The risks associated with abortion remained elevated even after controlling for prior mental health, age, and poverty. But among women with prior mental health issues, psychiatric hospitalization was nine times more likely for those who had abortions. In contrast, among women without prior mental health issues, abortion was linked to only a 50% increased risk of psychiatric hospitalization.
The study from the Charlotte Lozier Institute (CLI) found that over 60% of women who had an abortion report a high level of external pressure to abort from one or more source. The study also found that these same women report higher levels of subsequent mental health and quality of life issues.
Pregnancy can bring about many emotions; sometimes excitement and fear can be conflated when a woman is left without ample support to contend with these feelings, and result in a heartbreaking decision.
Brittany found herself in this situation, and feeling she had no other choice she took the first abortion pill. Later she became convinced that God interceded on behalf of her baby.
The mechanism of abortion pill reversal is essentially the same mechanism often used to prevent miscarriage… the hormone progesterone. Only in this case, it’s aimed at reversing the effects of the abortion pill regimen. If a woman decides after taking the first of the two drugs in the regimen (mifepristone) that she doesn’t want to go through with the abortion process, she may be able to try abortion pill reversal.
Each year, about 700,000 aborted children’s remains enter the water systems, and water treatment plants are not designed to handle medical waste.
The abortion pill is often described as a “safe and effective way to end an early pregnancy,” at least according to Planned Parenthood. But is it? Recently, the Ethics and Public Policy Center released a study that analyzed insurance data codes for over 865,000 cases in which women took mifepristone (the abortion pill) and found that “serious adverse events” for the drug occurred at a rate approximately 22 times higher than the rate reported on the Food and Drug Administration’s (FDA) label for the drug.
A new, first-of-its-kind study asserts that serious adverse events from mifepristone, the first drug in the abortion pill regimen, occur at a rate approximately 22 times higher than the rate reported on the Food and Drug Administration’s (FDA) label for the drug.
Published percentages for ER visits on mifepristone’s 2023 label indicate that 2.9 to 4.6% of women who take it end up in the emergency room, indicating that abortion pill ER visits could be in the tens of thousands every year. In addition, the FDA’s medication guide acknowledges that as many as seven percent (7%) of women will need surgery after taking mifepristone “to stop bleeding” or to complete the abortion… These percentages, against Guttmacher Institute’s updated 648,500 annual abortion pill data from 2023, reveal that each year, 39,000 to 45,400 women may need additional surgery, and 19,400 to over 32,000 women may report to an emergency department after taking abortion-inducing drugs.
The emergency room visitation rate for abortion complications appears to have increased since the U.S. Food and Drug Administration removed guardrails on the use of the abortion pill.
“It really felt like peer pressure in there,” she said of her discussion with the technician.
After consuming the first abortion pill, Lynette later sat in her home questioning her choice, and then she began scrolling through her phone. She tried to force herself to vomit, but she was unable to do so.