depo

Hormonal Birth Control Plus Poor Diet Is a Recipe for Disaster

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I am a 29 year old female who began experiencing a decline in my health at 25 years old. This was in 2020. At that point, I had been on hormonal birth control for nearly 10 years. I suspected the birth control was contributing to my ill-health but my doctor disagreed and continued to prescribe different forms to alleviate my symptoms. That did not work and only made things worse. When Depo-Provera was added, I completely crashed and have not recovered, nearly two years later.

When I first began to experience extreme fatigue, abdominal bloating, irritability, restlessness, and massive amounts of hair falling out, I went to my primary care doctor who could find no reason for it on basic bloodwork, except for a low vitamin D level (27mg/mL). They checked CBC, CMP, autoimmune markers, B12, a complete thyroid panel, Lyme titers, mono titers, and iron levels. Since everything was basically normal, my primary care doctor blamed it on my stressful job. At the time, I was working in the emergency room on the night shift. I was not getting the best sleep, and not eating that well either. I was lucky to eat one meal a day and then maybe a snack especially on my busy shifts. On my days off, I was so exhausted that I would eat maybe twice a day. My diet consisted of easy meals like grilled chicken, salads, granola bars, processed cereals, pizza, chicken nuggets, chips, bananas here and there, and overall not a lot of fruits or vegetables.

Enter Depo-Provera

Fast forward to the fall of 2021, after these symptoms persisted, my doctor decided to switch my birth control to the Depo-Provera shot. After taking this shot, havoc was wreaked on my body and brought me down to a level of non-functioning that I never knew existed. Over the next couple months and after taking only one depo shot, I began to experience debilitating symptoms of headaches, fatigue, achy joints/all over body pain that eventually progressed into episodes of heart-racing anytime I would change position. I also experienced shortness of breath, chest pain, difficulty swallowing, a complete loss of appetite, GI issues, brain fog, severely decreased ability to concentrate, severe restless leg syndrome, insomnia, and neurological symptoms so extreme it felt like my brain was “short circuiting” for lack of a better word.

One side of my body would become extremely numb, tingly, and feel weak without any clear deficits. I experienced severe muscle weakness, where it would feel like my body was doing everything it possibly could to keep me upright and breathing. It was so bad, I felt as though I couldn’t even grip my phone and just talking on the phone to family felt like I was dying. I could barely concentrate. I developed severe visual issues, a condition called visual snow syndrome, and still am dealing with it with no improvement. I also developed tinnitus and have a constant high pitched ringing in my ear. I am unable to handle any type of stress, multi-tasking, or any emotional upset without truly feeling like my body is dying from severe neurological symptoms. I became scared to leave the house alone because of these debilitating symptoms. I lost over 30 pounds from feeling so awful and a complete loss of any desire to eat. I would have to force myself to put in fluids or food.

Over the course of many months, I saw multiple neurologists, neuro-ophthalmologist, cardiologist, electrophysiologist, primary care doctor, ENT, TMJ specialist, otologist, binocular vision specialist, rheumatologist, had numerous ER visits, two hospital admissions. I even participated in vestibular/neurological physical therapy over the course of several months. I had multiple head MRIs and CTs of my head and neck, MRIs of my spine, and so much bloodwork looking for autoimmune causes. I had a colonoscopy, a camera down my nose to look at my throat, an audiogram, a sleep study, a tilt table test, an echocardiogram, a stress-echocardiogram, and they even attempted a lumbar puncture on me as well. Conditions such as blood clots, multiple sclerosis, any type of cancer or tumor, etc., were ruled out and the only thing they came up with was a diagnosis of Postural Orthostatic Tachycardia Syndrome (POTS), a suspicion for “some type of migraine variant” and a deficiency in vitamin D and phosphorus on my bloodwork.

Could This Be Thiamine Deficiency?

Fed up and worsening, I paid out of pocket to go to a natural medicine doctor who did heavy metal and mold testing on me along with hormone testing. Nothing really turned up there and so I took it upon myself to order a full vitamin and mineral panel paying over a grand out of pocket. This panel revealed that my serum thiamine was one point away from being flagged as low (8 nmol/L). I then returned to my primary care and two different neurologists to ask if a thiamine deficiency could be the problem or at least part of it, especially after my own research and the known research that birth control depletes many B vitamins. All of the doctors told me that there was no possible way I could have a thiamine deficiency since it is added to so many foods in the United States. They also told me that I could just take a B complex vitamin if I was worried. Even after I told them I was hardly eating because I felt so sick and that when I was eating it was mostly foods like processed toast, frozen chicken nuggets, cans of soup, and other things of that nature, they still dismissed the idea of thiamine deficiency.

