Dr. Dan L. Edmunds, Ed.D,B.C.S.A.,DAPA.

Dr. Dan L. Edmunds, Ed.D,B.C.S.A.,DAPA.
e-mail: batushkad@yahoo.com

Tuesday, November 06, 2007

10 REASONSTO SAY NO TO PSYCHIATRIC DRUGS

1. Premium Non Notre...or...Do no Harm.

* Drugs create altered states of mind by artificially increasing or decreasing neuro-functioning, and this causes harm to neuroconnections (e.g. downregulation, upregulation, tardive dyskinesia, EPS, Allostatic load, etc…) See reference list.

2. Use least intrusive method possible when treating.

* It is less intrusive to conduct psychotherapy than to administer a psychotropic mood and thought altering drug that always carries negative side effects. Drugs “work” by causing brain pathology and disrupting the normal neurotransmitter functioning and levels. See reference list.

3. Psychotherapy is MORE EFFECITVE than Drugs, especially in the long run.

* Psychotherapy is more effective than medication, especially in the long run, and psychotherapy plus medications show no greater benefit than therapy alone.(There are numerous studies showing this effect, most notably: Effectiveness of Psychotherapy: Michigan State Study. Seligman, M., **Consumer Reports, 1995.)

* Even exercise shows greater benefits for symptom reduction than anti-depressant medications. (Mercola, J., British Journal of Sports Medicine, April 2001: 35: p.114-117.)

* Psychotherapy can work better than drugs even for insomnia. (U.S. News and World Health Report, December 3, 2004. Visit www.behavioralhealth.typepad.com)

* Recovery rates are almost 3 times better in unindustrialized countries than in the U.S., where we use psychotropic drugs to “treat” patients. It is quite simple as to why we suffer more by attempting to suppress our suffering with technology. Freud stated “civilization is the root of our neurosis.”

Harrison, G., Hopper, K., Craig, T., Laska, E., et al. (2001). Recovery from psychotic illness: a 15- and 25- year international follow-up study. British Journal of Psychiatry, 178, 506-17.

Hopper K. & Wanderling J. (2000). Revisiting the developed versus developing country distinction in course and outcome in schizophrenia: results from ISoS, the WHO collaborative follow-up project. International Study of Schizophrenia. Schizophrenia Bulletin, 26(4), 835-46.

Hopper, K., Harrison, G., Aleksander, J., & Sartiorius, N. (2004, In Press). Recovery from schizophrenia: An international perspective. Madison, Connecticutt: International Universities Press, Inc.

Indian Journal of Medical Research, August 2004; WHO studies published in 1992 and 1996; US SAMHSA; Washington Post.

Jablensky, A., Sartorius, N., Ernberg, G., Anker, M., Korten, A., Cooper, J. E., Day, R., Bertelsen, A. (1992). Schizophrenia: Manifestations, incidence and course in different cultures, a World Health Organization ten country study. Psychological Medicine Monograph Supplement 20, 1-95.

Leff, J., Sartorius, N., Jablensky, A., Korten, A., & Ernberg, G. (1992). The international pilot study of schizophrenia: five-year follow-up findings. Psychological Medicine, 22, 131-145.

Murphy, H. B. & Raman, A.C. (1971). The chronicity of schizophrenia in indigenous tropical peoples: Results of a 12 year follow-up survey in Mauritius. British Journal of Psychiatry, 118, 489-97.

* Psychological interventions are at least as effective as pharmacological treatments for depression (Antonuccio et al., 1995; DeRubeis et al. 1999.)

* Even for people diagnosed Schizophrenic (no or minimal drug usage references):

Alanen, Y.O.; Ugelstad, E.; Armelius, B.A.; Lehtinen, K.; Rosenbaum, B.; and Sjostrom, R., Eds. (1994) Early treatment for schizophrenic patients: Scandinavian psychotherapeutic approaches. Oslo, Norway: Scandinavian University Press.

