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Re: Dosage?

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Missy,

Hi! Just to see if it will help him in any way. You know, Don't leave any

stone unturned! Hope things are going good for you. JJ is doing fine, Hes been

doing a lot of swimming and bike riding.

Take care and write back when you can, Lois

Missy wrote:

> From: " Missy " <missya@...>

>

> Hi, Lois! Missy, Princess Shelby's Mommy, here. I just wanted you to know

> that I'm not ignoring your post about pepcid--I just don't have an

> answer. Why are you going to give JJ the pepcid (just very curious!).

>

> Best wishes!

> Missy

> dosage?

>

> >From: lois noland <jlois@...>

> >

> >Hello everyone,

> > I posted this before but did not get any replys sooooo I'am asking

> >again. I want to try pepcid ac on JJ but don't know the right dosage and

> >how long I can try it. JJ is 11 years old and about 70 pounds. And

> >replys will be apprchated. Thanks!!!!!!!!

> > Lois (mom to JJ bug)

> >

> >

> >------------------------------------------------------------------------

> >ONElist: bringing the world together.

> >

> >Join a new list today!

>

> ------------------------------------------------------------------------

> ONElist: where real people with real interests get connected.

>

> Join a new list today!

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Guest guest

Hi, Lois! Missy, Princess Shelby's Mommy, here. I just wanted you to know

that I'm not ignoring your post about pepcid--I just don't have an

answer. Why are you going to give JJ the pepcid (just very curious!).

Best wishes!

Missy

dosage?

>From: lois noland <jlois@...>

>

>Hello everyone,

> I posted this before but did not get any replys sooooo I'am asking

>again. I want to try pepcid ac on JJ but don't know the right dosage and

>how long I can try it. JJ is 11 years old and about 70 pounds. And

>replys will be apprchated. Thanks!!!!!!!!

> Lois (mom to JJ bug)

>

>

>------------------------------------------------------------------------

>ONElist: bringing the world together.

>

>Join a new list today!

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Guest guest

Lois,

According to what has already been posted, the dosage is 1 mg/kg

twice a day.

1 pound = 2.2 kg

70 pounds/2.2 = 31.8 kg

So the dose is 32 mg twice a day (daily total = 64 mg).

Amy

------------------ Reply Separator --------------------

Originally From: " Missy " <missya@...>

Subject: Re: dosage?

Date: 06/08/1999 11:34am

From: " Missy " <missya@...>

Hi, Lois! Missy, Princess Shelby's Mommy, here. I just wanted you to

know

that I'm not ignoring your post about pepcid--I just don't have

an

answer. Why are you going to give JJ the pepcid (just very curious!).

Best wishes!

Missy

dosage?

>From: lois noland <jlois@...>

>

>Hello everyone,

> I posted this before but did not get any replys sooooo I'am asking

>again. I want to try pepcid ac on JJ but don't know the right dosage

and

>how long I can try it. JJ is 11 years old and about 70 pounds. And

>replys will be apprchated. Thanks!!!!!!!!

> Lois (mom to JJ bug)

>

>

>---------------------------------------------------------------------

---

>ONElist: bringing the world together.

>

>Join a new list today!

----------------------------------------------------------------------

--

ONElist: where real people with real interests get connected.

Join a new list today!

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Guest guest

Amy, thanks alot!!! Lois

Amy Holmes wrote:

> From: Amy Holmes <aholmesmd@...>

>

> Lois,

>

> According to what has already been posted, the dosage is 1 mg/kg

> twice a day.

>

> 1 pound = 2.2 kg

>

> 70 pounds/2.2 = 31.8 kg

>

> So the dose is 32 mg twice a day (daily total = 64 mg).

>

> Amy

>

> ------------------ Reply Separator --------------------

> Originally From: " Missy " <missya@...>

> Subject: Re: dosage?

> Date: 06/08/1999 11:34am

>

> From: " Missy " <missya@...>

>

> Hi, Lois! Missy, Princess Shelby's Mommy, here. I just wanted you to

> know

> that I'm not ignoring your post about pepcid--I just don't have

> an

> answer. Why are you going to give JJ the pepcid (just very curious!).

>

> Best wishes!

> Missy

> dosage?

