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Hey all, just read about the mom on the verge of tears, and I can

totally relate tonight.

I was out with my ASD son at a park to watch the local Zoo bring

animals there for the kids to see and it really just struck me how

sick he looks compared to the other kids there.

We have not started the Valtrex protocol yet, but have been using the

Monolaurin and I am talking to our DAN doc tomorrow to go over the

possibility of Valtrex.

Our son is now on Amphoterician B yeast meds and also the Transfer

Factors supps and also probiotics right now and 1 drop of NCD

Zeolites per day. Ever since using the Monolaurin, his stools have

become more regular, however today he had some diarreah accidents

when I increased the dose by one cap.

Just looking at him tonight, pale pale face with dark circles under

his eyes and just this look like he was " not there " and he kept

holding his tummy just broke my heart.

It makes me feel like such a bad mom, like I just can't seem to get

his puzzle figured out. I have been trying to figure it out ever

since his diagnosis 2 years ago and just recently started seeing the

DAN doc for guidance. But is has still been so difficult.

We can barely afford all these tests everyone is talking about, the

cost to see the DAN doc is very very hard on us and anything extra

has been very very hard to pay for, so we are trying our best and

hope that the Valtrex protocol might be what he needs, but yet we

just don't know.

I am convinced his immune system is completely messed up and that he

deserves so much better, yet sometimes I feel really overwhelmed and

don't have any confidence in myself with this.

If anyone can e-mail me on or off line to help me with advice,

insights, that sort of thing, it would really cheer me up.

I just need someone to help me through this who knows this protocol.

Thanks,

Jen

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