contraceptives

Why I Made a Documentary About the Birth Control Pill

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I began using the birth control pill in my early 20’s. After 3 years of using the pill, I decided it was time to stop. I didn’t expect the process of coming off birth control to be so harsh. I was wrong. The withdrawal symptoms were unlike anything I had ever felt before. I developed extremely high blood pressure, had tingling and weakness throughout my body, brain fog, and a frightening sense of depersonalization. Not a single doctor could give me any information about what was causing these symptoms, when they would end, or even if they would end. In fact, most of the physicians I saw denied that pill withdrawal was a thing. They said that my symptoms were anxiety and suggested an antidepressant. I knew that couldn’t be the cause of these unique, first-time symptoms. I felt like there was no hope in sight. Through research, I found that I was not alone. There were many women who experienced similar symptoms while withdrawing from hormonal contraceptives, In fact there were thousands of women just like me.

I wrote an article about my full experience coming off the birth control pill and published it on this website, here. Since then, the article has received hundreds of comments from women who developed similar withdrawal symptoms. I decided to make a documentary about hormonal birth control in an effort to help spread awareness, and, to comfort other women who were struggling. Filming a documentary with no crew, no production money, and no experience, will fully test one’s sanity, but I was determined to uncover and document the health effects of hormonal contraceptives. After 4 years of work, I released the documentary entitled, “Hormoneously Alone,” on YouTube.  It can be found here.  I learned a lot from filming this documentary, and over the next few months, I will be writing a series of articles about the topics discussed in the film as well as other information that I was not able to include.

Ninety-eight percent of the female population will use a hormonal contraceptive in their lifetime. This is likely because it is 99% effective at preventing pregnancy when taken regularly. Using the pill alleviates worry and it is easy to use. In the US alone, this means that about 13 million women use hormonal birth control, with 6 million between the ages of 15-24 and 7 million between the ages of 25-34. I also learned that about 60% of women who have taken the pill have done so for other issues unrelated to pregnancy. Acne, bloating, and cramps are some of the main catalysts for using the pill.

What you may not know, and what I did not know before I began taking the pill, is up to 60% women who use hormonal contraceptives, whether for the prevention of pregnancy or for other reasons, stop taking the pill within 6 months because of side effects.  Unfortunately, there is little research on pill withdrawal and why it effects some women and not all. Through my own research, I’ve personally estimated that about 15% of women will experience withdrawal symptoms.  This is troubling because these withdrawal symptoms seem to only be recognized by the women who use these products. There are few experts in women’s health who understand pill withdrawal. Most doctors and gynecologists seem unaware of these effects. This leaves most of us struggling to recover on our own.

If a significant amount of women use hormonal contraception at some point in their lives, and the side effects both on and off the pill are not well studied, do we really know enough about the well-being of the girls and women who use them? With teenagers especially, are we doing more harm to the developing brain and body when we prescribe artificial hormones for things like acne and painful or irregular periods? Given the large number of girls and women who use the pill, do we as a society, not just as women, understand what we are committing to when we take the pill? From what I experienced and what I learned while producing the documentary, even though the pill has been on the market for over 60 years, we still do not fully understand the implications of using artificial hormones. Over the next few articles, I will be tackling some of these big issues that many women wonder about while on the pill, and off the pill. Hopefully, what I have learned will help others make more informed decisions and feel empowered to know what’s right for their body, and their body only.

Hormoneously Alone – A Birth Control Documentary

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More people than ever are reading Hormones Matter, a testament to the need for independent voices in health and medicine. We are not funded and accept limited advertising. Unlike many health sites, we don’t force you to purchase a subscription. We believe health information should be open to all. If you read Hormones Matter, like it, please help support it. Contribute now.

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Why Aren’t Women Tested for Factor V Leiden and Other Clotting Disorders?

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When I had a stroke at age 28, my doctors did some tests and found that I have a fairly common clotting disorder called Factor V Leiden. They told me that this, combined with birth control pills, are what caused me to have the cerebral venous thrombosis (stroke). It didn’t occur to me then to ask what Factor V Leiden actually was. Or to ask why I hadn’t been testing for inherited clotting disorders before I was put on medication that increased my risk for blood clots. These things didn’t occur to me until much later, after I learned to walk again.

