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Can you post the results of his hair test and get some feedback? You

are so wise to begin intervention for your son now.

>

> Hi everyone,

> I am going to try to make this as short as possible...I bet you've

> heard that before, ha ha. Who has a short story here?!

>

> We have a three year old with SPD, well that is where it started

> anyway, then we unraveled a slew of food allergies, 23 to be exact -

> oh, plus two that we have been able to add to that list since having

> his IgG done in September of 08. So we are free of many foods in

> addition to GF/CF and corn-free. We continue to struggle with

> " symptoms " . This lead me to start researching the WHY of it all. I

> believe he also has yeast issues and who knows what else. So we

> decided to do the Doctor's Data hair elements test. And here I am!

>

> I used the counting rules and it looks like he has a high

probability

> of mercury poisoning. This is the part that got us:

> " If the number of items entirely inside the middle band (white and

> green) is 11 or less it indicates a high probability of abnormal

> mineral transport and it indicates a high probability of mercury

> poisoning. " He is at exactly 11!

>

> Regarding the specific levels - his antimony, nickel, titanium,

> copper, cobalt and zirconium are high and low are calcium, sodium,

> potassium, vanadium, molybdenum, boron, strontium and rubidium.

>

> Sooooo, we did see a dr who is on the DAN! list (The Woodlands in

> Quakertown, PA), but we didn't really even realize we were seeing

one

> and why we were there in the first place. That is when we decided

on

> the IgG test. Visiting him (an hour away) is covered under our

> insurance, but the test wasn't. So, now my concern is that we won't

> be covered for chelation and testing, if that is the direction we

need

> to go. He doesn't seem to be on the same page as what I am reading

in

> Children with Starving Brains, so I wonder if I should even bother

> using him anyway. We can't afford to pay a doctor out of pocket for

> this, so where does that leave us? Do we get more testing from

here?

> Do we attempt chelation naturally on our own? What is next? I am

> desperate to help our wonderful son and want to have consistently

> normal days again. I am exhausted and drained, we have a 7 month

old

> as well and I just wish I could enjoy them both while they are

little.

> This craziness creeps into my days and has me wishing for bedtime

> more than I like to admit.

>

> I have a blog that I started recently when we were just getting

going

> on the GFCF diet, feel free to check it out -

> http://grayson-youarewhatyoueat.blogspot.com/

>

> Should I post the results of the hair elements test here to be sure

> that I am reading it right? And I guess the big question is, WHAT

> NOW?? I bought and started treating him with Liver Life from

BioRay,

> but he can't seem to ramp up past 8-9 drops and I can't even get

near

> the NDF Plus for chelating, he is highly aggrevated by it, so we are

> avoiding it until I can ramp up the Liver Life more. I am stuck

here

> at this cross roads now though, the test has my mind reeling!

>

> Oh and our list of supplements currently are:

> Cod Liver Oil

> Kirkman hypoallergenic multi vitamins

> HLC MindLinx by Pharmax probiotics

> DMG

> liquid calcium magnesium citrate

> additional magnesium

> zinc/C drops

> Biotin and/or Lauricidin with NoPhenol between meals for yeast

> chewable AFP and Zyme Prime enzymes with meals

>

> Lucky for me, the kid swallows pills like a champ!! Who would'a

known

> that a three year old could swallow pills like him and he doesn't

even

> need water!

>

> Since some of his elements came in low, should I be adjusting our

> supplements?

>

>

>

>

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Hi ,

Welcome to the list. Comments interspersed.

S S

New here and confused

Posted by: " jessicagalligani " jessicagalligani@... jessicagalligani

Thu Feb 5, 2009 7:18 pm (PST)

Hi everyone,

I am going to try to make this as short as possible...I bet you've

heard that before, ha ha. Who has a short story here?!

We have a three year old with SPD, well that is where it started

anyway, then we unraveled a slew of food allergies, 23 to be exact -

oh, plus two that we have been able to add to that list since having

his IgG done in September of 08. So we are free of many foods in

addition to GF/CF and corn-free.

*Have you considered NAET? www.naet.com

We continue to struggle with

" symptoms " . This lead me to start researching the WHY of it all. I

believe he also has yeast issues and who knows what else. So we

decided to do the Doctor's Data hair elements test. And here I am!

