressed, no denial either. Your nation will and is getting worse, thats just reality
NvaGivUp, No implication intended that *you* were leading the discussion towards rage and/or politics. I was just admonishing myself not to launch into a wild political rant! At the same time , I am not saying that we patients should withdraw from political engagement and let our country go to hell. Just saying that this particular website is not the place for me to "let loose." There are countless other sites where I can vent politically if I am so inclined.
Hmmm this brings up a question for me living in USA. I am trying to find affordable prices for Rivastigmine and Amitiza. Will be enrolling in Medicare Pt D for first time next week and the plans consider those 2 drugs Non Preferred Brand and are expensive. I have researched pharmacy discount cards, medical school clinical trials, access to samples, and mail order from Canada. Haven't finished looking for manufacturer to ask for help first try at that brought up India, Germany, China, and Switzerland just as places the drug is manufactured, nothing about help. Any thoughts?? We can't move to Australia😃
Try goodrx.com
Thanks for suggesting goodrx. I tested for xadago. With coupon, 30 xadago tabs are only just over $700.00 usd.
That's still a hefty price to pay! It seems to me our PD meds are going to cost more in 2018! I take Neupro, Rytary, Rasagiline and 2 blood pressure meds Isradipine and Lisinipril. I am one year away from Medicare. Right now I can afford Rytary at $50 month and other meds about $10 month but when I look up GoodRX I see prices for the above even with a 90 day supply are much more in 2018.
I have seen the push in a lot of media in the US to create fear of socialised medicine like it's some precursor to communism. Our system in New Zealand isn't perfect by any means but I'm happy with paying $5/prescription and $30 to see the Dr. If I have to go to hospital it's all free. Don't have to worry about insurance.
Even the language I think is chosen to induce fear. What is called socialised health care is known as universal health care in the countries that have it.
I think we Americans confuse "socialism" as anti-Democracy. I think we often confuse capitalism with democracy, and think capitalism IS democracy.
USA is on the slippery slope sadly. Even conservative wikipedia rates USA's democracy as 'flawed' and Australia / NZ as 'true'. This flawedness flows onto things like healthcare which in the USA is a big pharm $ making racket. The type of rorting going on in the USA is bad for the world, seriously. We resist it here.
I dread the day that I may need more medication than I take now....probably, I will not take it. Won't be able to afford it.
It's a bit of a myth that Aussie health care is free. If you earn over a certain amount you have to pay for private health insurance or be taxed a similar amount. In my case that's $4800 a year for a family of 4. We also pay a 2% Medicare on our salary if it's over a certain amount. I pay out of pocket expenses of $50 per GP visit and $80 per neuro visit. Meds are subsidised so I pay only $38 a month for azilect for example. My integrative GP is considered a luxury and I pay around $200 to see her!
If you have less money, or just chose to, you can use the public health system which is very good and virtually free (you basically see the same doctors but may have to wait longer) and you get cheaper meds if you are a pensioner etc.
I'm really happy to pay this knowing my fellow Australians are being looked after, and also that I will be too if I can no longer work. I can't imagine making people sell their house to treat their kids cancer.
Arnt we smug!!
Not really accurate Astra if you have PD and get a pension the costs are nil for GP. I was an RN and the public system is good. Also the last 5 months all my meds are free due to being over the safety net threshold. All my tests scans etc are free.
My point exactly. It's free if you need it to be, otherwise you pay what you can afford.
I think it's s great system, and I have huge admiration for the RNs I have met, especially those looking after my aging parents.
Aye us is the UK have it good also if not working free prescriptions if working you can pay for a Pre Paid Certificate £104 a year and can pay it over 10 months at 10.40 per month and then be entitled to as many meds as needed.
Everybody is entitled to free healthcare (GPs,Consultants etc...) and all the scans required that would cost a bomb (MRI, CT, DAT SCAN etc...) only downfall can be wait time around about 4 months for me to see my 1st Neuro...You can however go private if you have the cash.