Re: READY to START for my 2 boys!! ANDY...others with experience...is this corre

[Guest guest]

>

> Four years ago, we considered chelation therapy and started my youngest son on

TD-DMPS noticing NO change at all. We did this for 2 years. (I heard later

that this turned out to be a scam?---Dr. Buttar anyone?) We did this based on a

heavy metals test (hair test) where the kids were off the charts in metals

except none showing for mercury.

It would be exceptionally useful to actually see the hair test. I don't suppose

you can post it in the files section?

>We were told that sometimes mercury doesn't show if it doesn't spill. Is this

true? Our oldest son's neurologist at Loma told us that if we were to

chelate him that we could dislodge the mercury from his brain and it would

" relodge " somewhere else, possibly causing him to seize even worse....so we

opted out. Is this true?? Can chelating with DMSA and ALA worsen his seizures?

If done wrong. Not if done properly.

What is happening is the neurologist is telling lies as almost all doctors do to

try to control you. This is one of the very difficult things for most people to

accept and understand - doctors are taught in medical school and residency that

they are SUPPOSED to make things up to scare you so you don't do anything other

than regular mainstream medicine.

It's pretty easy to verify this - just put the neuro on the spot to describe

specific cases where s/he has observed this and keep asking questions until you

get a clear picture or s/he gets mad.

Do note that DURING the actual chelation cycles he may be more prone to having

seizures, but this is easily controlled by using enough medication or reducing

chelator amounts to a low enough level. Similarly there may be temporary issues

during the 'detox hump,' but since you already chelated him that should have

already happened (unless the TD-DMPS you got didn't actually contain any active

DMPS).

> Subsequently, this influenced our decision to NOT chelate. Now we regret it

since time has passed and we have only placed small bandages (like gf/cf diet,

hbot (made it worse) amongst all the other problems.

HBOT is actually more risky for this than chelation. It is still worthwhile in

certain specific situations.

> After reading a ton of material on the internet on Cutler Protocol, and

reading through only partially in the book Amalgam Illness:Diagnosis &

Treatment, (I plan to finish soon), I would like to start my boys immediately

with chelating. I can say that their guts have improved greatly over the last 4

years, to the point that I just started reintroducing wheat and all grains back

into their diet, but their behaviors have worsened to some extent and I am

finding my oldest son more aggressive and I am afraid I am losing them both to

this disease.

Sounds like you need to take the grains back out.

This is part of the " GFCF religion. " The GFCF diet does NOT cure anything at

all. It only holds the symptoms at bay as long as you continue the diet. Of

course, when the kids reach adolescence they become rebellious and don't follow

the diet, so people who have relied on it then have their children get

catastrophically worse, become unmanageable and have to institutionalize them

when the children often could have gotten all better if they'd been chelated

earlier on - and after chelation most of them would not need the GFCF diet.

Yours apparently still need it, but really do need to chelate.

>

>

> So this is what I have gleaned from my initial reading (please those with

experience let me know if I have this right and if I need to add more

supplements???):

>

>

> k

>

> Age: 10 years, 3 months

>

> Weight: 97.5 lbs.

>

> Supplements currently on:

> P5P, 50 mg (2x/day)

B complex (like B50) is usually adequate if given 3-4 times a day.

> Vitamin C, 500 mg (1x/day)

this needs to be 3-4 times a day.

> GABA, 500 mg(1x/day)

GABA only lasts a few hours. All the antiseizure meds are like it in action and

should be used instead in the presence of frank seizures.

> Taurine, 1000 mg (2x/day)

> Magnesium (.9cc injection 1x/day)

Give Mg by mouth several times a day, sometimes that is adequate and it will

always help even if injections are needed.

> Natural Calm, 325mg/2tsp (Magnesium tea...sometimes before bed if seizures are

prevalent)

> 1 Super Papaya Enzyme Plus with meals

> 1 tsp coconut oil 3x/day

They need zinc too. Maybe 50 mg once or twice a day.

>

> Other Issues to Consider: k had 1 febrile seizure at 14 months of age.

At 28 months of age, k was hospitalized for seizure disorder and has had a

total of 5 hospitalizations and thousands of seizures since. He has been on at

least 10 different anticonvulsants with little or no success in stopping the

seizures but leaving only lasting behavioral problems. The last drug he was on

was the worst (Ativan: Lorazepam) which is a benzodiazepine that took 6 months

to wean him off of. His seizures average about 3/week now down from and average

of 22/week when he was on the medication!

