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I also took the Melisa test. I think it is great

because it gives unambiguous results and doctors can't

dismiss it out of hand. You can ask them if they have

heard of it before you tell them about it (100% of the

time the answer is no), and then hand over the 30-40

pages of papers Melisa has published on mercury and

metals allergy. They still treat you like a kook but

it is clear to all concerned it is because they are in

denial, not because you are crazy (which is also

unfortunately sometimes true!)

In my case mercury had killed off all the memory cells

which would normally react to it. It nuked part of my

immune system.

Dave

--- Freeman vf@...> wrote:

> > And it's good to hear that dramatic recovery is

> possible without noticing

> > an immediate benefit from amalgam removal.

>

> To be honest, amalgam removal made me feel worse.

> It was about 5 months before I started to feel

> better. Is one of those things *YOU HAVE TO DO*

> I you ever hope to get better.

>

> > I haven't felt any better

> > since mine were replaced in October and I'm hoping

> chelation will do

> > the trick eventually.

>

> *IT TAKES TIME... A LONG TIME*

>

> Amalgam removal is just the beginning of

> a *LONG* process, eternal if you don't

> chelate. If you remove your amalgams

> and don't chelate you will not get better

> soon, if at all!

>

> > Did you only do 5 rounds of chelation in 3 years?

>

> Due to my amalgam illness, I was bed redden, and

> unable to work (semi-homeless actually). I was

> unable to stand, much less endure the rigors

> of the workplace. My fiancee left me (with the

> words:

> " Dating a homeless man isn't sexy " , if I recall

> correctly),

> my friends left me (Ha! is all in your head...),

> I ballooned to 420lbs (eating disorder 'they' said),

> I lost my job due to the illness, and the

> depression,

> desperation, and apathy left me with nothing but

> the strength to plot my own death. So, no income,

> no chelation. I went from working as a highly paid

> software engineer, to working as a part-time janitor

>

> at my local hospital. I could only afford to chelate

> once or twice a year (It's very hard to survive

> on $130 dollars a week.)

>

> Amalgam illness is just like any other illness when

> it comes to the economics of health care:

>

> You are too week to work so you are broke,

> you are too broke to get better. This was

> the story of my life for the past 3 years.

>

> Fortunately, after the 5 rounds of chelation

> I was able to get a better job and work

> more hours. Not full time, but enough to avoid

> sleeping in the park. Now I'm saving for my

> 6th round.

>

> > (If so, how long were these rounds?)

>

> 7 days on.

>

> > Did you wait several years after amalgam removal

> > before starting chelation?

>

> My first round of chelation was about a year or

> a year and a half after amalgam removal. It took

> me a while to get my bearings and the money to

> start. I was *REALLY* sick!

>

> > What did you use -- DMSA, DMPS, ALA, other?

>

> I presently only use ALA. I've used ALA/DMSA my 3rd

> round of

> chelation and my suicidal ideation came back

> with a vengeance. I felt really sick, like I was

> about to die. So I have not used DSMA sciense

> then.

>

> > If I may ask, are you continuing to chelate, or do

> you think you've

> > plateaued and will no longer benefit from

> additional chelation?

>

> I'm saving money to chelate again. I'm still very

> sick and unable

> to be productive in the workforce. Chelation is a

> long process, I

> don't feel a plateau coming anytime soon. With every

> chelation

> round my body gets better, sometimes in very subtle

> ways. I little

> better sleep, a little more cheer, a little more

> endurance.

> Most improvements come v e r y s l o w l y. . .

>

> One of the most interesting pieces of information

> I discovered about my self, came as a gift 2

> Christmas

> ago, when a very sweet person gave me for Christmas

> a go at the Melisa Allergy Blood Test.

> http://www.melisa.org

> The Melisa blood test tests for hypersensitivity to

> metals.

> The test was about $300. After I submitted my blood

> sample,

> one of the doctors called me and informed me that

> I was hypersensitive to Mercury. I got one of the

> highest readings the lab has ever seen. When the

> doctor

> called me he asked me: " You are hypersensitive to

> Mercury,

> are you feeling ok? We are concerned. " , I busted out

> laughing!

>

> It seems I have a genetic predisposition to be

> highly allergic

> to mercury. Go figure.

>

> I hope this diatribe helps somebody down the road,

> as I've been helped by the graces of God and the

> many

> knowledgeable people in this forum.

>

> Mad love,

>

> Vince.

>

> On Thu, 31 Jan 2008 01:35:41 -0000

> " xbluehens " xbluehens@...> wrote:

>

> >

> >

> > > The more I chelate the better I feel.

> > > After 3 years of amalgam removal, and

> > > 5 chelation rounds my depression is

> > > about 85% gone.

> >

> > What a dramatic and encouraging testimony. Thanks

> for sharing. And

> > it's good to hear that dramatic recovery is

> possible without noticing

> > an immediate benefit from amalgam removal. I

> haven't felt any better

> > since mine were replaced in October and I'm hoping

> chelation will do

> > the trick eventually.

> >

> > Did you only do 5 rounds of chelation in 3 years?

> (If so, how long

> > were these rounds?) Did you wait several years

> after amalgam removal

> > before starting chelation? What did you use --

> DMSA, DMPS, ALA, other?

> >

> > If I may ask, are you continuing to chelate, or do

> you think you've

> > plateaued and will no longer benefit from

> additional chelation?

> >

> > Thanks,

> > Darren

>

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Since we don't have a lab in the US that does this, where did you guys send

yours? Did your doctor or dentist order it for you? How much did it cost (I

know it depends on how many things you have tested)? What other things did you

test for? Did you have the test done BEFORE amalgam removal or AFTER? Before

or after any chelating? It also says that things that affect the immune system,

like HC, will affect the results. I wonder why more people don't do this? If

anybody else has done this, please respond. I can't remember hearing/reading

what Andy thinks about this either, anybody else remember?

Sorry about the 20 questions! But metal allergy helps explain why different

people are affected differently by different amounts of exposure. So there are

two aspects to being toxic, one is allergy/sensitivity, and the other would be

the amount of exposure. So someone who is very sensitive, will have symptoms

even from a small exposure. And someone who isn't as sensitive, can still be

toxic just due to the amount of exposure they have had. But this is why it can

vary so much.-----------Jackie

http://www.melisa.org

In frequent-dose-chelation Sherratt wrote:

I also took the Melisa test. I think it is great

because it gives unambiguous results and doctors can't

dismiss it out of hand. You can ask them if they have

heard of it before you tell them about it (100% of the

time the answer is no), and then hand over the 30-40

pages of papers Melisa has published on mercury and

metals allergy. They still treat you like a kook but

it is clear to all concerned it is because they are in

denial, not because you are crazy (which is also

unfortunately sometimes true!)

In my case mercury had killed off all the memory cells

which would normally react to it. It nuked part of my

immune system.

Dave

--- Freeman vf@...> wrote:

> One of the most interesting pieces of information

> I discovered about my self, came as a gift 2

> Christmas

> ago, when a very sweet person gave me for Christmas

> a go at the Melisa Allergy Blood Test.

> http://www.melisa.org

> The Melisa blood test tests for hypersensitivity to

> metals.

> The test was about $300. After I submitted my blood

> sample,

> one of the doctors called me and informed me that

> I was hypersensitive to Mercury. I got one of the

> highest readings the lab has ever seen. When the

> doctor

> called me he asked me: " You are hypersensitive to

> Mercury,

> are you feeling ok? We are concerned. " , I busted out

> laughing!

>

> It seems I have a genetic predisposition to be

> highly allergic

> to mercury. Go figure.

>

>

>

> Vince.

>

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