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>I am chelating on 12.mg of ala and dmsa and noticed that I am more

> sensitive to the smell of oil esp when pumping gas and now at my own

> home downstairs near the boiler. I smell oil and other dont seem to.

> What can I do for this at the moment and what might this mean? On

> most of the recommended supplements, flax oil, mag, calcium, etc. Thanks

It is common for your smell to improve on/after chelation. This is a good

thing usually as it often means it is returning to normal.

Was it bad before?

It can also be due to zinc supplementation.

Adrenaline also sensitizes you to smells (if I'm correct?) and the chelation

could be increasing your adrenal stress and thus adrenaline and this smell.

Or you are just clearing metals out of your smelling receptors.

DeanSA

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>I am chelating on 12.mg of ala and dmsa and noticed that I am more

> sensitive to the smell of oil esp when pumping gas and now at my own

> home downstairs near the boiler. I smell oil and other dont seem to.

> What can I do for this at the moment and what might this mean? On

> most of the recommended supplements, flax oil, mag, calcium, etc. Thanks

It is common for your smell to improve on/after chelation. This is a good

thing usually as it often means it is returning to normal.

Was it bad before?

It can also be due to zinc supplementation.

Adrenaline also sensitizes you to smells (if I'm correct?) and the chelation

could be increasing your adrenal stress and thus adrenaline and this smell.

Or you are just clearing metals out of your smelling receptors.

DeanSA

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i interpreted this smell to be part of ongoing mcs (mult chem

sensitivites); which I believe in turn is usually part of fast phase 1-

slow phase 2 liver metabolism .AI protocol is niacinamide, grapefruit

juice and selenomethionine. This has helped me a lot

see page 28, 110 of AI

I had my amalgam fillings out three weeks ago and occasionally still

get an industrial gasoline like taste/smell in my mouth. It happened

this week while I was in canada and out in the middle of nowhere (ie

there would be no such pollutants in the air) so my thought is its

part of the toxic sludge being released from my body. I am on round 3

of dmsa

I thought someone had said calcium was not a good supplement to take??

-- In frequent-dose-chelation , " email4ebay2005 "

wrote:

> I am chelating on 12.mg of ala and dmsa and noticed that I am more

> sensitive to the smell of oil esp when pumping gas and now at my own

> home downstairs near the boiler. I smell oil and other dont seem to.

> What can I do for this at the moment and what might this mean? On

> most of the recommended supplements, flax oil, mag, calcium, etc.

>Thanks

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,

I live in a houseful of people with MCS, what is the AI protocol? How bad

was you MCS, can you give me more detal?

Thanks,

Glenn

In a message dated 12/7/2007 4:19:02 P.M. Eastern Standard Time,

mle_ii@... writes:

Thanks not chelating yet. I have 6 more amalgams to get removed, 3

are being removed next week and 3 more in the first week of January.

I am so glad I'm getting these amalgams out. The first 3 he removed

he noticed some decay and said that they were at the end of their

life. He removed 2 more of them on Wednesday and found a lot of

decay and when he took them out he said they almost fell out they

were so bad.

That leaves 3 on my lower left and 3 on my upper right. So almost

half of them gone so far.

Plus they look a lot better too. :)

Mike

>

> Hi Mike

> My MCS is I would say 90% better on the AI protocol

> It was so bad i could hardly function, smelling fumes everywhere,

> headaches and anxiety...now its just occasionally so I know this

> stuff (AI) really works.

>

> are you chelating right now

>

>

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,

I live in a houseful of people with MCS, what is the AI protocol? How bad

was you MCS, can you give me more detal?

Thanks,

Glenn

In a message dated 12/7/2007 4:19:02 P.M. Eastern Standard Time,

mle_ii@... writes:

Thanks not chelating yet. I have 6 more amalgams to get removed, 3

are being removed next week and 3 more in the first week of January.

I am so glad I'm getting these amalgams out. The first 3 he removed

he noticed some decay and said that they were at the end of their

life. He removed 2 more of them on Wednesday and found a lot of

decay and when he took them out he said they almost fell out they

were so bad.