I used the counting rules and it looks like he has a high probability

of mercury poisoning. This is the part that got us:

" If the number of items entirely inside the middle band (white and

green) is 11 or less it indicates a high probability of abnormal

mineral transport and it indicates a high probability of mercury

poisoning. " He is at exactly 11!

Regarding the specific levels - his antimony, nickel, titanium,

copper, cobalt and zirconium are high and low are calcium, sodium,

potassium, vanadium, molybdenum, boron, strontium and rubidium.

*Have you identified and reduced/removed sources of exposure?

www.danasview.net/metals lists sources of exposure.

Sooooo, we did see a dr who is on the DAN! list (The Woodlands in

Quakertown, PA), but we didn't really even realize we were seeing one

and why we were there in the first place. That is when we decided on

the IgG test. Visiting him (an hour away) is covered under our

insurance, but the test wasn't. So, now my concern is that we won't

be covered for chelation and testing, if that is the direction we need

to go.

*Whether you chelate with the DAN or on your own (many of us do) make sure you

use Andy Cutler's protocol.

He doesn't seem to be on the same page as what I am reading in

Children with Starving Brains, so I wonder if I should even bother

using him anyway. We can't afford to pay a doctor out of pocket for

this, so where does that leave us?

*Many of us chelate without a doc. DMSA and ALA are available without a

prescription.

Do we get more testing from here?

Do we attempt chelation naturally on our own? What is next? I am

desperate to help our wonderful son and want to have consistently

normal days again. I am exhausted and drained, we have a 7 month old

as well and I just wish I could enjoy them both while they are little.

This craziness creeps into my days and has me wishing for bedtime

more than I like to admit.

I have a blog that I started recently when we were just getting going

on the GFCF diet, feel free to check it out -

http://grayson-youarewhatyoueat.blogspot.com/

Should I post the results of the hair elements test here to be sure

that I am reading it right? And I guess the big question is, WHAT

NOW?? I bought and started treating him with Liver Life from BioRay,

but he can't seem to ramp up past 8-9 drops and I can't even get near

the NDF Plus for chelating,

*NDF is not a good idea. Get DMSA and ALA instead. DMSA is available from

www.vrp.com, ALA at most health food stores and pharmacy but you have to look

for the low dose.

he is highly aggrevated by it, so we are

avoiding it until I can ramp up the Liver Life more. I am stuck here

at this cross roads now though, the test has my mind reeling!

Oh and our list of supplements currently are:

Cod Liver Oil

Kirkman hypoallergenic multi vitamins

HLC MindLinx by Pharmax probiotics

DMG

liquid calcium magnesium citrate

additional magnesium

zinc/C drops

Biotin and/or Lauricidin with NoPhenol between meals for yeast

chewable AFP and Zyme Prime enzymes with meals

Lucky for me, the kid swallows pills like a champ!! Who would'a known

that a three year old could swallow pills like him and he doesn't even

need water!

You'll want to chase the ALA with water anyway and make sure he's well hydrated.

Since some of his elements came in low, should I be adjusting our

supplements?

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

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>>We can't afford to pay a doctor out of pocket for

> this, so where does that leave us? Do we get more testing from here?

> Do we attempt chelation naturally on our own?

I used ALA for my kids, without a doctor.

>>I can't even get near

> the NDF Plus for chelating, he is highly aggrevated by it,

Try something else. I used ALA for chelating, and it worked very well

here.

> Biotin and/or Lauricidin with NoPhenol between meals for yeast

Lauricidin caused so much yeast overgrowth here that I had to

discontinue it and use something else to address viruses. So in my

experience, it does nothing for yeast, except increase the yeast.

Dana

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Oh no, Lauricidin INCREASED yeast for you guys? That isn't good.

Maybe that is why he's acting out. He does better on the Biotin, I

just switched it back to Biotin again today and he's doing better now.

He was a mess on the Lauricidin and I couldn't figure it out. Now

that you mention it, that is probably our trigger! SIGH The book

Children with Starving Brains recommends alternating yeast treatments

and we can't use GSE and most of the OoO has olive oil in it which he

can't have either, except for the super expensive and highly

concentrated kinds. I just haven't been able to drop another $50 on a

supplement that might not work. We have a number of things piling up

that don't work for him, it's such a waste of money and products! I

know, I should sell them on the Autism for Sale site, I just haven't

had the time.

Thanks, you always manage to find me on all the groups, Dana!! You

are like an angel sent from above, helping us all as you do!

> >>We can't afford to pay a doctor out of pocket for

> > this, so where does that leave us? Do we get more testing from here?

