(A4e3a1b) non-surgical abortions


The so-called "contraceptive" pill is an abortifacient, as are the I.U.D. and the "morning after pill". ******* As of this date, 04-03-15, this folder contains 3 items. ******* item 1 THE DANGERS OF THE "MORNING AFTER" PILL ******* item 2 MORNING AFTER ABORTION PILL UPDATE ******* item 3 HOLLY PATTERSON'S PARENTS SAY ABORTION DEATHS WIDELY UNDERREPORTED ************************************************************************************************************************ ******* item 1 THE DANGERS OF THE "MORNING AFTER" PILL ******* From: [email protected] ******* Date: Mon, 15 Mar 2004 ******* Dear Colleague: ******* This May, the American Federal Drug Administration (FDA) is expected to either approve or disapprove over-the-counter (OTC) availability of so-called "emergency contraception"(EC), the morning-after pill (MAP). ******* Last week, PRI's Weekly Briefing focused on the risks of MAP to adolescents. Morning-after pills are dangerous not only to teens, but to all women. ******* Given these dangers, we urge the FDA to disapprove OTC distribution of the morning-after pill. ******* Steven Mosher, President, PRI Weekly Briefing, 12 March 2004, Vol. 6 / No. 10 ******* In the mid-nineties, the World Health Organization (WHO) began to realize that increased access to routine methods of contraception led to increased rates of abortion. So a new method of post-coital "contraception" was zealously sought and promoted: the morning-after pill.(1) ******* Despite subsequent WHO studies which described routine post-coital contraception as "unsuitable primarily because of the high incidence of cycle disturbances",(2) efforts to approve and market MAP globally continued. Today, these efforts have washed up on our shores, in the form of Women's Capital Corporation/Barr Laboratories' application to the FDA to approve MAP for over-the-counter distribution. Women's Capital Corporation is the manufacturer of the Plan B morning-after pill. ******* As the evidence shows, these efforts are motivated by ideology and profit, not by concern for the health and well-being of women. ******* Even the notorious abortion promoter, David A Grimes, MD, who was a presenter for Plan B's manufacturer before the FDA advisory committee in December 2003, acknowledged in a 2002 interview that MAP have a serious negative effect on a woman's menstrual cycle: "Repeated use of EC wreaks havoc on a woman's cycle", Grimes said, "so the resulting menstrual chaos acts as a powerful deterrent to using this method too often."(3) In fact, the menstrual chaos Grimes warns about does not deter women from repeated and routine use of MAP, as studies have shown. But MAP-induced menstrual irregularities do make it hard for women to determine whether or not they are pregnant or experiencing delayed menses. ******* At home and abroad, the abortion, family planning, and population control groups which seek to promote MAP ignore the scientifically-proven risks of levonorgestrel (the sole active ingredient of Plan B MAP). These well-documented adverse side effects include significant weight gain (on average 15 pounds), depression, ovarian cyst enlargement, gallbladder disease, high blood pressure, respiratory disorders,(4) increased risk of ectopic pregnancy (5) and death. In some women, these serious adverse effects of levonorgestrel-type MAP could lead to further health risks for bulimia, anorexia, or clinical depression. ******* While these risks are multiplied with increased use, the advocates of MAP promote its increased, frequent, and repeated use. From the makers of Plan-B, MAP "can be provided as frequently as needed",(6) as if it were candy or Tums. The wholesale promotion by the profiteers is undercut by solid evidence, and warnings advising women and physicians to limit usage, or to not use it at all.(7) Norplant, the drug very similar to Plan B, was linked to severe medical problems which were never adequately studied or acknowledged by the FDA or the drug manufacturer (please see PRI's Norplant Information page, posted at http://www.pop.org/main.cfm?id=197&r1=2.25&r2=9.00&r3=0&r4=0&level=2&eid=368). ******* While public awareness of the dangers of MAP was steadily growing in the US, the international abortion community stepped up to the plate. In 2003, the International Consortium for Emergency Contraception stated that "Medical and behavioral research conducted to date does not provide any basis for limiting the number of times that women use ECPs [emergency contraceptive pills], in a year or in a month. . . . Women should use ECPs as often as needed."