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  IGNAZ SEMMELWEISS and AUTISM:
when prevailing paradigms resist change
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by Teresa Binstock
Researcher in Developmental and Behavioral Neuroanatomy
My writings do not constitute medical advice.
Instead, they represent a seeking to understand autism-spectrum disorders
and their causes and associated traits.
The story of Ignaz Semmelweiss sheds light upon why the NIH and NIMH are
impeding progress in research about causes, diagnostics, and treatment in autism and
similar syndromes.
      By clinging to an oversimplified and outmoded model of autism (ie,
it's gotta be genetic), the stubborn persistence of several research administrators in
the NIH and NIMH means that funding for autism and autism-spectrum syndromes remains
funneled into the hands of a small group of researchers who pledge (via
NIH-grant contracts) to conduct their research in accord with the model wherein "it's
gotta be genetic" (1). This funding pattern imposes a serious limitation on
research that ought be occurring, given the growing amount of new data which indicate
that *more than* genetic-aspects need be considered.
      The relationship between (a) the offically approved though outmoded
paradigm and (b) subsequent funding patterns is worth re-stating: The persistence of
the NIH and the NIMH in focusing almost entirely upon a genetic-theory of autism
means that a goodly amount of data continues to be ignored, shunted from
view, and unfunded -- even as the primary genetics-model researchers are blessed with
abundant funding despite decades of non-success (1). For instance, the data from
Wakefield, Warren, Singh, Shattock, Oleske et cetera are important, as are patterns
amidst parental anecdotes -- eg, gastrointestinal atypicalities, vaccination effects,
extraodrinarily recurrent otitis et cetera. 
      However, as recent years have shown, despite the many new data and
anecotes, the NIH and NIMH are resistant to change. The new data remain virtually
ignored, the parents' anecdotes treated as if mere hearsay. Not surprisingly, in the
face of this bureaucratic intransigence, the goal of changing and improving the NIH and NIMH in
regard to autism funding will require increased effort.
      Toward that goal, the data and fate of Ignaz Semmelweiss reveal much
about challenges to well-entrenched medical paradigms, about how new data are
ignored, and proponents of new data and alternative paradigms are treated. In short, when a
medical model becomes institutionalized and its primary spokespersons
become set in their well funded ways, such institutions and individuals strongly resist
change. 
A fine rendition of the Semmelweiss story is presented in Jeanne
Achterberg's book Woman as Healer:
 

"ON CONTROLLING GERMS
"By the end of the nineteenth century, the work of Lister, Pasteur, Koch,
and other 'microbe hunters' led to the germ theory of disease, and to knowledge of
sepsis and antisepsis. Hospital procedures and sanitation dramatically improved.
      "Even before the germ theory, another man -- Ignaz Semmelweiss
(1818-1865) -- was successful in learning to control the spread of pueperal (childbed) fever,
caused by Streptococcus pyogenes. His is a long, sad story, representing
the worst that can happen when one challenges the prevailing mode of thought.
      "Semmelweiss reasoned that dirty hands were the cause of pueperal
fever. He noted that wards staffed by medical students had about a 10 percent
mortality rate due to fever, while those staffed by midwives had... 3 percent... He also
knew that medical students went straight from autopsy chambers to laboring mothers.
They [the med students] never washed their hands, but wiped them, instead, on aprons
already coated with body fluids.
      "Semmelweiss ran several experiments requiring students to wash their
hands with soap and water and rinse them in chlorinated lime solution before
entering the wards. With each study, the death rate dropped to less than 1.5 percent,
only to return to the previous high levels when the [hand washing] procedures were
curtailed. 
      "Semmelweiss's work should have proven to be a boon to motherhood and
life. Not so. His colleagues greeted his paper with jeers and scathing attacks on
his character. They simply refused to believe that their own hands were the
vehicle for disease. Instead, they attributed it to a spontaneous phenomenon arising
from the 'combustible' nature of the parturient woman. Semmelweiss's academic rank was
lowered, his hospital priveleges restricted. Despondent, he was committed
to an insane asylum, where he died of blood poisoning, a disease not unlike the
puerperal fever he had almost conquered." (2)
 

