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BEWARE...
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THINK
AGAIN BEFORE YOU GO FOR BREAST ENLARGEMENT
SURGERY....
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Breast
augmentation surgery, according to the American
Society of Plastic Surgeons (ASPS), was the fourth most
popular invasive surgical procedure among cosmetic plastic surgeries performed in 2000. In a press release
dated July 12, 2001, the ASPS says that breast augmentation
was performed on 212,500 women last year.
Meanwhile,
millions of women have been subjected to the ill effects
of these modern day vanity contraptions that were bought
in good faith.
Before
reading the page below I'll request you to go through
the The
Real Story of Glenda
, a Silicon
Implant Victim.This is from her web page at
http://www.geocities.com/Heartland/Hills/2596/silicone.html
Remember
!!
- Silicone
gel implants were banned
in 1992 by FDA.
- If
you have (or had) a ruptured silicone breast implant,
you will be denied Health Insurance Coverage.
- Saline-filled
implants tend to have a higher
rate of leaking and deflation than silicone
gel implants, which means more frequent surgery to
replace them.
- In a study published
in the Lancet medical journal, Dr Lori Brown of the
Food and Drug Administration (FDA) says: "There is
emerging consensus that both the incidence and prevalence
of breast-implant rupture
are much higher than previously suspected."
- 21%
overall increase in cancers
for women with implants, compared to women of the
same age in the general population.
- Implant patients
were three times as likely
to die from lung cancer, emphysema and
pneumonia as other plastic surgery patients.The
study is based on medical records and death certificates
of almost 8,000 women with breast implants, including
silicone gel implants and saline implants, and more
than 2,000 other plastic surgery patients. ( National
Cancer Institute (NCI), Boston University, Abt Associates,
and the Food and Drug Administration, with Dr. Louise
Brinton from NCI as lead author. )
Breast
Implant Dangers
3%
suffer leakage within three years (deflated implant)
Occasionally,
breast implants may break or leak. The saline fill
is salt water and will be absorbed by the body without
ill effects. Older implants with silicone gel can
leak also. If this occurs, one of two things may occur.
If breakage of the implant shell that has a contracture
scar around it, then it may not feel like anything
has happed. If the shell breaks and there is not a
contracture scar, then leakage into the surrounding
tissue results in a sensation that the implant is
deflating. The leaking gel may collect in the breast
and a new scar may form around it. In other cases
gel can migrate through the lymphatic system to
another area of the body. Breaks may require a
second operation and replacement of the leaking implant.
If the gel has migrated it may not be possible to
remove all of the silicone gel. This silicone gel
is the what some say is related to the initiation
of connective tissue disorders.
One
study they reviewed showed that 63.6% of breast
implants which had been in place for between one and
25 years had ruptured or were leaking. (http://news.bbc.co.uk/1/hi/sci/tech/33450.stm)
For
silicone gel and saline-filled implants, some causes
of rupture or deflation include : damage by surgical
instruments during surgery, overfilling or underfilling
of the implant with saline solution (specific only
to saline-filled breast implants), capsular contracture
,closed capsulotomy , stresses such as trauma or intense
physical manipulation ,excessive compression during
mammographic imaging, placement through umbilical
incision ,site injury to the
breast, normal aging of the implant ,unknown/unexplained
reasons.
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FDA completed
a retrospective study on rupture of silicone gel-filled
breast implants. This study was performed
in Birmingham, Alabama and included women who
had their first breast implant before 1988. Women
with silicone gel-filled breast implants had a
MRI examination of their breasts to determine
the status of their current breast implants. The
344 women who received a MRI examination had a
total of 687 implants. Of the 687 implants in
the study, at least two of the three study radiologists
agreed that 378 implants were ruptured (55%).