> > Do we attempt chelation naturally on our own?

>

>

> I used ALA for my kids, without a doctor.

>

>

> >>I can't even get near

> > the NDF Plus for chelating, he is highly aggrevated by it,

>

>

> Try something else. I used ALA for chelating, and it worked very well

> here.

>

>

> > Biotin and/or Lauricidin with NoPhenol between meals for yeast

>

>

> Lauricidin caused so much yeast overgrowth here that I had to

> discontinue it and use something else to address viruses. So in my

> experience, it does nothing for yeast, except increase the yeast.

>

> Dana

>

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I won't have the graph bars in the copy and paste, is this good enough?

Aluminum 7.3 < 8.0

Antimony 0.13 < 0.066

Arsenic 0.050 < 0.080

Barium 0.19 < 0.50

Beryllium < 0.01 < 0.020

Bismuth 0.10 < 2.0

Cadmium 0.016 < 0.070

Lead 0.23 < 1.0

Mercury 0.09 < 0.40

Platinum < 0.003 < 0.005

Thallium < 0.001 < 0.002

Thorium < 0.001 < 0.002

Uranium 0.027 < 0.060

Nickel 1.5 < 0.20

Silver 0.05 < 0.20

Tin 0.17 < 0.30

Titanium 1.2 < 1.0

Calcium 120 125- 370

Magnesium 22 12- 30

Sodium 7 20- 200

Potassium < 3 12- 200

Copper 25 11- 18

Zinc 170 100- 190

Manganese 0.24 0.10- 0.50

Chromium 0.71 0.43- 0.80

Vanadium 0.018 0.030- 0.10

Molybdenum 0.046 0.050- 0.13

Boron 0.19 0.70- 5.0

Iodine 0.92 0.25- 1.3

Lithium 0.010 0.007- 0.020

Phosphorus 189 150- 220

Selenium 0.77 0.70- 1.1

Strontium 0.11 0.16- 1.0

Sulfur 46300 45500- 53000

Cobalt 0.031 0.004- 0.020

Iron 15 7.0- 16

Germanium 0.035 0.030- 0.040

Rubidium 0.007 0.016- 0.18

Zirconium 2.3 0.040- 1.0

> >

> > Hi everyone,

> > I am going to try to make this as short as possible...I bet you've

> > heard that before, ha ha. Who has a short story here?!

> >

> > We have a three year old with SPD, well that is where it started

> > anyway, then we unraveled a slew of food allergies, 23 to be exact -

> > oh, plus two that we have been able to add to that list since having

> > his IgG done in September of 08. So we are free of many foods in

> > addition to GF/CF and corn-free. We continue to struggle with

> > " symptoms " . This lead me to start researching the WHY of it all. I

> > believe he also has yeast issues and who knows what else. So we

> > decided to do the Doctor's Data hair elements test. And here I am!

> >

> > I used the counting rules and it looks like he has a high

> probability

> > of mercury poisoning. This is the part that got us:

> > " If the number of items entirely inside the middle band (white and

> > green) is 11 or less it indicates a high probability of abnormal

> > mineral transport and it indicates a high probability of mercury

> > poisoning. " He is at exactly 11!

> >

> > Regarding the specific levels - his antimony, nickel, titanium,

> > copper, cobalt and zirconium are high and low are calcium, sodium,

> > potassium, vanadium, molybdenum, boron, strontium and rubidium.

> >

> > Sooooo, we did see a dr who is on the DAN! list (The Woodlands in

> > Quakertown, PA), but we didn't really even realize we were seeing

> one

> > and why we were there in the first place. That is when we decided

> on

> > the IgG test. Visiting him (an hour away) is covered under our

> > insurance, but the test wasn't. So, now my concern is that we won't

> > be covered for chelation and testing, if that is the direction we

> need

> > to go. He doesn't seem to be on the same page as what I am reading

> in

> > Children with Starving Brains, so I wonder if I should even bother

> > using him anyway. We can't afford to pay a doctor out of pocket for

> > this, so where does that leave us? Do we get more testing from

> here?

> > Do we attempt chelation naturally on our own? What is next? I am

> > desperate to help our wonderful son and want to have consistently

> > normal days again. I am exhausted and drained, we have a 7 month

> old

> > as well and I just wish I could enjoy them both while they are

> little.

> > This craziness creeps into my days and has me wishing for bedtime

> > more than I like to admit.

