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I think it represents the highly private nature of HCV and a not unreasonable desire not to give any personal details to an anonymous website, at least not without checking it out in detail first.
If you don’t have forced registration to post then you get over run by spam bots, but then registration requires giving up an email address. I suppose not everyone is familiar with using “burner” email addresses for such purposes.
I seem to spend half my day clicking the “Unsubscribe” button on emails.
The actual number is the number of different sessions browsing content in the last 600 seconds. Each device creates its own session so it’s actually a count of devices rather than people, although the numbers are similar. Right now it looks like:
That’s just awful LG. I guess I have been lucky in my journey, my GP is very supportive, medical staff are fabulous and certainly not judgmental. Bendigo Base still haven’t given me an appointment however I have spoken to the Nurse at the Liver Clinic and told her about my generics etc. To say she was excited is an understatement,……everyone I have told about my HepC including workmates have been incredibly supportive….as I said I think I have been very very lucky and it makes me really sad and mad to hear about the way those of you that have been treated badly.
Keep on keeping on!
Hi Tiana
I also have genotype 1b. I only have two weeks left of treatment Sof/Led (12 week treatment). I have suffered from insomnia all the way through but energy levels just keep getting better every day. It’s so nice to to feel like I want to fall asleep at work
A few headaches but nothing a Neurofen didn’t cure, and yes, lots of water is the key. Sounds like you have had a bit of a rough trot to start with but I’m sure it will only get better and better as you go along. Keep on keeping on.
Cheers
Lynne
1 round of DAAs is going to feel like 1 round with a powder puff rather than 2 rounds with Mike Tyson.
For GT3 it looks like this:
Sofosbuvir Daclatasvir
NAIVE
default: svr: 97%, trials: UN-NAMED IIb (24wk) 89% (16/1
ALLY-3 97% (73/75) AASLD-2015 96% (24/25) Aggregate 97% (97/100)
w24: svr: 100%, trials: AASLD-2015 100% (29/29)
F4
default: svr: 65%, trials: ALLY-3 58% (11/19) AASLD-2015 70% (23/33) Aggregate 65.4% (34/52)
w24: svr: 90%, trials: AASLD-2015 86% (116/135) overall but Child-Pugh A 90% (90/100)
riba24: svr: 81%, trials: AASL-2015 81% (39/4
FAIL
default: svr: 86%, trials: ALLY-3 94% (32/34) AASLD-2015 86% (89/103) (bias by F3/F4)
FAIL+F4
svr: 64%, trials: ALLY-3 69% (9/13)
w24: svr: 86%, trials: AASLD-2015 86% (89/103)
riba24: svr: 80%, trials: AASLD-2015 80% (28/35)
If my viral load is not UND at 6 weeks, half treatment…
Maybe it is recommended to prolonged the treatment with 4 weeks, with a total of 16 weeks?
I don’t know, I am a little bit disappointed.
Any advice will be appreciated.
Thanks!You are 1b F0-1 and treatment naive. That gives you a 99% chance of SVR with 12 weeks Sof/Led:
ION-1 100% (67/67) ION-3 98% (43/44) Aggregate 99.1% (110/111)
Not bad odds.
To reassure you here are some real results from a patient of mine…
Week 0 7.8 million
Week 2 598
Week 4 76
Week 5.5 < 15 Week 8 0 Week 12 0 SVR 4 0 SVR 12 0 Lots of testing because she was a doctor and one of my first patients. 5.5 weeks because she went on a cruise! Personally if I wanted an insurance blanket I would add some Simeprevir rather than treat for longer. The odds are on your side and you are chasing the last 1-2%. http://fixhepc.com/forum/experts-corner/602-100-dare-to-dream-the-impossible-dream.html
