Hi dt - you previously mentioned "tipping points". I do believe we are heading towards one...
Yeah, of course national health services or insurance companies should be paying for our treatments, but thanks to the extortionate price charged by Gilead they obviously have to prioritise who they treat. Imagine the headlines stink if liver cancer or cirrhosis patients went untreated while a good treatment exists and is available (well, don't even imagine it - it is happening now in Australia!).
I totally agree with all the cost-saving arguments about getting insurance companies to pay for health tourism, but they will never do it.
Apart from embarrassing the heck out of said health services and insurance companies, we just have to keep pressing on with legal alternative solutions.
Of course, fixHepC cannot do anything illegal. So...
* Find a good doctor in Australia or India or wherever who will write a prescription
* Find a friend in Bangladesh or India or Australia who can receive the prescribed meds legally. Get them to post it onwards to you or your friend in need.
* Christmas is approaching! Lots of little parcels should be flying around the world!
* Write to CBS or the BBC or Al Jazeera or any other news agency and tell them the story!
That will be your tipping point!
(ps. from now on, I think I am going to write "thanks to the extortionate price charged by Gilead" in every one of my posts)
Diagnosed Jan 2015: GT3, A0+F0/F1. Fatigue + Brain-Fog.
Started Sof+Dac from fixHepC 10-Nov-2015. NO sides.
Pre-Tx: AST 82, ALT 133, Viral Load 1 900 000.
Week4: AST 47, ALT 58. VL < 15 (unquantifiable).
Week12 (EOT): AST 30, ALT 26, VL UND
Week16 (EOT+4): AST 32, ALT 28, GGT 24, VL UND
Week28 (EOT+16): AST 26, ALT 22, GGT 24, VL UND
Ever grateful to Dr James.
Relapsed somewhere after all that... Bummer!
Jan 2018: VL 63 000 (still GT3).