What’s the big deal with AB2109?

 

All of us have noticed the big push from health care as of late and have read pages upon pages of tactics that they list and publish, to try and push vaccines on the total population. So is it any surprise that they are trying to change laws in order to make it more difficult to say no? Of course it isn’t and neither is it a surprise that they will make more $money$ because of this new bill.

Now while I am sure that it didn’t all start with Dr. Richard Pan, his name is on this bill so he is taking the brunt of the backlash. Despite the numerous postings of upset parents, practitioners and even people around the globe… he does not respond, but continues to post articles as if they don’t exist. Maybe he thinks if he holds out long enough, the bill will pass and they’ll all disappear.  But we’ll have to wait to see how that pans out.

There are a few who don’t get what the big deal is and protest that this isn’t forced vaccination so people shouldn’t be complaining. So what better thing to do than clearly outline what is so bad about this new bill.

Currently in order to get a philosophical exemption, one has to simply write and sign a piece of paper and send it to the appropriate place. The new suggestion is that in addition to that piece of paper, parents must also go to a doctor and listen to them lay out the benefits and risks of vaccinations, the doctor must write a letter, sign it and then the parent must write another letter and sign that one. This must also happen again once the child reaches grade 7 and applies to children who are homeschooled as well.

So now not only can’t you just opt-out, you have to sit in a doctor’s office and risk catching something, but you must also listen to them tell you; how wonderful vaccines are, how the only risk is a sore arm, maybe a possible fever and that you are putting your child and everyone else at risk by not vaccinating cause your child is now a cesspool of disease.

Before I move on to the next point of contention, I want to touch a bit on these papers that have to be written and signed, according to the new bill. Most of us are familiar with the general working of doctor’s offices these days. As it stands, most doctors don’t even discuss vaccines but instead simply state that your child is due for them. There is never an option given to opt out and most people are not aware that it is even possible to do so. Most offices don’t keep you in for the appropriate time to watch for an allergic or otherwise reaction after injection and most doctors have absolutely no clue, what the signs of a reaction are. Multiple stories from families all ring the same ‘the doctor would not even consider that a reaction was possible’ ‘the doctor kept denying that it could be the vaccine, despite all other possibilities being ruled out’ ‘my baby turned blue and stopped breathing and he just kept saying, it’s not the vaccine, it’s not the vaccine’.

I’m getting to my point I swear.

With doctors continually denying risks and not being aware of current studies how can they properly inform parents of the benefits and risks when they are so biased, uneducated and opinionated on the subject.  With that in mind we come to the signed papers. I have not found anywhere that it states what is to be written on that document. It would be nice to assume that it will say something like, risk/benefits were explained and medical intervention was denied. In reality it could be very different. Doctors could write that risk/benefits were explained and parent refuses, putting child and community in danger. Then the parent is required to sign a paper showing that they basically agree to the doctor’s paper. If a parent is being required to sign such a thing…… no wonder there is backlash about this.

People refusing to inject their children with a manufactured product didn’t do so lightly and didn’t do so out of laziness or lack of funds. People refusing are educated on vaccines, diseases and how to properly treat them without the need of synthetic materials. Doctors, hell a lot of people are dismissing real concerns as some passing trend. Maybe if they started acknowledging these concerns, actually listening and investigating; we wouldn’t have such a misunderstanding from health care professionals. It’s not from lack of trying, more and more people are not only learning about what is happening: they are seeing it with their own eyes.

