Is our Hope in Congress?

tmr-homepage-final4The autism epidemic continues to skyrocket, but the head of the Congressional Interagency Autism Coordinating Committee (IACC) investigating all the factors involved, claims they have no power and can do nothing. Anne Dachel summarizes the recent disappointing meeting. At least, concerned, knowledgeable parents, and those working with autism families, were disappointed. I’m guessing the pharmaceutical companies and others supporting the vaccine industry were also watching and listening, and probably came away with relief that they continue to be safe – for the moment.

Listening to a recording of the speech given by Megan Davenhall at the September 2014 IACC meeting gives me hope, but not hope in what Congress can or will do, hope in what a grassroots movement of parents can do.  This impassioned, yet calm, rational, and highly thoughtful plea describes the dilemma faced by autism parents who have helplessly watched their child regress after vaccines, live with the enormous daily challenges of vaccine induced autism, and helplessly watch Congress give lip service to the concept of exploring causes and treatments.

And the head of this illustrious gathering of highly educated congressional committee members, Thomas Insel, MD (Director of NIMH) sums it all up by saying,

We have no money. We have no resources. We are just a bully pulpit. We have no recourse. The public doesn’t understand this. We can have honest exchanges like this and listen.

Summary: ‘Basically, we are powerless to effect chang don’t get your hopes up.’ But he does mention the real powers in the room, the NIH, the CDC and others who hold all the power and money in this debate. That, folks, is the problem. Those with the money do not have the will to explore and expose the cause and effective treatment to prevent autism.

  • They do have the money to continue to heavily lobby congress with their point of view.
  • They do have the money to heavily influence doctors to continue to give too many vaccines too early.
  • They do have the money to advertise their shots through every means possible, including the March of Dimes.
  • They do have the money to publish fraudulent research (#CDCwhistleblower) and the money to keep the mainstream media from reporting on it.

Money talks. Every time a child gets a vaccine it keeps the wheels of the machinery working. Even if a child is injured by a vaccine, it still generates revenue because they become a lifelong client for medical services – an infinite variety of medical services.

Megan Davenhall, President of The Thinking Moms Revolution, and many others have been relentless in leading a charge FOR TEN YEARS to inform those in authority – this committee of esteemed health experts who hold important positions, and who they thought were able to make a difference. These are mainly parents who live with the reality of vaccine induced brain damage causing medically induced autism EVERY SINGLE DAY.

They had hoped their pleas and volumes of information provided to Congress was going to make a difference. I believe we are reaching a tipping point. But Congress is not our hope. It is going to take a grassroots movement of EVERYONE to make a change. The autism parents’ burden is too great. They need those of us who are informed and aware to help them.

The recent autism statistics were 1:23 ten-year olds are autistic. In 1980 it was 1:10,000. At this rate, even if your child remains unscathed, chances are a significant number of his friends and peers will be. October is Autism Awareness month. Share. Those of us outside of this debate need to be informed and we need to speak up to expose this greed induced epidemic.

This autism is extremely different… It’s pain.  It’s bowel disease.  It’s mitochondrial dysfunction.  It’s seizures.  It’s immune deficiency.  And in many cases, it is a silent plea for help through head banging, and self-injurious behaviors and aggression.  Parents have been searching for treatment for these co-conditions for years. We pay out-of-pocket because insurance won’t cover the staggering cost of healing the many physical ailments our children suffer from.  Our kids who fall into this model of autism, the ones who are healthy and become urgently ill, need to be treated with respect and like human beings who are sick. Their physical symptoms need to be addressed by medical professionals in the same ways that they would be handled in a person without autism.

 

Parents have been telling you for years that there was some trigger that sent their healthy child into a physical and developmental tailspin. They watched this happen to their kids. And we’re ignored. You ignore our firsthand eyewitness accounts of damage to our children. You hold these meetings that accomplish nothing. And [you] give us the mic a few times a year and we tell you, ‘Autism is medical.’ This version of autism that the parents come here and talk to you about. Let me be clear on that. Our children get better when we treat the medical problems they have. Their behaviors that land them on the spectrum in the first place, improve when they get healthier. And you don’t hear us. You give us fifteen minutes of your day and interrupt parents who travel on their own dime to come here and speak to you. If they go over their allotted three minutes, they get interrupted–as long as we end the meeting by five. Megan Davenhall

The Age of Autism has volumes of information if you care to learn more.

30 ways in 30 Days, Exploring Vaccines: Day 14