The relationship between (a) Semmelweiss's data and recommendations and (b)
his medical school's professors, bureaucrats, and their colleagues has
parallels in the modern-days relationship between (i) new data from parental anecdotes and
from a few, daring autism researchers, and (ii) the espoused beliefs of and funding
patterns enforced by key personnel within the NIH, the NIMH, and their
affiliated subsidiaries we think of as "medical school research facilities". Let us
consider two parallels between how Semmelweiss was treated and how the NIH and NIMH
react to new data in autism-spectrum syndromes:
      1: Initially and for many years, new data are strongly ignored; then,
they are resisted; and finally, if a person espouses those data and is persistent in
seeking to explore their ramifications, then he or she becomes shunned and
excluded. That these reactions occur leads to a second ramification significant to autism
research in the 1990s and beyond.
      2: Despite the new data and its acceptance by many individuals, the
data and *ramifications* of that data tend to remain ignored by highly placed medical
bureaucrats. As a result, medical practices that ought change because of
the new data's signficance do not change; and people entrenched within the old
paradigm (now made outmoded by the new data) do their best to enforce the old paradigm --
and do so despite the fact that the new data suggest better methods of treatment,
diagnostics, or research.

During Semmelweiss's era, advances in agriculture and in sanitary practices
(ie, events progressing *outside* of medical schools and teaching hospitals) were
alleviating much human suffering, but women amidst childbearing were not so
fortunate; they continued to die at needlessly high rates. After
summarizing health-related progress in the 19th Century, Achterberg writes:
      "None of the advances in health affected the abominably high infant and
maternal mortality rates, however. The risks to life in giving birth and
being born were exacerbated to epidemic proportions as increasing numbers of women
gave birth in hospitals." (2)

      In other words, there was a very real cost -- prolonged human
suffering, even numerous deaths -- because despite the data collected and shared by Dr.
Semmelweiss, medical-research officials of his day were defiantly resistant to change.
      Similarly, keeping Dr. Semmelweiss's fate in mind, we wonder in 
regard to autism, how many years will new data be ignored? In how many U.S. medical
school research facilities will promising research be steered away from or squelched?
      What will be required to cause the NIH and NIMH to quit acting like the
officials who suppressed Semmelweiss and instead to begin acting like sincere
scientists who appreciate new data, even as paradigms must adapt or be
replaced.

My own hunch is that the NIH and NIMH will not change from within; the senior
practitioners of the "it's gotta be genetic" model have too much influence.
Just as Semmelweiss and his data were suppressed, so too will the NIH/NIMH
autism-research insiders continue to act against the the growing body of new data in
autism; the NIH's pro-genetic old-timers will cling to their paradigm and its funding.
As a result, change within the NIH and NIMH will have to be initiated from
outside those tax-supported corporations.

As a goal for 1999 and beyond, I offer that parents and their
organizations and foundations increase the pressure brought to bear upon the NIH and the NIMH in
regard to how autism-research funds are allocated. The "it's gotta be
genetic" model is no longer the only paradigm worthy of funding; and not to fund other
models and other data in autism is no longer scientifically valid. The NIH and the
NIHM are re-enacting the Ignaz Semmelweiss scenario wherein new data are ignored on
behalf of an old-guard and its outmoded paradigm; autism children and their parents
deserve far more. The paradigm-shift in autism must occur more rapidly, even within
the NIH.
 

Teresa Binstock
Researcher in Developmental and Behavioral Neuroanatomy
 

(1) See autism-list posts by Ray Gallup or Bob Jensen for further
discussion and important points.
(2) Jeanne Achterberg; p110-111; Woman As Healer. Shambhala Publications,
Inc.; Boston, 1990.
      Teresa comments: this is an excellent, readable book offering many
insights about the history of healing, herbs, and midwifery, focusing upon the role
of women, including during the Inquisition, when women with knowledge of healing and
herbs ofter were killed as "witches".
 
 

Any information obtained here is not to be construed as medical or  legal advice. The decision to
vaccinate and how you implement that decision is yours and yours alone.


 


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