This means that 69% of the 344 women had at least
one ruptured breast implant. Of the 344 women,
73 (21%) had extracapsular silicone gel in one
or both breasts. Factors that were associated
with rupture included increasing age of the implant,
the implant manufacturer, and submuscular rather
than subglandular location of the implant. A summary
of the findings of this study is also available
on FDA's website at http://www.fda.gov/cdrh/breastimplants/studies/biinterview.pdf
and http://www.fda.gov/cdrh/breastimplants/studies/birupture.pdf.
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capsular contracture
The
most common complication of breast implants is capsular
contracture, a tightening of the scar tissue that
the body produces around the implant as a natural
part of healing. Additional surgery may be required
either to remove the scar tissue or to remove—and
perhaps replace—the implant. In a prospective clinical
study of saline-filled breast implants conducted by
Mentor, the cumulative, 3-year, by patient rates of
a first occurrence of capsular contracture Grades
III and IV were 9% for the 1264 augmentation patients
and 30% for the 416 reconstruction patients. In a
prospective clinical study of saline-filled breast
implants conducted by McGhan, the cumulative, 3-year,
by patient rates of a first occurrence of capsular
contracture Grades III and IV were 9% for the 901
augmentation patients and 25% for the 237 reconstruction
patients.
Silicone Immune
Toxicity Syndrome
There are several
forms of the chemical in breast implants that can
cause a problem in the human organism.  Silicon
(Si) is the basic element and probably causes immune
system changes.  Silica or SiO2 is the form it
is mined from the earth.  Silicone gel is a synthetic
material containing 38% silicon.  The silica is
45% silicon. There is slow leakage ("bleeding") of
the silicone gel from the implants through the semi-permeable
membrane envelope and also into and through the capsule
that surrounds the implants.  This is picked up
by the microphages (scavenger cells) of our immune
system and is broken down inside these cells which
travel all over the body.  The gel breaks down
inside these cells, which travel all over the body.
 The gel breaks down into Silica and Silicon which
causes an immune system dysregulation.  Thus,
there are antibodies produced against the silicon
and also against the silicon and protein complex (organ
systems) so that you get autoimmune illness.
Silicone Immune
Toxicity Syndrome for further reading go to http://www.ephca.com/sits.htm
Below
is the List of Chemicals which experts have
analyzed to be in the explanted breast implant
shell envelopes and gels.
Methyl Ethyl
Ketone, Cyclohexane, Isopropyl Alcohol ,
Denatured
Alcohol ,Acetone ,Urethane, Lacquer thinner
,Ethyl Acetate ,Epoxy Resin, Epoxy hardener,
Amine, Printing ink, Toluene, Freon ,Silicone,
Lofol (formaldehyde), Flux Metal, cleaning acid,
Eastman 910 glue (Cyanoacyryiates) ,Talcum Powder,Color
Pigments as release agents Oakite (a cleaning
solvent), Ethylene Oxide (ETO), Carbob black,
Xylene, Hexane, Hexanone 2, Antioxidant (rubber)
,Zinc Oxide ,Naphtha (rubber solvent), Phenol
Benzene-Known carcinogen!!!!
ALSO.....
Polyvinyl Chloride (Liquid Vinyl) This ingredient
was used in all medical devices made at Edwards
Lab, from tubing to gel.
Methylene
Chloride/Dichloromethane. This breaks down in
the body so blood cannot carry oxygen. It metabolizes
carbon monoxide poisoning and causes central
nervous system depression.
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Loss
of sensation in the nipple or breast
Some women report
loss of sensation in their nipple, but they may also
become overly sensitive. Loss of sensation is more
common in breast lift-implant procedures. The area
around incision may also have small patches of numbness,
or increase sensitivity. These symptoms usually disappear
within time, but may be permanent in some patients.
It usually takes at least a full year to find out
what the final sensation will be.
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Breast
Enlargement
The
clinical studies were conducted over eight months during
2002. 124 women, ranging from 17 to 48 years of age, were
randomly selected for natural breast enhancement
study.
87%
of the women in the SUCCESS group had a measured breast
enlargement of 0.5-2.0 cm..
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