LLMDs and MMS

Discussion in 'Lyme Disease Archives' started by LdyM, Oct 14, 2008.

  1. LdyM

    LdyM New Member

    Hi fellow Lymies,

    Just curious what your LLMDs think of MMS? Aware of it as yet, etc.?

    **LdyM
  2. victoria

    victoria New Member

    have a hard enough time dealing with the protocol(s) per ILADS. Few if any advise it. However, that doesn't stop people from trying it as one of many alternatives... including people I know who got good results altho not suffering as badly from lyme.

    Waynesrhythm has posted about it here and on main board...so you might want to put MMS in the search box on this board as well as on the main board as Rich Vank has had some interesting things to say about it as well....

    hope that helps. If you can't find it, let us know... not sure if the new board is working well yet with search features, the old one 'may' work better (immunesupport url), but haven't tried to compare.

    all the best,
    Victoria




  3. LdyM

    LdyM New Member

    Thank you Victoria. Yes, I've been reading their interesting posts, and was just wondering what their MDs thought of it for Lyme. Are the LLMDs even aware of MMS?

    Best, LdyM
    [This Message was Edited on 10/15/2008]