That leaves 3 on my lower left and 3 on my upper right. So almost

half of them gone so far.

Plus they look a lot better too. :)

Mike

>

> Hi Mike

> My MCS is I would say 90% better on the AI protocol

> It was so bad i could hardly function, smelling fumes everywhere,

> headaches and anxiety...now its just occasionally so I know this

> stuff (AI) really works.

>

> are you chelating right now

>

>

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Strange that you mention the smelling of oil/gasoline. Everyonce in

a while, in fact this happened last night while walking our dog, I

get a powerful scent of gasoline/oil and wondered why. I thought

perhaps there had been a car nearby that was burning oil or someone

just had their house oil tank filled nearby.

I seem to have a poor sense of smell, though I cannot tollerate

strong scents very well. My taste seemed to be not as good as it

used to as well.

Mike

>

> i interpreted this smell to be part of ongoing mcs (mult chem

> sensitivites); which I believe in turn is usually part of fast

phase 1-

> slow phase 2 liver metabolism .AI protocol is niacinamide,

grapefruit

> juice and selenomethionine. This has helped me a lot

>

> see page 28, 110 of AI

>

> I had my amalgam fillings out three weeks ago and occasionally

still

> get an industrial gasoline like taste/smell in my mouth. It

happened

> this week while I was in canada and out in the middle of nowhere

(ie

> there would be no such pollutants in the air) so my thought is its

> part of the toxic sludge being released from my body. I am on round

3

> of dmsa

>

>

> I thought someone had said calcium was not a good supplement to

take??

>

>

>

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Hi Mike

My MCS is I would say 90% better on the AI protocol

It was so bad i could hardly function, smelling fumes everywhere,

headaches and anxiety...now its just occasionally so I know this

stuff (AI) really works.

are you chelating right now

> Strange that you mention the smelling of oil/gasoline. Everyonce

> in a while, in fact this happened last night while walking our

> dog, I get a powerful scent of gasoline/oil and wondered why. I

> thought perhaps there had been a car nearby that was burning oil

> or someone just had their house oil tank filled nearby.

> I seem to have a poor sense of smell, though I cannot tollerate

> strong scents very well. My taste seemed to be not as good as it

> used to as well.

>

> Mike

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Hi Mike

My MCS is I would say 90% better on the AI protocol

It was so bad i could hardly function, smelling fumes everywhere,

headaches and anxiety...now its just occasionally so I know this

stuff (AI) really works.

are you chelating right now

> Strange that you mention the smelling of oil/gasoline. Everyonce

> in a while, in fact this happened last night while walking our

> dog, I get a powerful scent of gasoline/oil and wondered why. I

> thought perhaps there had been a car nearby that was burning oil

> or someone just had their house oil tank filled nearby.

> I seem to have a poor sense of smell, though I cannot tollerate

> strong scents very well. My taste seemed to be not as good as it

> used to as well.

>

> Mike

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In frequent-dose-chelation mle_ii wrote:

Strange that you mention the smelling of oil/gasoline. Everyonce in

a while, in fact this happened last night while walking our dog, I

get a powerful scent of gasoline/oil and wondered why. I thought

perhaps there had been a car nearby that was burning oil or someone

just had their house oil tank filled nearby.

I seem to have a poor sense of smell, though I cannot tollerate

strong scents very well. My taste seemed to be not as good as it

used to as well.

--------I believe the senses, like taste and smell, are related to zinc

deficiency, and high levels of zinc supplementation is suggested for mercury

toxic people. So this may improve as you chelate and supplement enough

zinc.-------Jackie

Mike

>

> i interpreted this smell to be part of ongoing mcs (mult chem

> sensitivites); which I believe in turn is usually part of fast

phase 1-

> slow phase 2 liver metabolism .AI protocol is niacinamide,

grapefruit

> juice and selenomethionine. This has helped me a lot

>

> see page 28, 110 of AI

>

> I had my amalgam fillings out three weeks ago and occasionally

still

> get an industrial gasoline like taste/smell in my mouth. It

happened

> this week while I was in canada and out in the middle of nowhere

(ie

> there would be no such pollutants in the air) so my thought is its

> part of the toxic sludge being released from my body. I am on round

3

> of dmsa

>

>

> I thought someone had said calcium was not a good supplement to

take??

