**TO MUNCH**

Discussion in 'Lyme Disease Archives' started by zipk, Apr 5, 2009.

  1. zipk

    zipk New Member

    Hi Munch:

    I was just looking at your history. Did Dr. C treat your CPN as well? If not, who? One of your Chicago docs?

    Thanks,
    Zip
  2. munch1958

    munch1958 Member

    I couldn't find anyone in Chicago to treat CFS & FM so I made 7 trips to Detroit. Dr C made copies of all of my labs from Detroit. So I can't say if he would have run the tests for CPN.

    The cpnhelp.org website has lots of info about CPN. Have you checked there? Most of those treatments are the exact same ones that Dr C prescribed for me. I had some stringy gunk that I was coughing up (gross - huh?). I'm sure it was from CPN. That didn't go away until I got on IM Claforan.

    Do you have it too?
  3. zipk

    zipk New Member

    I became ill in 2000 and used MDLabs out of NJ to test for infections. I came up negative for CPN. I was just curious.

    Has Dr. C addressed your viral infections at all?

    Thanks,
    Zip
  4. zipk

    zipk New Member

    I just saw your responses to Lisaloo regarding the viral treatment. Thanks!

    Z
  5. zipk

    zipk New Member

    Hi Munch.

    Which doc helped you with the nebulized glutathion and b12?

    THanks again,
    Zip
  6. zipk

    zipk New Member

    bumping...
  7. munch1958

    munch1958 Member

    Prescribes my B12 shots and glutathione for nebulizer.