What the frack is going on:
http://www.youtube.com/watch?v=oHQu3SeUwUI

Gasland Trailer:
http://www.youtube.com/watch?v=dZe1AeH0Qz8

Really, you play tennis outside of the courts, i don't?

I'm just saying that if you really want people to listen, then you need to approach this from an un-bias side. I know dogs will go there an probably pee on the fence, or are you proposing that you want this to be part the dog free area? I'm OK with that, i just don't want to smell/sit in pee or poop anymore.

and the space around the outside of the tennis courts? should be green right?

My check was cashed in October 07'
We just got our tree yesterday! Yah! So happy to have it even though it took forever...
(I was told that their records showed we 'd already received it, that's why it took so long. Maybe their is a mix up for you too...)

David Kirby:
Government Concedes Vaccine-Autism Case in Federal Court - Now What?

Link: http://www.huffingtonpost.com/david-k ... ncedes-vacci_b_88323.html

Sorry to load up this thread, but someone asked...

The info is on the web, I know now someone is gonna ask for the source?

Type the name of the vaccines as listed above with the word "description" after and you will get a list of the ingidients or be directed to a page that has them.

Some have links to the unfamiliar terms.

M-M-R* II (Measles, Mumps, and Rubella Virus Vaccine Live) is a live virus vaccine for vaccination against measles (rubeola), mumps and rubella (German measles).

M-M-R II is a sterile lyophilized preparation of (1) ATTENUVAX* (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived from Enders attenuated Edmonston strain and propagated in chick embryo cell culture; (2) MUMPSVAX* (Mumps Virus Vaccine Live), the Jeryl Lynn** (B level) strain of mumps virus propagated in chick embryo cell culture; and (3) MERUVAX* II (Rubella Virus Vaccine Live), the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts.1,2

The growth medium for measles and mumps is Medium 199 (a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum) containing SPGA (sucrose, phosphate, glutamate, and human albumin) as stabilizer and neomycin.

The growth medium for rubella is Minimum Essential Medium (MEM) [a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum] containing human serum albumin and neomycin. Sorbitol and hydrolyzed gelatin stabilizer are added to the individual virus harvests.

The cells, virus pools, fetal bovine serum, and human albumin are all screened for the absence of adventitious agents. Human albumin is processed using the Cohn cold ethanol fractionation procedure.

The reconstituted vaccine is for subcutaneous administration. Each 0.5 mL dose contains not less than 1,000 TCID50 (tissue culture infectious doses) of measles virus; 20,000 TCID50 of mumps virus; and 1,000 TCID50 of rubella virus. Each dose of the vaccine is calculated to contain sorbitol (14.5 mg), sodium phosphate, sucrose (1.9 mg), sodium chloride, hydrolyzed gelatin (14.5 mg), human albumin (0.3 mg), fetal bovine serum (< 1 ppm), other buffer and media ingredients and approximately 25 mcg of neomycin. The product contains no preservative.

Before reconstitution, the lyophilized vaccine is a light yellow compact crystalline plug. M-M-R II, when reconstituted as directed, is clear yellow.

VARIVAX(R) - (Varicella Virus Vaccine Live (Oka/Merck))

Description

VARIVAX(R) (Varicella Virus Vaccine Live (Oka/Merck)) is a preparation of the Oka/Merck strain of live, attenuated varicella virus. The virus was initially obtained from a child with natural varicella, then introduced into human embryonic lung cell cultures, adapted to and propagated in embryonic guinea pig cell cultures and finally propagated in human diploid cell cultures (WI-38). Further passage of the virus for varicella vaccine was performed at Merck Research Laboratories (MRL) in human diploid cell cultures (MRC-5) that were free of adventitious agents. This live, attenuated varicella vaccine is a lyophilized preparation containing sucrose, phosphate, glutamate, and processed gelatin as stabilizers.

VARIVAX, when reconstituted as directed, is a sterile preparation for subcutaneous administration. Each 0.5 mL dose contains the following: a minimum of 1350 PFU (plaque forming units) of Oka/Merck varicella virus when reconstituted and stored at room temperature for 30 minutes, approximately 25 mg of sucrose, 12.5 mg hydrolyzed gelatin, 3.2 mg sodium chloride, 0.5 mg monosodium L-glutamate, 0.45 mg of sodium phosphate dibasic, 0.08 mg of potassium phosphate monobasic, 0.08 mg of potassium chloride; residual components of MRC-5 cells including DNA and protein; and trace quantities of sodium phosphate monobasic, EDTA, neomycin, and fetal bovine serum. The product contains no preservative.

