Guest guest Posted March 31, 2012 Report Share Posted March 31, 2012 Yes, it is SUCH a challenge, isn't it, Jodie? So much trial and error, and opposite opinions out there. I'm not dealing with autism or a child with autism, so I don't read all of that information but my LLMD treats primarily autistic kids, so I pick up on some of that. He put me on the SCD actually based on some labs, but how much he currently uses it with his kids, I don't know. He treats each person very individually. My impression is that a large number of lymies have the kind of gut issues Angie describes and we've all talked about here. I think it would have occurred for her regardless of the coil use, but that is just my opinion. And all the ideas for it that have been mentioned have merit and a lyme patient might do them all and still struggle. And maybe that's why this thread has been so active. Sherry > > > > > > Hi...the SCD diet feeds parasites.....so if they are a part of the issue, I wouldn't do SCD. Seen that one happen with many children with Autism ...the other forum I'm on! Jodie > > > Quote Link to comment Share on other sites More sharing options...
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