Posted by
danielferres on
URL: https://www.es-forum.com/Anybody-here-been-diagnosed-with-ES-by-a-medical-doctor-tp1546201p1546242.html
Hi Giorgio,
The EMF Testing costs about $500, the first visit cost $187 and
letters with diagnostics can cost from $25 to $250.
I'm not sure of the parameters of the EMF testing and I need to
receive more information from them. I mean the magnetic field and
electric field in the place I did the testing.
They said that I'm sensitive to 50Hz and 60Hz EMFs but I do not
know if they mean at all intensities or the sensitivity could
start at some V/m or mGs.
They do not test for microwave radiation only ELF electromagnetic fields.
I also did some skin testing that showed some food alergies (most of
them). I did also blood testings, orine testings...
Dr Rea thought that I could have chemicals and I did the
organophosphates and pyretroids testing, giving negative results.
Then I had to do the CPST (Clhorinated pesticides) but I didn't do
it because I prefered to do other tests.
I did RBC elements and Hair elements, RBC was OK and Hair
Elements showed Uranium (moderate) and Silver (Very High) but
both elements could be only in Hair and not in blood so is
not conclusive. I used a silver cap and this means that it could
have silver in the hair for this reason.
As an hypothesis for Uranium, it could come from the tap water I used
in the shower in Los Angeles.
I also think that hair analysis may not show some toxic elements that
have been long time in the body, and are not in the blood.
I think that I could have mercury, MSG and aspartame because it was
showed in an ART Testing (Klinghardt) I did in last December.
I did the Organix and RBC Fatty Acids testing from MetaMetrix labs,
it gives some interesting information about your metabolism and
supplement requirements, But I received the results later and
I could need now a physician to help me to interpret it.
I did sauna theraphy during some days. Some days I feel really
better after it.
They use an specific protocol reading the weight, pulse, pressure
before exercising and after the sauna.
I took Alhpa Ketoglutamic, L-Glutathione, Vit C, and niacin (a dose is
staring at 25mg first day, increasing 25mg until you have a
niacin flush, red burning skin).
I did 15-20 min exercise (you decide the time), then I did
sauna for 15-30 min (starting 15 min, increasing 5 min next day,
depending on your tolerance). I started at 140F then 150F and I
finished at 160F. They have 3 saunas (2 dry, 1 infrared)
I tried also the Limphatic Drainage therapy, it is 80$ session,
it seems that offers good results for MCS people but I didn't
notice the effects.
The first time I was there I was staying in a hotel for 50$, but was
highly EMF polluted, electric and magnetic fields, and a cell phone
tower at 50metres.
The next time I used cheap place in a relatively low emf (They had
only Wireless in the living room, but is possible to get a room far
from there) in Dallas for 20$ in a hostel at 45 min using rail and metro.
I tried also the environmental housing which is $110 (two beds),
is really good for environmental alergies with ceramic floor and
filtered water in the shower and tap water, air filters in each room...
it is OK for ELF EMFs and you can turn OFF the electrical installation
of the room if you want. In the microwave range I detected 20-40mV/m
in a room in the base floor. Not bad, but I think it maybe too much
for me.
Here I put information I have about costs of all treatments and the
therapies.
===============================================================
Cost of treatment at EHCD
Initial History and Physical = $ 187.00
Return visits = $83.00
Skin Testing = $23.00 an item
Foods 30= $690.00
Pollens 13 = $299.00
Molds and Mold Mixes (19) = $437.00
Dust/Mite = $64.00
Peptides, hormones, terps = $800.00 App.
Smuts, etc., danders
Chemicals 10 = $230.00
Any combination of these items can be tested.
Sauna = $37.00 a session
Sauna is usually 5 days a week for a minimum of 2-3 weeks. Optimally
participation occurs for 6 weeks.
Participation is dependent on chemical or metal in blood or urine lab
analyses.
Oxygen therapy (18 days) = $1062.00 ($59.00 daily)
Participation is dependent upon findings of elevated venous blood gases.
Autogenous Lymphocytic Factor = $500.00
Required Lab analyses = $700.00
Monthly Treatment Cost = $150.00 for 30 day
Yearly Treatment Cost = $2400.00
IV therapy (1) = $200.00 - $500.00
Usually 2 a week for 3 weeks
Laboratory analyses vary from =$500.00 - $2,500.00
Participation in any program is dictated by symptoms, physician
assessment, and laboratory analyses. Any program initiated at the
clinic can be continued at home.
Treatments options vary with each patient.