> >

> > I have a blog that I started recently when we were just getting

> going

> > on the GFCF diet, feel free to check it out -

> > http://grayson-youarewhatyoueat.blogspot.com/

> >

> > Should I post the results of the hair elements test here to be sure

> > that I am reading it right? And I guess the big question is, WHAT

> > NOW?? I bought and started treating him with Liver Life from

> BioRay,

> > but he can't seem to ramp up past 8-9 drops and I can't even get

> near

> > the NDF Plus for chelating, he is highly aggrevated by it, so we are

> > avoiding it until I can ramp up the Liver Life more. I am stuck

> here

> > at this cross roads now though, the test has my mind reeling!

> >

> > Oh and our list of supplements currently are:

> > Cod Liver Oil

> > Kirkman hypoallergenic multi vitamins

> > HLC MindLinx by Pharmax probiotics

> > DMG

> > liquid calcium magnesium citrate

> > additional magnesium

> > zinc/C drops

> > Biotin and/or Lauricidin with NoPhenol between meals for yeast

> > chewable AFP and Zyme Prime enzymes with meals

> >

> > Lucky for me, the kid swallows pills like a champ!! Who would'a

> known

> > that a three year old could swallow pills like him and he doesn't

> even

> > need water!

> >

> > Since some of his elements came in low, should I be adjusting our

> > supplements?

> >

> >

> >

> >

>

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Is it normal to have fluctuating numbers on different tests? We had

the wrong hair toxic elements test done initially so we had the

correct one done which means I have two reports within 3-4 weeks to

compare. Many of his levels bounced around. Some went down and some

jumped way up, like the nickel. I had trouble getting the second

sample from his head since I had just cut off most of his hair for the

first test, so I was scraping the strands together to make it for the

second test. Could I have contaminated it with something? I used the

same clippers for both hair cuts.

>

> Hi everyone,

> I am going to try to make this as short as possible...I bet you've

> heard that before, ha ha. Who has a short story here?!

>

> We have a three year old with SPD, well that is where it started

> anyway, then we unraveled a slew of food allergies, 23 to be exact -

> oh, plus two that we have been able to add to that list since having

> his IgG done in September of 08. So we are free of many foods in

> addition to GF/CF and corn-free. We continue to struggle with

> " symptoms " . This lead me to start researching the WHY of it all. I

> believe he also has yeast issues and who knows what else. So we

> decided to do the Doctor's Data hair elements test. And here I am!

>

> I used the counting rules and it looks like he has a high probability

> of mercury poisoning. This is the part that got us:

> " If the number of items entirely inside the middle band (white and

> green) is 11 or less it indicates a high probability of abnormal

> mineral transport and it indicates a high probability of mercury

> poisoning. " He is at exactly 11!

>

> Regarding the specific levels - his antimony, nickel, titanium,

> copper, cobalt and zirconium are high and low are calcium, sodium,

> potassium, vanadium, molybdenum, boron, strontium and rubidium.

>

> Sooooo, we did see a dr who is on the DAN! list (The Woodlands in

> Quakertown, PA), but we didn't really even realize we were seeing one

> and why we were there in the first place. That is when we decided on

> the IgG test. Visiting him (an hour away) is covered under our

> insurance, but the test wasn't. So, now my concern is that we won't

> be covered for chelation and testing, if that is the direction we need

> to go. He doesn't seem to be on the same page as what I am reading in

> Children with Starving Brains, so I wonder if I should even bother

> using him anyway. We can't afford to pay a doctor out of pocket for

> this, so where does that leave us? Do we get more testing from here?

> Do we attempt chelation naturally on our own? What is next? I am

> desperate to help our wonderful son and want to have consistently

> normal days again. I am exhausted and drained, we have a 7 month old

> as well and I just wish I could enjoy them both while they are little.

> This craziness creeps into my days and has me wishing for bedtime

> more than I like to admit.

>

> I have a blog that I started recently when we were just getting going

> on the GFCF diet, feel free to check it out -

> http://grayson-youarewhatyoueat.blogspot.com/

>

> Should I post the results of the hair elements test here to be sure

> that I am reading it right? And I guess the big question is, WHAT

> NOW?? I bought and started treating him with Liver Life from BioRay,

> but he can't seem to ramp up past 8-9 drops and I can't even get near

> the NDF Plus for chelating, he is highly aggrevated by it, so we are

> avoiding it until I can ramp up the Liver Life more. I am stuck here

> at this cross roads now though, the test has my mind reeling!

