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Re: Fragrances

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,

Some people are prescribed oxygen for chemical sensitivities and find that it

helps them when they are in public venues. I personally just can't go

anywhere any more, due to all of the toxics out there, even when I'm having a

good enough CFIDS day to go out.

Reducing exposures in your own home is really critical, I think. Needs

(www.needs.com) is the best source for fragrance free and nontoxic

everything. They send out a free catalogue. Magick Botanicals makes a full

line of fragrance free shampoo, soap, hairspray, etc., and there are other

companies that make fragrance free options as well. The best way to find

things is to go to a natural foods store and look for " fragrance free " on the

label -- " unscented " is deceptive, as it sometimes means the product has

chemical masking agents to hide the scent.

Baking soda and vinegar work wonders for many household chores, and steam

cleaners are also great. You can clean most things with steam alone. Baking

soda and vinegar are an excellent substitute for laundry detergent as well.

Good luck!

Peggy

In a message dated 5/25/02 9:56:18 PM,

writes:

<<

Avoidance is difficult.

I've only recently realized the impact that fragrances have on me. Before, I

didn't know what it was that made me ill when I was exposed to them. Now

it's quite clear.

>>

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Many of my more " weird " or more peripheral symptoms reflect my overall

condition;

scents, temperature, changes in the barometer. The tireder and sicker I am

the more sensitive to everything.I am sure there are other symptoms but I

can't think of 'em right now.

Adrienne

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We are currently having problems with fragrances and avoidance makes

sense. I know it's hard and there is the problem of isolation,

believe me, I understand.

I have been sensitive to synthetic fragrances for about 14 years,

but noticed that after several months of treatment for

hypercoagulation (heparin and nonprescription anticoagulants), an

apparent side effect was a reduction in sensitivity. So much so

that Ken commented that I wasn't fleeing from synthetic scents

anymore. I had also had been on antibiotics for mycoplasma for

several months prior to the improvement in MCS. Maybe a

coincidence, who knows.

The MCS became very bad again after a particularly bad and prolonged

exposure in January, and interestingly, an ISAC panel done shortly

after the exposure showed a dramatic increase in my prothrombin

fragments. Our daughter showed very similar changes in her ISAC

panel results and she had also become much more sensitive to

fragrances.

Of course, we are hoping that the prescription and nonprescription

anticoagulants that we are taking will have the added benefit of

reducing the MCS problems. We'll see...

Also, someone on another group recently reported that after taking

antibiotics for Lyme she noticed that her MCS had improved as well.

Interesting...

Laurie

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I use an industrial type respirator & it really filters out all the toxins.

I get it from a Place called on Safety company but I am sure you can

find a place that carries them nearby if you look in the yellow pages.

I made myself a badge to wear that says

I am allergic to smoke perfume & chemicals

so people will know why I am wearing it.

The badge really helps educate people & I find a lot of sales clerks & other

people end up telling me they have problems with perfumes also.

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Hi ,

I really sympathise with your fragrance problem. I

have had problems with scents for all of my life

although I didn't have a name for it as a child.

I bought a filter type mask from a local health-food

type store and find this a real asset to use on public

transport/in shops etc. It does attract some strange

looks (and the occasional rude comment) but it means

that I can get around a bit more.

Kindest regards,

Annette

__________________________________________________

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Laurie,

No disrespect or flaming intended......just a thought re: your post:

" improvement in MCS. Maybe a coincidence, who knows.... hoping that the

prescription and nonprescription anticoagulants that we are taking will

have the added benefit of reducing the MCS problems. ...abx...she

noticed that her MCS had improved as well. Interesting... "

I have to remind myself when my symptoms are lessoned--just because we

can no longer sense and turn and avoid does it then mean the toxic

effects are no longer poisonous or toxic to our systems...and then, is

our MCS really improved or cured..I have been kicked back just recently

as I threw caution to the wind and ignored triggers cause I have been

sooo good about avoidance over the years--DUH ;-( , resulting in my son

of 19 telling me he would take away my car keys for the next month and I

was not permitted to leave the house and expose myself for at least two

more weeks to anything and I was not allowed to get my blood drawn at

the hospital ever again-only at the doctors or resource lab ;-) --this

recent reaction from a 10 minute non-avoidance of trigger exposure

really concerned him this time-- I have been down more than 2 weeks

trying to kick it and regain my mcs " normal " which for is cfs without

the sensitivities....Anyway do YOU really feel that heperan (sic)

alleviates MCS and then maybe abx too? Ken and you are two of my

trusted information sources--no references or referrals needed ;-)

Thanks, Carol

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Hi Carol,

Ken and I strongly suspect that the heparin helped. Our MD is also

interested, because of the changes in our ISAC panel results after

the prolonged exposure we were subjected to.

That doesn't mean that we think caution would no longer be necessary

though. Before the recent exposure that gave us such problems, I

believe I had improved enough that the chance exposures out in

public were not making me feel ill - I didn't automatically flee

from them, but I was still careful to avoid any prolonged

exposures. A difference of a few seconds of exposure maybe - but I

felt more free to be out in public with other people.

This is all so unknown and apparently so complex, I wouldn't presume

to know the answers. I'm not suggesting that someone take heparin

to try to improve their MCS, but it would be very interesting if

other people who are taking it for hypercoagulation notice

improvements in MCS.

Laurie

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Annette Barclay wrote:

> I bought a filter type mask from a local health-food

> type store and find this a real asset to use on public

> transport/in shops etc. It does attract some strange

> looks (and the occasional rude comment) but it means

> that I can get around a bit more.

>

Annette, I find that the filter masks designed for " nuisance odors " which have a

layer of activated charcoal embedded in them work alot better than plain dust

and pollen masks when it comes to

fragrances, diesel fumes, and smoke.

I've been buying them from Gempler's in bulk (NAYY...)

--

el (andrea@...) Nevada City, CA, USA

" ...wake now! Discover that you are the song

that the morning brings... "

" One is taught by experience to put a premium

on those few people who can appreciate you

for what you are. " - Gail Godwin

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  • 5 months later...

Carol, I had to give up wearing perfume because I'm allergic to something in

it. Back when I used to have migraines, I'd get one every time I was around

someone with strong perfume for any length of time.

Sue in NC

on 10/28/02 5:43 PM, Carol at carol@... wrote:

> Has anyone ever noticed that some fragrances exacerbate their symptoms? I

> can take a little perfume, but too much throws my system out of whack. I

> would think it's chemicals, but even aromatherapy with natural oils

> (chamomile, lavender) has this effect. I was just curious if anyone else

> has this symptom.

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Hi Carol,

I have always had reactions to certain perfumes and

aftershaves but I think that it is due to allergies.

Anything with rose, magnolia, or honeysuckle are the

worst. They cause me to get dizzy and have headaches.

Iris

--- Carol <carol@...> wrote:

> Has anyone ever noticed that some fragrances

> exacerbate their symptoms? I

> can take a little perfume, but too much throws my

> system out of whack. I

> would think it's chemicals, but even aromatherapy

> with natural oils

> (chamomile, lavender) has this effect. I was just

> curious if anyone else

> has this symptom.

>

> Love to all,

> Carol

>

>

>

>

>

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