Life Dynamics and Jill Stanek: Groundbreaking Legal Means to Stop Child Predators

As many pro-lifers know, Jill Stanek has joined with Life Dynamics to report news on the life issues. She’s now reporting on a groundbreaking push by Life Dynamics to hold the abortion industry accountable for concealing the sexual abuse of minors.
This blog has repeatedly referred to the first study, done more than 10 years ago by Life Dynamics, which revealed that over 90 percent of abortion clinics, who were called by an actress portraying a 13 year old girl with 22 year old boyfriend, showed a willingness to flout the laws requiring reporting of suspected sexual abuse of minors. Many of these abortion clinics even provided the methodology to conceal the sexual abuse.
Now Life Dynamics has mailed CDs to 53 thousand personal injury attorneys to educate them on the state laws pertinent to this issue, and the possibility of bringing suit against school officials, health care professionals and clinics which provide services to minors who have been sexually abused by adults, and fail in their legal requirement to report such abuse to the state.
Jill Stanek reports that Mark Crutcher’s phone at Life Dynamics has been ringing incessantly ever since launching this campaign.

Your friendly Pharmer suggests that further rich ground for the lawyers exists and that fear of litigation can dissuade retail pharmacies from stocking Plan B and Ella.

The government can force retailers to sell these drugs to the sexual predators, only if they stock the drug.
In the future, lawsuits might be the tool to stop the government from forcing retailers to stock these drugs. None of the businesses could survive a group of civil lawsuits for aiding sexual predators.

Currently good target states for this kind of litigation are Washington, Oregon and of course, New York. The large retail pharmacy chains would run screaming to the State Boards of Pharmacy for relief from the governments requirement to sell these drugs to minor females and their rapists.

Life Dynamics Facebook Announcement of the Campaign to Educate Personal Injury Attorneys.

WND Article explains Life Dyanamics Campaign to Legally Restrain the Enablers of Child Sex Abuse

 

Caution to People Who Rejoice over 2009 CDC Abortion Data

New CDC data shows bungled abortion reporting in 2009.

Everyone is all abuzz over the 5% reduction in abortions shown in the 2009 CDC data. Instead they should be digging a bit deeper to see if the data really represents reality. Some pro-lifers target the reporters who expected an increase in abortions due to the economy. It’s true that poverty for women rose in 2009 and continues to do so.

The CDC is only able to count reported abortions, and therefore the data is necessarily incomplete. State laws requiring abortion reporting to a central agency vary from non-existent to un-enforceable.

The opportunity to induce home abortions and have them completed at hospitals has increased. These events cannot be reported as abortions unless the mom admits to doing something illegal, or accuses someone else of doing something illegal to her. Internet commerce has made home abortion chemistry much more accessible than in the past. Therefore it is unlikely that any numbers reported by the CDC are available. More recently Ulipristal acetate (Ella) has become available with online prescribing, providing a newer home abortion option using accumulated doses.

It should be noted that even without the above consideration, the CDC data on surgical plus mifepristone abortion is not comprehensive.

So far the joyful articles reporting the CDC abortion data of 2009 did not mention the LIMITATIONS section of the report, part of which is quoted below. Note that the CDC only reports 65 -69% of the abortions which are reported by the Alan Guttmacher Institute. Read on:

“The findings in this report are subject to at least four limitations. First, because reporting requirements are established by the individual reporting areas (17), the collection of data varies, and CDC is unable to obtain the total number of abortions performed in the United States. During the period covered by this report, the total annual number of abortions recorded by CDC was 65%–69% of the number recorded by the Guttmacher Institute (12,59), which uses numerous active follow-up techniques to increase the completeness of the data obtained through its periodic national census of abortion providers (12). Although most reporting areas collect and send abortion data to CDC, this information is given to CDC voluntarily. Consequently, during 2000–2009, seven of the 52 reporting areas did not provide CDC data on a consistent annual basis, and for 2009, CDC did not obtain any information from California, Delaware, Maryland, or New Hampshire.***** In addition, whereas most of the reporting areas that send abortion data to CDC have laws requiring medical providers to submit a report for every abortion they perform to a central health agency, in New Jersey and the District of Columbia, medical providers submit this information voluntarily (16). As a result, the abortion numbers these areas report to CDC are incomplete.††††† Moreover, even in states that legally require medical providers to submit a report for all the abortions they perform, enforcement of this requirement varies (60). Consequently, several other reporting areas tend to provide CDC with incomplete numbers.”

http://www.homeabortion.info/index.html

The Reason for FDA Approval of Ella, Ulipristal Acetate is HERE

RU—Serious? Jennie McCormack, the Next “Roe”? Good Grief | LifeNews.com.