I spent most of the first two years after my stroke getting on with my life. It wasn’t until I was searching for a topic for my thesis that I revisited what happened to me. I had no idea that birth control pills could be so dangerous and I certainly didn’t know that I could have an inherited genetic condition which would make them exponentially more dangerous for me. “How many women have the same condition?” I wondered. “Why don’t we test them before they are put on hormones?” These are some of the questions I sought to answer with my research.

What is Factor V Leiden?

Factor V Leiden (FVL) is a 20,000-year-old mutation common in the general population and a major genetic risk factor for thrombosis. It’s the most common genetic clotting disorder, accounting for around half of all cases. It’s most commonly found in Caucasians (3-8%).

Patients with Factor V Leiden can be either:

  • Heterozygous: inherited one mutated gene from a parent

or

  • Homozygous: inherited two mutated genes, one from each parent

What Does It Do?

As my hematologist described, FVL doesn’t cause blood clots but once activated, it dangerously accelerates clotting. Researchers aren’t clear on why some people with FVL activate and others don’t but there is almost always a precipitating factor—surgery, trauma, immobility, use of hormones, etc.

According to a review in Blood, the journal for the American Society of Hematology, women with heterozygous FVL who also use oral contraceptives have an estimated 30 to 50-fold increased risk of blood clots, while women with homozygous FVL have a several hundred-fold increased risk.

It is the most common genetic cause of primary and recurrent venous thromboembolism in women.

We know that taking estrogen can increase the risk of blood clots, stroke, and heart attack in women. And estrogen, when taken by someone with FVL, can significantly increase the risk of blood clots. Whether women are taking synthetic estrogen in the form of oral contraceptives, or hormone replacement therapy or have increased concentrations of the endogenous estrogens due to pregnancy, they are at much greater risk of clotting.

FVL accounts for 20-50% of the venous thromboembolisms (VTE) that are pregnancy related. In the United States, VTE is the leading cause of maternal death. In addition to causing VTE in pregnant women, FVL has been linked to miscarriage and preeclampsia.

Perhaps the women most at risk for blood clots are those that have been placed on hormone replacement therapy (HRT). A recent review of data from several studies found that women taking hormone replacement therapy were at an increased risk of blood clot and stroke. Worse yet, women with FVL who are also on HRT were 14-16 times more likely to have a VTE.

Despite these risks, women are not systematically tested for FVL before they are prescribed oral contraceptives, before or during pregnancy, or before commencing HRT.

What Women Know about Birth Control and Blood Clots

Part of my thesis research included a survey to assess what women understand about the risks of birth control pills and clotting disorders. Over 300 women who had taken birth control pills participated. What I found was that most women do not understand the side effects of hormonal birth control, nor are they familiar with the symptoms of a blood clot.

As for clotting disorders, nearly 60% of the women surveyed had no knowledge of these conditions. When asked whether they knew about clotting disorders BEFORE they took birth control pills that number increases considerably.

Over 80% of women were taking a medication without the knowledge that they could have an undiagnosed genetic condition that would make that medication exponentially more dangerous.

This shouldn’t come as much of a surprise give that this information is not found in advertisements for birth control pills, on non- profit websites about birth control pills and their risks, or on literature provided with the prescriptions.

Why Aren’t Women Tested for Clotting Disorders?

The most common reason I found in my research for not testing women were cost-benefit analyses measured in cost per prevention of one death.

Setting aside the moral argument that you cannot put a price on a human life, because clearly the government and corporations do just that. (It’s $8 million in case you were wondering.) The cost of taking care of taking care of victims of blood clots is not insignificant.

Each year thousands of women using hormonal contraceptives will develop blood clots. The average cost of a patient with pulmonary embolism (PE) is nearly $9,000 (for a three-day stay not including follow-up medication and subsequent testing).

A hospital stay as a stroke patient is over twice that at nearly $22,000 (not including continuing out-patient rehabilitation, medications, testing, etc.). As a stroke survivor, I can tell you that the bills don’t stop after you leave the hospital. I was incredibly lucky that I only needed a month of out-patient therapy. Most patients need considerably more and will require life-long medication and testing. It’s important to note that due to the increasing cost of healthcare, the figures in these studies (PEs from 2003-2010; strokes from 2006-2008) would be exponentially higher now.