>

> Oh and our list of supplements currently are:

> Cod Liver Oil

> Kirkman hypoallergenic multi vitamins

> HLC MindLinx by Pharmax probiotics

> DMG

> liquid calcium magnesium citrate

> additional magnesium

> zinc/C drops

> Biotin and/or Lauricidin with NoPhenol between meals for yeast

> chewable AFP and Zyme Prime enzymes with meals

>

> Lucky for me, the kid swallows pills like a champ!! Who would'a known

> that a three year old could swallow pills like him and he doesn't even

> need water!

>

> Since some of his elements came in low, should I be adjusting our

> supplements?

>

>

>

>

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No, we need the color of the bar and whether it's to the right or left.

>I won't have the graph bars in the copy and paste, is this good enough?

>

>Aluminum 7.3 < 8.0

>Antimony 0.13 < 0.066

>Arsenic 0.050 < 0.080

>Barium 0.19 < 0.50

>Beryllium < 0.01 < 0.020

>Bismuth 0.10 < 2.0

>Cadmium 0.016 < 0.070

>Lead 0.23 < 1.0

>Mercury 0.09 < 0.40

>Platinum < 0.003 < 0.005

>Thallium < 0.001 < 0.002

>Thorium < 0.001 < 0.002

>Uranium 0.027 < 0.060

>Nickel 1.5 < 0.20

>Silver 0.05 < 0.20

>Tin 0.17 < 0.30

>Titanium 1.2 < 1.0

>Calcium 120 125- 370

>Magnesium 22 12- 30

>Sodium 7 20- 200

>Potassium < 3 12- 200

>Copper 25 11- 18

>Zinc 170 100- 190

>Manganese 0.24 0.10- 0.50

>Chromium 0.71 0.43- 0.80

>Vanadium 0.018 0.030- 0.10

>Molybdenum 0.046 0.050- 0.13

>Boron 0.19 0.70- 5.0

>Iodine 0.92 0.25- 1.3

>Lithium 0.010 0.007- 0.020

>Phosphorus 189 150- 220

>Selenium 0.77 0.70- 1.1

>Strontium 0.11 0.16- 1.0

>Sulfur 46300 45500- 53000

>Cobalt 0.031 0.004- 0.020

>Iron 15 7.0- 16

>Germanium 0.035 0.030- 0.040

>Rubidium 0.007 0.016- 0.18

>Zirconium 2.3 0.040- 1.0

>

>

>> >

>> > Hi everyone,

>> > I am going to try to make this as short as possible...I bet you've

>> > heard that before, ha ha. Who has a short story here?!

>> >

>> > We have a three year old with SPD, well that is where it started

>> > anyway, then we unraveled a slew of food allergies, 23 to be exact -

>> > oh, plus two that we have been able to add to that list since having

>> > his IgG done in September of 08. So we are free of many foods in

>> > addition to GF/CF and corn-free. We continue to struggle with

>> > " symptoms " . This lead me to start researching the WHY of it all. I

>> > believe he also has yeast issues and who knows what else. So we

>> > decided to do the Doctor's Data hair elements test. And here I am!

>> >

>> > I used the counting rules and it looks like he has a high

>> probability

>> > of mercury poisoning. This is the part that got us:

>> > " If the number of items entirely inside the middle band (white and

>> > green) is 11 or less it indicates a high probability of abnormal

>> > mineral transport and it indicates a high probability of mercury

>> > poisoning. " He is at exactly 11!

>> >

>> > Regarding the specific levels - his antimony, nickel, titanium,

>> > copper, cobalt and zirconium are high and low are calcium, sodium,

>> > potassium, vanadium, molybdenum, boron, strontium and rubidium.

>> >

>> > Sooooo, we did see a dr who is on the DAN! list (The Woodlands in

>> > Quakertown, PA), but we didn't really even realize we were seeing

>> one

>> > and why we were there in the first place. That is when we decided

>> on

>> > the IgG test. Visiting him (an hour away) is covered under our

>> > insurance, but the test wasn't. So, now my concern is that we won't

>> > be covered for chelation and testing, if that is the direction we

>> need

>> > to go. He doesn't seem to be on the same page as what I am reading

>> in

>> > Children with Starving Brains, so I wonder if I should even bother

>> > using him anyway. We can't afford to pay a doctor out of pocket for

>> > this, so where does that leave us? Do we get more testing from

>> here?