>

>

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Thanks not chelating yet. I have 6 more amalgams to get removed, 3

are being removed next week and 3 more in the first week of January.

I am so glad I'm getting these amalgams out. The first 3 he removed

he noticed some decay and said that they were at the end of their

life. He removed 2 more of them on Wednesday and found a lot of

decay and when he took them out he said they almost fell out they

were so bad.

That leaves 3 on my lower left and 3 on my upper right. So almost

half of them gone so far.

Plus they look a lot better too. :)

Mike

>

> Hi Mike

> My MCS is I would say 90% better on the AI protocol

> It was so bad i could hardly function, smelling fumes everywhere,

> headaches and anxiety...now its just occasionally so I know this

> stuff (AI) really works.

>

> are you chelating right now

>

>

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The Ai protocol (an Andy Post) from what I think was the previous

site used by this forum was niacinamide, grapefruit juice and

selenomethionine

I ended up taking amd still do

1500 mg of niacinamide (3* a day)

375 mg (3* a day) of grapefruit deed extract

1000 mcg of selenomethionine

My understanding is that the first two supplements slow down phase 1

amd I think the selenomethionine mops up mercury (it binds to it and

renders it inert or something like that

I believe sulphur problems just take the MCS problems to another

level.

My sensitivity to these smells happened about 2.5 years ago and came

about along the same time that I managed to have liver fluke

parasites. The MCS seemed to have initailly came about when we moved

office spaces and our window opened onto a busy street in SF and our

offices were right above the garage under the building so lots of

fumes. However noone else in my office could really smell the fumes

like I could. All this time (last two years) ) I thought most of my

symptoms were lyme and parsites which they probably were but also MCS

Then about a year ago, I went to this practitioner whose big deal

was going on a very limited organic diet of ...water, chicken, eggs

and green vegetable drink (natural blend). I also gravitated to a

heavy sulphur food diet (eggs, broccolli, leaks, cauliflower etc

etc,as that was all I could eat) He also prescribed chorella and

cilantro. This combinaton made everything much orse.

This F'ing dummy had me convinced that I would have to move out into

the Oregon bush/coast to survive, as " he had seen it before " ...this

option was even more depressing

My MCS became so bad I could hardly manage...bad back and head

burning, shortness of breath, extreme anxiety and depression

(suicidal), I did not want to live... could not think straight ,

paying bills (any task for that matter) was too overwhelming...lost

40 pounds

Taking these supplements literally bought me back from the brink

Good luck

> >

> > Hi Mike

> > My MCS is I would say 90% better on the AI protocol

> > It was so bad i could hardly function, smelling fumes

everywhere,

> > headaches and anxiety...now its just occasionally so I know

this

> > stuff (AI) really works.

> >

> > are you chelating right now

> >

> >

>

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Share on other sites

The Ai protocol (an Andy Post) from what I think was the previous

site used by this forum was niacinamide, grapefruit juice and

selenomethionine

I ended up taking amd still do

1500 mg of niacinamide (3* a day)

375 mg (3* a day) of grapefruit deed extract

1000 mcg of selenomethionine

My understanding is that the first two supplements slow down phase 1

amd I think the selenomethionine mops up mercury (it binds to it and

renders it inert or something like that

I believe sulphur problems just take the MCS problems to another

level.

My sensitivity to these smells happened about 2.5 years ago and came

about along the same time that I managed to have liver fluke

parasites. The MCS seemed to have initailly came about when we moved

office spaces and our window opened onto a busy street in SF and our

offices were right above the garage under the building so lots of

fumes. However noone else in my office could really smell the fumes

like I could. All this time (last two years) ) I thought most of my

symptoms were lyme and parsites which they probably were but also MCS

Then about a year ago, I went to this practitioner whose big deal

was going on a very limited organic diet of ...water, chicken, eggs

and green vegetable drink (natural blend). I also gravitated to a

heavy sulphur food diet (eggs, broccolli, leaks, cauliflower etc

etc,as that was all I could eat) He also prescribed chorella and

cilantro. This combinaton made everything much orse.

