Phoenix Rising tells QMUL: release the PACE trial data
Mark Berry, Acting CEO of Phoenix Rising, presents the Board of Directors’ open letter to Queen Mary University of London (QMUL) urging them to release the PACE trial data, and hopes that other non-UK organisations will join British charities in the same request...
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Starting IVIG

Discussion in 'Antivirals, Antibiotics and Immune Modulators' started by dsdmom, Oct 6, 2010.

  1. dsdmom

    dsdmom Senior Member

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    It looks like I will be starting ivig - possibly next week. The first time I have it done I need to go 5 days in a row. I am a bit nervous and am wondering what to expect. For those of you who have gotten ivig, were you pretty miserable and if so, for how long? Should I expect to be out of commission for a week or 2? I'm most worried about a headache I guess.

    It was approved based on neuropathy, so it is not for CFS per se.
     
  2. ukxmrv

    ukxmrv Senior Member

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    I was fine with IVIG, took Benadryl which my doctor recommended. Sadly, no effect on my ME symptoms.

    Hope that it goes well for you!

    XMRV+
     
  3. dsdmom

    dsdmom Senior Member

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    Thanks for your input!
    What were you taking it for? Do you remember your dose? And how often?
     
  4. heapsreal

    heapsreal iherb 10% discount code OPA989,

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    australia (brisbane)
    dsdmom, how did the IVIG go??

    cheers!!!
     

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