I’m not a statistician but I can do some basic math and while I wasn’t able to find data for the United States (surprise, surprise), the health ministry in France recently conducted a study that showed that the birth control pill causes 2,500 blood clots a year and 20 deaths.  The United States has 9.72 million women using the pill compared to France’s 4.27 million. This doesn’t include the patch, ring, injectable, or hormonal IUD, but for the sake of keeping things simple, let’s just use the pill. So we have over twice the pill-users as France, which means twice the blood clots (5,000) and twice the deaths (40). If we assume that half of the blood clots are PE and half are stroke, we come up with a whopping $77.5 million in hospital bills for these blood clots (not counting life-long treatment). Now adding the cost-of-life determined by the government (40 women times $8 million= $320 million) and we end up with nearly $400 million a year in damages caused by the pill. For the cost of only one year of damages, all 10 million women could have a one-time $40 blood test which would result in considerably fewer blood clots.

Furthermore, the research in my thesis shows that women would be willing to not only take these tests, but also to pay for them!

Of the 311 who answered the question, 82.3% (or 256) said they would be willing to take the test. Only 7.2% said no, with the other 10.6% “not sure.” More than 60% of respondents would be willing to pay for the test (up to $50).

In addition, the cost of a blood test is directly proportional to how frequently it is performed. An increase in testing will result in a decrease in the cost of testing.

Women Deserve Better

Putting aside the monetary costs for a moment, what about the emotional and physical toll for women who suffer these dangerous and debilitating blood clots? There is no excuse for women to suffer strokes, pulmonary embolisms, DVTs, multiple miscarriages, and still births because they have an undiagnosed clotting disorder.

That said, requiring a test before prescribing hormones to women would raise awareness of the dangers of these drugs and may reduce the overall number of women using them. Which leads one to wonder if the absence of testing for women is really just a public relations strategy.

Perhaps one of the most devastating cautionary tales of not testing for clotting disorders comes from Laura Femia Buccellato. Her daughter Theresa was 16 years old when she was killed from a blood clot caused by (undiagnosed) Factor V Leiden and birth control pills. Would Theresa be with us today if she had had a simple blood test? Would I have had a stroke? When we will demand better?

We Need Your Help

More people than ever are reading Hormones Matter, a testament to the need for independent voices in health and medicine. We are not funded and accept limited advertising. Unlike many health sites, we don’t force you to purchase a subscription. We believe health information should be open to all. If you read Hormones Matter, like it, please help support it. Contribute now.

Yes, I would like to support Hormones Matter.

Image by fernando zhiminaicela from Pixabay.

This article was first published in September 2016.

Deconstructing Contraceptives: What Do We Really Know?

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Over the last several weeks, I have been preparing a report regarding our research on birth control and blood clots. In doing so, I have been reviewing past work and stumbled upon my notes for the presentation that landed the grant allowing this research to begin. The talk was filmed, but the video is behind a paywall. So, I decided to post the notes and the presentation. Enjoy.

Birth Control, Big Money and Bad Medicine: A Deadly Trifecta in Women’s Health

As I considered how to put this presentation together, I struggled with where to begin, what to leave in, what to leave out. There is so much that needs to be understood about contraceptives that we could fill a week of lectures and discussions. What I kept coming back to, however, is the notion that if I can teach you how to think about contraceptives, or for that matter, any medical treatment, if I can teach you how to question and evaluate the research, how to find the answers that you need; if I can give you a foundation and a framework for understanding the science, the economics and the politics of this medication, then each of you can find your own answers, and perhaps, if you are so inclined, contribute back to the knowledge base, so that we all have a better understanding of these issues. And so it is from that perspective that I have decided to approach this discussion. I want to give you a foundation and a framework from which to build your own house of knowledge. Sounds a little corny, doesn’t it, but bear with me, learning how to think critically about medical science might just save your life or the life of a loved one.

The Framework of Knowledge

I have a background and a natural inclination towards philosophy. In other words, I tend to think about things a bit more deeply than perhaps I should. This gets me into trouble sometimes.

One of the questions that plague my thinking is ‘how we know what we think we know’. I find that more often not, pondering from where and from whom the knowledge, the science, the politics, even the historical interpretations come from, tells us a lot about what it is we know exactly and what we really have no business claiming knowledge of.

With hormonal contraceptives, and indeed, the entirety of women’s health, when we deconstruct what is known and detach it from how we know it, or at least how we think we know it, it becomes very clear, very quickly, that our knowledge is severely limited.

