Withdraw of Consent

It want to make it very clear that I do not consent to medical treatment and that any need for care is being created through fiduciary abuse and munchousen by the chemical industry.

In 1997, when I was 17 I consented to a medical experiment, that I was mislead into believing was a legitimate study of the safety and effectiveness of the allergy vaccine. We talked with Dr. Strimas who explained how allergies can add up to cause reactions. After years of getting the shots I started having panic attacks and realised that avoidance was effective, will exposure was stressful and made things worse.

I later developed Hashimoto's Thyroiditis after a traumatic instance of medical rape, where I was exposed to allergens against my will in abusive settings, denied safe food, and forced to ingest a dangerous immunosuppressant know as Risperdal. After I was diagnosed with Hashimoto's Thyroiditis I was switched to thyroid medicine and sent to an extremely noisy environment. I later noticed a neck breaking autoimmune reactions to sound, or degenerative disk disease.

I had a heck of a time getting medical records and finding safe placement for someone with my condition. I discovered my doctor had died, right before the allergy vaccine had proven "safe and effective". The obituary said he was in on his way to a meeting, but did not mention how he had died. Rumor it was a suicide, I don't feel the vaccine was safe or effective.

I am fully withdrawing all consent form the study. I do not approve of the methodology and I do not feel the vaccine is safe.

Boundaries Agreement

I will support Mary in taking full physical possession of her body and doing what she feels is necessary to maintain personal health.

I understand that Mary did not choose to spend her childhood sitting in her own urine and feces will doctors and psychologists abused Mary exploiting her for financial gain and slandering her with science doctrine used to promote defective products.

I understand that Mary is fully capable of budgeting and taking care of money, when she has enough to afford what she needs, but is still unable to gain control of what is rightfully hers from the medical/chemical industry.

I understand that Mary's needs are significantly increased by her physical disabilities and I will trust her when she tells me she is being harmed even if I do not understand.

I understand that Mary has education that did not even exist when I was in school, and I will not talk down to Mary by questioning her decisions or treating her like she is in any way less than people who had the physical stamina and ability to write and get better degrees or jobs.

I will avoid worshiping doctors in front of Mary, because I understand that they drugged her raped her and left her sitting in urine and blood, and it is cruel to make Mary relive that traumatic childhood experiences.

I understand that Mary wants to gain more control over her hands and I will try not to pressure Mary any into situation that cause neurological regression.

I will avoid endangering Mary's life by denying sleep or pushing her into environments where she does not feel safe.

Psychologists Are Stealing Our Lunch Money

Bullying is a big problem for children with Autism. What do you do if your desk beats you up and the psychologists steal your lunch money? This is the reality for children Ehlers Danlos syndrome. The condition affects collagen production making it painful to sit at a desk and difficult to write. People with Ehlers Danlos syndrome bend easily and could benefit from regular physical activity and diets that promote coligon building and the reduction of swelling to compensate. Psychological tests are regularly imposed on these children at public expense. Psychologists have become bullies abusing these children and recommending poisons, will ignoring serious physical issues with their food and environment. This is the worst kind of bullying the child is made to feel their is something wrong with them, when really they are just being starved and physically abused by people who overestimate the value of their "knowledge".

All children deserve more choices of food and how they spend their time. Lack of funding is no excuse, children should come first. Stop paying these ignorant bullies to tell 6 year olds they are behind, get these kids safe food and let them have good choices of suitable activities. Forcing a child to sit still is abuse, let children have active options.

Our Research

I have found that a significant portion of the research they have done in our name is not accessible to us. Please make this research publicly available to us in the least restrictive environment possible. Many of us are not receiving enough money to cover our basic needs and can not afford to buy a second time, the research that was paid for with our money. Also I feel researchers and fundraisers who have stood up for our rights, are being killed for what they know and want to protect them from harm.

Please make all the research publicly available as soon as possible.

Thank you,

Mary Tormey

I posted this in honor of recently deceased UCLA professor. RIP William S. Klug (Bill Cipher). I hope you inspire many generation to continue your work with genetics, orbital theory, and 3 dimensional modeling.
Concepts in Genetics
https://biologyrules1.files.wordpress.com/2015/03/concepts-of-genetics-w-s-klug-et-al-10th-edition.pdf

Our Money

I can see there is a lot of funding going out in the name of disabled people. It seems a blank check is written for "healthcare", will our basic needs and rights are ignored.
The Department of Justice appears to be to cover up their negligence in overlooking the many charities and government organisations that fraudulently claim to help people with disabilities, but instead waste money for the disabled, preventing them from meeting basic needs. Such as having a home or paying for electricity. Hospitals are using expensive drugs and service to embezzle money from vulnerable populations, that are being denied their right to live in the least restrictive environment possible. This breach of fiduciary duty, insurance fraud, and abuse of members of a vulnerable populations. The department of justice has living wage employees, yet claims to lack the resources to investigate.


For additional information:
To give you an idea of how money for us is being misspent.
Govt. Spends More on Disability than Food Stamps, Welfare Combined
http://www.breitbart.com/big-government/2013/03/25/govt-spends-more-on-disability-than-food-stamps-and-welfare-combined/

Let me point out that benefits are not adequate, and people are being diagnosed and treated for profit. Many of these people are victims of civil rights violations, who were damaged by Welfare funded drugs. I am an able bodied person who collects a disability after being found "gravely disabled" will being held in a captive environment without legal representation or just cause, and made gravely disabled by a minty blue children's medication, I never consented to take. I have audio sensitive seizures and hashimoto's issues and motor skill problem caused with welfare money, I did not even legally qualify for.
"How Americans Game the $200 Billion-a-Year 'Disability-Industrial Complex'"
http://www.forbes.com/sites/theapothecary/2013/04/08/how-americans-game-the-200-billion-a-year-disability-industrial-complex/#234505ce1f54

A politician who is apparently fails to understand economics, promoting health insurance plans without understanding how this interferes with religious freedom, product choice and the basic right to life. Humans obviously had God given rights to everything they needed well before the invention of money now. Adding money as a barrier to this is a problem no matter who pays. The public funds research and should have access to it, without having to pay for vain marketing or profits.
BERNIE SANDERS ON HEALTHCARE
http://feelthebern.org/bernie-sanders-on-healthcare/

This reminds me of the grade school, I saw how the money was being spent on redundant tests to see if I qualified for services. They wasted a huge amount of money on vague repetitive tests to show, obvious issues with written comunications. Actual servicse provided costed nothing, I gave oral ansewers had extra time on tests and got assistance from other students.
http://atlas.newamerica.org/individuals-disabilities-education-act-cost-impact-local-school-districts