Today it is extremely apparent that our son has lost eye contact.
When I informed BioRay, the company that makes NDF, the co-founder
told me to stop using it. I told her that we obviously already had.
She then asked, "What would you like us to do?" Well, for
starters...not look to me to tell you what you should be doing,
especially when it's obvious that you have not done enough testing on
your product. Secondly, don't market your product to parents of
autistic children and doctors of autistic children if you have no
idea how this will affect autistic children.

The co-founder of BioRay, Stephanie, insinuated that it was my fault
because I gave him too high of a dose. I reminded her of their dosage
specifications...the one I followed. She then informed me that those
specifications are not meant for autistic children. BUT you see,
they have not set specifications for autistic children, so we have a
big problem.

She's right about one thing: it is my fault. I'm so ashamed I let
this happen to my baby boy...a whole year of progress...gone.

Please do not use NDF. The risk is too high. And if you are patients
of the Pfeiffer Treatment Center, please ask them not to recommend
it. The company co-founder has admitted to me that they do not have
the funds to do proper research. This stuff shouldn't be anywhere
around our kids.

I just wanted you to know...