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Chrissy

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Hi not really sure how this all works but here we go.

I have read a few posts and I can't believe that some have to wait due to the fact that their insurance is holding things up. I have been an epileptic for 33 years and have three with epilepsy, none of use have ever had trouble when it came to things being covered by insurance.

I feel for all that have this problem. Australia must be pretty good when it comes to our health cover. Our doctors have always been helpful, too even try to copy with problems with insurance on top of the epilepsy as well would be difficult.
 
Hi Chrissy! I completely agree with you. I am very grateful for our health care system, it's not perfect but I read so much on here that shows it could be a lot worse.
 
Hey - also Australian, so i definitely agree with you both! And yeah, it's just amazing what a drama people have - the worst I have to deal with is waiting for a few months to get an appointment with a neurologist (although it would be quicker if it was an emergency of course) and that's only because I live in little Tasmania and we don't have a huge supply of neuros here!
 
I thought America would be ahead of us but when it comes to medical I really feel for them. E isn't a new problem. My heart and thoughts go out to all that have the struggle. It was hard enough when I was young buy with my own girls I haven't had a problem
 
Sorry if it's a really personal question, but you mentioned that you have 3 children who have epilepsy - would you mind if I asked a bit about it in a private message? it's a topic that has come up with me recently.
 
I suppose its different for all sorts of different places. In the UK we have the NHS. On the bright side its free but on the downside waiting times can be horrendous.
 
As another Aussie on the board I feel as most of you here. I don't think we will ever have a perfect system but I am so glad for what we have. I know that in some parts of the country (particularly rural areas) you would probably have a hard time accessing bulk billed services or waiting extreme lengths of time to see a specialist but I know that here in Sydney I haven't had any major issues when i've needed to see someone. Access to free public health care is a right and not a privilege and as far as I am concerned it can only benefit the country as a whole to have a healthy population.
 
All systems can be a struggle on occasion because there is always a crack. I have been fortunate because I also have Epileptologist who is a researcher. Then again the US can be a true maze of medical care.

On another note according to my family I am not allowed to go to Australia. Odds are I would never return because I would like it that much. Also just wondering we have a store that sells Kangaroo meat. Is there a good way to eat kangaroo?

Sorry for going off track.
 
Hi Lola Lolushka, you can send a private message that is fine with me. Yes I do have three girls with epilepsy and if am able to help anyone I will.
 
Hi Knothing, I don't actually eat Kangaroo but my cats love it. Some people do but I am not one of them. I like to stick to the norm lamb, beef and chicken.
 
Not an aussie here, lol... I have pretty decent insurance here in the states. but last year, when I first was diagnosed, I spent a good amount of money, up to my maximum out of pocket, which was $2500. It was all mainly on the MRI's, EEG's, And video EEG. still working on paying that off. Already a good chunk into my max this year as well.

Insurance has definitely taken a turn for the worse in the last couple of years (jee.. wonder why...ummm obama care maybe??). at least the price of all my meds are pretty cheap with my ins.

Hopefully.. things will get better in the coming years here in the US.

cheers!
 
I really feel for you. My insurance doesn't cover everything but a partial part of everything. my meds are not covered but they only come to around the $40 per month which is overall really good. The children's medication is expensive but due to their pension they get it cheaper. Hope things do get better for you in he States.
 
Umm, I personally would say the best way to eat Kangaroo meat is not at all. I mean, there are people who eat it and you can buy it at the supermarket or butchers but I don't like the idea of eating our national emblem. Plus, I can't understand how it is possible for anyone to assure that they aren't poisoned or diseased in anyway as it's not like Kangaroos are 'farmed'. I do believe that Kangaroo meat is very healthy from all accounts but whilst it seems there are still plenty around they have reached 'quasi extinction levels' http://www.gopetition.com/petitions/kangaroo-extinction.html. so the practice is not really appealing to me.
 
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I'm not too happy with the American healthcare system either. I was diagnosed with 'psychosomatic tendencies' and not taken seriously, at least until I crashed my car. Then when I went to the ER having a suspected seizure, all they did was x-ray my chest because I was a smoker? No EEG or at least something brain-related? I think I'm going to have to look into moving to Australia...
 
Hey Trinity,

I see what you mean about eating the emblem - ALTHOUGH - I have eaten Kangaroo before... It was cooked beautifully, tasted FANTASTIC and really enjoyed it until I found out what I was eating... :)
 
I've eaten it before as well - my sister tricked me into it by pretending it was beef. My parents barbecue kangaroo kebabs on Australia Day and all I can think is how terribly unpatriotic. I would hate to see the extinction of our national emblem for the sake of filling out bellies with tasty (yes, I know it's tasty) food.
 
Yeah that's what they think. My Dad does lots of things he thinks are funny - i'm sure that is the ONLY reason they eat kangaroo on Australia Day, especially since they know I don't like it. LOL
 
Roo meat

The funniest thing I have come across, is that I did rescue with kittens. When I sold two I mentioned to the new owners that they liked kangaroo mince and the guy told me that they eat Roo meat too. I just imaged the kittens taking their food.
 
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