May-Thurner Syndrome

On top of all of the debilitating POTS and neurological symptoms, throughout my time on birth control I had complained to my GYN about persistent left sided pelvic pain. It felt like my labia was swollen and at times like something was bulging into my pelvic area. In 2019, I had a CT scan of my abdomen and pelvis done due to some GI symptoms I was having. An incidental finding on it was suspicion for pelvic congestion syndrome (PCS). The report stated that I had very prominent peri-uterine vessels and a dilated left gonadal vein. I took these results to my GYN at the time who clearly stated “PCS is a fake diagnosis and you don’t need to do anything with that.” Since I was young, in my early 20s, I didn’t take it too seriously. Again as time went on, I continued to have the pain and over the years my GYN kept changing my birth control and mentioned endometriosis and small ovarian cysts as possible causes. The birth control would help a little bit for a while but then I would have irregular bleeding and the pain would always come back. It wasn’t until after I took the Depo shot and came off of the hormones that things became worse.

I began to have severe left pelvic pain that persisted for months. I had transvaginal ultrasounds every 6 to 8 weeks to monitor recurring small cysts that they swore were not the cause of my pain. I was tested for PCOS and was negative for that too. It wasn’t until the end of 2022, that I had another transvaginal ultrasound and this one read as having a hydro-salpinx. I had a new GYN at the time who referred me to get an MRI done of my pelvis. This MRI came back as also showing “likely hydro-salpinx” on the left. Since I was having such severe pain, I was referred to a GYN surgeon who said in extremely painful cases it is recommended to take out the tube and it was pretty much nonfunctional when it was as swollen as mine. I elected to proceed with the surgery, as the pain was so extreme. Funny enough, after the surgery when the pathology came back there was no hydro-salpinx and my surgeon said he did not see any endometriosis when he performed the laparoscopy. He said he believed my MRI may have been misread since he did not see any indication of hydro-salpinx during the procedure.

As if that wasn’t enough, after the procedure I had a severe neurological reaction to the scopolamine patch they put on me during the procedure. I had so much testing for this. I was even in the hospital for 5 days with what they thought was “scopolamine patch withdrawal” even though I only had the patch on for 3 days like they told me to wear it.

Fed up and still in pain, I let it go for a few more months thinking it was just “scar tissue” from the surgery or some other easy explanation. It wasn’t until my POTS doctor recommended me to wear an abdominal binder/compression device around my stomach that things worsened so much that I was forced to figure this out. I began having severe left pelvic, hip, and leg pain after wearing this device for only 3 days. I went to the ER because the pain was so bad, but they could only find a small ovarian cyst on my left ovary. They didn’t even consider doing any other work-up. I was then sent to an orthopedic to look at my hip and back to my GYN. Neither could really give an explanation for this pain. Finally enough was enough, I went to a vascular doctor on my own accord to get this PCS, which no one seemed to take seriously, looked at.

At the vascular surgeon’s office, they did a vascular scan of my pelvis and abdomen and were quickly shocked to find that my left iliac vein was almost completely compressed causing my peri-uterine vessels to get almost no blood flow. They diagnosed me with something called May-Thurner Syndrome and said that they usually only see severe cases like mine in women who have had “5 or 6 babies.” I was 28 at the time with one previous ectopic pregnancy many years ago. They quickly scheduled me to get a stent of my left iliac vein placed, as my left leg had begun swelling bigger than my right due to the limited blood flow.

On the day of surgery, my left leg was 2 inches bigger than the right and I was in severe pain. They did a venogram with internal ultrasound and were able to tell me my left iliac vein was 85% compressed. So basically, I was getting no flow through it and hardly any return through that vein up to my heart. They also informed me that the birth control was probably masking the problem but also could have been worsening it when I was on estrogen-containing birth control. They said I was extremely lucky that I did not develop a blood clot, especially when I had taken Beyaz for several years. Now, I am on blood thinners for several months post stent, while waiting to see if this helps with my POTS symptoms at all. So far, I have not seen any improvement except that my leg is no longer swollen.

Still Seeking Answers

I don’t know if thiamine deficiency could be causing my issues, but I have not received any answers other than POTS and my recently discovered May-Thurner Syndrome. I have seen so many doctors and spent so much money with no improvement in my health. This all severely worsened after I took the Depo shot. I have been unable to work for months, was bed bound for a long time, and was completely unable to eat during the worst of my symptoms. Now, I am at least able to move around more than I was and leave the house for doctor appointments, but I am still not working and I am still searching for answers. I would like to feel better and get back to some type of semi-normal life.

