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Hi Jeff, hopefully some of the rain from your parade falls into my glass (only just) half full, I could use it.
My understanding is that raised AFP can mean a lot of things but sudden increases are always worth close scrutiny. The drop is apparently probably good too but mostly gives me a low base to watch for increases over the next few months.
When you say “the pointy end” I believe you mean at the forefront of scientific research!
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Thanks beaches, this year the festivities fall just after EOT so there will be much (low carb) feasting but rather limited sacraments.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
… Dog-bites?
Probably that or horses is how it got into the human population in the first place but dogs haven’t been domesticated long enough for it to have been a common vector within our species. On the other hand, injuries during hunting or just the scratches and cuts of general living plus huddling together for warmth at night pre-fire? Scarification? And all baby boomers will have seen the opening sequence to 2001: A Space Odyssey so will realise that even before battle axes, blood stuck to the nearest available branch/club.
So if its been around since ancient times, how has that been determined? Have mummys been found to have HepC?
I don’t believe so. Basically it’s figured it out from the RNA sequence evidence that was used to draw up the graphic I posted. If you know what Genotypes/subtypes are around now and their relationship to each other genetically plus how often the virus successfully mutates on average, you can work backwards to determine at what points the branches in the genetic tree occurred and how long it has been around.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Thanks Price, that was something I wondered about from the data I’d seen. So this is a great reminder that I had planned to review in more detail rather than just skimming.
I guess the current riba cohort size in the DAA reviews is too small yet to provide any confidence but my AFP has dropped to 4.5 under Tx. Maybe something there?
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
fretboard wrote:………so how did the various genotypes come about? Just asking cause that area always confuses me.
Okay, so I’ll try and give this a go from an evolutionary genetics perspective:
As Vororo says HCV has been around for a long time. Basically we probably started out with either one (or possibly a very few) strain of HCV which crossed the barrier from some other host into the human population. Viruses don’t breed though so they basically replicate themselves with each generation being the same as the previous one.
The exception to this rule is when they mutate into something different but in almost all cases the mutation will be weaker than the original strain and won’t be as successful at replicating so will die out or be killed off by its hosts immune system ending that new strain before it has a chance to spread into other hosts. But very, very occasionally the mutation will be successful. It will be good at replicating itself accurately and may have an advantage over the original in how it manages to evade our immune system. So it will continue to thrive and may get lucky enough to spread into other peoples bloodstreams. If it does that often enough then that strain will likely continue into the future as a new genotype or subtype. Now, the chances of genotype 1b mutating into 3a are so infinitesimally small that basically “it ain’t gonna happen!”. But what will happen is that 1a will become 1ax or 1ay or if it is different enough it will create a new genotype, say GT8 or whatever we decide to call it.
Here you have to remember that because HCV is only spread by blood to blood contact it has a linear transmission path so in ancient times you would find that all the people infected in an area would have the same or similar genotypes/subtypes. Until you throw in population movement, migration and now modern jet travel, etc. then we start to get a mix of types across the world.
Below is a great picture that shows the main genotypes by their place of origin/greatest commonality. The interesting thing to note is that while there are 7 main genotypes there are many, many more subtypes. Some of these subtypes have or will die out, other new ones will be created. This is a bit like human genetics in that there are people who are blue eyed, and of these some will have blonde hair. So we have blue eyed/blondes but even within this grouping there will be some with straight hair, some with wavy hair, some with curly hair and some with frizzy hair. Each of the Geno-subtypes is a bit like that. But to keep things simple and because all the genotype 1a subtypes are very similar, we just say they are 1a. (Or blue eyed/blondes).
Hopefully all that makes sense as a very simplistic explanation. Please discuss amongst yourselves and there will be a test in the morning.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Congratulations Sonix!