The next point and it’s a biggie….. what if you cannot find a doctor to sign? Nothing in this bill states that a doctor must sign a paper allowing exemption and according to the new bill, without a signature you cannot get an exemption and therefore you child cannot attend school. This is where the mandatory vaccination line comes into play. Now follow along here…. Your child must attend school or you can be charged. If you cannot find a doctor to sign an exemption than your child cannot go to school, forcing you to have to vaccinate in order to gain attendance. Homeschooling is not an option because this bill also applies to homeschoolers. Since an increasing number of parents are now using chiropractors and naturopaths etc. and these doctors are not able to sign the exemption, they are left to seek out a doctor to sign. If no doctor in their area will sign (since it is a new trend to not allow unvaccinated patients in their offices) they have to travel in order to find one. What if this is not possible? Do they then have to go against their belief and vaccinate their child because, they have no other option. This is why parents are protesting this as mandatory vaccinating. They know all too well what their old doctors are like and how hard it will be just to say “no thanks, we’re good”

You all know my opinion; opt in not out!

I left the best part for last, because it’s something I noticed right away and here is why. With every new vaccine, drug or medical treatment; there is always a cost analysis to determine if it is viable to put to market. If a procedure costs more than it would profit, it is usually shelved. Vaccines are always checked to make sure that it is profitable and marketable. I saw this very early on when I started learning to read studies, so I noticed right away that there was some noting at the bottom of the bill, stating that any costs could be deferred and it got me thinking about how this bill could possibly be profitable. It didn’t take long of course, to see where the money was going to go and yes this bill will be making people money. Think about it.

Every parent in California, wishing to get a philosophical exemption will have to pay in order to receive one, because seeing a doctor there is not free, even for something that is mandatory.(this bill makes it mandatory to see a doctor in order to sign) Since it is being estimated by health care professionals that more people are getting exemptions and “putting people at risk” than it surely must be a lot of people right? All those people now having to pay for an exemption really adds up. Not only do they have to pay now but if their child is young, then they have to pay AGAIN when that child reaches grade 7. Next they’ll put in place a new bill making them return for another exemption for high school and it could go on like this. It’s obvious why they are doing this and it’s a very simple reasoning. Doctors are losing money and fast. Many people do not realize how many well baby appointments are recommended, all occurring when a vaccination is due. Not only are they paid for the visit but they make money on each vaccine given as well. If more people are not getting vaccinated and therefore not needing to go for well baby visits, then doctors are not receiving that money anymore. This new bill will ensure that, that money lost is partially made up, while also hoping that parents will crumble and give in to vaccines.

A final point of contention in this bill, that I nearly forgot to write about (it is 2am here) is that it sets precedent. I touched on before that people all over the globe are protesting on Dr. Pan’s facebook page and this is the reason why. If this passes, then more states will likely try to pass the same. Following in its footsteps could be other countries and that’s what worries people. Better to nip it in the bud now before we have a full out bloom that could eventually lead to a very real, very deadly and completely mandatory vaccination rule.

For now I am glad to be living in Ontario where all I have to do is pay $25 to get a form notarized and I don’t have to listen to someone less educated in vaccines than I, tell me that they are completely safe and nothing bad will happen to my child.

For now at least.

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It’s Not Something You’re Simply Born With

Oh Autism Speaks, how you annoy me so. I haven’t seen you in my news feed for awhile but today you have graced me with your presence. This is what they put out today and surprise, surprise it’s another piece on genetics. I have to state first of all that this illusion of prenatal testing is ridiculous. We have not pin-pointed a gene or any way to determine whether a child has autism shortly after birth or prenatally. Even though this article states that it has a test for autism, please be aware that this is just a money grabbing scheme. They know a few genes that they have pin-pointed-among the hundreds of other ‘multiple variations’ that have been claimed- that not only occur in those with autism, but those also with other disorders and regular people. If you took 100 people without autism, you will find these noted genes among them. They don’t have autism, so claiming that this test is anything but a giant ploy is ludicrous. Please know that even if they do find ‘something’ they have no treatments. They have therapies and medications that turn your child into a zombie. There are actual treatments that you can spend your money on and they will actually help as opposed to $1,500+ for them to tell you, yes here it is, now let’s make you pay for intensive therapies and pump your kid full of anti-psychotics. Go ahead if that is how you want to do things but I honestly feel sorry for the child. I have spent an immense amount less than that and in 2yrs my son has made tremendous progress, but I’m also not one to look for that easy way out, the one pill cure all that most of these parents are blindly dreaming about. It is not gonna happen; this is far too complex a disorder for a simple quick fix solution. The only quick fix is stopping the increasing number of children affected, but since no one is looking at the actual cause and too focused on genetics, this isn’t happening any time soon.

