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Re: How do I know?

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Hi Audrey

This is a tricky one. I was disappointed not to see the dramatic improvements

some have seen when starting enzymes BUT we came off diet with first dose and

no regression. That kept me going, then I tried to be very objective, not

easy being a mum as well and I realised we had improved stools and skin after

anout 3 weeks. So I knew something was happening. For Sam, 4 at the time (we

have been on HNI since June 2001), it turned out to be yeast overgrowth

masking big improvements but we had small continual sustained improvements

which continue to this day and big ones in socialbility and eye contact when

we treated the yeast. I'm very very glad I stuck with it.

How old is your child, are they on diet, have you seen anything physical like

the improved stool to give you a clue to any effect. My advice would be, if

you can afford it, give it 2 months, minimum 3 weeks on full dose with all

food and reassess. We were saving money by being off diet so that covered

costs and some for us. Good luck with whatever you decide

Mandi in UK

> My son has been on enzymes (pep and zyme) for a good three weeks now-

> full doses at all three meals for 2 weeks. I have been keeping very

> detailed notes about his days. I'm just not sure I am seeing enough

> improvement to warrant continuing with the expense each month (tight

> budget-though this would not matter if were seeing enough

> improvement). How do you guys decide whether or not to continue. I

> would like to hear from both sides if you have the time. Thanks.

>

> Audrey

>

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My son has been taking enzymes for roughly a month. Changes are very

subtle. He seems much happier. Laughs at more appropriate times. Not

as resistant to transitions. Also, seems to help dark circles under

the eyes. (I have been trying to get rid of these since he was three.

He's six now.) I will continue with the enzymes. In fact I think I

will add the No-Fenol in a few weeks. I think we have phenol problems

that are still causing behavior problems.

Even though improvements with enzymes are subtle and slow, I think I

see enough improvement to try and remove the Concerta and lower the

Zyprexa. The changes I have seen are hard to attribute just to

enzymes because I have been doing other things also. Like added Super

Nu Thera vitamins and Epsom salt baths. Just this weekend started

adding MSM. Also, added Cod Liver Oil and Flaxseed Oil.

I'm excited about the subtle improvements and will continue on and

hope for added improvements.

Spencer's Mom,

> Hi,

>

> My son has been on enzymes (pep and zyme) for a good three weeks

now-

> full doses at all three meals for 2 weeks. I have been keeping

very

> detailed notes about his days. I'm just not sure I am seeing

enough

> improvement to warrant continuing with the expense each month

(tight

> budget-though this would not matter if were seeing enough

> improvement). How do you guys decide whether or not to continue.

I

> would like to hear from both sides if you have the time. Thanks.

>

> Audrey

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Guest guest

> Hi,

>

> My son has been on enzymes (pep and zyme) for a good three weeks

now-

> full doses at all three meals for 2 weeks.

Do you give enzymes with all his snacks also?

> I have been keeping very

> detailed notes about his days. I'm just not sure I am seeing enough

> improvement to warrant continuing with the expense each month (tight

> budget-though this would not matter if were seeing enough

> improvement). How do you guys decide whether or not to continue.

My kids are highly metal toxic, so the improvement I saw with enzymes

was " good " , but my kids still reached a plateau even with enzymes.

The good thing for me, and why I am continuing them, is that enzymes

allow me to feed my kids foods. They tolerate only four foods without

enzymes, and no supplements. And with enzymes I can feed them most

foods, and a few supplements. Chelation is vastly improving my kids,

but I still think the enzymes are important, otherwise I would have

almost nothing I would be able to feed them, and they would not

receive necessary nutrition.

You can consider stopping the enzymes, and see if you see any

regression. You can also consider that you are still feeding your

child a food which the enzymes are not helping with, so that would

mask the effectiveness of the enzymes. Or perhaps your child does not

have food issues. Consider metals tho, because that is my children's

main issue.

http://www.autismchannel.net/dana/chelate.htm

Dana

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Guest guest

That is a hard question especially if your child's skills and or behaviors

are inconsistent- sometimes good and sometimes bad or what. i would suggest

that you pick a few areas in your mind that you would like to see

improvement in- areas that if your son would improve on, the enzymes would

be worth it.

for example, i decided that if Michoel would wake up in the morning in a

better mood than he usually does, the enzymes are worth it, even if he isnt

go great the rest of the day. I mean, he HAS been better the rest of the day

too- but i'v decided the minimum i would have to see to stick to these

enzymes was better mood upon wakening. You might decide on things like more

eye contact, better speech, or anything else. That you keep any eye on those

areas.

Rivky

[ ] How do I know?

> Hi,

>

> My son has been on enzymes (pep and zyme) for a good three weeks now-

> full doses at all three meals for 2 weeks. I have been keeping very

> detailed notes about his days. I'm just not sure I am seeing enough

> improvement to warrant continuing with the expense each month (tight

> budget-though this would not matter if were seeing enough

> improvement). How do you guys decide whether or not to continue. I

> would like to hear from both sides if you have the time. Thanks.

>

> Audrey

>

>

>

>

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Guest guest

I would add in the No-Fenol before you give up...

[ ] How do I know?

Hi,

My son has been on enzymes (pep and zyme) for a good three weeks now-

full doses at all three meals for 2 weeks. I have been keeping very

detailed notes about his days. I'm just not sure I am seeing enough

improvement to warrant continuing with the expense each month (tight

budget-though this would not matter if were seeing enough

improvement). How do you guys decide whether or not to continue. I

would like to hear from both sides if you have the time. Thanks.

Audrey

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  • 1 year later...

Hi a & welcome to our group:

We have some very helpful " severity assessment forms " from Cranial

Tech in our " files " section " severity assessment forms " . This might

help you determine how mild or severe your son's plagio is. I'd

recommend you reposition him right now to avoid any further

flattening & help round out his flatness right now. He's at a great

young age to get results from repositioning. We have very helpful

repositioning info in our " files " section " repositioning

headquarters " and many helpful product repositioning links in

our " links " section.

My daughter's plagio was pretty severe, she was born with it as

her's began in utero, so our ped pointed her plagio out to us at

just her 2 week chk up.

Good luck, keep us posted.

Debbie Abby's mom DOCGrad

MI

> Hi I have a 2 month old son and I've notice that he has a

littleflat

> spot on his right side...now how do I know if the mild flattening

is

> normal or not? I will ask the ped we go for his 2 month well visit

> next week but i guess what I'm asking is every child with a flat

spot

> diagnosed to having plagio????

> a

> 9/10/03

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Make sure you keep an eye on the flat spot and if it is not going

away or even getting worse, try to demand a further assessment w/ a

Cranial Tech site or a neurosurgeon. So many docs say that the flat

spots will round out on their own--many do just that, but sometimes

further treatment is required. The earlier the problem is addressed,

the more successful treatment is going to be. In the meantime,

welcome to the group and good luck with repositioning and tummy time!

Kim--Gus' mom

DOC Band 8/21/03

> Hi I have a 2 month old son and I've notice that he has a

littleflat

> spot on his right side...now how do I know if the mild flattening

is

> normal or not? I will ask the ped we go for his 2 month well visit

> next week but i guess what I'm asking is every child with a flat

spot

> diagnosed to having plagio????

> a

> 9/10/03

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