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.

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The Depo Decline

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Learning About Depo the Hard Way

In 2010, I was 32 years old, and a preschool and elementary school teacher. I was looking for birth control to prevent pregnancy. I tried several different birth control pills previously, but reacted badly on every single one of them. The pills increased my blood pressure significantly and gave me migraines. I also tried both the hormonal and non-hormonal IUDs. Each of them gave me chronic bacterial vaginosis. This persisted for the entire 6 years that I used these devices. My doctor told me that the Depo Provera shot would be a good option for me since it didn’t have any estrogen in it and I wouldn’t have those terrible side effects. She said the only side effect would be a 5-10lb weight gain. I stupidly and regretfully took her advice and got the depo shot. I wish I could take that day back because it has ruined the past 10 years of my life. I had the shot on August 18, 2010 and I still do not feel well, almost 10 years later. That shot left me with numerous autoimmune and endocrine problems. I should mention, I was healthy before all of this began.

Within a week of the Depo shot, I began feeling off and not like myself. I developed unusual and extreme hunger. I was very moody and irritable, extremely tired, and experienced daily headaches and migraines. It only got worse from there. Within three months, I gained 25 pounds.  I called my doctor’s office and told them I would not be returning for another shot. I told the receptionist about the side effects that I was having.

I began having all sorts of weird health problems that were totally out of the norm for me. As I mentioned, I was healthy prior to depo and never had to go to the doctor except for my annual check-up. I felt like I was going crazy because my doctor said “Depo can’t do this to you.” When I asked why I was having all these problems all of a sudden, she assured me it wasn’t from Depo. What was it from then? I have never been given an answer.

I have spent thousands of dollars on trying to heal my body and have seen over 20 doctors and specialists to try to find out what this shot did to me including: endocrinologist’s, rheumatologist, gastroenterologist’s, podiatrist’s, dermatologists, chiropractors, naturopathic doctors, physical therapist, massage therapists, psychologist, infectious disease doctor, vitamins and supplements. My health never returned. I’m only able to function at about 20-25% of what I was prior to depo. This is despite trying everything I do to heal my body through research and books and doctors.

It has been a decade from hell and because of all these health problems from depo, I lost my job, my family and my house. This shot poisoned my body and wreaked havoc on my mind and body. I’m 100% convinced from the newest research conducted and reading “The Dangers of Depo” book that it did irreversible damage to my body at a cellular level. My body, my mind, my thyroid and adrenals and my cells were never able to recover and heal from this shot.

This past decade has been a literal nightmare. This shot needs to be banned. I’m only writing all of this to warn other women to stay away from this poison. I wouldn’t wish what happened to me on anyone. It has destroyed my once happy and successful life.

Surviving Depo Together

Last year I started a Facebook group “Depo Provera =Endocrine Disorders” support group to help other women who are experiencing endocrine problems after getting the Depo Provera shot. In little over a year, we have 589 members. These are women who have become ill with various endocrine problems since getting the depo shot.

We are all very supportive and help each other. Most of us have family and friends that really don’t understand what it’s like to get so ill from a pharmaceutical. So it has been very comforting knowing we have each other to talk to and other women who know and understand what we are going through. That was my goal when I started this support group. I wanted to see how many other women worldwide were experiencing severe health problems from depo and offer a safe place for us to share stories, concerns, advice and anything helpful. We have an amazing group of ladies and I met some wonderful women through my Depo group. Their support and encouragement pushed me to go public with my Depo story. I’m a very private person. I didn’t want everyone in the world knowing about my horrific experience and my life crumbling. It’s embarrassing to me, but I’m doing this because I feel knowledge is POWER! The more we inform women about the dangerous Depo-Provera birth control shot the better.

With social media and the internet hopefully women will research Depo Provera before getting it and realize how dangerous it can be. Then make an informed decision prior to getting it. Had myself, and thousands of other women been informed about these issues, we would have never gotten this shot. So I’m writing this to help as many women as I can to be informed and to warn them as to what can happen if they chose to get depo.

I hope my story helps women. That is the only reason I am sharing it. I don’t want anyone to go through what I’ve been through.

Depo Provera Side Effects

Below are just some of the dozens of diagnoses, odd symptoms and lab results that I have had since receiving Depo Provera.