The very first line tells all, about the motives behind this organization and general researchers of autism.

“A burst of research into the genetics of autism has given scientists insight into the basis for the disorder. Now, some companies aim to capitalize on these findings by developing DNA screens that might one day provide a diagnosis at birth”

Do any of you actually believe that this research is about helping people? Look up the word ‘capitalize’ in the dictionary. This is all about $$$$. Do you honestly believe that the Down syndrome test, which is ‘offered’ repeatedly during the prenatal process, is just there because they care? They make money off of every test done and then for that second test they make thousands more. Do you think sticking a needle into your womb is free just because you don’t see the money coming out of your pocket?

Ok enough of that, you get the point. It’s all about making the dough and maybe as a side effect a possible few kids and families may be helped, but I doubt it.

“That specifically targets the developmental disorder, searching the genome for either irregular CNVs or single-nucleotide polymorphisms (SNPs) that could explain the symptoms.”

So what specific genes are named in autism because last I heard there were 100s of different possible combinations, with absolutely no chromosomal abnormalities? Are they just looking for irregular or duplicate genes and claiming autism? Can they no grasp the fact that SOMETHING has to affect these genes, these bits of DNA to change?

“These tests are not giving any answers and they are costing thousands of dollars “a microarray costs, on average, $1,500, and that’s without the bells and whistles such as doctor visits and additional gene sequencing”

These researchers are making millions looking at an end result.

“Therapies—a market that UK-based research publisher Global Data expects to top $5 billion in the US in 2018”

Why not do something productive in terms of genes and test children at birth and then after regression? Test the difference between parents who believe that their children were born with autism and those who watched their children regress after numerous vaccines.

Then this load of malarkey “These abnormalities remain difficult to detect until a child is around four years of age or older”… Really cause myself and other parents can tell you differently and correct me if I`m wrong but aren`t most children diagnosed around 18mths-2yrs old after nearly a year of actively trying to get a diagnosis. Isn`t that part of the whole vaccines don`t cause autism argument, that children are diagnosed right at the time of vaccines?

They go on and on about treatments and yet they only mention therapies. There is a huge difference and yet still many, many people –even professionals- still use the two interchangeably.

“The diagnostic holy grail is a molecular test that can pinpoint the disorder at birth to hook children into therapies straightaway”

Yes and yet after all this money spent you still have nothing, absolutely squat really. How long did it take to find out the problem with Down syndrome? If it were strictly a genetic problem, we would have no problem finding it. Before I move on I absolutely have to point out the horrific fact that our health system is absolutely burning itself alive. We can test for Down syndrome so why can’t we figure out why it’s happening? It’s like with vaccines, instead of actually addressing measles or any other, we use our ‘prevention’ methods and cross our fingers that it works and no one ever gets said disease again because we have no clue what to do when that happens. Wow we are truly f**ked, seriously over half of these parents have no idea how to take care of sick children. Look at how many are hospitalized due to dehydration…DEHYDRATION…seriously wtf, we should be teaching people what to do when they or their children become sick instead of focusing every ounce of energy into prevention and if that fails; more prevention. Here take this vaccine and you’ll never have to worry about your child getting sick ever again. Yes I am fully aware that this is not word for word what they are saying; I am however equally aware that this is the mindset people are getting because of the message that is being delivered. Don’t believe me, look at the flu shot. Beside the fact that we’ve seen the studies showing this vaccine to be pointless in preventing the flu and only reducing symptoms by %4, the message is ‘don’t wanna get sick and miss work, school etc. Get the flu shot, save your life and others’. So people go on down to Walgreens, the grocery store or wherever they are putting these disgusting stands and get their shot with full thinking that they are not going to get sick. A few days late they have the full blown flu and have absolutely no idea what to do because all they were told was get this and don’t get sick; no one says what you should do if you actually do get sick cause no one gets sick anymore because we have these wonderful magical vaccines right?