>> > Do we attempt chelation naturally on our own? What is next? I am

>> > desperate to help our wonderful son and want to have consistently

>> > normal days again. I am exhausted and drained, we have a 7 month

>> old

>> > as well and I just wish I could enjoy them both while they are

>> little.

>> > This craziness creeps into my days and has me wishing for bedtime

>> > more than I like to admit.

>> >

>> > I have a blog that I started recently when we were just getting

>> going

>> > on the GFCF diet, feel free to check it out -

> > >

><http://grayson-youarewhatyoueat.blogspot.com/>http://grayson-youarewhatyoueat.\

blogspot.com/

>> >

>> > Should I post the results of the hair elements test here to be sure

>> > that I am reading it right? And I guess the big question is, WHAT

>> > NOW?? I bought and started treating him with Liver Life from

>> BioRay,

>> > but he can't seem to ramp up past 8-9 drops and I can't even get

>> near

>> > the NDF Plus for chelating, he is highly aggrevated by it, so we are

>> > avoiding it until I can ramp up the Liver Life more. I am stuck

>> here

>> > at this cross roads now though, the test has my mind reeling!

>> >

>> > Oh and our list of supplements currently are:

>> > Cod Liver Oil

>> > Kirkman hypoallergenic multi vitamins

>> > HLC MindLinx by Pharmax probiotics

>> > DMG

>> > liquid calcium magnesium citrate

>> > additional magnesium

>> > zinc/C drops

>> > Biotin and/or Lauricidin with NoPhenol between meals for yeast

>> > chewable AFP and Zyme Prime enzymes with meals

>> >

>> > Lucky for me, the kid swallows pills like a champ!! Who would'a

>> known

>> > that a three year old could swallow pills like him and he doesn't

>> even

>> > need water!

>> >

>> > Since some of his elements came in low, should I be adjusting our

>> > supplements?

>> >

>> >

>> >

>> >

>>

>

>

>

--

Ralph Nader on the need for moral courage:

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We need colors on everything and over or under 50% on the essentials.

S S

Re: New here and confused

Posted by: " jessicagalligani " jessicagalligani@... jessicagalligani

Fri Feb 6, 2009 12:13 pm (PST)

I won't have the graph bars in the copy and paste, is this good enough?

Aluminum 7.3 < 8.0

Antimony 0.13 < 0.066

Arsenic 0.050 < 0.080

Barium 0.19 < 0.50

Beryllium < 0.01 < 0.020

Bismuth 0.10 < 2.0

Cadmium 0.016 < 0.070

Lead 0.23 < 1.0

Mercury 0.09 < 0.40

Platinum < 0.003 < 0.005

Thallium < 0.001 < 0.002

Thorium < 0.001 < 0.002

Uranium 0.027 < 0.060

Nickel 1.5 < 0.20

Silver 0.05 < 0.20

Tin 0.17 < 0.30

Titanium 1.2 < 1.0

Calcium 120 125- 370

Magnesium 22 12- 30

Sodium 7 20- 200

Potassium < 3 12- 200

Copper 25 11- 18

Zinc 170 100- 190

Manganese 0.24 0.10- 0.50

Chromium 0.71 0.43- 0.80

Vanadium 0.018 0.030- 0.10

Molybdenum 0.046 0.050- 0.13

Boron 0.19 0.70- 5.0

Iodine 0.92 0.25- 1.3

Lithium 0.010 0.007- 0.020

Phosphorus 189 150- 220

Selenium 0.77 0.70- 1.1

Strontium 0.11 0.16- 1.0

Sulfur 46300 45500- 53000

Cobalt 0.031 0.004- 0.020

Iron 15 7.0- 16

Germanium 0.035 0.030- 0.040

Rubidium 0.007 0.016- 0.18

Zirconium 2.3 0.040- 1.0

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>

> I am new here and I have been struggling with the decision of TKR

> bilatteral for a few weeks now. I am only 36 yrs old, lots of sports

> injuries over the years and weight is an issue as well.

> <snip>

> How much time does one

> truely need for recovery, before they go back to work? 6 weeks? Any

> input would be great.

>

> Deena

>

Hi, Deena. I think it can rarely be done in 6 weeks, but plan for

more, maybe a lot more. Take your time to be able to do your PT, which

is hard to do while working, even if you are able to work from home.