Alanen, Y.O.; Lehtinen, V.; Lehtinen, K.; Aaltonen, J.; and Rakkolainen, V. (2000) The Finnish model for early treatment of schizophrenia and related psychoses. In: Martindale, B., Bateman, A., Crowe, M., and Margison, F., Eds. Psychosis:

Psychological approaches and their effectiveness. London: Gaskell. (The centerpiece of their approach is rapid in-home family and social network intervention to avoid hospitalization and medicalization.) Ciompi, L., Duwalder, H.-P., Maier, C., Aebi, E., Trutsch, K., Kupper, Z., & Rutishauser, C. (1992). The pilot project "Soteria Berne": Clinical experiences and results. British Journal of Psychiatry, 161(suppl. 18), 145-153. (A replication of Mosher and co-workers Soteria Project in California. Similar results-about 2/3rds of newly diagnosed psychotics recovered without neuroleptic drug treatment)

Lehtinen, V. et. al. (2000). Two-Year Follow-up of First Episode Psychosis Treated According to an Integrated Model: Is immediate neuroleptisation always needed? European Psychiatry, 15(5): 312-320. (44% of the randomly assigned subjects received no neuroleptic drug treatment-vs. 6% of the controls- over the two-year period and their outcomes were comparable or better than those treated with drugs.)

Matthews SM, Roper MT, Mosher LR, and Menn AZ. (1979) A non-neuroleptic treatment for schizophrenia: Analysis of the two-year post-discharge risk of relapse. Schiz. Bull. 5: 322-333. (Soteria treated patients-as compared with hospital treated-had a significantly lower rehospitalizaton rate over two years despite few being neuroleptic maintained. First cohort analysis)

Mosher, L.R. & Bola, J.R. (2000) The Soteria Project: Twenty-five Years of Swimming Upriver. Complexity and Change, 9: 68-74. (Soteria patients-43%- who received no neuroleptics over the two year follow-up period did substantially better than those who did. As a group the Soteria treated patients had better outcomes than a control group that received "usual" hospital and drug treatment. The subgroup of "poor prognosis" subjects treated at Soteria had better outcomes than the Soteria group as a whole. First combined cohort analysis)

Mosher LR & Menn A Z (1978) Community residential treatment fornschizophrenia: Two-year follow-up. Hosp Comm Psych 29: 715-723. (Better psychosocialoutcomes for Soteria treated 1st and 2nd episode patients compared with control subject receiving "usual" treatment. First cohort.)

Mosher LR, Vallone R, and Menn AZ .(1995) The treatment of acute psychosis without neuroleptics: Six-week psychopathology outcome data from the Soteria project. Int. J. Soc. Psych. 41: 157-173. (2nd cohort: as was true of the 1st cohort, at six weeks the Soteria group had improved as much without meds as the hospital group-all of whom received neuroleptics.)

Tuori, T. et al (1998) The Finnish National Schizophrenia Project 1981-1987: 10 year evaluate on of its results. Acta. Psychiatrica Scandinavica 97: 10-18. (In the presence of comprehensive "need adapted"psychosocial treatment, drugs are unneccesary for the most part and may, in fact, prevent recovery.)

4. No Evidence for Biological Basis, so Why Use Biological Intervention?

* "There is no definitive lesion, laboratory test, or abnormality in brain tissue that can identify mental illness." in Surgeon General's report on mental health December, 1999.

* “psychiatry is the only medical specialty that…treats disorders without clearly known causes…including disabling diseases such as schizophrenia.” In American Psychiatric Association. (1998). Textbook of Psychopharmacology.Washinton, DC: American Psychiatric Press, AND American Psychiatric Association. (1999). Textbook of psychiatry. Washington, DC: American Psychiatric Press. (Texts used by Psychiatry Students)

*"Brain Disease Hypothesis for Schizophrenia Disconfirmed by All Evidence" by Al Siebert, PhD., Ethical Human Sciences and Services, Vol 1, No. 2 1999

* “there are no data to indicate that ADHD is due to a brain malfunction...After years of clinical research and experience with ADHD, our knowledge about the cause or causes of ADHD remain largely speculative." Nov. 1998 National Institute Health (NIH) Consensus Conference on ADHD concluded (see quote above).

* Leo, J. & Cohen, D., Broken Brains or Flawed Studies: A Critical Review of Neuroimaging Research, In The Journal of Mind and Behavior, Winter 2003, Volume 24, Number 1, pp 29-56

* Joseph, J. (1998). The equal environment assumption of the classical twin method: A critical analysis. Journal of Mind and Behavior, 19, 325-358.


