Re: EMF Sensitivity - Porphyria?

[Guest guest]

Porphyria can be treated with Rife frequency technique.

***************************

Porphyria

Several rare disorders due to the inability to create heme, a component of

hemoglobin. This causes skin and

nerve symptoms including abnormal sensitivity to light, skin lesions and

scarring, delirium, seizure, coma, and

abdominal pain. The neurological aspects of this condition are typically

precipitated by drugs such as barbiturates.

Since the liver, bone marrow, cellular metabolism, and other basic parts of the

body are involved, also try other

symptom pictures.

698, 780 frequencies in Hertz.

*************************

Even on a computer, one can generate these frequencies with f.i. NCH Tone, and

burn them to an audio CD.

Each frequency for 5 minutes.

Greetings,

Claessens

member Verband Baubiologie

www.milieuziektes.nl

www.milieuziektes.be

www.hetbitje.nl

checked by Norton

EMF Sensitivity - Porphyria?

Hi all

I by chance came across an article the other day saying that estrogen is be

avoided in porphyria, as it makes it worse. My severe EMF problems started last

year not long after I started on estrogen therapy, so I wondered what porphyria

was (as it's about the only thing I haven't tested for on the lab's main test

page).

So apparently there are different types of porphyrias and they're mostly

genetic. Some of them make your skin extremely sensitive to sunlight because of

porphyrincs in the skin, these can also damage your liver, others lead to muscle

weakness, etc, and on googling, I found those people are also really sensitive

to fluorescent lights.(And I'm guessing EMF generally, even if they don't all

know it).

Then I found a book by a professor Rochlitz, who asserts that porphyria

is the root cause of CFS, MCS, ES etc, and is very much undiagnozed. According

to him, it can also be triggered by infections, heavy metals, etc. He says the

routine tests for it are unreliable, you need DNA testing to see if you have one

of the mutations causing the different types.

This is his book:

http://www.wellatlast.com/whatsnew.html

(I haven't bought it yet, but I'm planning on doing so).

This ia a summary of it:

http://www.thefreelibrary.com/Porphyria+Link+to+Environmental+Illness.-a02432904\

47

This is an Nexus article re, which I haven't bought either:

http://www.nexusmagazine.com/index.php?page=shop.product_details & flypage=flypage\

..tpl & product_id=1992 & category_id=214 & option=com_virtuemart & Itemid=44

Anyway, there's a site

http://www.cpnhelp.org/

where the subscribers are treating chlamydia pneumonia (not the same as the

SCD chlamadia T) as the cause of most cases of CFS, MS, etc. They do this with

pulsed antibiotics. But apparently Cpn also causes secondary porphyria, which

is worsened by killing it with antibiotics. They treat this with glucose, high

carb diets, activatged charcoal, increased b vits (especially b12) and Questran:

http://www.cpnhelp.org/secondaryporphyria

(These antibiotics would obviously also be addressing other infections such as

Lyme, Rickettsia, mycoplasma, etc), and I guess the porphyria treatment also

addressing other causes.

This is a discussion on their forum about EMF sensitivity, some have gotten

over their's by this antibiotic and porphyria traetment:

http://www.cpnhelp.org/computers_emfs_cold_feet

Another , new treatment for porphyria is Tegamet (Cimetidine ):

http://www.theannals.com/cgi/content/abstract/31/3/365

http://www.ncbi.nlm.nih.gov/pubmed/8915698?dopt=Abstract

Here's a Facebook chat about people using it for porphyria and some reporting

losing much sensitivity to the sun and to fluorescent lights:

http://www.facebook.com/topic.php?uid=2445760941 & topic=11831

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

[Guest guest]

Hi

Yes, but there are about eight (if not more) different types of porphyria and

they all have different symtoms etc.

I don't know which one this professor is referring to, must order the book and

wait for it to come to SA..

But wouldn't rife be contraindicated for ESers. I was doing a lof of rife, becks

blood electrifier, zapper and I think it contributed to my becoming ES (and I've

read of others too).

>

> Porphyria can be treated with Rife frequency technique.

> ***************************

> Porphyria

>

> Several rare disorders due to the inability to create heme, a component of

hemoglobin. This causes skin and

>

> nerve symptoms including abnormal sensitivity to light, skin lesions and

scarring, delirium, seizure, coma, and

>

> abdominal pain. The neurological aspects of this condition are typically

precipitated by drugs such as barbiturates.

>

> Since the liver, bone marrow, cellular metabolism, and other basic parts of

the body are involved, also try other

>

> symptom pictures.

>

> 698, 780 frequencies in Hertz.

>

> *************************

>

> Even on a computer, one can generate these frequencies with f.i. NCH Tone, and

burn them to an audio CD.

>

> Each frequency for 5 minutes.

>

> Greetings,

> Claessens

> member Verband Baubiologie

> www.milieuziektes.nl

> www.milieuziektes.be

> www.hetbitje.nl

> checked by Norton

>

>

>

>

>

>

> EMF Sensitivity - Porphyria?

>

>

> Hi all

>

> I by chance came across an article the other day saying that estrogen is be

avoided in porphyria, as it makes it worse. My severe EMF problems started last

year not long after I started on estrogen therapy, so I wondered what porphyria

was (as it's about the only thing I haven't tested for on the lab's main test

page).