To maintain potency, the lyophilized vaccine must be kept frozen at an average temperature of -15 degrees C (+5 degrees F) or colder and must be used before the expiration date (see HOW SUPPLIED, Stability and Storage). Storage in any freezer (e.g., chest, frost-free) that reliably maintains an average temperature of -15 degrees C (+5 degrees F) or colder and has a separate sealed freezer door is acceptable.

ActHIB?
Haemophilus b Conjugate Vaccine
(Tetanus Toxoid Conjugate)

DESCRIPTION
Caution: Federal (USA) law prohibits dispensing without prescription.

NOTE: Haemophilus b Conjugate Vaccine (Tetanus Toxoid Conjugate) - ActHIB? is identical to Haemophilus b Conjugate Vaccine (Tetanus Toxoid Conjugate) - OmniHIB? (distributed by SmithKline Beecham Pharmaceuticals); and is manufactured by Pasteur M?rieux S?rums Vaccins S.A.

ActHIB?, Haemophilus b Conjugate Vaccine (Tetanus Toxoid Conjugate), produced by Aventis Pasteur SA, is a sterile, lyophilized powder which is reconstituted at the time of use with either saline diluent (0.4% Sodium Chloride) or Aventis Pasteur Inc. (AvP) Diphtheria and Tetanus Toxoids and Pertussis Vaccine Adsorbed (whole-cell pertussis vaccine D.P. or Tripedia?, AvP Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed (DTaP) (when reconstituted known as TriHIBitTM) for intramuscular use only. The vaccine consists of the Haemophilus b capsular polysaccharide (polyribosyl- ribitol- phosphate, PRP), a high molecular weight polymer prepared from the Haemophilus influenzae type b strain 1482 grown in a semi-synthetic medium, covalently bound to tetanus toxoid.1 The lyophilized ActHIB? powder and saline diluent contain no preservative. The tetanus toxoid is prepared by extraction, ammonium sulfate purification, and formalin inactivation of the toxin from cultures of Clostridium tetani (Harvard strain) grown in a modified Mueller and Miller medium.2 The toxoid is filter sterilized prior to the conjugation process. Potency of ActHIB? is specified on each lot by limits on the content of PRP polysaccharide and protein in each dose and the proportion of polysaccharide and protein in the vaccine which is characterized as high molecular weight conjugate.

When ActHIB? is reconstituted with saline diluent, each single dose of 0.5 mL is formulated to contain 10 ?g of purified capsular polysaccharide conjugated to 24 ?g of inactivated tetanus toxoid, and 8.5% of sucrose.

When ActHIB? is combined with AvP DTP vaccine by reconstitution, each single dose (0.5 mL) is formulated to contain 10 ?g of purified capsular polysaccharide conjugated to 24 ?g of inactivated tetanus toxoid 8.5% of sucrose 6.7 Lf of diphtheria toxoid, 5 Lf of tetanus toxoid, and an estimate of 4 protective units of pertussis vaccine. Thimerosal (mercury derivative) 1:10,000 is added as a preservative to AvP DTP vaccine. (Refer to product insert for AvP whole-cell DTP.)

When ActHIB? is combined with Tripedia? (TriHIBitTM) by reconstitution for booster dose, each single dose (0.5 mL) is formulated to contain 10 ?g of purified capsular polysaccharide conjugated to 24 ?g of inactivated tetanus toxoid, 8.5% of sucrose, 6.7 Lf of diphtheria toxoid, 5 Lf of tetanus toxoid and 46.8 ?g of pertussis antigens. Thimerosal (mercury derivative) 1:10,000 is added as a preservative to Tripedia?. (Refer to product insert for Tripedia?.)

The reconstituted vaccine, using saline diluent, appears clear and colorless. The reconstituted vaccine, using AvP DTP vaccine, appears whitish in color. TriHIBitTM, the reconstituted vaccine, using Tripedia? is a homogenous white suspension.