Diagnoses

  • Hashimoto’s autoimmune thyroiditis
  • miscarriages
  • Chronic Epstein Barr virus
  • Cytomegalovirus
  • Lyme disease
  • Skin cancer (3 times) leg, face, low pelvic region
  • Fibromyalgia
  • Arthritis in lower back
  • Degenerative disk disease
  • Bone spurs on spine
  • Facet syndrome in my low spine – I have severe lower back and neck pain
  • Autoimmune disease
  • PCOS
  • Nodules on thyroid, cysts on liver and kidney, cysts on right ovary, fibroid on uterus
  • Pre-diabetes
  • Sleep apnea and low oxygen while sleeping and trouble breathing during the day

Labs

  • Adrenal fatigue -low cortisol/ACTH
  • C reactive protein is very high
  • Sedimentation rate is very high, and indicator of high inflammation
  • Absolute basophils very low
  • Anion gap high

Symptoms

  • Food sensitivities and Food intolerances to gluten, dairy, soy, sugar
  • High blood pressure 169/115
  • Pain/throbbing in bicep/elbow
  • Throbbing pain on thyroid
  • Bloating, swollen stomach, diarrhea -IBS/D
  • Ringing in ears-tinnitus 24/7
  • Dry eye syndrome
  • Heavy bleeding (menorrhagia)
  • Debilitating fatigue, always tired, malaise, not feeling awake for hours after waking up, falling asleep a lot during the day, sleeping 12-15 hours per day, my body feels limp and I get worn out doing simple things like laundry
  • Night sweats
  • Brain fog, headaches, anxiety, nervousness, irritability
  • Getting very dizzy and passed out twice
  • Feet and hands falling asleep a lot, my fingers are stiff- right thumb freezing and won’t move
  • Teeth grinding while asleep
  • Plantar fasciitis-feet: severe pain on bottom of feet and left outer side of my foot making it hard to walk especially when I miss my menstrual cycle
  • Toenail fungus
  • Poor healing: cuts and incisions do not heal.
  • I can’t handle normal stress at all. I get very sick and then I can’t get rid of colds. My immune system doesn’t work and I end up staying sick for months and years.
  • Extreme 80 lb Weight gain
  • Iron and ferritin are deficient
  • Vitamin B low
  • Vitamin D deficiency

Basically, I am falling apart, one piece at a time, and no one seems to be able to help. Doctors mostly dismiss my declining health. The power of informed choice was taken away from me since I was not informed of the real risks. Depo carries a black box warning, which is the most stringent warning short of an outright ban. Had I been aware of this, I would have never gotten this shot. It is completely unfair, unjust, and unethical for doctors and nurses to administer this shot to unsuspecting women without adhering to their legal obligation of disclosing the very real, serious, and in some cases like mine and many others, permanent side effects that this form of birth control is responsible for.

If you are suffering with endocrine related side effects due to Depo Provera, please join my Facebook group, “Depo-Provera=Endocrine Disorders Support Group.”

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. 

If you would like to share your story: Contact Us.

Image credit: Wallpaper Cave.

This article was first published on June 17, 2020. 

The Depo Health Storm

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It was the winter of 2017 and life was busy. I was 38 years old, married for almost 13 years, a mother of 10-year-old identical twin girls, and an almost 9-year-old daughter. I was in my 15th year of teaching and had been a successful literacy coach for the past five. l thrived being busy and always seemed to get everything done, even when it seemed impossible. I would describe myself as strong-willed, determined, passionate, intense, competitive, a perfectionist, controlling, aware, empathetic, and more importantly, always prided myself on my resilience. Unfortunately, I would soon learn the power of Depo and how even the strongest of wills would concede to it.

The Depo Black Box Warning – Ignored

In early February 2017, I made an appointment with Planned Parenthood, specifically to get the Depo Provera birth control injection. I didn’t have a gynecologist or the patience to look for one near me, so I thought this was the easiest and quickest way to get what I needed and continue with my busy life. I’m extremely impatient as well. That moment stopped me dead in my tracks. It was February 22, 2017, and at that moment, everything as I knew it would change.

I was brought into a room and a nurse walked in. We didn’t discuss anything besides when I casually asked what the side effects were, thinking I’d hear the same things I had always heard. Her only warning was that I might spot a little but that it was normal. Then, right before she gave me the injection, she pulled out two forms and asked me to sign them without telling me what they were. I just figured it was a formality, so I signed them and never thought anything of it. It was not until about 7 months later when I looked again and saw that the forms stated that I was given Depo’s written black box insert, which is the most stringent warning short of an outright ban, and that I was verbally warned of the very serious and dangerous side effects. Months later, I learned that medical professionals, injecting Depo, are legally obligated to disclose both the written and verbal warnings, before administering the shot. The next thing I knew, she injected my right upper thigh with Depo Provera.