Jennie McCormack aborted her 5 month unborn baby using mifepristone and misoprostil which she purchased online.
She was charged for illegally obtaining those drugs, doing a home abortion, and violating the ban on abortions after 20 weeks. She is appealing her convictions with the 9th Circuit Court of Appeals.

The FDA approved Ella for use as a morning after pill in an effort to provide another avenue for procurement of drugs for home abortions. Ella, ulipristal acetate, is a chemical analog of RU-456, mifepristone, and, in sufficient doses, operates by the same mechanism. Ella can be obtained from an online pharmacy in Utah, and doing so would circumvent one of the laws which McCormack has broken in her home state of Idaho.

For NYT, Evaluating Birth Control Mechanisms is Classed as POLITICAL SCIENCE

Science at Issue in Debate on Morning-After Pill – NYTimes.com.

Pharmer is immensely amused by the NYT Political Science article purporting that Plan B, levonorgestrel (a progestin – synthetic progesterone analog) delays ovulation but has no effect upon post fertilization mechanisms. This claim certainly has a relationship to political ideology, but not to pharmacological science.

There is the suggestion that Plan B can operate to impede ovulation even when taken 72 hours after intercourse.

The usual life of sperm is 48 hours, and The usual lifespan of secondary oocytes (eggs) is 1 day. The most fertile time for a woman is the day of, and the day after ovulation.

Laughably entertaining is the suggestion that there is no time for levonorgestrel to affect thickness or receptivity of the uterine lining, but there is time for it to always work by delaying ovulation. Scroll back up to the lifespan of the gametes and THEN ponder that it takes about 7 days for the early human embryo to travel down the fallopian tubes into the uterus and implant in the uterine lining.

Seven days is not long enough for the morning after pill to affect feedback inhibition, transport, endometrial tissue, and implantation processes, yet 48 hours is claimed to be long enough to exert a perfect 100 percent mechanism for delaying ovulation so that sperm and ‘egg’ don’t meet.  (Remember when a woman is most fertile, the day of and the day after ovulation?)   It’s pathetic when leftist ideology replaces scientific analysis and inquiry in such a blatantly obvious manner.

James Trussell (population controller of Princeton) has changed his tune about the efficacy of Plan B. Now he wants to say that the pill is ridiculously ineffective, so that condoms, rhythm, and withdrawal are far superior in efficacy as birth control. This is what he needs to admit in order to claim that the Plan B doesn’t work if a woman has ovulated.

Progesterone hormones have multiple mechanisms of action. Progesterone receptors are found in various tissues, and their preponderance and activity undergo cyclic changes. These hormones largely affect gene expression. These effects are not instantaneous. The physiological effects of progestins on reproduction vary with the timing of their use. The morning after pill’s modes of action will vary depending on when in the cycle and how long after intercourse they are used.

One cannot prescribe progestins to patients to mitigate hypermenorrhea (excessive bleeding), and at the same time claim that they don’t affect the uterine lining.

Progestins given on a scheduled basis fail to prevent ovulation in about half of patients. This has been attached to the labeling of progestin only pills, which have been used to control excessive bleeding, as well as to prevent pregnancy.

Plan B is a progestin. Ella is a selective progesterone receptor blocker (like mifepristone, RU456). Each one will affect the reproductive processes in different, dose dependent and time dependent ways. Political Science author Pam Belluck needs to consider the drugs separately when attempting to evaluate them mechanistically.

Plan B, levonorgestrel, like ALL hormones, operates on many physiological processes, by many different means.

If the leftists ever manage to develop effective birth control drugs which operate ONLY by preventing the union of sperm and egg, we may proceed with the constitutional amendments to accurately define human life with no further impediments.

More at Jill Stanek’s place. and right HERE.

Stanek weekend question: Why would a group promoting emergency contraception encourage men to buy it? – Jill Stanek

Stanek weekend question: Why would a group promoting emergency contraception encourage men to buy it? – Jill Stanek.

