Not really. Some scientist or Rosie O'Donnell will come up with another culprit and probably, many kids will be misdiagnosed or it will be high fructose corn syrup that apparently contains traces of mercury. I have a feeling that the link between mercury and HFCS is a way to push the ban on the sweetener.
Not sure the autism industry will give up so easily. There will always be a reason and many parents will find something else to blame.
I tried to define autism and discovered there is a wide range of warning signs. We use to call many of these warning signs, "just being a kid." I am not sure most diagnosed autistic children are actually autistic.
Apparently, "A comprehensive evaluation requires a multidisciplinary team, including a psychologist, neurologist, psychiatrist, speech therapist, and other professionals who diagnose children with ASD." Yet many parents read the warning signs on some web site and decide since their little ones were vaccinated, Bingo. The bad guy is preservatives.
I will not be one bit surprised if we eventually learn that either autism does not widely exist in the population or it is something else. Seems easy to simply say to a parent, "your child is autistic."
Or believe Jenny McCarthy that thinks the link is undeniable, case closed. She has NO CLUE or scientific background. No medical degree or time spent in a research lab or other skills that allow her to make any sort of serious comments on causality. She is a parent suffering and looking for reason.
For all she knows, her child is ill because of genetics; a leading "cause" of the problem.
And so many parents likely agree with McCarthy. Or the British study--apparnelty well regarded at the time--that turned out to be an elaborate fraud.
Look, I feel sadness for parents with sick kids, but I also feel sorry for the parent that seeks to blame one industry or product for their kid's problems sans any legitimate proof either way. Parents look for answers and often turn to crackpots that serve their own needs and goals rather than the truth.
I apologize in advance for the long winded reply. This is a subject near and dear to my heart.
I'm sorry, but I take issue with much of what you're saying here.
Yes, there are some parents out there that are looking to blame someone or something for the issues that their children have, but most of us just want to help our children live happy and productive lives. Oftimes, you need a diagnosis to do that.
Autism, like many other disorders comes in varying degrees of severity. Children can be very high functioning or severely disabled. That doesn't mean there is nothing wrong with the high functioning kids. Dr's are not as eager as you think to slap our kids with the autism label. Try defining cerebral palsy. I can guarantee you'll find many different symptoms from very mild to severe.
Take my daughter for example. She has been diagnosed with a mild form of autism and a mild, but rare type of c.p. The diagnosis process as you say, was long and complicated, and the most painful thing I have ever had to go through as a parent. You are required to document every one of your child's flaws and weaknesses. You have to speak with countless Dr's and therapists. It's exhausting for everyone involved, and heartbreaking for the parents. You must be brutally honest if you expect to find an answer. Now, most people upon first meeting her have no idea that there is anything amiss. But given time, they begin to notice the quirks. Now that she's older, those quirks are more readily apparent. Socially, she's far behind her peers, which can make school difficult. Things that come naturally for most, we have to teach her, and that takes time. It's very frustrating for her to have to learn to remember to read and interpret social cues. Sure, her symptoms are less severe than many, but that doesn't make them less real.
Personally, I think the rise in diagnosis rates stems from an increase in awareness. I know many adults who, if born today, would most likely be diagnosed with autism.
As for the c.p., we are pretty sure that was caused by the hormone used to develop the lungs in utero, or the vacuum assisted birth. When the drug was administered, the link between it and c.p. Had not yet been verified. (in fact I'm not 100% certain they have proven it definitively) It wasn't until a year later that research was published. However, even had we known of the link, we still would have taken the risk. When your choices are having a pre-term child who is unable to breath, or having one who can but has a small risk of c.p., you choose breathing. I'm not going to run out and sue the Dr's and drug companies for trying to make sure my baby would live.
Again, I apologize for the long post, and these are just my thoughts and opinions on the issue as a parent who has had to go through the process.