So moving on to thee best part of the article…
“We think that 80–90% of what causes autism is really the genetics. But pinning down the genetic cause of autism has been difficult. Known mutations comprise fewer than 20% of all cases of ASD’s”

These guys really have alot of nerve don’t they? They can only find known mutations –none specified, hell -none is ever specified- in less than 20% yet they, in basically the same sentence they try and claim that 80-90% of what causes autism is genetically based. It will take you a hundred years and you still won’t be able to prove that statement, that very poor assumption. If you just look at the increase you will see that 80-90% of what causes autism is ‘outward influence’ and if you close your eyes really, really hard…….you can hear the doctors whisper in your ear that it’s all genetics, you parent are to blame with your poor genes and choice in poor gened mate because he read an article somewhere 5 yrs ago.

Oh but my uncle, grandfather, parent or other has it, I think. Interesting that you can now diagnose everyone including Bill Gates to fit this idea laid out before you. Instead of nodding your head and thinking fondly of the quirky uncle on your mom’s side, why don’t you actually take a look? Maybe it’s all malarkey, maybe just maybe they came into the same situation as your child and what causes their autism is the same. Who the heck is to say, certainly not me because while my family – both side- are insane, quirky, do things other people would never have the balls to do type of people, none have autism, none flap their hands when they get excited, all of them speak and they do not have anything close to the physical issues my son has. Now I’m not saying that every autism is like my sons, not every child has autism because of vaccines- since the issue is much deeper than that- but I certainly am saying that no child is just born with genes like theirs unless there was exposure to something during pregnancy.

I also do love- not- how they pup every one up with ‘autism is caused by genes’ when they have this;

“Found in less than 1% of individuals with ASD. But this mutation alone isn’t the final word on an autistic diagnosis. Some people with the 16p11.2 deletion or duplication have no or few autistic symptoms”

So in short normal speak: you have squat. No wait, in fact, you have even more questions like why does this make sense to warrior parents and not you guys

“And many rare variants associated with autism present schizophrenic, epileptic or bipolar symptoms instead,”

Hmmm maybe they have the secret recipe? No I think they have just been doing a better job than you guys with far, far less money than you have at your fingertips. They know that autism and the above are not strictly psychiatric disorders, they know that these are things that can affect the whole body and that these are things that you are not simply ‘just born with’.

It’s actually quite sad when you think about it, all these people, families, loved ones told that this is the way things are and there is nothing that can be changed. Now we know that it is possible to have hope, that we can make lives better for these people. Take the ‘Gardisil Girls’ for example, there seemed to be no hope and yet when treated for the cause- or as much as we know at this point- these girls get better. The same type of treatment that is helping thousands of children with autism and that can help thousands more.

This is a false hope “A microarray screening for CNVs pinpointed the probable genetic basis for Lily’s autism”… the beginning of the article mentions this little girl as though they were going to reveal the secret to this genetic test that would diagnose at birth, yet now with proper wording you see that it is all just an illusion. They are hoping to come across one child –or group of children- that will unlock it all for them and we know that isn’t going to happen. These children have different causes and are each affected by so, differently and to such extremes it is hard to categorize them under the same diagnosis. One thing stands ever simply though. There is a cause. In this day to continue to doubt that is to pull the blinds shut and let the world move on without you; because we are. Children are recovering. They are not cured, because we can only do so much and we don’t have the money to research this properly. We can only continue our work while we watch millions spent on areas of research that are not helping a single child or family. Not one. Not ever.