Found at the backupyourbirthcontrol site was encouragement for males to buy emergency contraception for their sex partners.  There seems to be huge support and encouragement people to have sex with those whom they don’t really like.  Jill Stanek’s weekend question got right to the heart of the matter, and bears repeating.

Plan B One-step (levonorgestrel 150 mcg) is the form which is available over the counter, and which may be purchased by both males and females.
Here is a Blast from the Past from pharmacy academics who favored the availability of the original Plan B  for use in  underage females.  This was the intended result of bringing the drug over the counter.
(If you read the entirety of  THIS article, you can appreciate the utter incompetence of one of the academics referenced in the Blast from the past link.)

It’s  important to remember that these morning after pills are NOT very effective.  The efficacy  is about 60 percent per SINGLE use.   Used repeatedly, the drugs are an absolute joke for preventing pregnancy.  Encouraging reliance upon the morning after pills (Ella included) is really an efficient  way to sell surgical or later forms of chemical abortions.   Encouraging guys to believe that the pill can increase their access to sex is a smart marketing move for the abortionists.  It also places the health and well being of girls and women at risk, since males can give them the drug without their consent.

It is a public service for Jill Stanek to have asked this question about the marketing of morning after pills to males.  This question needs to be repeated whenever and wherever possible, to highlight the rationale behind the morning after pills.

Ella  (ulipristal acetate, analog of RU-486 mifepristone) is available for morning after use by an ONLINE PRESCRIBING process.   It’s easy to obtain fraudulently and doses can be accumulated for later chemical abortions initiated at home.   This mechanism was allowed by the FDA in order to make up for the shortfall of physicians willing to do surgical abortions.

The only positive aspect of this scenario is that it is ultimately self-limiting.  Enhanced by the immunosuppressive qualities of the progestins, Chlamydia trachomatis and other STD organisms can help to prevent further propagation of people with this socially destructive mindset.

Idaho Pharmacist Refused to Dispense Planned Parenthood Prescription Cleared of Wrongdoing

Planned Parenthood continues its harassment of an Idaho Pharmacist who refused to dispense an order for methergine, nor give a referral.

The media, acting as mouthpiece for Planned Parenthood’s version of the story gives the following outline.

The pharmacist took a call from planned parenthood about an order for methergine (which is used to stem bleeding after delivery, miscarriage, abortion). The pharmacist is said to have asked if this was related to an abortion procedure. The planned parenthood nurse would not answer, citing the privacy of the patient.
The pharmacist allegedly refused to take the order, and also did not refer the nurse to another pharmacy. She is said to have hung up the phone on planned parenthood.  (smile). And ask yourself why planned parenthood is doing abortions without this hemostatic drug on the premises. Isn’t that dangerous?

We do not have the pharmacist’s version of the story. We do have the people at Second Hand Smoke weighing in on this case, and pondering whether the pharmacist did the right thing, and was within the scope of Idaho pharmacy practice standards. As many of them had insufficient data and background to address this topic,  Pharmer was only too happy to assist them in their cogitations as follows:

Someone thinks that oral methergine is going to sufficiently address the kind of uncontrolled bleeding that can kill a patient in minutes.

Another person thinks that pharmacists should not have the patient’s medical history.

Without information as to what is being treated, the pharmacist can’t check the safety and appropriateness of the prescription. Under these conditions, the prescription should not be filled.

There are some people who should avoid health care practice due to incompetence.

At my place of employment I correct numerous physician orders each shift. This is a necessary part of my job function as a pharmacist. I also tell the physicians and nurses how to use the meds (to avoid these errors). When I was a retail pharmacist, I obtained changes in prescriptions on a regular basis. I refused to fill some prescriptions due to dangerous drug interactions, etc. I refused to stock and dispense Redux, which is now off the market, because I knew better than the FDA, at the time, that taking this drug was not worth the risk.

The pharmacist in this case was correct to refuse a prescription from a prescriber who was unwilling to verify that the prescription was within the scope of his or her practice. Pharmacists need that information to know if the prescription is legitimate and “legal to dispense”. In addition, prescriptions from Planned Parenthood should be scrutinized to see if they really have been authorized by a licensed prescriber. It appears from the story that the Planned Parenthood agent was not being cooperative with respect to providing information relevant to the prescription, and the pharmacist may have had good legal and clinical reason to avoid taking the order. Not much is really known about this case since the info is coming mainly from planned parenthood, and its media mouthpiece.

