Re: Therapy needs---Cheryl

[Guest guest]

I will... And thank you Dr. ! I now have a starting point and

that makes it so much easier to get going. I will look into NACD

further. A week ago, I didn't even know what it was.

>

> Please read and take to heart Dr. 's words and take her study

> and post to your appointment. It will help your dr. help you. It is

> going to take a while for you to figure out the allergens involved,

> if that is part of your deal. You need trial eliminations and

testing

> for that. It will take a while (and some serious pushing) for you

to

> get the testing in the malabsorption folder but you must do it,

along

> with genetic testing. You need to know if the gut is involved, to

> what extent, and genetics will guide you as to the need for

> permanence with some dietary stuff, whether or not something more

> serious like FOD and/or mito is at issue, and how your child

compares

> to the syndrome seen on the board by the responders. You also need

to

> know if environmental allergens, vaccine injury and/or metal are

part

> of this.

>

> Therapy plays a role and seems your most immediate concern as you

> need it while you address the above. One thing I learned just last

> night is the one truly dyspraxic child who had definite milk and

> gluten issues along with allergy stuff, is that while it may not

have

> aapeared that she was processing all that was done with her (2

months

> ago she tested out at age 3 in preschool despite being 5 and being

> there for 2 years) she was. One month free of most but not all

> allergens has that same child testing at 2nd grade level. So the

> information was there, in a holding pattern, in her brain. One

month

> on the right diet (as much as they can tell so far) she is setting

> the table and saying " OK, let's see, I need a for for daddy, etc.).

>

> So, as for therapy:

>

> Get as much as you can for free and do as much as you can on your

own

> and consider NACD. Janice has posted on this extensively.

> Neuroplasticity will allow your child's brain to develop in spite

of

> what is blocking it and you need all the help you can get. Do all

you

> can, doo it now and do it frequently, intensely, and for as long a

> duration as you can.

>

[Guest guest]

You can do this Cheryl and so can your boy. Don't you ever forget

that!

> >

> > Please read and take to heart Dr. 's words and take her

study

> > and post to your appointment. It will help your dr. help you. It

is

> > going to take a while for you to figure out the allergens

involved,

> > if that is part of your deal. You need trial eliminations and

> testing

> > for that. It will take a while (and some serious pushing) for you

> to

> > get the testing in the malabsorption folder but you must do it,

> along

> > with genetic testing. You need to know if the gut is involved, to

> > what extent, and genetics will guide you as to the need for

> > permanence with some dietary stuff, whether or not something more

> > serious like FOD and/or mito is at issue, and how your child

> compares

> > to the syndrome seen on the board by the responders. You also

need

> to

> > know if environmental allergens, vaccine injury and/or metal are

> part

> > of this.

> >

> > Therapy plays a role and seems your most immediate concern as you

> > need it while you address the above. One thing I learned just

last

> > night is the one truly dyspraxic child who had definite milk and

> > gluten issues along with allergy stuff, is that while it may not

> have

> > aapeared that she was processing all that was done with her (2

> months

> > ago she tested out at age 3 in preschool despite being 5 and

being

> > there for 2 years) she was. One month free of most but not all

> > allergens has that same child testing at 2nd grade level. So the

> > information was there, in a holding pattern, in her brain. One

> month

> > on the right diet (as much as they can tell so far) she is

setting

> > the table and saying " OK, let's see, I need a for for daddy,

etc.).

> >

> > So, as for therapy:

> >

> > Get as much as you can for free and do as much as you can on your

> own

> > and consider NACD. Janice has posted on this extensively.

> > Neuroplasticity will allow your child's brain to develop in spite

> of

> > what is blocking it and you need all the help you can get. Do all

> you

> > can, doo it now and do it frequently, intensely, and for as long

a

> > duration as you can.

> >

>