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Viewing 15 posts - 1 through 15 (of 19 total)
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  • #2816
    Rowan
    • Topics: 2
    • Replies: 5
    • Total: 7
    • Novice
    @rowan

    I have had HCV for longer than I can remember. I was initially diagnosed in 1994 and had to convince doctors that I had never used injecting drugs nor had a tattoo, piercing or blood transfusion. I was not believed. In 1995 a professor of hepatology placed me on a trial using Interferon only. It was an ordeal and I suffered depression. Unfortunately I never met the criteria for continuation although my Liver Function Tests showed a major improvement. In 1995 I had “bridging fibrosis’ which is a step away from cirrhosis. Fast forward to 2015 and I have mild cirrhosis, fibroscan has jumped from 7 to 12 in under a year and my fatigue has skyrocketed. For me time was running out and although the government may eventually come to the party with treatments I feel that they might rather want to spend the money on a nice bomb for the Air Force. I cannot afford to wait and am deeply indebted to Dr Freeman and his team at the buyers’ club. These people show that we can be a compassionate Nation. My meds are in the country and soon I will embark on a journey so many have successfully done before. Thankyou to all for sharing your stories.

    #2817
    Avatar photoJoy
    • Guardian Angel
    • ★★★★★
    @joy

    Hi Rowan, welcome to the generic rebels club, and all the best with your treatment.

    #2821
    Joan
    • Topics: 3
    • Replies: 68
    • Total: 71
    • Recovery Champion
    • ★★★★
    @joan

    Hi Rowan I too am awaiting arrival of drugs..will join you on the journey.


    GT2B Diagnosed 1989
    Started Tx 6.Nov.2015
    F3 Fibroscan 17: April.2015
    Alt PreTx: 186 Ast PreTx: 157 VL PreTx: 733,000 27.10.2015
    Alt Week 4: 14 Ast Week 4: 28 VL Week 4: UND 7.12.2015

    #2825
    Avatar photoBloot
    • Topics: 3
    • Replies: 65
    • Total: 68
    • Recovery Champion
    • ★★★★
    @bloot

    G’day Rowan
    I’m eagerly awaiting my tx as well
    My wife says she wants to fly to Tasmania and hug Dr Freeman and the buyers club people
    I think she just wants a holiday lol

    Good luck mate – you’re doing the right thing
    We’ll keep each other up to date with how we are going


    52 y.o. G3a for about 30 years
    Previous tx 2004 interferon/ ribavarin
    2004: ALT 624 AST 263

    Pre tx test 23/10/15: ALT 153 AST 128 VL 11 849 493
    6/11/15: Sof/ dac started
    26/11/15: ALT 41 AST 41
    7/12/15: ALT 36 AST 30 Virus undetected

    2004 biopsy F3
    Fibroscan appt Jan 11 2016.

    #2828
    Ann Bee
    • Topics: 1
    • Replies: 30
    • Total: 31
    • Treatment Warrior
    • ★★★
    @ann-bee

    Hi Rowan,
    happy you found this great bunch. What genotype are you? It is amazing how quickly we are all clearing the virus with minimal side effects, certainly compared to the other toxic substances used. Good luck

    #2882
    Joan
    • Topics: 3
    • Replies: 68
    • Total: 71
    • Recovery Champion
    • ★★★★
    @joan

    Hello Rowan
    Welcome I too am awaiting to start treatment I look forward to sharing stories.


    GT2B Diagnosed 1989
    Started Tx 6.Nov.2015
    F3 Fibroscan 17: April.2015
    Alt PreTx: 186 Ast PreTx: 157 VL PreTx: 733,000 27.10.2015
    Alt Week 4: 14 Ast Week 4: 28 VL Week 4: UND 7.12.2015

    #2883
    Avatar photoLondonGirl
    • Guardian Angel
    • ★★★★★
    @londongirl

    Good luck Joan – You will be on the mend soon I’m sure.
    All the best for minimal sides and a complete recovery.
    LG

    ps I am only 42 kgs – not on treatment yet.


    GT1a Dec14 F2/8.7 VL 900000-2.5M
    Jan16 Hepcivir-L MonkMed/Redemption
    Baseline: VL 913575 Alt 76 Platelets low
    Wk2 VL1157 Alt 23
    DET Wk 8 VL 32 Alt19 ‘In the slow lane’
    June16 Fibro 5.7 F0/1 LIF 1.5
    Wk 11 VL<12 Alt 13 Det/Unq
    Extending tx 12 wks Mylan Sofo/Dac MonkMed
    Wk 14 VL <12 Det/Unq
    Wk 16 VL UNDETECTED
    Wk 22 + 4 Wks Sunprevir FixHepC
    Wk 24 UNDETECTED Alt 13
    Wk 12 post tx SVR12 Wk 26 SVR24
    Thank-you Tim, Dr Debasis @ MonkMed & Dr Freeman @ Fix HepC

    #2889
    Avatar photocrazy8
    • Topics: 0
    • Replies: 49
    • Total: 49
    • Recovery Champion
    • ★★★★
    @crazy8

    G’day to you Rowan, like you I have doubts about PBS listing of these drugs, but honestly, who wants to wait six months for a ‘maybe’ when good chances are in that time you could be cured and have all new problems to consider ..Like what toppings you want on your pizza. :whistle:

    Anyways I start my Tx soon as well so good luck to all of us eh!, and I don’t care about how this virus was contracted, nobody deserves to live with this hanging over their heads.