If a woman came to me AFTER the fact with a prescription for methergine, I would fill it, (and have done that in retail practice). At that time, the drug is not a part of the abortion procedure.

I would not fill a prescription which could be preliminary or a part of the actual abortion regimen.

With the availability of Ella, (ulipristal acetate) which operates in the same way as RU-486- (mifepristone), there will be many related conundrums for hospitals which don’t normally do abortions. Ulipristal at 0.5mg/kg is used as a morning after pill. The doses can be combined to use for later chemical abortions. Expect many “miscarraiges”, “missed ABs”, D&Cs to be followed up at legitimate hospitals after the woman has used ulipristal to kill her baby in the embryonic stage of development. This is a significant reason for bringing Ella to market as a morning after pill: to allow its “off label” use and finish up chemical abortions at legitimate facilities, thus dodging much of the stigma and personal $ cost associated with abortion. It is also a means to deal with the decreasing supply of abortionists.

The Idaho board has ruled that the pharmacist broke no state laws in alleged refusal to fill the prescription.

Planned Parenthood continues to harass the pharmacist by threatening to file a complaint with federal agencies.  This  is not likely to go anywhere, as this part of pharmacy practice is governed by state law.

Planned Parenthood also stuck its nose in the business of  the Pharmer  by intervening in an employment issue in which it had no legal standing.  This organization has a long history of using your tax money  (which accounts for at least a third of its income) to harass pro-life health care professionals in many different states.

Planned Parenthood has, for many years been involved in canvassing operations to locate pro-life pharmacists.  Pharmer has  received calls  to this end, and told the callers to do their own research.   Planned parenthood has sent people to “sting” CPCs and pro-life health care professionals.   For us, there is poetic justice in seeing the work of LiveAction.org, and seeing it reveal publicly  what we’ve heard all along from their dissatisfied clientele.

*Compare the Planned Parenthood complaint to the Idaho Pharmacy Board with the media feed on this issue.    Hook- Line and Sinker.

FDA Approves Ulipristal acetate as Expected

Watson is the generic drug manufacturer which is expected to distribute EllaOne in the US, now that the FDA has approved it for use as a morning after pill.

Headlining at Pharmacists for Life International is a low opinion of the FDA’s decision to spend time on this me-too analog of the abortive drug, mifepristone (RU486), and allow the marketing as a morning after pill.
Below is what Pharmer sent to Rob Stein of the Washington post, at his request. It’s possibly not translatable into language understandable by that newspaper’s readers.

On the sidebar and searchable on this blog is further information on Ulipristal acetate, coming soon to the US, for use in underage girls, (without parental consent) and by women who are ill-informed about the drug and its effects.

Reply to request for statement on the impending approval of Ulipristal:

Ulipristal Acetate, according to its developers, can kill embryos and fetuses, and is marketed in Europe as EllaOne. The low dose 30mg form, has been prioritized for approval by the FDA, which would have served us better by adequately addressing the current, rolling shortages of lifesaving and essential medications.

The embryocidal, ulipristal acetate doses may be accumulated by physicians or patients for medical abortions at home, sidestepping the so-called regulation of mifepristone/misoprostil (the other abortion drug). This will lead to additional life-endangering problems for the targeted adolescent girls and women.

The FDA is expected to continue in its long tradition of relegating females to bottom class health care status.

Reply when asked if pharmacists would refuse to dispense it:

Pharmacists were excused from handling mifepristone/misoprostil, and most were relieved to be sheltered from the ethical and legal liabilities.
The majority would not like providing information and dispensing ulipristal, since it is an analog of mifepristone. Expect attempts to force pharmacists to do so.

If you were to juxtapose the issue of severe drug shortages and the approval of this ‘me-too’, abortifacient in a survey of pharmacists, the majority would express the opinion that the FDA is nearly useless.

Personal note to Rob Stein concerning the FDA’s action:

In my place of employment is a gigantic board listing the shortages and outages of essential medications, such as antibiotics, pain relievers, anaesthetics and drugs for sedation.This problem has been significant for years, and has worsened considerably in the last year, impeding our ability to provide vital care for our patients.

The FDA has placed the approval of this duplicate analog of mifepristone ahead of need to address this severe health care issue. My disrespect for the FDA is profound and beyond the ability to verbalize.