Bill in MN

Bilateral TKR a little over a year ago.

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I would get a second and third opinion that you only have the option

of a TKR. After 4 or more excellent ortho docs told me that was the

only thing they could do to fix my knees, then I resigned myself to

it. I would not take the word of just one surgeon.

I assume Euflexxa is like Synvisc and others, an HLA substance they

inject into your knees. If this stuff works for you to where you

still have a life, a lot of people really benefit from it and it

does postpone surgery. It didn't work on me, my knees were shot.

I decided to get TKR when I noticed I was making excuses to go out

and do things, because of knee pain, and my quality of life was

diminished.

Personally I wouldn't have a bilateral, too tough emotionally and

physically. But there are people who do.

Good luck

Hollie

> I am new here and I have been struggling with the decision of TKR

> bilatteral for a few weeks now. I am only 36 yrs old, lots of

sports

> injuries over the years and weight is an issue as well. I have

been

> getting Euflexxa injections in both knees every 6 months and

steroid

> injections every other three months this has been going on for

about a

> year now. I was told by a surgeon last week that I need both

knees

> replaced and I should not wait any longer due to compromising the

> ligaments. Is this true? Has anyone heard anything like this?

My

> theory is why not buy myself as much time possible if the

injections

> are working some what. And they are, I am 3 weeks out from

injection

> #3 of Euflexxa and still have pain but it is minimal, can't do

stairs

> but hey thats ok. Any suggestions? Ideas? How much time does

one

> truely need for recovery, before they go back to work? 6 weeks?

Any

> input would be great.

>

> Deena

>

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Hi Deena,

I wouldn't do both knees at once - just my own personal suggestion. That

said, if you can't do STAIRS, how do you get around? And if you can't do

stairs, you can't really get good exercise - and good exercise is vital to

the health of your whole body. If you can do a complete exercise program,

walk several miles, and go up and down stairs, then you don't need knee

replacement yet. But if your knees are keeping you from doing any one of

those things, the rest of you is suffering.

claire

Callahan Goodman

I am new here and I have been struggling with the decision of TKR

bilatteral for a few weeks now. I am only 36 yrs old, lots of sports

injuries over the years and weight is an issue as well. I have been

getting Euflexxa injections in both knees every 6 months and steroid

injections every other three months this has been going on for about a

year now. I was told by a surgeon last week that I need both knees

replaced and I should not wait any longer due to compromising the

ligaments. Is this true? Has anyone heard anything like this? My

theory is why not buy myself as much time possible if the injections

are working some what. And they are, I am 3 weeks out from injection

#3 of Euflexxa and still have pain but it is minimal, can't do stairs

but hey thats ok. Any suggestions? Ideas? How much time does one

truely need for recovery, before they go back to work? 6 weeks? Any

input would be great.

Deena

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Deena,

I agree with , I wouldn't get both knees done at the same time

either. It's been 5 months since I had my left TKR and my right one is

scheduled for March 17, and I can barely wait! The difference is

unbelievable. I also have weight issues and my doctor didn't think that

I should do both at once. The impatient part of me says " I wish I had "

but the thinking part of me knows that it was the right choice. It also

helps to have the comparison of the " new " knee vs. the " old " knee. I

went back to work last time at 5 weeks, but since I will need to be

using my leg to drive, I will wait the 6 weeks this time. I thought 5

was too early, but it was time off work and money situation.. Anyway,

it's been a struggle for the past 5 months to have to still deal with

pain in my right knee, so I would suggest that if you are doing well

with the first knee, do the other one as soon as you feel confident.

(again, mine was an insurance thing.) You will be so glad you did it!

Good luck! =)

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>

> Deena,

> I agree with , I wouldn't get both knees done at the same time

> either. It's been 5 months since I had my left TKR and my right one is

> scheduled for March 17, and I can barely wait! The difference is

> unbelievable.

Regarding doing one at a time vs. two at once - that is mostly between

you and your doctor, but a lot of the choice is whether you are up to

it or not. When I made the choice, I was talking with two surgeons,

One wanted to do two, the other, one at a time. My dad was pretty sick

with cancer at the time, and a long-time friend of the family came

over to visit him. This man had two done at once, a couple of years

before, and had just come back from a week of skiing in Colorado. And

he was 80 years old! Since he was now my hero, I asked him if he had

any regrets about doing two, and in his words, " it is the only way to

go! " Based on his comments and his success, I went ahead and

scheduled the bilateral.