This F'ing dummy had me convinced that I would have to move out into

the Oregon bush/coast to survive, as " he had seen it before " ...this

option was even more depressing

My MCS became so bad I could hardly manage...bad back and head

burning, shortness of breath, extreme anxiety and depression

(suicidal), I did not want to live... could not think straight ,

paying bills (any task for that matter) was too overwhelming...lost

40 pounds

Taking these supplements literally bought me back from the brink

Good luck

> >

> > Hi Mike

> > My MCS is I would say 90% better on the AI protocol

> > It was so bad i could hardly function, smelling fumes

everywhere,

> > headaches and anxiety...now its just occasionally so I know

this

> > stuff (AI) really works.

> >

> > are you chelating right now

> >

> >

>

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> > >

> > > Hi Mike

> > > My MCS is I would say 90% better on the AI protocol

> > > It was so bad i could hardly function, smelling fumes

> everywhere,

> > > headaches and anxiety...now its just occasionally so I know

> this

> > > stuff (AI) really works.

> > >

> > > are you chelating right now

> > >

> > >

> >

>

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congrats. How many LA did you need?

>

> > Strange that you mention the smelling of oil/gasoline. Everyonce

> > in a while, in fact this happened last night while walking our

> > dog, I get a powerful scent of gasoline/oil and wondered why. I

> > thought perhaps there had been a car nearby that was burning oil

> > or someone just had their house oil tank filled nearby.

>

> > I seem to have a poor sense of smell, though I cannot tollerate

> > strong scents very well. My taste seemed to be not as good as it

> > used to as well.

> >

> > Mike

>

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sorry Letsdetox, what is LA?

I started the AI protocol in September/07 and I really felt much

better (to where I could at least participate in life and work)

after a few weeks. However i also stopped the sulphur foods at the

same time and the chorella and cilantro. I think like with many of

our symptoms its a combination of things that are wearing us down

Also just to clarify and thank for her clarification

on grapefruit seed extract versus grapefruit juice

I only just started the grapefruit seen extract when I came home for

a few weeks holiday to Canada..but for the last 3 months I had been

taking grapefruit juice (about 3 glasses a day). Now that i know

these two are not the same I will get back on grapefruit juice

Another interesting thing (dysfunction) I experienced and am not

sure if it was related to the MCS or mercury mobilization from

chorella/sulphur foods and cilantro or was just a function of

mercury toxicity was sensitivity to electro-magnetic fields (EMF).

One time about 2 years ago, my head started burning when I was using

my cell phone and I never thought anything more of it until my

previous health practitioner suggested I purchase a electro-magnetic

measuring meter. It confirmed certain areas of my house/work

area/streets and auto's that had high readings.

I know at the height of my MCS problems this past summer I had spent

a few days in my girlfriends car driving up to Oregon and back. My

symptoms got a lot worse(very agitated/much anxiety) during this

trip. I got very nutty and stressed out. This was just before I

started in the AI protocol

Also my new work area in my office shows higher readings of EMF

(i just moved offices) and I have felt a little nasueaus/anxious

when working at it before I left for this family trip to Canada

Its very intersting that my Prius does not give the same high

readings (of EMF) that other cars do. I know overall there is not

much that can be done with these fileds as they are very pervasive

in our communities but I truly feel that until the mrcury comes out

of my head and body, these fields will continue to irritate me

I just know how my body reacts to things after being ill for 3-4

years and so I try to avoid long drives in cars and working at my

computer.

> > Hi Mike

> > My MCS is I would say 90% better on the AI protocol

> > It was so bad i could hardly function, smelling fumes

> > everywhere, headaches and anxiety...now its just occasionally so

> > I know this stuff (AI) really works.

> >

> > are you chelating right now

> >

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Sorry, i mean how many LA rounds did you need?

> > > Hi Mike

> > > My MCS is I would say 90% better on the AI protocol

> > > It was so bad i could hardly function, smelling fumes

> > > everywhere, headaches and anxiety...now its just occasionally

so

> > > I know this stuff (AI) really works.

> > >

> > > are you chelating right now

> > >

>

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