The Depo Storm: From Weight Gain to Total Debilitation

Within days, I just didn’t feel right. I began noticing that I was unusually moody and tired, and felt overall, puffy. Soon after the shot, I started struggling with my weight, which was highly unusual. I’m barely 5 feet tall and have always been petite, and more importantly, had always been able to control my weight. Furthermore, I led a healthy lifestyle of watching what I ate and working out often. But in only 2 months, I had exceeded my all-time highest weight. I now weighed the same as I did when I was 9 months pregnant with my youngest daughter. My concern prompted me to return to Planned Parenthood and speak with the same nurse who had administered the injection. I told her what was going on and she replied, “I’ve never heard of such a thing.” Those words repeated over and over in my head to this very day. I told myself it would be over soon and that I’d be back to my old self once the shot “wore off” in three months, which was May 2017. Well, May came and went and my symptoms only got worse. This is when I realized there was no “expiration date,” and that once Depo is in your body, you can never take it out.

Months passed, and in September 2017, my physical health took a sharp turn for the worse. I experienced memory loss, profuse sweating day and night, extreme itchiness, and frequent hives, and was very easily startled. I also developed dizziness, water retention, constipation, vaginal infections, muscle weakness, heart palpitations, shortness of breath, hair loss, no sex drive, depression, anxiety, no menstrual cycle or ovulation, bloating, dry skin, severe tooth decay, sore breasts, toenail infections, incontinence, and debilitating exhaustion.

One day at work in early November 2017, I started getting itchy hives. It only started as a few, but within hours, I was covered from head to toe in the itchiest and biggest welts I’ve ever had. I drove myself to the emergency room and my husband met me later on. I was given Benadryl and told I must’ve had an allergic reaction to something. I now know it was Depo wreaking havoc on my body…and that was just the beginning.

On November 19, 2017, I watched my sister pass away from a painful battle with cancer. This loss shook my world. My emotional stress was at an all-time high, and I quickly spiraled into a deep depression. As a controlling person by nature, I was losing all of it and fast, and that alone took a huge mental toll on me. I could no longer control my emotional, mental, or physical health, and didn’t have the stamina to do the job I was once successful at and loved. I became an emotionally unstable mother and wife, was in a constant state of fight or flight, and my exhaustion was literally beyond comprehension.

No matter how hard I fought to be “normal,” my body and mind just weren’t responding in their “normal” ways. I was unrecognizable in every way and could no longer continue lying to myself that nothing was wrong, that I was imagining all these symptoms, or that one day this poison would “be out of my system.”  Those were all lies I told myself trying to maintain some sense of normalcy and sense of control over the things I no longer had. I doubted my inner strength and resigned myself to the fact that this was the way life was going to be from now on and tried to accept that. And the only thing I felt like I had left was the memory and mourning of both the death of my sister and the determined person I identified as my entire life. I constantly reflected on the mass destruction it had over my life but didn’t have the physical strength or mental capacity to even consider addressing any of it.

Summoning the Strength to Self-Diagnose: Depo Destroyed My Thyroid

Almost one year later, in January 2018, as I sat slumped in the usual corner of my couch, in the deepest depression and defeat I once couldn’t even fathom and trying to become familiar with this new person I had inadvertently become, I felt one last glimmer of hope and truly believe my sister gave me strength, from the other side.  So, I began researching my symptoms…all of them, and they all pointed to either menopause or hypothyroidism. But I knew there was no way I could be menopausal when before Depo, my cycle was like clockwork, I ovulated every single month, and was overall, very healthy.  So, I diagnosed myself with hypothyroidism and focused all my attention there.

In February 2018, after I self-diagnosed, I decided it was time to start seeing doctors to get an official diagnosis and begin getting my health back. I noted every single symptom to prepare for my appointments, thinking being prepared would bring me closer to a diagnosis. I first started out seeing hormone specialists, otherwise known as endocrinologists. Other doctors I saw included 2 primary physicians and a rheumatologist, to rule out lupus. Well, my visits with these doctors proved that all the preparation in the world meant nothing at all. I was never heard. Instead, I was dismissed, told I was probably peri-menopausal, told I was experiencing all 25-plus symptoms because I had just turned 40. I was even told to see a psychiatrist! To boot, all blood results were “normal.” Although I questioned my sanity more than once, the knowledge I had acquired told me differently. I just knew there had to be an answer. I figured if I could narrow down the reason why I was sick, then why couldn’t someone else? So, my search continued.