Please list all the ones that were tried, tell us what the neurologist says is

causing the seizures, what exact type the neurologist says they are, and provide

the actual EEG interpretive report discussing what they saw when they did an

EEG.

> And, sometimes he will have 2 weeks with NO seizures and then 4 or 5 days

with about 8 seizures/day. Is it okay to chelate even though he is having

seizures?

You don't really have a choice if heavy metals are causing them and you want

them to stop.

It sounds like there may be some unrecognized trigger. Are you familiar with

chemical sensitivity? Do you think he is chemically sensitive?

>

>

>

> Proposed Schedule for k

>

>

> Start 12mg DMSA and 12mg ALA at the same time. For us, Monday 9am, 12pm,

3pm, 6pm, 9pm, 12pm, 3pm, 6am until Thursday, 9pm bedtime.

>

> Rest from Thursday at 9pm, Friday, Saturday and Sunday starting back at 9am

Monday morning with the above schedule

>

> Add ?????? supplements to his protocol

>

>

>

This is fine.

>

>

> Andy

>

> Age: 7 years, 5 months

>

> Weight: 47.5 lbs.

Use comments above from k for Andy too.

It is pretty likely both of them would benefit from some form of adrenal

glandular, such as Thorne brand, Allergy Research Group/Nutricology brand, or

Standard Process brand. I'm only naming brands because it isn't that common a

supplement and these 3 lines carry it, any brand should be fine.

>

> Supplements/Medicine currently on:

> Fluconazole, .75ml 1x/day, 40mg/ml concentration

Did you ever try this on k?

> P5P, 100 mg (2x/day)

> Vitamin C, 500 mg (1x/day)

> Taurine, 1000 mg (2x/day)

> Glutagenics, 1tsp/day (1tsp = 3500mg L-Glutamine, 500mg Licorice Root, 50 mg

Aloe Leaf Extract)

> Natural Calm (Magnesium tea...sometimes before bed if seizures are prevalent)

> 1 Super Papaya Enzyme Plus with meals

> 1 tsp coconut oil 3x/day

>

> Other Issues to Consider: Andy has chronic constipation and is dependent on

suppositories. I'm not sure if this is anxiety related since he acts like he is

trying to hold back from pushing, but there may be other issues. Andy is one of

the highest yeast kids that his ex-DAN! doctor ever had.

Use more magnesium by mouth and also anything that enhances bile flow, lecithin,

milk thistle extract (several times a day) glycine, etc.

>

>

> Proposed Schedule for Andy

>

> Start 12.5mg DMSA and 12.5mg ALA at the same time. For us, Monday 9am, 12pm,

3pm, 6pm, 9pm, 12pm, 3pm, 6am until Thursday, 9pm bedtime. We are wanting to

use liquid ALA throughout the night to help Andy stay asleep and powdered ALA

during the day mixed in applesauce to save on cost.

This is fine.

>

> Rest from Thursday at 9pm, Friday, Saturday and Sunday starting back at 9am

Monday morning with the above schedule

>

> Add ?????? supplements to his protocol

>

As above. And please provide more information.

Andy

http://www.noamalgam.com/index.html

Amalgam Illness: Diagnosis and Treatment

http://www.noamalgam.com/hairtestbook.html

Hair Test Interpretation: Finding Hidden Toxicities

http://www.noamalgam.com/nourishinghope.html

Nourishing Hope for Autism: Nutrition Intervention for Healing Our Children

http://www.noamalgam.com/biologicaltreatments.html

Biological Treatments for Autism and PDD

[Guest guest]

Andy-

Were you saying here that HBOT is actually more risky for possibly increasing

seizures than chelation (or done incorrectly chelation)? Just want to be sure I

am following the conversation correctly. If there is not a seizure issue what's

your take on HBOT and who it may be appropriate for? Thanks-

" There is a crack in everything and that is how the light gets in. "

Leonard Cohen

From: AndyCutler@...