PRESCRIBING INFORMATION
PEDIARIX?
[Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed,
Hepatitis B (Recombinant) and Inactivated Poliovirus Vaccine Combined]
DESCRIPTION
PEDIARIX? [Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed, Hepatitis B
(Recombinant) and Inactivated Poliovirus Vaccine Combined] is a noninfectious, sterile,
multivalent vaccine for intramuscular administration manufactured by GlaxoSmithKline
Biologicals. It contains diphtheria and tetanus toxoids, 3 pertussis antigens (inactivated pertussis
toxin [PT] and formaldehyde-treated filamentous hemagglutinin [FHA] and pertactin
[69 kiloDalton outer membrane protein]), hepatitis B surface antigen, plus poliovirus Type 1
(Mahoney), Type 2 (MEF-1), and Type 3 (Saukett). The diphtheria toxoid, tetanus toxoid, and
pertussis antigens are the same as those in INFANRIX? (Diphtheria and Tetanus Toxoids and
Acellular Pertussis Vaccine Adsorbed). The hepatitis B surface antigen is the same as that in
ENGERIX-B? [Hepatitis B Vaccine (Recombinant)].
The diphtheria toxin is produced by growing Corynebacterium diphtheriae in Fenton medium
containing a bovine extract. Tetanus toxin is produced by growing Clostridium tetani in a
modified Latham medium derived from bovine casein. The bovine materials used in these
extracts are sourced from countries which the United States Department of Agriculture (USDA)
has determined neither have nor are at risk of bovine spongiform encephalopathy (BSE). Both
toxins are detoxified with formaldehyde, concentrated by ultrafiltration, and purified by
precipitation, dialysis, and sterile filtration.
The 3 acellular pertussis antigens (PT, FHA, and pertactin) are isolated from Bordetella
pertussis culture grown in modified Stainer-Scholte liquid medium. PT and FHA are isolated
from the fermentation broth; pertactin is extracted from the cells by heat treatment and
flocculation. The antigens are purified in successive chromatographic and precipitation steps. PT
is detoxified using glutaraldehyde and formaldehyde. FHA and pertactin are treated with
formaldehyde.
The hepatitis B surface antigen (HBsAg) is obtained by culturing genetically engineered
Saccharomyces cerevisiae cells, which carry the surface antigen gene of the hepatitis B virus, in
synthetic medium. The surface antigen expressed in the S. cerevisiae cells is purified by several
physiochemical steps, which include precipitation, ion exchange chromatography, and
ultrafiltration.
The inactivated poliovirus component of PEDIARIX is an enhanced potency component.
Each of the 3 strains of poliovirus is individually grown in VERO cells, a continuous line of
monkey kidney cells, cultivated on microcarriers. Calf serum and lactalbumin hydrolysate are
used during VERO cell culture and/or virus culture. Calf serum is sourced from countries the
USDA has determined neither have nor are at risk of BSE. After clarification, each viral
suspension is purified by ultrafiltration, diafiltration, and successive chromatographic steps, and
1
inactivated with formaldehyde. The 3 purified viral strains are then pooled to form a trivalent
concentrate.
The diphtheria, tetanus, and pertussis antigens are individually adsorbed onto aluminum
hydroxide; hepatitis B component is adsorbed onto aluminum phosphate. All antigens are then
diluted and combined to produce the final formulated vaccine. Each 0.5-mL dose is formulated
to contain 25 Lf of diphtheria toxoid, 10 Lf of tetanus toxoid, 25 mcg of inactivated PT, 25 mcg
of FHA, 8 mcg of pertactin, 10 mcg of HBsAg, 40 D-antigen Units (DU) of Type 1 poliovirus,
8 DU of Type 2 poliovirus, and 32 DU of Type 3 poliovirus.
Diphtheria and tetanus toxoid potency is determined by measuring the amount of neutralizing
antitoxin in previously immunized guinea pigs. The potency of the acellular pertussis
components (inactivated PT and formaldehyde-treated FHA and pertactin) is determined by
enzyme-linked immunosorbent assay (ELISA) on sera from previously immunized mice.
Potency of the hepatitis B component is established by HBsAg ELISA. The potency of the
inactivated poliovirus component is determined by using the D-antigen ELISA and by a
poliovirus neutralizing cell culture assay on sera from previously immunized rats.
Each 0.5-mL dose also contains 4.5 mg of NaCl and aluminum adjuvant (not more than
0.85 mg aluminum by assay). Each dose also contains ≤100 mcg of residual formaldehyde and
≤100 mcg of polysorbate 80 (Tween 80). Neomycin sulfate and polymyxin B are used in the
polio vaccine manufacturing process and may be present in the final vaccine at ≤0.05 ng
neomycin and ≤0.01 ng polymyxin B per dose. The procedures used to manufacture the HBsAg
antigen result in a product that contains ≤5% yeast protein.
PEDIARIX is formulated without preservatives.
The vaccine must be well shaken before administration to obtain a homogeneous, turbid,
white suspension.
Diphtheria and Tetanus Toxoids Adsorbed Combined Bulk (For Further Manufacturing Use)
is manufactured by Novartis Vaccines and Diagnostics GmbH & Co. KG, Marburg, Germany.
The acellular pertussis antigens, the hepatitis B surface antigen, and the inactivated poliovirus
antigens are manufactured by GlaxoSmithKline Biologicals, Rixensart, Belgium. Formulation,
filling, testing, packaging, and release of the vaccine are performed by GlaxoSmithKline
Biologicals.