>

> >From: lois noland <jlois@...>

> >

> >Hello everyone,

> > I posted this before but did not get any replys sooooo I'am asking

> >again. I want to try pepcid ac on JJ but don't know the right dosage

> and

> >how long I can try it. JJ is 11 years old and about 70 pounds. And

> >replys will be apprchated. Thanks!!!!!!!!

> > Lois (mom to JJ bug)

> >

> >

> >---------------------------------------------------------------------

> ---

> >ONElist: bringing the world together.

> >

> >Join a new list today!

>

> ----------------------------------------------------------------------

> --

> ONElist: where real people with real interests get connected.

>

> Join a new list today!

>

> ------------------------------------------------------------------------

> Give back to your community through " Grow to Give. "

>

> Deadline is June 19. See homepage for details.

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  • 1 year later...
Guest guest

Hi Lynne,

I could be wrong, I'm not a doc, but that seems awfully high. I wouldn't take it unless I felt this doc knew what he was doing. Are you sure he's into the AP?

I'm on Minocin at a very low dose three times a week and clindy on Tuesdays, and that's more than enough to keep in mild herxes off and on and mostly on the weekends, which is okay, because a lot of times I just sleep it off.

You could look at the AP protocol yourself and decide how much is the right dosage that way and let your doctor know you know. I'm sorry I can't help you that way...I'm a regular klutz in the doc's office I have so much resentment when I'm there. Just having an appointment makes me cranky.

Good luck.

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  • 3 months later...

Hi Becky,

Most speech therapists have not heard of EFA supplementation for

childhood apraxia, or of EFAs at all any more than the average person

has heard of EFAs. The use of EFAs to help apraxia/dyspraxia in

children was started by parents just within the last few years. It is

not as yet recognized as an effective treatment in the professional

literature ... but we are working on that. Trials to scientifically

test the effectiveness of EFAs for apraxia in children are just in the

planning stages now, but at least the scientific community is beginning

to take a look at it.

I don't know how long Pro-EFA brand of supplement has been available,

but EFA supplements have been around for some time as a general dietary

supplement and as a (scientifically backed) nutritional treatment for

things like depression. They aren't exactly mainstream, though. Like

ginseng for memory and St 's Wort for mild depression, EFAs are

still primarily in the health food stores and are considered

" alternative. " Unlike other supplements, EFAs are not well known.

Millions of people worldwide have been helped with mild depression by

taking St 's wort, and most people have at least heard of it. The

medical community generally acknowledges St 's wort now, even though

it is still considered alternative. Folic Acid is another example of a

substance that most people had never heard of not that long ago, and

now, it is helping mothers deliver healthier babies as far as the word

has spread. Maybe someday, children with apraxia everywhere can be

helped by supplementing with EFAs, even if it's considered alternative.

Maybe most people will have heard of them and know they're natural

things the body needs, that most people don't get enough of, that are

important for brain development.

If just those basic facts were known by most educated people, more

children with apraxia would probably be supplemented with EFAs, and

maybe fewer children would develop speech and language disorders in the

first place, as mothers supplemented themselves during pregnancy and

breastfeeding.

You might print some of

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Van den Beemt <van@m...> wrote:

> Most speech therapists have not heard of EFA supplementation for

> childhood apraxia, or of EFAs at all any more than the average

person

> has heard of EFAs. The use of EFAs to help apraxia/dyspraxia in

> children was started by parents just within the last few years. It

is

> not as yet recognized as an effective treatment in the professional

> literature ... but we are working on that. Trials to scientifically

> test the effectiveness of EFAs for apraxia in children are just in

the

> planning stages now, but at least the scientific community is

beginning

> to take a look at it.

Thanks Deborah for all the information. I have another question,

though, will my son be on this supplement the rest of his life or can

we eventually ween him off it. Thanks again.......

Becky in NJ

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Hi Becky,

This I really don't know. I would put it to Dr. Agin or Dr. Katz.

Could one of you share whether the need for supplementation is long

term? Does anyone know at this point? Are there any references to long

term need in studies of Omega-3 or other EFAs with other disorders?

Thanks,

Deborah L. Van den Beemt, MS, CCC-SLP

in NH/VT

> Thanks Deborah for all the information. I have another question,

> though, will my son be on this supplement the rest of his life or can

> we eventually ween him off it. Thanks again.......

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