Date: Sat, 13 Feb 2010 20:17:58 +0000

Subject: [ ] Re: READY to START for my 2 boys!! ANDY...others with

experience...is this corre

>

> Four years ago, we considered chelation therapy and started my youngest son on

TD-DMPS noticing NO change at all. We did this for 2 years. (I heard later

that this turned out to be a scam?---Dr. Buttar anyone?) We did this based on a

heavy metals test (hair test) where the kids were off the charts in metals

except none showing for mercury.

It would be exceptionally useful to actually see the hair test. I don't suppose

you can post it in the files section?

>We were told that sometimes mercury doesn't show if it doesn't spill. Is this

true? Our oldest son's neurologist at Loma told us that if we were to

chelate him that we could dislodge the mercury from his brain and it would

" relodge " somewhere else, possibly causing him to seize even worse....so we

opted out. Is this true?? Can chelating with DMSA and ALA worsen his seizures?

If done wrong. Not if done properly.

What is happening is the neurologist is telling lies as almost all doctors do to

try to control you. This is one of the very difficult things for most people to

accept and understand - doctors are taught in medical school and residency that

they are SUPPOSED to make things up to scare you so you don't do anything other

than regular mainstream medicine.

It's pretty easy to verify this - just put the neuro on the spot to describe

specific cases where s/he has observed this and keep asking questions until you

get a clear picture or s/he gets mad.

Do note that DURING the actual chelation cycles he may be more prone to having

seizures, but this is easily controlled by using enough medication or reducing

chelator amounts to a low enough level. Similarly there may be temporary issues

during the 'detox hump,' but since you already chelated him that should have

already happened (unless the TD-DMPS you got didn't actually contain any active

DMPS).

> Subsequently, this influenced our decision to NOT chelate. Now we regret it

since time has passed and we have only placed small bandages (like gf/cf diet,

hbot (made it worse) amongst all the other problems.

HBOT is actually more risky for this than chelation. It is still worthwhile in

certain specific situations.

> After reading a ton of material on the internet on Cutler Protocol, and

reading through only partially in the book Amalgam Illness:Diagnosis &

Treatment, (I plan to finish soon), I would like to start my boys immediately

with chelating. I can say that their guts have improved greatly over the last 4

years, to the point that I just started reintroducing wheat and all grains back

into their diet, but their behaviors have worsened to some extent and I am

finding my oldest son more aggressive and I am afraid I am losing them both to

this disease.

Sounds like you need to take the grains back out.

This is part of the " GFCF religion. " The GFCF diet does NOT cure anything at

all. It only holds the symptoms at bay as long as you continue the diet. Of

course, when the kids reach adolescence they become rebellious and don't follow

the diet, so people who have relied on it then have their children get

catastrophically worse, become unmanageable and have to institutionalize them

when the children often could have gotten all better if they'd been chelated

earlier on - and after chelation most of them would not need the GFCF diet.

Yours apparently still need it, but really do need to chelate.

>

>

> So this is what I have gleaned from my initial reading (please those with

experience let me know if I have this right and if I need to add more

supplements???):

>

>

> k

>

> Age: 10 years, 3 months

>

> Weight: 97.5 lbs.

>

> Supplements currently on:

> P5P, 50 mg (2x/day)

B complex (like B50) is usually adequate if given 3-4 times a day.

> Vitamin C, 500 mg (1x/day)

this needs to be 3-4 times a day.

> GABA, 500 mg(1x/day)

GABA only lasts a few hours. All the antiseizure meds are like it in action and

should be used instead in the presence of frank seizures.

> Taurine, 1000 mg (2x/day)

> Magnesium (.9cc injection 1x/day)

Give Mg by mouth several times a day, sometimes that is adequate and it will

always help even if injections are needed.

> Natural Calm, 325mg/2tsp (Magnesium tea...sometimes before bed if seizures are

prevalent)

> 1 Super Papaya Enzyme Plus with meals

> 1 tsp coconut oil 3x/day

They need zinc too. Maybe 50 mg once or twice a day.

>

> Other Issues to Consider: k had 1 febrile seizure at 14 months of age.

At 28 months of age, k was hospitalized for seizure disorder and has had a

total of 5 hospitalizations and thousands of seizures since. He has been on at

least 10 different anticonvulsants with little or no success in stopping the

seizures but leaving only lasting behavioral problems. The last drug he was on

was the worst (Ativan: Lorazepam) which is a benzodiazepine that took 6 months

to wean him off of. His seizures average about 3/week now down from and average

of 22/week when he was on the medication!