* Joseph, J. (1999). A critique of the Finnish Adoptive Family Study of Schizophrenia. Journal of Mind and Behavior, 20, 133-154.

5. Psychotropic Drugs Create, not correct, Chemical Imbalances & Disorders.

* Psychotropic drugs create potential permanent Downregulation and Upregulation: increasing the susceptibility to having the very symptoms or problem they are attempting to reduce. Dr. Peter Breggin, MD, Harvard Graduate, Psychiatrist and Researcher, Breggin, P. & D. Cohen. (2000). Your Drug May Be Your Problem: How and Why to Stop Taking Psychiatric Medication. New York: Perseus Books. Also see Grace Jackson, M.D.(2005) Rethinking Psychiatric Drugs: A guide to Informed Consent.

* Untreated Initial Psychosis: Relation to Cognitive Deficits and Brain Morphology in First-Episode Schizophrenia, by Ho, Alicata, Ward, Moser, O'lLeary, Arndt, and Andreasen, American Journal of Psychiatry 2003; 160:142-148. This studies' "results suggest that large-scale initiatives designed to prevent neural injury through early intervention in the prepsychotic or early psychosis phase may be based on incorrect assumptions that neurotoxicity or cognitive deterioration may be avoided.

6. Many Psychotropic Drugs Increase Risk of Suicide-Aggression.

* Taking almost all of the SSRI antidepressants increase the patient’s risk of having and acting upon suicidal thoughts, agitation and akathisia. Dr. David Healy, MD, medico-legal expert witness/researcher, former Director of North Wales Dept. of Psychological Medicine and Secretary of British Association of Psychopharmacology, author of over 120 peer reviewed articles and 12 books.

7. We Don’t Really Know If The Drugs Are Safe or Risks All Known.

* “Our current drug approval system has demonstrated that we don’t always understand the full magnitude of drug risks prior to approval of products.”

Dr. Steve Galson, director of FDA’s Center for Drug Evaluation and Research,reported in the N.Y. Times, Nov. 6, 2004, in FDA’s Drug Safety System Will Get Outside Review.

* Since 1997, almost two dozen prescription drugs have been taken off the market due to serious side effects–some causing numerous deaths. (http://www.pbs.org/wgbh/pages/frontline/shows/prescription/hazard/)

* Whitaker, R., The case against antipsychotic drugs: a 50-year record of doing more harm than good, Medical Hypotheses, Volume 62, Issue 1 , 2004, Pages 5-13.

8. Drugging your problem is MORE Expensive.

* Psychotherapy is Less Costly Than Drugs, basically because suppressing the problem does not help you work through, solve, HEAL, AND because therapy produces natural brain changes (Antonuccio et al. 1997; Cuijpers, 1997; Smith et al, 1997.) Especially since psychological treatments can be successfully delivered in a group format or even as bibliotherapy with minimal therapist contact.

* Pharmacotherapy alone increases vulnerability to depression relapse (Hollon et al, 1991; Segal et al, 1999) and there is virtually no evidence of antidepressant efficacy in children (Ambrosini et al, 1993; Hazell et al., 1995.)

9. Drugs simply do not work.

* Greenberg et al in 1992 outlined how effects of medication were significantly smaller than normally reported.

* Approximately 75%-90% of sugar pills were EQUALLY EFFECTIVE as SSRI-Antidepressant drugs, and that when the sugar pill-placebo gave a side effect,there was NO CLINICAL DIFFERNCE BETWEEN THE DRUG AND THESUGAR PILL. (J. Moncrieff & I. Kirsch, July 16, 2005, British Medical Journal, doi:10.1136/bmj.331.7509.155 2005;331;155-157 BMJ.

* Kirsch, I,. & J. Thomas, at el, The Emperor's New Drugs: An Analysis of Antidepressant Medication Data Submitted to the U.S. Food and Drug Administration,, In Prevention & Treatment, Volume 5, Article 23, posted July 15, 2002.

10. Saying Yes to a Psychotropic Drug is almost Never an Informed Choice.

1 comment:

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