    GT 3, F3, Contracted 1993 Tx Naive
    V/L 1,267,000 AST 67 ALT 65 6/10/15
    commence Sof/Dac (Mesochem) 6/11/15
    AST ALT normal 24/11 *
    *V/L UNDETECTED 24/11*

    #2908
    Rowan
    • Topics: 2
    • Replies: 5
    • Total: 7
    • Novice
    @rowan

    Ann Bee

    I am a Geno 1A.

    I see from yr sig that treatment is going well. good luck.

    Cheers, Rowan

    #2926
    neilo
    • Topics: 1
    • Replies: 11
    • Total: 12
    • Acolyte
    • ★★
    @neilo

    Hi Rowan
    My drugs should arrive shortly too. Best of luck with your treatment. I’ll let our community know how I go.
    Thanks again Dr Freeman and Greg Jefferys.


    G1 Had since 1979-80?? Started Sof/Dac through Buyers Club on 5/11/15 Liver biopsy done 2005 and 2010 both F1. Fibroscan done 19/10/15 F0.
    Week 4 viral load UND and Bloods normal
    Finished Tx on 27/1/16. Bloods normal.
    Week 6 SVR 10/3/16 UND Bloods normal.
    Week 12 SVR 21/4/16 UND Bloods normal

    #7523
    Rowan
    • Topics: 2
    • Replies: 5
    • Total: 7
    • Novice
    @rowan

    Hi Everyone.

    It has been about 4 weeks plus on SOF/DAC/RBV. Initially I felt invigorated slightly and was coping well with medications. But since day 4 to now (day 34) it has been a roller-coaster of slight nausea, insomnia, lethargy, some aches and feeling OK for a while. Some nights I have an elevated temperature, lymph nodes enlarged and restless legs. (Rinse and repeat!)

    Bloods were done yesterday and am waiting for results on 25th. Hoping that it is just side effects but have to admit feeling deflated when things didn’t rapidly improve on day 17 as some have reported. I guess we are all different and each journey is unique.

    Good luck to all and thanks again to FixHepC for making it possible.

    (G1A, previously treated, ALT/AST in the 200s at start, 73 Kgs, VLoad unknown)

    #7533
    Avatar photoLondonGirl
    • Guardian Angel
    • ★★★★★
    @londongirl

    Hi Rowan, Well done you and from what I read, yes, we are all different.

    Also, from what I have read, the Ribavarin can make you feel poorly the longer you take it, tired and some nausea.
    Have also read you must take it with some fat and many suggest you drink a natural pro-biotic yogurt drink to help the stomach.

    Best wishes for the best outcome.


    GT1a Dec14 F2/8.7 VL 900000-2.5M
    Jan16 Hepcivir-L MonkMed/Redemption
    Baseline: VL 913575 Alt 76 Platelets low
    Wk2 VL1157 Alt 23
    DET Wk 8 VL 32 Alt19 ‘In the slow lane’
    June16 Fibro 5.7 F0/1 LIF 1.5
    Wk 11 VL<12 Alt 13 Det/Unq
    Extending tx 12 wks Mylan Sofo/Dac MonkMed
    Wk 14 VL <12 Det/Unq
    Wk 16 VL UNDETECTED
    Wk 22 + 4 Wks Sunprevir FixHepC
    Wk 24 UNDETECTED Alt 13
    Wk 12 post tx SVR12 Wk 26 SVR24
    Thank-you Tim, Dr Debasis @ MonkMed & Dr Freeman @ Fix HepC

    #7536
    dope-on-a-rope.jpgDr James
    • Guardian Angel
    • ★★★★★
    @fixhepc

    The evidence favouring Ribavirin is fading. For GT3 it has faded. With GT1a you would need to be cirrhotic to need Ribavirin and even then 24 weeks Sof/Dac would be my personal choice due to the Riba sides.


    YMMV

    #7537
    Avatar photoLondonGirl
    • Guardian Angel
    • ★★★★★
    @londongirl

    Thank-you Dr F, I will not be taking Ribavarin.


    GT1a Dec14 F2/8.7 VL 900000-2.5M
    Jan16 Hepcivir-L MonkMed/Redemption
    Baseline: VL 913575 Alt 76 Platelets low
    Wk2 VL1157 Alt 23
    DET Wk 8 VL 32 Alt19 ‘In the slow lane’
    June16 Fibro 5.7 F0/1 LIF 1.5
    Wk 11 VL<12 Alt 13 Det/Unq
    Extending tx 12 wks Mylan Sofo/Dac MonkMed
    Wk 14 VL <12 Det/Unq
    Wk 16 VL UNDETECTED
    Wk 22 + 4 Wks Sunprevir FixHepC
    Wk 24 UNDETECTED Alt 13
    Wk 12 post tx SVR12 Wk 26 SVR24
    Thank-you Tim, Dr Debasis @ MonkMed & Dr Freeman @ Fix HepC

    #7540
    avatar876.jpegGaj
    • Guardian Angel
    • ★★★★★
    @gaj

    Hi Rowan,

    I’m on the same meds as you and the Riba will be the main culprit. Due to delays in arrival of the Riba I started on the Sof/Dac first and added the Riba 16 days later. Definitely noticed the difference and fairly similar sides to you. Lethargy, intermittent aches, lots of insomnia and leg cramps a couple of nights. No nausea but as LondonGirl suggests I do take the Riba with some fat. Full fat milk on my cereal and fruit in the morning and whatever I’m eating in the evening although if it is low/no fat I will have a glass of milk or chunk of cheese at the same time. Having said that, I do feel much better overall than pretreatment, both physically and psychologically.

    …..and it looks like a chat with my specialist soon about the latest evidence!


    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
    :cheer: :cheer: :cheer:

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