Forum Replies Created
-
AuthorPosts
-
Can I just say I find that link that Vororo posted to the Hep C trust guidance page about generics amazing. It shows times are changing as to how generics are viewed.
Trying to find a phone no. I have for an interested journalist to do my bit in the activist stakes……Hi Deborah, from another Deborah! And Welcome.
Yes to living in the UK and been through the Redemption trial. Also London Girl has and there are others from the uk some who have bought via here but not on Redemption.
Are you thinking that you may come back to the uk and get the drugs delivered and a bit of monitoring ( have you got family here?)
Monkmed who are in partership with Fixhepc will guarantee to get your drugs to you here via FedEx. Getting a doctor / hospital to be supportive here is the tricky bit, but some people have managed it. Private monitoring/ blood tests are expensive. Personally I liked the feeling of being under the wing of the NHS, also had some high BP problems.
But things are improving I believe and for people going down this route it is becoming more known about and accepted in the NHS.
Vororo posted an interesting link from The Hep C Trust which,as he says, is a pretty conservative organisation.http://hepctrust.org.uk/buying-hepatitis-c-drugs-online-%E2%80%93-what-you-need-know
For an online appt. with GP2U for a script ( there is a link on the homepage here) you will need to know your genotype and your fibrosis level.
All the best to you, hope this helps,
DebYou must be so relieved!
Congratulations! Well done
Congratulations Emilio!
Fantastic news for you!
All the best!Hallelujah Chorus, Love it LG, it sure has been a long time coming, and all the sweeter for it
Congratulations and loads of love
Debs xxxxThanks Dr James for clarifying so many questions. I am going for the “poor mans SVR 4” this week And I think I am fine with that until my 12 week SVR test. Just feeling a bit achy and tired and don’t know why, reading people’s posts is quite reassuring ( Phoenix, thanks!) And obviously this post with all the good information for us EOT ers. Thanks again Dr James.
It’s good to read of peoples experiences on this forum, because we are all different.
Thankyou Phoenix for being honest and posting this. I had a little smile at your turn of phase for the title as that would be my sentiments exactly! ( apart from the UND as haven’t had the test yet.) I find your post quite reassuring.
I am going for a liver function test next week as I asked my gp for one and won’t get a VL test until 12 weeks post EOT, as per NHS standard.
Cheers, and really glad you remain undetected. Congratulations!Sounds great! What we all want to hear
Congrats LynneGAJ, have a lovely evening, enjoyed the song and the sentiment behind it is pretty emotional
I bet you are pleased to not be rattling when you walk anymore! (I think it was you said that?)
I hope everything will be coming up roses for you………They just keep on rolling in! Congratulations Neilo!
All the best for your new life!Hi Banoru,
You definitely need to know your genotype, so check that with your doctor.
I’m not sure about the other issue, I can’t remember being asked for anything like a Medicard, could someone else shed some light?And you may find it tricky to get one in England. Best to use a service such as GP2U in which you have an online appointment and get your script. Doesn’t cost very much. You will find a link to it through this site (or google it.) You need to know your genotype and level of fibrosis.
Cheers
Any other questions just ask, all the best.Well done Ariel, Congratulations!
Knew you would with those LFTs
Trailblazer Nadia, I remember you from the uk hepc forum before you switched your blog to here. An inspiration, wishing you all the best for the future
Debs X -
AuthorPosts