(8) No evidence was provided to back up this outlandish, politically motivated, assertion. ******* The international abortion community made MAP a routine part of its emergency health battery for displaced peoples. In Albania, a prominent clinic director lamented that young people especially "use it every time they have sexual intercourse."(9) ******* The "fear of pregnancy" factor in other countries has been used by international abortion peddlers to promote the chemical with no safeguards or restrictions, leading some women into taking increased dosages. One study from Hungary reported women taking 4-5 pills (3.0 to 3.75 mg total, which is 4-5 times the approved dose) as a first dose, followed by one .75 mg pill 12 hours later.(10) ******* Clearly, over-the-counter distribution of MAP would occasion misuse and overdose. Still, presenters for Women's Capital Corporation/Barr Laboratories blankly assured the FDA advisory committee that MAP are completely safe with "no potential for overdose . . . ." (11) ******* The total number of women damaged by MAP throughout the developing world is untallied. Today this threat is aimed at American women. ******* No doubt, the greatest risk of MAP is loss of human life. Packaging for MAP omits clear warnings of the risks and abortion-inducing function of the chemical. Women must be informed of the total risks of MAP, to themselves and their children. ******* Over-the-counter approval of MAP would unleash great harm on American women. The FDA should act to protect women and children by denying OTC approval for Plan B or any other MAP product. ******* ENDNOTES ******* 1. "Fuller Information and More Choice - The Responsible Way Ahead", Progress in Reproductive Health Research, 1995, No. 35, part 2. World Health Organization. Available at: www.who.int/reproductive-health/hrp/progress/35/news35_2.en.html. ******* 2. Mitchell D. Creinin, MD, "Emergency Contraception: More Than a Morning After Pill", Medscape General Medicine, 1999. Available at: www.medscape.com/viewarticle/408799. Without oversight of any medical professional, OTC/MAP will enable possible routine use by women and adolescents. ******* 3. Laurie Barclay, MD, "Over-the-Counter Emergency Contraception: A Newsmaker Interview with David A. Grimes, MD", Medscape Medical News, 2002. Available at: www.medscape.com/viewarticle/442258 Dr. Grimes is Vice President of Biomedical Affairs, Family Health International, Research Triangle Park, North Carolina. ******* 4. "Contraceptive Implants Come of Age", Progress in Reproductive Health Research No. 61, World Health Organization. Available at: www.who.int/reproductive-health/hrp/progress/61/news61.html. ******* 5. "A Communication to All Doctors from the Chief Medical Officer", Chief Medical Officer Update No. 35, U.K. Department of Health, January 2003. Available at www.doh.gov.uk/cmo/cmo_35.htm#20. ******* 6. "Health Professionals", Plan B Clinical Information. Available at: http://www.go2planb.com/section/health_professionals. ******* 7. G. Ugocsai, et al., "Scanning Electron Microscopic (SEM) Changes of the Endometrium in Women Taking High Doses of Levonorgestrel as Emergency Postcoital Contraception." Contraception 66: 433-437 (2002). The study also urges counseling for EC users "as the main side effect of breakthrough bleeding frequently occurs." ******* 8. "Repeated Use of Emergency Contraception: The Facts", International Consortium for Emergency Contraception, Policy Statement, July 2003. Available at www.cecinfo.org. ******* 9. Etlava Sahatci, "Lessons Learned From Family Planning and Contraception Programs in CEE/NIS Region,” 2002 Schweitzer Seminar Series, Albert Schweitzer Institute/Open Society Institute, Quinnipiac University. Available at www.quinnipiac.edu/x3363.xml. ******* 10. G. Ugocsai, et al. The short-term and long-term safety risks of such overdoses are unknown. Whether most women, especially adolescents, who overdose would seek medical care afterward is also unknown. ******* 11. Transcript, Nonprescription Drugs Advisory Committee in Joint Session with the Advisory Committee for Reproductive Health Drugs Meeting, Food and Drug Administration, December 16, 2003, P. 35. Transcript available at: www.fda.gov/ohrms/dockets/ac/03/transcripts/4015T1.pdf. ******* � 2004 Population Research Institute. Permission to reprint or use in any form granted. Credit requested. __________ If you would like to make a tax-deductible donation (U.S.A. only) to PRI, please go to https://pop.org/donate.cfm. All donations (of any size) are welcomed and appreciated. _________ PRI P.O. Box 1559 Front Royal, VA 22630 USA ******* Phone: (540) 622-5240 Fax: (540) 622-2728 ******* Email: [email protected] ******* Media Contact: Vince Criste ******* (540) 622-5240, ext. 206 ************************************************************************************************************************** ******* item 2 MORNING AFTER ABORTION PILL UPDATE ******* Date: Mon, 23 Feb 2004 ******* From: "Elliot Institute" ******* Dear Friend, ******* I've written before about the way women are being deceived about the morning after abortion pill. I hope you will take this occassion to review the following two articles. ******* "The Best Kept (ugly little) Secret in America" ******* www.afterabortion.org/PAR/V6/n4/birthcontrol.htm ******* The Morning After Abortion Pill Act ******* http://www.afterabortion.org/leg/Morningafter.htm ******* Now, I would also like to share with you the document below from pharmacist John Wilks. It gives a better and more up-to-date summary of the little known medical risks regarding use of the morning after abortion pill. ******* Wilks' list of risks underscores the fact that we are witnessing yet another population control experiment in which women are being treated with less respect than guinea pigs. At least in experiments involving guinea pigs only a limited number are exposed to the risks of an untested treatment and the experiment has a planned ending at which point the results are evaluated. In this case, unlimited numbers of women are being exposed to the dangers of this abortifacient and there is not even a plan to measure complications and determine its safety. The plan is simply, push it on the public and hope for the best. ******* For population controllers it is sufficient to prove that any new contraceptive/abortifacient successfully prevents births without causing immediate maternal death. As long as the method successfully prevents births, they will relentlessly promote it as the "latest best option" -- as has been done with the Pill, IUD's, Norplant, Depo Provera, et cetera. What we are witnessing is a shell game of dangerous birth control options. When women grow disenchanted with the side effects and cost of one, offer them another. ******* Meanwhile, effective, safe, and free natural family planning (NFP) methods based on periodic abstinence are mocked and dismissed because (a) pharmaceutical companies can't make money off of them, and (b) NFP methods underscore the importance of marriage, communication, and respect for life. ******* Enough of my commentary.... Here are the facts... ******* Yours for Life in Christ, ******* David C. Reardon, Ph.D. ******* P.S. I've been asked by CWA to also share with you the link below to documents they have compiled regarding the morning after pill abortion controversy. ******* http://www.cwfa.org/articles/5000/CWA/life/index.htm ------------------------- ******* WHY THIS PHARMACY DOES NOT SELL POSTINOR-2; THE "MORNING-AFTER" PILL MAP) ******* 1. Scientific studies have provided strong evidence indicating that for many women the �morning-after� pill (MAP) does not stop a pregnancy from occurring. Researchers have said that this drug acts in at least two ways to end a pregnancy that began at fertilization: ******* * By damaging the lining of the womb so that implantation of the human embryo � the unseen patient - cannot occur. [1] ******* * Research in mice has also indicated that if an embryo attaches to the womb, the body reabsorbs it, thereby ending the embryos life. [2] ******* Because the MAP can act via these two methods, it must be classified as an abortifacient � a drug that can cause an abortion.[3] The fact that the MAP reduces the expected pregnancy rate by 87% supports the claim that it frequently acts to end the life of a human embryo. [4] ******* Therefore, due to the danger to the health of the human embryo caused by the MAP, my Code of Professional Conduct, parts 1.1 and 1.2 forbids me from selling this drug.[5] ******* 2. The �morning-after� pill is also very dangerous to a woman�s health. Scientific reports have proved that: ******* * The �morning-after� pill causes an increase in the incidence of ectopic pregnancies (lodgement of the human embryo in the Fallopian tube rather than in the womb.) [6] In one of these cases the affected Fallopian tube had to be surgically removed. As a result these women have a greatly reduced possibility of a future pregnancy. ******* * The �morning-after� pill can also have serious interactions with prescribed medications. The British Medical Journal has reported that the �morning-after� pill can interfere with warfarin medications. [7] [8] ******* * Dr. Ellen Grant, writing in the Lancet (2001) has expressed the concern that �� 5% of women have a genetic susceptibility to thromboembolic disease (blood clots).