> So apparently there are different types of porphyrias and they're mostly

genetic. Some of them make your skin extremely sensitive to sunlight because of

porphyrincs in the skin, these can also damage your liver, others lead to muscle

weakness, etc, and on googling, I found those people are also really sensitive

to fluorescent lights.(And I'm guessing EMF generally, even if they don't all

know it).

>

> Then I found a book by a professor Rochlitz, who asserts that

porphyria is the root cause of CFS, MCS, ES etc, and is very much undiagnozed.

According to him, it can also be triggered by infections, heavy metals, etc. He

says the routine tests for it are unreliable, you need DNA testing to see if you

have one of the mutations causing the different types.

>

> This is his book:

>

> http://www.wellatlast.com/whatsnew.html

>

> (I haven't bought it yet, but I'm planning on doing so).

>

> This ia a summary of it:

>

>

http://www.thefreelibrary.com/Porphyria+Link+to+Environmental+Illness.-a02432904\

47

>

> This is an Nexus article re, which I haven't bought either:

>

>

http://www.nexusmagazine.com/index.php?page=shop.product_details & flypage=flypage\

..tpl & product_id=1992 & category_id=214 & option=com_virtuemart & Itemid=44

>

> Anyway, there's a site

>

> http://www.cpnhelp.org/

>

> where the subscribers are treating chlamydia pneumonia (not the same as the

SCD chlamadia T) as the cause of most cases of CFS, MS, etc. They do this with

pulsed antibiotics. But apparently Cpn also causes secondary porphyria, which

is worsened by killing it with antibiotics. They treat this with glucose, high

carb diets, activatged charcoal, increased b vits (especially b12) and Questran:

>

> http://www.cpnhelp.org/secondaryporphyria

>

> (These antibiotics would obviously also be addressing other infections such

as Lyme, Rickettsia, mycoplasma, etc), and I guess the porphyria treatment also

addressing other causes.

>

> This is a discussion on their forum about EMF sensitivity, some have gotten

over their's by this antibiotic and porphyria traetment:

>

> http://www.cpnhelp.org/computers_emfs_cold_feet

>

> Another , new treatment for porphyria is Tegamet (Cimetidine ):

>

> http://www.theannals.com/cgi/content/abstract/31/3/365

> http://www.ncbi.nlm.nih.gov/pubmed/8915698?dopt=Abstract

>

> Here's a Facebook chat about people using it for porphyria and some

reporting losing much sensitivity to the sun and to fluorescent lights:

>

> http://www.facebook.com/topic.php?uid=2445760941 & topic=11831

>

>

>

> ------------------------------------

>

>

[Guest guest]

> Then I found a book by a professor Rochlitz, who asserts that

> porphyria is the root cause of CFS, MCS, ES etc

I thought porphyria was merely a symptom of heavy metal poisoning,

just like can be... (?)

Marc

[Guest guest]

Hi Marc

Normally it's genetic, and the symptoms are rather obvious (except for the skin

one, where exposure to the sun can make the skin swell and ache, but without

blistering and thus the diagnosis is often mised).

But infections, etc, can cause secondary porphyria. And the lab tests araare

inaccurate and only test for some of them (there is about 8).

And according to that professor these porphyrins are the root cause of the

symptoms of CFS , MS, MCS, ES, etc.

And two of those links I posted have people getting better from ES - one

treating Cpn with antibiotics and the secondary porphyria with gluose, activated

charcoal, carbs, etc, and the other group were treating conventionally diagnozed

porphyria with Tegamet.

>

> > Then I found a book by a professor Rochlitz, who asserts that

> > porphyria is the root cause of CFS, MCS, ES etc

>

> I thought porphyria was merely a symptom of heavy metal poisoning,

> just like can be... (?)

>

> Marc

>

[Guest guest]

Re Bill's post:

> I would stay away from zappers myself... I think the theory

> (Prof. Sam Milham) that ALS is usually caused by diathermy/TENS

> treatment (even Lou Gehrig himself probably had diathermy for

> his back; his trainer is known to have used it on others) looks

> very plausible. These symptoms usually start many years later.

TENS treatment is probably pretty much the same as Tennant's Biomodulator

treatment that's directly aimed at raising voltage/pH...

I believe treatments like that can worsen inflammation... Tennant also mentions

not to use his Biomodulator on inflamed body parts.. That makes sense because

inflammation is simply too much pH/voltage...

These things like TENS and Biomodulator emit a lot of different natural

frequencies to raise body voltage. They work probably the same as the sun for

instance... The sun also raises your voltage/pH but don't sit in the sun all day

or... Especially if you have (brain) inflammation...

Qi Gong masters also give Chi/energy, which is imo the same as raising

voltage... Qi Gong therapies are considered to be not good for inflammation...

So also not good for CFS patients, CFS patients have got inflammation (brain,

gut,...).

.

>

> >

> >

> > > Normally it's genetic, and the symptoms are rather obvious

> > >

> > > But infections, etc, can cause secondary porphyria.

> >

> > Ahh, thanks!

> >

> > As for your concerns about zapping, I've tried a few zappers,

> > and never found them to increase my ES symptoms at all.

> >

> > Marc

> >

> >

>

>

>