Had a hard time posting this on another thread, but it is related...

I think you should investigate vaccines more. Most if not all board members stating vaccines are safe have large amounts of stock in the companies producing them and have much to gain.
Yes, there is a time and place for some...
But really, really do your research before you inject formaldehyde, rat poison, mercury, aborted fetus tissue, monkey, feces, and other neurotoxins into your body.
Statistically, you are more likely to obtain the disease from the vaccination or complication there of. Also studies show that most of the disease we are being inoculated for was on the decline before vaccinations were introduced.
Like I said, perhaps there is a time and a place. But be an informed consumer. Don't take your doctors word as truth either, they too have $$$ to gain. My doctor promised emphatically there were none of the listed ingredients above in vaccinations he wanted to give my child. I had to beg for the ingredient list. Sure enough, they were on the list. I highlighted them, brought the pamphlet/list back, and have never been asked about them again.
The drug companies now say they do not use mercury in the manufacturing of vaccines anymore. So did they recall all the vaccines previously made. Nope! They are dispensing them to the public until they run out. They haven't said what is being used in it's place. Is it possibly worse? Unless an ingredient is considered an "active" ingredient, It does not have to be listed.
Many people that have done research and exposed the faults with vaccines have had their license revolked and laboratories taken away. Hmmm. I find that extremely suspicious.
Please do your research and truly know what you are putting into your body. Learn how your immune system works. Learn how vaccines work/don't work. You know my opinion.
I'm sure I'm gonna "get it" for this post. I know my beliefs are the minority, but I had to say something.
But ask yourself why you believe in vaccinations. Is it because it's what is familiar, comfortable, what you grew up believing, what your parents told you to do, what your doctor told you to do? Or is it because you have investigated them with the same effort (or more) you would use when buying a car? How many people have actually taken the time to educate themselves on this? Pro or Con. At least it would be an informed decision and not a decision based on fear. How real is the fear? Many of the outbreaks since the introduction of vaccinations were caused by the vaccinations. Go figure? You've gotta look deep for this information because the CDC and drug companies do not want the public to now this.
If you do vaccinate, do not get the "cocktail" vaccinations. They have not been studied for safety!!!!!!!! They have only been studied individually. And do not vaccinate if your immune system is compromised. (Cold, fever, other illness)
If you have a newborn and are vaccinating. You should know that your child is a guinea pig, no vaccines have ever been tested for safety on infants. All research is for children ages five and six. That's the earliest age study. Since 1983 the number of vaccines the CDC recommends for our children has TRIPLED!
Really, are they ALL necessary?

My friend just sent me this e-mail..

"I called up this department:

Department of Fire and Emergency Services
465 Marin Boulevard
Jersey City, NJ 07302
Tel: (201) 547-4239
Fax: (201) 547-4398

Armando Roman, Director
William Sinnott, Fire Chief



and asked how this could be demolished so quickly when there should be an investigation. He said that they've already investigated. I said, "so what caused the fire?" He said he couldn't tell me, it's part of an ongoing investigation. FISHY"