� When these women take the �morning-after� pill � which is equal in strength to taking 50 regular birth control tablets � a blood clot might form. [9] ******* * There is concern that the very high dose of hormone taken in the �morning-after� pill might �kick-start� cervical cancer if a woman is already infected with human papilloma virus. [10] ******* In summary, because of these dangerous medical consequences associated with the �morning-after� pill and my professional duty-of care responsibilities, we do not sell Postinor-2. ******* John Wilks B.Pharm., MPS, MACPP Consultant Pharmacist. February 18th 2004 --------------------------------------------------------- ---------- ******* [1] Ugocsai G, Rozsa M, Ugocsai P. Scanning electron microscope (SEM) changes of the endometrium in women taking high doses of levonorgestrel as emergency postcoital contraception. Contraception. 2002;66:433-437 ******* [2] Shirley B, Bundren JC, McKinney S. Levonorgestrel as a postcoital contraceptive. Contraception. 1996:52(2):277-81 ******* [3] Moore KL, Persaud TVN. The Developing Human: Clinically Orientated Embryology (6th edition. Philadelphia: W.B. Saunders Company 1998), ******* [4] Wellbery C. Emergency Contraception. Arch Fam Med 2000; 9:642-64 ******* [5] Policy � Code of Professional Conduct. Pharmaceutical Society of Australia. Endorsed by National Council March 1998. ******* [6] Sheffer-Mimouni G, Pauzer D, Maslovitch S et al. Ectopic pregnancies following levonorgestrel contraception. Contraception. 2003;67:267-269 ******* [7] Ellison J, Thomson AJ, Greer IA. Apparent interaction between warfarin and levonorgestrel used for emergency contraception. BMJ. 2000;321:1382 ******* [8] Richards D. An Important drug interaction � an alternate mechanism. BMJ Rapid responses. 22 December 2000 ******* [9] Grant E. Adverse reactions and emergency contraception. Lancet. 2001;357:1201 ******* [10] Chen Y-H, Huang L-H, Chen T-M. Differential effects of progestins and estrogens on long control regions of human papillomavirus types 16 and 18. ******************************************************** ******* SUBSCRIPTION INFORMATION ******* To SUBSCRIBE, just send a blank email to ******* [email protected] ********************************************************************************************************************* ******* item 3 HOLLY PATTERSON'S PARENTS SAY ABORTION DEATHS WIDELY UNDERREPORTED ******* From: [email protected] ******* Date: Fri, 27 Feb 2004 05:02:13 EST ******* Washington, DC (LifeNews.com) -- The parents of Holly Peterson, who died after using a chemical abortion drug she obtained from Planned Parenthood, say they believe the number of women who have died after using the abortion pill is "widely underreported." ******* The statement comes after a state health agency found that the abortion business and a medical center that treated Holly before her death improperly reported Holly's abortion death to authorities. "We are appalled by the lack of reporting and accountability of Planned Parenthood and ValleyCare Medical Center to report Holly's death to the State of California DHS," Monty Patterson and his wife Helen said in a statement Wednesday. "If hospitals and abortion clinics don't feel they should be responsible to report a death to the state, what makes the FDA or the drug manufacturer believe they will consistently and accurately receive reports on adverse events or deaths related to drugs," the Patterson's added. A report released Tuesday by the California Department of Health Services in their investigation into the death of Holly Patterson reveals that Planned Parenthood failed to follow its own internal policies for informing women on how to use the RU 486 abortion drug that was responsible for Holly's death. ******* http://www.lifenews.com/nat353.html *********************************************************************************************************************

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The following warning is a prophetic message given to me, Frank Wagner, in November of 1974. ******* LISTEN TO THE CRY OF THE ABORTED CHILDREN. THEIR CRY IS NO. THEIR CRY IS A CRY OF TERROR. HEED THEIR CRY. ******* This prophecy is now being fulfilled. ******* For details about the source, meaning and fulfillment of this prophetic message go to ******* http://ca.geocities.com/fwagner4/index.html ******* email me at *** [email protected] ***

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