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Hi Vororo,
The fully disposable syringe was invented by Colin Murdoch, a New Zealand pharmacist, in the year I was born (1956). Obviously it took a while after that to come into common let alone universal use. I have early childhood memories of GP inoculations being given by syringes that were shiny and “clinked” when returned to the little metal tray they used and just the fact that they put it back on the tray would indicate it probably wasn’t disposable. This occurred prior to migrating from UK to Aust so very early sixties when I was maybe 3-6 yr old?
Having said that and while it doesn’t matter much anyway, I can state that I’m a gentle soul and with conviction that it isn’t possible that I contracted HCV from method (b), which leaves (a) unless (d) applies.
There are also some interesting studies of how it appears to have spread outwards into the community from Glasgow hospitals post WW2.
So while I suspect us BBs have caused some interesting patterns and swirls in the dissemination of HCV, the research does seem to indicate that the greatest spread has occurred due to knowledge/technology/military issues rather than allegedly “moral” ones.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Hi Norman,
I wonder if the problem with the doctors you approached is that they are reluctant to discuss this area with a blind caller over the phone. You may find them more willing to discuss during a face to face meeting where they have a copy of your medical records to refer to.
Depending on the current status of your illness, and assuming you don’t have cirrhosis or other complications then once you have a prescription your own GP would likely be able to monitor your treatment progress based on the linked cheat sheet.
http://fixhepc.com/forum/forum-gp-cheat-sheet.html
Anyway, both Hazelriannon & Chapel are located in New Zealand as is Tina from page 11 who is also an active member here. They don’t appear to be online at the moment but will no doubt be along soon to provide further advice as to doctors in your country now that they know where you are located.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Hi Hope,
Yes, I just came back to state that I along with 18% of others was still detected at week 4, this did not worry me at all because I knew I would (and did) reach undetected. Here is the link for Dr James thread.
http://fixhepc.com/forum/viral-load-and-svr/287-viral-load-on-treatment-what-to-expect.html
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Hi Hope,
I am so sorry to hear that you have been subject to such appalling behaviour by your doctor. A doctor is supposed to put the best interests and privacy of their patient first. Yelling at you in the corridor so everyone can hear and scaring you is most definitely NOT in your best interests or good for your health!
Secondly it would seem that the “everybody” at Barcelona that she was talking about didn’t include Professor Laurent Castera who is the EASL Secretary General (and the host at Barcelona) who stated:
“There is a clear role for generic treatments such as these for people with Hepatitis C across the world. The implications of increased availability of these drugs could be enormous, presenting more people with the possibility of a ‘cure’ for what is often a debilitating condition,”
Or perhaps the numerous links to various reports as listed in the first post on the following thread and many others:
http://fixhepc.com/forum/media-news/924-upi-on-board.html
Now, those are all well respected people, journals and medical media reports. Can your doctor show you ANY evidence to support their claim about what everyone was saying/doing? Something in writing or in the media that supports these verbal claims? Otherwise, I would suggest he/she has absolutely no plausibility in his/her claims.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
”Hit wrote:Don’t all laugh …
If it doesn’t take much time can someone please give a brief tutorial on how To upload music to this thread
Click on reply, click on the little film strip icon amongst the selectable edit icons and you will get the below screen. Copy and paste the URL for the YouTube video you want to use into the URL box and click on “insert video”. Enter any comments in the text box below it and then click on “submit”. Hope that makes sense.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
”James-Freeman-facebook” wrote:Hi Jeff,
With your history of HCC you have a 1:3 chance of seeing it back, on average within 3.5 months so make sure you have an AFP every month for the next 6 months and an ultrasound, triple phase CT, or MRI if the is any substantial increase.
Don’t skip this!
Thanks Dr James, I’m also already on three monthly scans for at least 12 months. Monthly AFP as well makes sense given this new information.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Great news Michael!
Looking forward to hearing of your SVR.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Fantastic news jay kim! .
Well on the way.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Hi Fernandez, to find Private Messages click on your user name or go to your profile. You will find the PM link on the left hand side under your details.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
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