For example, did you know that most of the science on contraceptives was developed over 50 years ago before the thalidomide tragedies changed FDA regulations regarding women’s health? Did you know that after thalidomide, research involving women of childbearing potential was all but prohibited until the late 1990s?

The post-thalidomide regulations, when combined with the political quagmire that is female reproduction, all but eliminated research and development on hormonal contraceptives, with the large pharmaceutical industries preferring to make only slight changes to dosage or delivery method and focus almost entirely market saturation over all else.

Probably not, unless you study this stuff. But knowing this, understanding how we know what we know about hormonal contraceptives can tell us a lot about these products, even if you don’t know the science.

So, hormonal contraceptives didn’t get the safety research they deserved. Indeed, they did not and continue not to because of the perceived economic and political costs associated with contraceptive science is greater than the perceived benefits.

Why fund new science, when the old science is already approved and the market is mature, in the sense that women and physicians alike consider hormonal contraceptives safe, but more importantly, a necessary component of reproductive health?

The Objectivity Bias

Back to the topic of how we know what we know, not only do we have to consider the science behind these drugs, but we also must consider in what context the science emerged and whether and how that context introduces a bias that impedes our understanding.

I would argue that bias is inevitable, even fundamental to the scientific endeavor, even though we claim objectivity. Consider, for example, the process of research design. What questions are asked and not asked are dependent entirely on the researcher’s individual constructs about what the problem is. Defining the problem, or even whether there is a problem to be investigated, is informed by education, culture, society, advertising, marketing, and in more modern times, by research funding availability. In many ways, bias permeates every aspect of the scientific endeavor. And yet, we hold tightly to this notion that delineating science from every other pursuit of knowledge, is its objectivity, its lack of bias.

In science, in particular, we have exalted the notion of objectivity above all else. The experiments we do are meant to eliminate subjectivity, to eliminate chance and the variables that might confound our data so that we can say with some confidence that this or that treatment is safe and effective.

While these are laudable goals that have contributed largely to the great advancements we have in all fields of science and technology, I think, in some ways, we have taken this reliance on objectivity too far, so much so that we have lost the humanity, and indeed, the humility in our scientific endeavors. This fealty to what I would argue is a contrived reliance of objectivity, to controlled but abstracted data calculations, not only severely limits the scope of our understanding but also poses real risks to human and organismal health. We see evidence of this every day, when human illness mediated by a particular drug or environmental toxicant is viewed only in terms of averages. That is, when a drug evokes a reaction in only small fraction of those who use the medication, but appears not evoke that reaction in others (though I would argue that it evokes other reactions that we are simply not recognizing), then those reactions, those costs, are viewed as inconsequential. They are not statistically significant and because we forget that statistical significance is different that clinical significance, because supplant statistical significance, a mathematical abstraction for clinical and human significance, we fail to recognize the dangers of a particular medication.

And so when I approach medical science, or really anything, it is always with those two things in mind – how we know what we think we know, and how biases, mine and others, influence that knowledge. It is from that perspective, we’ll take our foray into the contraceptive conundrum.

My Biases

Because I believe biases are so important – let’s begin with my biases. We’ll then look at the biases in modern medicine and statistics and how those biases have informed how we know what we know about hormonal contraceptives. Finally, we’ll tackle what is known and what is not known about what hormonal contraceptives do and do not do to the body.

You already know a little about me from the bio I submitted and from the brief introduction. But let me insert myself into the research, give you some idea of the lens through which I understand medical research in general, and hormonal contraceptives, in particular. I stand here today as a woman who has used oral contraceptives and experienced side effects from them (but at the time had no clue about the connections between my health issues and the contraceptives, nor did any of the physicians I sought help from).

I am mom of 21 year old twins, a wife of 26 years and a lifelong jock (even at the ripe old age).

I am as a research scientist. I love figuring out how things work, and to me, figuring out how things work means not only going to down to the smallest possible unit of function – the molecule, the chemical pathways, but mapping the systems involved, not just of the target organ but across the entire body. I think I was an engineer in a former life.

I am writer, as I mentioned, with philosophical tendencies.

I am business owner, whose business involves understanding women’s health and healthcare.

Finally, I am fierce women’s health advocate. For too long, questions about women’s health have been ignored. I want to change that.

I should also mention, as someone who is involved in medication adverse events research, listening to patient stories, seeing the devastation that some of these medications can evoke, and then investigating the mechanisms by which these reactions can occur, I have become increasingly wary of pharmaceutical promises. Admittedly, in that regard, I am probably more biased than others. It is difficult not to be.