And you wonder while all the warriors are pissed off.

“Despite extensive data collection and genomic screening, these microarrays can only identify an associated genetic abnormality in 8–25% of known clinical cases of autism, depending on whom you ask”

So even if we take their highest calculation of 25%, we still have that amount of children with a genetic abnormality that does not point to autism because this abnormality exists in other diagnoses and also regular everyday people. Still let’s throw them a bone and say good job, pat on the back for you. You took $1,500 from this family all to either confirm there suspicions, get tested earlier for therapies or….what? What treatment can you put together from this information? Earlier therapy, sure that’s a good thing I cannot disagree with however, even with those few extra months or years of therapy, you are only going to get so far. What these people aren’t saying out loud is that this test is not foolproof. Imagine taking your baby in, spending this money and getting back a positive result only, your child doesn’t have autism. Maybe there is no harm in that situation, but imagine the time and money spent, not to mention what impact this or any type of diagnosis has on a child. Then what of the other 75% that may be tested and will be told that their child is fine, only to later receive a diagnosis of autism.

I have to note that this article is truly annoying in that they keep relating to finding these ‘genes’ as the cause.
“But we’re still left with 75% of kids who still have an unknown cause.” No correction, you are STILL left with 100% of kids with an unknown cause and 25% of children that have similar gene abnormalities, which may or may not be related to autism.

“Despite the relatively low diagnostic yield, CNV-probing chromosomal microarrays are the recommended genetic test for autism by the American Society of Human Genetics and the Boston-based Autism Consortium”

Of course they are what else do you have? After how many years and how many billions of dollars, what have you come up with? After say ten years and possibly a million dollars –I am estimating extremely high- parents and others have come up with treatment plans and centers that are actually giving kids back their lives. – In a functional respect- They have also started centers for therapies, groups and so many things that actually help.

I’m so glad that they mentioned Fragile X in here because it’s another hot button issue for me. A gene doesn’t spontaneously break; I’ve talked to parents of children who have been diagnosed with Fragile X after a vaccine reaction. Same story; healthy child, meets milestones then regression day after vaccines, only this time it shows on a test as Fragile X. Saying that Fragile X is the cause is again, absurd. What happened to this gene and other genes is an end result. Our genes reflect our state and are impacted by such. Saying that this is the cause leads people to think ‘oh its genes, nothing we can do’ when that is not true. These kids could actually be getting treatment that would make their lives easier and instead they are basically left in their own world and struggling when it doesn’t have to be that way.

“Most of the time, mutations associated with autism are formed de novo in the autistic person.”

I would love to see where they got this from and until I do, I call BS on this. If this were true to the degree that they are stating it, then there would already be prenatal testing and autism wouldn’t be such a hot topic as it is.

Thinking that it is strictly genes is very detrimental to families. There will be few families willing to have another child based on the information being spat and the risk of inheritable autism. The whole family is missing out when it does not have to be so. I took what I know about autism –my sons specifically- and I made a prevention plan when I got pregnant again. My daughter doesn’t have autism and maybe it is just a coincidence, but apparently so are children dying 30min after receiving a vaccine. Who am I to claim truth when I have no money to do research to back up my claims, yet neither do they. Even ground for now I guess, let’s move on.

“Even at the end of the day, the complete genome sequences of 10,000 autistic diagnoses still won’t be able to predict definitively what the detailed clinical outcome will or won’t be,” says Scherer. For that reason, experts emphasize the necessary role of clinical geneticists, like Schaaf, to help interpret the data and make it clear that genes aren’t the be-all and end-all”

*Applause* And even if it was 100% foolproof, it still would not help us with prevention or treatment. It still will not help these children or their families

Finding the cause in genes in order to diagnose earlier or prenatally; is a waste of time, money and resources

We need to know the cause in order to find the cure. We need to stop looking at everything but the obvious.

Let’s open the box and see what’s inside