Please list all the ones that were tried, tell us what the neurologist says is

causing the seizures, what exact type the neurologist says they are, and provide

the actual EEG interpretive report discussing what they saw when they did an

EEG.

> And, sometimes he will have 2 weeks with NO seizures and then 4 or 5 days

with about 8 seizures/day. Is it okay to chelate even though he is having

seizures?

You don't really have a choice if heavy metals are causing them and you want

them to stop.

It sounds like there may be some unrecognized trigger. Are you familiar with

chemical sensitivity? Do you think he is chemically sensitive?

>

>

>

> Proposed Schedule for k

>

>

> Start 12mg DMSA and 12mg ALA at the same time. For us, Monday 9am, 12pm,

3pm, 6pm, 9pm, 12pm, 3pm, 6am until Thursday, 9pm bedtime.

>

> Rest from Thursday at 9pm, Friday, Saturday and Sunday starting back at 9am

Monday morning with the above schedule

>

> Add ?????? supplements to his protocol

>

>

>

This is fine.

>

>

> Andy

>

> Age: 7 years, 5 months

>

> Weight: 47.5 lbs.

Use comments above from k for Andy too.

It is pretty likely both of them would benefit from some form of adrenal

glandular, such as Thorne brand, Allergy Research Group/Nutricology brand, or

Standard Process brand. I'm only naming brands because it isn't that common a

supplement and these 3 lines carry it, any brand should be fine.

>

> Supplements/Medicine currently on:

> Fluconazole, .75ml 1x/day, 40mg/ml concentration

Did you ever try this on k?

> P5P, 100 mg (2x/day)

> Vitamin C, 500 mg (1x/day)

> Taurine, 1000 mg (2x/day)

> Glutagenics, 1tsp/day (1tsp = 3500mg L-Glutamine, 500mg Licorice Root, 50 mg

Aloe Leaf Extract)

> Natural Calm (Magnesium tea...sometimes before bed if seizures are prevalent)

> 1 Super Papaya Enzyme Plus with meals

> 1 tsp coconut oil 3x/day

>

> Other Issues to Consider: Andy has chronic constipation and is dependent on

suppositories. I'm not sure if this is anxiety related since he acts like he is

trying to hold back from pushing, but there may be other issues. Andy is one of

the highest yeast kids that his ex-DAN! doctor ever had.

Use more magnesium by mouth and also anything that enhances bile flow, lecithin,

milk thistle extract (several times a day) glycine, etc.

>

>

> Proposed Schedule for Andy

>

> Start 12.5mg DMSA and 12.5mg ALA at the same time. For us, Monday 9am, 12pm,

3pm, 6pm, 9pm, 12pm, 3pm, 6am until Thursday, 9pm bedtime. We are wanting to

use liquid ALA throughout the night to help Andy stay asleep and powdered ALA

during the day mixed in applesauce to save on cost.

This is fine.

>

> Rest from Thursday at 9pm, Friday, Saturday and Sunday starting back at 9am

Monday morning with the above schedule

>

> Add ?????? supplements to his protocol

>

As above. And please provide more information.

Andy

http://www.noamalgam.com/index.html

Amalgam Illness: Diagnosis and Treatment

http://www.noamalgam.com/hairtestbook.html

Hair Test Interpretation: Finding Hidden Toxicities

http://www.noamalgam.com/nourishinghope.html

Nourishing Hope for Autism: Nutrition Intervention for Healing Our Children

http://www.noamalgam.com/biologicaltreatments.html

Biological Treatments for Autism and PDD

_________________________________________________________________

Hotmail: Free, trusted and rich email service.

http://clk.atdmt.com/GBL/go/201469228/direct/01/

[Guest guest]

>

> >

>

> > Four years ago, we considered chelation therapy and started my youngest son

on TD-DMPS noticing NO change at all. We did this for 2 years. (I heard later

that this turned out to be a scam?---Dr. Buttar anyone?) We did this based on a

heavy metals test (hair test) where the kids were off the charts in metals

except none showing for mercury.

>

>

>

> It would be exceptionally useful to actually see the hair test. I don't

suppose you can post it in the files section?

