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Week 11 on Valcyte

Discussion in 'Antivirals, Antibiotics and Immune Modulators' started by undcvr, Jan 20, 2011.

  1. undcvr

    undcvr Senior Member

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    A few days ago I got my blood test results back. Not only have I been feeling really lousy in the deep of winter and my HHV6 levels never dropped and my EBV came back too. I recently only convinced my doc to put me back on 1800mg Valcyte. This dose is what I foresee myself to be on for the next few months.

    So for now no short-term/immdiate side effects on Valcyte. I have countered all of that with SLO. It seems to be working. Long term, I dont know. All the Lerner studies show his patients being on Valcyte for 6 months or more. I am not sure if I want to be on it for that long given what it can do cytotoxically. I am considering Vistide but that can screw my kidneys. Ah, I love my life and the decisions I have to make while living it. Cant wait for it to be over.

    I am functionable, as long as I dont exert myself. That also includes walking in the cold, I just break out into a sweat perspiring profusely. Proboost seems to help with this on days that I take it. Otherwise as long as I stay indoor-bound and dont excercise I am pretty ok. Mind fog is still there.

    I am also looking into Avonex. PR mentioned that Dr Chia supposedly cured his son with beta-interferon and AVs. I have thought of this combo myself but it was with Pegasys and Ribivirin. Chia's theory seems sound and worth looking into if my insurance will pay. This way I dont have to go hunting for all the pathogens that I maybe infected with and just hit them all with one therapy, much more preferable and much less poking. I like.
     
  2. Ema

    Ema Senior Member

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    @undcvr, did you ever try Avonex?

    Ema
     
  3. undcvr

    undcvr Senior Member

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    no never did I understand that some herbs like licorice induce interferon production and it is the even better alpha interferon, i went that route instead
     
  4. Ema

    Ema Senior Member

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    I thought that licorice induced interferon gamma. Does it also induce interferon alpha?

    This article suggests that interferon alpha is no good for people with MS. Since ME/CFS and MS share so many commonalities, I wonder what the implication is for us.

    Have you seen studies showing the benefit of interferon alpha in ME/CFS?
     
  5. Ema

    Ema Senior Member

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  6. undcvr

    undcvr Senior Member

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    I cannot remember what tests I looked up but I have CFS and I took Licorice and Andrographis and they did help me, quite alot I would say
     

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