So it is this totality of experiences that color, not only my interpretation of data, but I think more importantly, the questions I ask about any given medication. When I look at the safety and efficacy of a drug, I want to know in real terms what the benefits versus the risks are to an individual.

Unfortunately, we don’t have that information for majority of medications on the market, especially for women, and most especially for hormonal contraceptives.

With that long introduction, let’s dig into the topic at hand.

Birth Control, Big Money and Bad Medicine: A Deadly Trifecta in Women’s Health from Hormones Matter

Add Your Experience to the Conversation

As a result of this presentation, we were awarded a grant to investigate the health risks associated with hormonal contraceptives. Some of the early results of the pilot study can be found here and here. You can help us delineate those risks further by adding your experiences to our growing database by taking part in the Real Risk Study and, if you are so inclined, sharing your health story on Hormones Matter.

Real Risk Study: Birth Control and Blood Clots

Lucine Health Sciences and Hormones Matter are conducting research to investigate the relationship between hormonal birth control and blood clots. If you or a loved one have suffered from a blood clot while using hormonal birth control, please consider participating. We are also looking for participants who have been using hormonal birth control for at least one year and have NOT had a blood clot, as well as women who have NEVER used hormonal birth control. For more information or to participate, click here.

Heart Attack and Death While Using Yaz Birth Control Pills

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Our daughter Anne L. Ammons died suddenly in her sleep Nov. 7, 2009.  Her family, friends, and acquaintances were shocked. Annie was a new lawyer who had recently been admitted to the Maryland Bar, but she was known for her athleticism. While in law school she was a physical trainer, and 8 minute, 5 mile runs were the norm for her until several months before her death.

Annie’s death remained a mystery for quite a while, since it took the Maryland state medical examiner 4 months to attribute her death to a microscopic heart attack.  It took her family–her parents, sister, brother, and brother-in-law only a week to discover Annie’s silent killer—the birth control pill Yaz.  All of the physical symptoms that Annie had been suffering since March, 2009, including the final one (sudden death) were and are a strong match for side effects listed in the FDA Yaz label.

Starting on Yaz

In March, 2009, after Anne regained health insurance through her employer, the nurse practitioner at her OB/GYN office prescribed Yaz off label when Anne complained of menstrual cramps and irregular periods. Anne had taken Yaz two years before, for about a year, until she lost medical coverage.

In May, Annie tore a muscle in her back and was prescribed extra strength ibuprofen. The Yaz product monograph warns in bold letters that women taking medications, such as ibuprofen, that may increase serum potassium should have their potassium levels checked while taking Yaz, but neither the doctor nor the pharmacy noticed this. About that time Annie also began complaining of hair loss and weight gain.

That summer Annie again saw the OB/GYN nurse practitioner for break through bleeding and a vaginal infection, both of which could be Yaz side effects. Anne was prescribed Diflucan, which is another medication that may increase potassium levels in those taking Yaz. The Yaz product monograph contains a warning about this as well, but again, neither her doctor nor her pharmacist noticed.

Dealing with Yaz Side Effects

As the summer progressed, Annie continued to gain weight. I, her mother, thought that it might be related to lunches out with her boss and wasn’t too worried. Her co-workers asked if she was pregnant; in retrospect, I think that she did look pregnant. Additionally, in August, Annie began complaining of insomnia and extreme fatigue; she saw a physician assistant at her newly acquired general practitioner’s office. She was prescribed Lunesta which she continued until the night of her death. This medication can affect heart rhythm so it may have also been a contributing factor in her death.

In September, a lab test showed elevated liver enzymes which can also be a Yaz side effect, and a condition that means that Yaz should be stopped.  When she revisited her GP, she was sent to an endocrinologist, who after hearing Annie’s symptoms and without ordering any tests stated that Annie’s weight gain was caused by fatty liver and prescribed metformin.  Also without any testing, basing her diagnosis on only Annie’s symptoms reporting and an inexplicable assessment of hirsutism, the endocrinologist wrote in her notes that Annie should stay on Yaz for PCOS (an off-label and unproven use). Later, several years after Annie’s death, the Maryland Board of Physicians would exonerate this endocrinologist of any wrong doing.