>

>

>

> >We were told that sometimes mercury doesn't show if it doesn't spill. Is this

true? Our oldest son's neurologist at Loma told us that if we were to

chelate him that we could dislodge the mercury from his brain and it would

" relodge " somewhere else, possibly causing him to seize even worse....so we

opted out. Is this true?? Can chelating with DMSA and ALA worsen his seizures?

>

>

>

> If done wrong. Not if done properly.

>

>

>

> What is happening is the neurologist is telling lies as almost all doctors do

to try to control you. This is one of the very difficult things for most people

to accept and understand - doctors are taught in medical school and residency

that they are SUPPOSED to make things up to scare you so you don't do anything

other than regular mainstream medicine.

>

>

>

> It's pretty easy to verify this - just put the neuro on the spot to describe

specific cases where s/he has observed this and keep asking questions until you

get a clear picture or s/he gets mad.

>

>

>

> Do note that DURING the actual chelation cycles he may be more prone to having

seizures, but this is easily controlled by using enough medication or reducing

chelator amounts to a low enough level. Similarly there may be temporary issues

during the 'detox hump,' but since you already chelated him that should have

already happened (unless the TD-DMPS you got didn't actually contain any active

DMPS).

>

>

>

> > Subsequently, this influenced our decision to NOT chelate. Now we regret it

since time has passed and we have only placed small bandages (like gf/cf diet,

hbot (made it worse) amongst all the other problems.

>

>

>

> HBOT is actually more risky for this than chelation. It is still worthwhile

in certain specific situations.

>

>

>

> > After reading a ton of material on the internet on Cutler Protocol, and

reading through only partially in the book Amalgam Illness:Diagnosis &

Treatment, (I plan to finish soon), I would like to start my boys immediately

with chelating. I can say that their guts have improved greatly over the last 4

years, to the point that I just started reintroducing wheat and all grains back

into their diet, but their behaviors have worsened to some extent and I am

finding my oldest son more aggressive and I am afraid I am losing them both to

this disease.

>

>

>

> Sounds like you need to take the grains back out.

>

>

>

> This is part of the " GFCF religion. " The GFCF diet does NOT cure anything at

all. It only holds the symptoms at bay as long as you continue the diet. Of

course, when the kids reach adolescence they become rebellious and don't follow

the diet, so people who have relied on it then have their children get

catastrophically worse, become unmanageable and have to institutionalize them

when the children often could have gotten all better if they'd been chelated

earlier on - and after chelation most of them would not need the GFCF diet.

>

>

>

> Yours apparently still need it, but really do need to chelate.

>

>

>

> >

>

> >

>

> > So this is what I have gleaned from my initial reading (please those with

experience let me know if I have this right and if I need to add more

supplements???):

>

> >

>

> >

>

> > k

>

> >

>

> > Age: 10 years, 3 months

>

> >

>

> > Weight: 97.5 lbs.

>

> >

>

> > Supplements currently on:

>

> > P5P, 50 mg (2x/day)

>

>

>

> B complex (like B50) is usually adequate if given 3-4 times a day.

>

>

>

> > Vitamin C, 500 mg (1x/day)

>

>

>

> this needs to be 3-4 times a day.

>

>

>

> > GABA, 500 mg(1x/day)

>

>

>

> GABA only lasts a few hours. All the antiseizure meds are like it in action

and should be used instead in the presence of frank seizures.

>

>

>

> > Taurine, 1000 mg (2x/day)

>

> > Magnesium (.9cc injection 1x/day)

>

>

>

> Give Mg by mouth several times a day, sometimes that is adequate and it will

always help even if injections are needed.

>

>

>

> > Natural Calm, 325mg/2tsp (Magnesium tea...sometimes before bed if seizures

are prevalent)

>

> > 1 Super Papaya Enzyme Plus with meals

>

> > 1 tsp coconut oil 3x/day

>

>

>

> They need zinc too. Maybe 50 mg once or twice a day.

>

> >

>

> > Other Issues to Consider: k had 1 febrile seizure at 14 months of age.

At 28 months of age, k was hospitalized for seizure disorder and has had a

total of 5 hospitalizations and thousands of seizures since. He has been on at

least 10 different anticonvulsants with little or no success in stopping the

seizures but leaving only lasting behavioral problems. The last drug he was on

was the worst (Ativan: Lorazepam) which is a benzodiazepine that took 6 months

to wean him off of. His seizures average about 3/week now down from and average

of 22/week when he was on the medication!

