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What to expect?

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Hi Stan and everyone,

I'm pretty new to this group and have been getting the emails in digest

form.

I started my son on Valtrex a week ago. We also give him MB12 injections

every other night, and he takes folinic acid along with several other

supps.

I'm emailing because I'm wondering what the " normal " stages are for a

child with autism who is taking this. So far, no reaction positive or

negative, except that my son has had more trouble falling asleep. He's

also been gigglier, so it's probably yeast, but, can anyone (Stan?) tell

me what to expect, and how long it takes for a child to get better, if

they do respond to Valtrex?

My son has Epstein-Barr and Strep viruses, systemically. Also, our DAN!

doctor said it's okay to use TD-LDN concurrently, so we're planning on

starting that in another week, when he'll also have us increase the

Valtrex dose.

Thanks!

Cate

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