About this time Annie and I discussed her illness.  She thought that she might have adrenal fatigue (a condition not recognized by mainstream doctors) or that she too might have Lyme Disease.  Her sister, after ten years of suffering, had recently been diagnosed.  Annie and her sister had done a lot of hiking together; some of Anne’s symptoms did match her sister’s. As summer turned to fall, the weight gain continued and Annie seemed depressed. Thinking of seasonal affective disease. I suggested that she change bedrooms to one with increased daylight. I also wondered if changes in our living situation were at play; she and I had been roommates for about a year while her dad was away at school.  In addition, I wondered whether anxiety about finding a job as a lawyer (she was working at TESST college as a librarian) was also affecting her. But, I felt assurance that Annie’s problems would be figured out, since Annie was seeking help from medical doctors.

High Potassium Levels Due to Yaz

By the middle of October Annie was interviewing for lawyer positions and working hard at TESST to make the library nice since their state accreditation was looming.  Her spirits seemed improved, but still the weight gain was continuing. One afternoon she showed me a lab chit that reported high levels of potassium.  After her death, we learned that drospirenone (the progestin part of Yaz) can cause potassium levels to rise so dangerously high that the heart stops.  This can be the causality for “sudden death” as mentioned in the label, and we think that it was a factor in our daughter’s death.

However, after death, the mineral composition of the blood changes rapidly; therefore, it is impossible to prove that high potassium levels were involved. At any rate, Annie and I were ignorant at the time of the high potassium level and thought that high potassium might even be good since we were all taught that eating bananas is good for you.  On another occasion during late October, Annie asked me if I thought that her eyes were jaundiced. Although I didn’t see it, this may have been the case, especially since her liver enzymes were elevated. Jaundice is another serious Yaz side effect listed in the product monograph. Another time, Annie complained that her heart had been racing and asked me if I had ever experienced such a symptom.

The Week Leading up to Annie’s Death

Then came the week before Annie’s death.  My husband Rick stayed home from work one morning with intestinal flu-like symptoms (he never stays home sick); the next day Annie reported having thrown up.  She said that she had a strange pain in her stomach; it just didn’t feel right.  We both deduced that it must be a flu since her dad had also been ill.  That night she complained of numbness in her left arm.  Annie and I both thought of her torn back muscle in May and of her neck surgery a couple of years prior and thought that the pain could be related to one of those conditions. I wanted to take her to the emergency room, but she strongly declined.  If only I had insisted; that numbness was most probably a sign of her tiny heart attack.  Months later the medical examiner would explain to me that her heart had showed signs of healing; she must have had a heart attack several days before she died.

The day before Annie died she asked for my input about whether she should attend a special friend’s birthday party the next night or if she should go to a OB/GYN doctor’s appointment.  We both decided on the birthday party.  Again, if only at the time we had known. However, given that her doctors had ignored some of the serious side effects of Yaz that she was already experiencing, it may be that nothing would have been different even if she had gone to the appointment.

She returned from the party late that Friday evening; I got up and we both had the best time watching a particularly funny episode of Jay Leno.  I awoke around 4 am and found her still asleep in the family room recliner. When we awoke around 8:00 am, she had gone to her room and we went out to perform Saturday morning errands.  When we returned, I could not rouse her; her father frantically tried CPR, but it was too late.

Tragedies Caused by Hormonal Birth Control

I have had a horrible time since my baby’s death especially since we have discovered that no one in a position of authority cares enough to stop the production of these dangerous hormonal birth control pills.  And it’s not only Yaz and its sister drospirenone pills that kill and maim (strokes, pulmonary embolisms, and heart attacks occur) but also other hormonal pills and devices put on the market since the early 2000’s cause similar tragedies.  A friend of ours whose daughter died due to Nuvaring-induced pulmonary embolisms, took MEDWATCH reports and worked with a statistician to discover that between 600 and 800 American women die each year as a result of hormonal birth control in the United States.  As we continue to tell our story and to advocate for change, I pray that one day our voices will be heard so that so many lives will not be taken or ruined.

Real Risk Study: Birth Control and Blood Clots

Lucine Health Sciences and Hormones Matter are conducting research to investigate the relationship between hormonal birth control and blood clots. If you or a loved one have suffered from a blood clot while using hormonal birth control, please consider participating. We are also looking for participants who have been using hormonal birth control for at least one year and have NOT had a blood clot, as well as women who have NEVER used hormonal birth control. For more information or to participate, click here.