>

>

>

> Please list all the ones that were tried, tell us what the neurologist says is

causing the seizures, what exact type the neurologist says they are, and provide

the actual EEG interpretive report discussing what they saw when they did an

EEG.

>

>

>

> > And, sometimes he will have 2 weeks with NO seizures and then 4 or 5 days

with about 8 seizures/day. Is it okay to chelate even though he is having

seizures?

>

>

>

> You don't really have a choice if heavy metals are causing them and you want

them to stop.

>

>

>

> It sounds like there may be some unrecognized trigger. Are you familiar with

chemical sensitivity? Do you think he is chemically sensitive?

>

> >

>

> >

>

> >

>

> > Proposed Schedule for k

>

> >

>

> >

>

> > Start 12mg DMSA and 12mg ALA at the same time. For us, Monday 9am, 12pm,

3pm, 6pm, 9pm, 12pm, 3pm, 6am until Thursday, 9pm bedtime.

>

> >

>

> > Rest from Thursday at 9pm, Friday, Saturday and Sunday starting back at 9am

Monday morning with the above schedule

>

> >

>

> > Add ?????? supplements to his protocol

>

> >

>

> >

>

> >

>

> This is fine.

>

> >

>

> >

>

> > Andy

>

> >

>

> > Age: 7 years, 5 months

>

> >

>

> > Weight: 47.5 lbs.

>

>

>

> Use comments above from k for Andy too.

>

>

>

> It is pretty likely both of them would benefit from some form of adrenal

glandular, such as Thorne brand, Allergy Research Group/Nutricology brand, or

Standard Process brand. I'm only naming brands because it isn't that common a

supplement and these 3 lines carry it, any brand should be fine.

>

> >

>

> > Supplements/Medicine currently on:

>

> > Fluconazole, .75ml 1x/day, 40mg/ml concentration

>

>

>

> Did you ever try this on k?

>

>

>

> > P5P, 100 mg (2x/day)

>

> > Vitamin C, 500 mg (1x/day)

>

> > Taurine, 1000 mg (2x/day)

>

> > Glutagenics, 1tsp/day (1tsp = 3500mg L-Glutamine, 500mg Licorice Root, 50 mg

Aloe Leaf Extract)

>

> > Natural Calm (Magnesium tea...sometimes before bed if seizures are

prevalent)

>

> > 1 Super Papaya Enzyme Plus with meals

>

> > 1 tsp coconut oil 3x/day

>

> >

>

> > Other Issues to Consider: Andy has chronic constipation and is dependent on

suppositories. I'm not sure if this is anxiety related since he acts like he is

trying to hold back from pushing, but there may be other issues. Andy is one of

the highest yeast kids that his ex-DAN! doctor ever had.

>

>

>

> Use more magnesium by mouth and also anything that enhances bile flow,

lecithin, milk thistle extract (several times a day) glycine, etc.

>

> >

>

> >

>

> > Proposed Schedule for Andy

>

> >

>

> > Start 12.5mg DMSA and 12.5mg ALA at the same time. For us, Monday 9am,

12pm, 3pm, 6pm, 9pm, 12pm, 3pm, 6am until Thursday, 9pm bedtime. We are wanting

to use liquid ALA throughout the night to help Andy stay asleep and powdered ALA

during the day mixed in applesauce to save on cost.

>

>

>

> This is fine.

>

> >

>

> > Rest from Thursday at 9pm, Friday, Saturday and Sunday starting back at 9am

Monday morning with the above schedule

>

> >

>

> > Add ?????? supplements to his protocol

>

> >

>

> As above. And please provide more information.

>

>

>

> Andy

>

>

>

> http://www.noamalgam.com/index.html

>

> Amalgam Illness: Diagnosis and Treatment

>

>

>

> http://www.noamalgam.com/hairtestbook.html

>

> Hair Test Interpretation: Finding Hidden Toxicities

>

>

>

> http://www.noamalgam.com/nourishinghope.html

>

> Nourishing Hope for Autism: Nutrition Intervention for Healing Our Children

>

>

>

> http://www.noamalgam.com/biologicaltreatments.html

>

> Biological Treatments for Autism and PDD

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

> _________________________________________________________________

> Hotmail: Free, trusted and rich email service.

> http://clk.atdmt.com/GBL/go/201469228/direct/01/

>

>