A few weeks later, I was talking with him about another matter related

to cars, and happened to ask him, " why is it the only way to go? " He

said, " because if I only did one, I would never have done the other. "

That said, now having done a bilateral, I wouldn't discourage you from

having both done, nor would I discourage you from the choice of one at

a time. The thing is, go into the choice with both eyes open, and with

realistic expectations.

For me, the main advantage of bilateral was that I'd only have to go

through the big surgery once. The recovery of the bilateral will take

longer than one knee, but I would argue that it is less than the total

time of doing two separately. The recovery and PT are obviously a

little more harsh with two at once. I noticed that when the people I

went through PT with could focus on only one knee, they got their

flexion back sooner.

Just a few disconnected thoughts...

Bill in MN

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I can understand your apprehension. I'm only 43 and just had total

hip replacement.

I also did the different steroid shots/injections as a last resort.

However, after doing the research, many of those injections on a

regular basis can do more harm than good. I strongly recco you

research the long term effects of continuing these injections vs. the

benefits/drawbacks of the surgery.

I can say without a doubt that I am SO pleased I had the surgery.

While it may not be the last resort for you, when you eventually do

have it done, you will wonder why you waited so long.

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I can only speak from friends' experiences who said that they were

glad they had gotten both knees done at once. Recovery was a little

harder in terms of mobility but once it was done, it was done. My

friend who had both knees done had someone at home to help her with

everything including the physical therapy for (I think) two weeks.

My other friend who needs both knees done also wants to have both at

the same time. The OS told her it would be a matter of how long it

took to do one knee as she has some respiratory difficulties and he

doesn't think it would be wise for her to have a prolonged operation

if he couldn't do them both in the " normal " time.

On Feb 13, 2009, at 4:06 AM, Bill wrote:

>

> >

> > Deena,

> > I agree with , I wouldn't get both knees done at the same time

> > either. It's been 5 months since I had my left TKR and my right

> one is

> > scheduled for March 17, and I can barely wait! The difference is

> > unbelievable.

>

> Regarding doing one at a time vs. two at once - that is mostly between

> you and your doctor, but a lot of the choice is whether you are up to

> it or not. When I made the choice, I was talking with two surgeons,

> One wanted to do two, the other, one at a time. My dad was pretty sick

> with cancer at the time, and a long-time friend of the family came

> over to visit him. This man had two done at once, a couple of years

> before, and had just come back from a week of skiing in Colorado. And

> he was 80 years old! Since he was now my hero, I asked him if he had

> any regrets about doing two, and in his words, " it is the only way to

> go! " Based on his comments and his success, I went ahead and

> scheduled the bilateral.

>

> A few weeks later, I was talking with him about another matter related

> to cars, and happened to ask him, " why is it the only way to go? " He

> said, " because if I only did one, I would never have done the other. "

>

> That said, now having done a bilateral, I wouldn't discourage you from

> having both done, nor would I discourage you from the choice of one at

> a time. The thing is, go into the choice with both eyes open, and with

> realistic expectations.

>

> For me, the main advantage of bilateral was that I'd only have to go

> through the big surgery once. The recovery of the bilateral will take

> longer than one knee, but I would argue that it is less than the total

> time of doing two separately. The recovery and PT are obviously a

> little more harsh with two at once. I noticed that when the people I

> went through PT with could focus on only one knee, they got their

> flexion back sooner.

>

> Just a few disconnected thoughts...

>

> Bill in MN

>

>

>

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  • 1 year later...
Guest guest

Hi there I am new here, have a 5.5 month old son with I guess brachy - his head

is kinda flat in the back and wide, but it isn't uneven and we don't have any

assymetry issues. We were referred to a plastic/neurosurgeon who said she

recommends a helmet but said to try keeping him off the back of his head for a

month before we decide - see if it rounds out at all.

Meanwhile I am obsessing...half of my friends and family say we should get the

helmet, and half say his head is fine and it's a waste of money. Me and my

husband don't know what to think. I don't think his head is all that

abnormal...a little big maybe, but his dad has a big noggin'. I need some more

opinions from people who know what they are talking about. I'll try to post some

pics. His name Is Jack...

Also, I know this is ridiculous, but I keep tearing up thinking about his poor

little head being in a helmet for 4 months. I know it's not that big of a deal

and it will probably fly by, but for some reason it hurts me...I'm scared he is

going to hate it!!

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