Housing in environmentally controlled, less-toxic housing = $110.00 a
night
==========================================================
Best regards,
Daniel
--- In
[hidden email], "giorgio" <CINCIRIPINI@...> wrote:
>
> Hi Daniel,
>
> how much did you spend for this diagnosis ?
>
> have you treated for any therapy ?
>
> My regards
> Giorgio
>
> --- In
[hidden email], "danielferres" <danielferres@> wrote:
> >
> > Hi,
> > Two months ago I've been diagnosed EHS by Dr William Rea of the
> > Environmental Health Center in Dallas.
> > I did some EMF testing showing sensibility to 50Hz and 60Hz EMF
> > fields.
> > I think that the protocol they use to do the testing is
> > probably the one reported in this article.
> >
http://www.aehf.com/articles/em_sensitive.html> >
> > Best regards,
> > Daniel
> >
> > --- In
[hidden email], Evie <evie15422@> wrote:
> > >
> > > Hi, Jon,
> > >
> > > Dr. Rae's patient consultant (Dr Rae of the Environmental Health
> > Clinic of Dallas) told me I "was probably ES" by phone. (Something
> I
> > had already strongly suspected.) When I asked--2 years ago--whether
> > Dr. Rae had a protocol for ES, she said he was trying to eliminate
> > toxins and felt they were responsible and that lymphatic overload
> was
> > somehow responsible. Again, this was something I already knew. I
> > asked whether he has had success in helping people recover from ES
> > symptoms, and she said only within the first 2 years; after that he
> > sees little improvement. I asked alot of other questions also,
> about
> > pesticides and liver detox pathway dysfunction. She mentioned to me
> > (again, remember this is 2 years ago) that he was working on the
> liver
> > detox pathway dysfunctions and had, at that time, not felt he had
> that
> > worked out. (At least this was my take on what she said.) So, it
> is
> > possible that we could get a dx of ES from Dr. Rae. Whether that dx
> > would hold up in the
> > > medical profession as a whole is debatable. I still had problems
> > getting a medical doc to accept celiac disease as a valid dx in
> 2003!
> > But, if I were to be treated or get a dx, that would be where I
> would
> > start. Dr. Rae gets some flack because his clinic's patient rooms
> are
> > not set up for ES. To his credit, tho, he set his rooms up so his
> MCS
> > patients would not react to woods, etc. (That is why so much metal
> > furniture.) He was working with MCS patients way before he was
> aware
> > of ES and so his rooms reflect that. I was told that many of his ES
> > patients travel there and live in their own RVs at a nearby
> > campground. This was all within the discussion I had with the
> patient
> > consultant 2 years ago. Things may have changed since then. This
> is
> > his site:
> > >
> > >
http://www.ehcd.com/> > >
> > > Diane
> > >
> > > prentice_jon <prentice_jon@> wrote:
> > > hmm, that is an interesting question, for people in the
> US
> > at least,
> > > I would like to know if that is possible, best I could do was
> find a
> > > doctor who was glad that I figured out what was causing my
> problem.
> > > I hope that being diagnosed ES here doesn't require that the
> doctor
> > > and the ES person are one and the same.
> > > Jon
> > >
> > > --- In
[hidden email], sheila wade <sheila_texas@> wrote:
> > > >
> > > > it is hard to find a dr & very Expensive! suffer myself & since
> > > p/t & hmo ins no diagnosis yet hoping someone will step fwd
> > > > thanks!
> > > > God Bless
> > > > Sheila
> > > >
> > > > Carol <YoRed24@> wrote:
> > > > The reason I ask is because a casting producer for a
> > > show on Discover
> > > > Health/Mystery Diagnosis is looking for people with unusual
> > > illnesses.
> > > > Prerequisites are that the patient needs to live in the US, a
> > > medical
> > > > doctor must have given you the diagnosis (no self-diagnosed
> > > > electrosensitives), and the doctor must practice in your area
> and
> > > be
> > > > willing to get involved.
> > > >
> > > > Here is the info:
> > > >
> > > > Please contact MYSTERY DIAGNOSIS at:
> > > >
> > > > eanniello@ or (212) 645-0904 and leave a message
> > > > on their hotline. Be sure to include your full name, phone
> number,
> > > > email address, and disease.
> > > >
> > > > I have severe electrosensitivities myself, but unfortunately I
> > > have not
> > > > been diagnosed "officially" by a medical doctor. If you are
> > > interested,
> > > > please write to the producer.
> > > >
> > > > Carol
> > > >
> > > >
> > > >
> > > >
> > > >
> > > >
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> > > >
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> > > >
> > >
> > >
> > >
> > >
> > >
> > >
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>