I then focused what little energy I had left on thyroid research, spending every waking moment, which wasn’t much after all considering I slept most of my days away, delving deep to learn as much as I could. I took notes on my phone and bookmarked more articles than I could count. I also read the books, “The Dangers of Depo: The World’s Most Dangerous Birth Control,” by Traci Johnstone and Dr. Poppy Daniels, and “In the Name of the Pill,” by Mike Gaskins, which I highly recommend. I joined several Depo Facebook Support groups and soon learned that I was not alone.  After I became what I considered to be an “expert,” in both thyroid and female hormones, my opinion on these support groups wasn’t always the most popular, and I even ended up getting kicked out of one of these groups for providing facts!! Regardless, all of this information confirmed that my symptoms were actually common, and this gave me the motivation to keep on moving forward.

Finally, Confirmation: Thyroid Conversion Disorder

In March 2018, I was no longer physically able to care for my daughters, take care of the house or myself, or do my job, but what I could do and had control over was arming myself with even more knowledge.  But this time, my research focused on natural remedies and non-conventional medicine. This leads me to a bioidentical hormone replacement doctor. He didn’t take insurance, but my level of desperation was at its peak, and there is no price on my health. I spent thousands of dollars in comprehensive testing, over a short period, but finally got a diagnosis…the thyroid diagnosis I had given myself months prior.  My main diagnosis was a Thyroid Conversion Disorder. Other diagnoses included: copper toxicity, essential nutrient deficiencies, a mitochondrial defect, high liver enzymes, candida, estrogen dominance, and low testosterone and progesterone. And there were quite a few other abnormalities in my blood cell levels, which still have not leveled out.  To paint you a better picture, my Thyroid Reverse T3 level was over 40, when between 7-15 is optimal. This is sometimes referred to as your “hibernation” hormone, which is when your metabolism shuts down, your core body temperature drops, and you gain fat to prepare like a bear hibernating in the winter.

In mid-April 2018, I began bio-identical hormone replacement therapy, thyroid medication, and hundreds of dollars in supplements and out-of-pocket doctor visits. That wasn’t the end of my journey, however, because although I was finally given a diagnosis, my thyroid disorder is so rare, that not even hormone specialists or the best of non-conventional doctors knew how to treat it correctly. So, my search continued.

In May 2018, having seen two more doctors, spending more money, and doing more obsessive research, I finally figured out how to treat my rare condition. I took this new information to a naturopathic doctor who shockingly had knowledge and experience treating my specific and rare condition. Since he couldn’t prescribe, he worked in conjunction with a prescribing doctor from the second-highest-ranking hospital in the nation. Within a week of starting treatment, I began feeling better. However, my sigh of relief was short-lived. I wound up having issues getting my thyroid medication from the prescribing doctor, who was neither comfortable treating my rare condition, nor cared to understand it, and especially since, as my naturopathic doctor said, “We have to play a game in order to get your medication because the big wigs at the hospital will question the doctor asking why he’s prescribing medication when your levels are not in range.”  My naturopathic doctor even went as far as admitting that the prescribing doctor knew nothing about thyroid, didn’t care to and that he was manipulating him into giving me my medication, which finally started making me feel human again. I wasn’t hopeful, nor did I feel like playing a game, especially after all I had been through. But I knew that if you truly understood my condition, or cared to, you’d know my levels will never be in range again and shouldn’t be, with the medication I am on. Apparently all that mattered were my numbers, which weren’t indicators of how I felt at all.  Again, my search continued.

In August 2018, I was interviewed by a Canadian reporter, Sandra Bartlett, who contacted me on one of the Facebook Depo Support Groups.  She was working on a podcast featuring five women’s stories about Depo and asked if I’d like to be part of it. I jumped at the chance. Sadly though, it would never be aired because she couldn’t find a doctor to explain, let alone acknowledge, that Depo does in fact, cause horrific effects. During this time, I met a girl online named Gretchen, who was basically telling my story verbatim. I saw the anger, resentment, and thirst for knowledge in her and we would later team up to create a Facebook support group for those who developed endocrine disorders as a direct result of Depo.  We continue to fight for stricter regulations on birth control and tirelessly work to spread awareness and truth about the very real and serious dangers of this poison.

In October 2019, only several months ago, and after another failed attempt at seeing a well-known and highly rated integrative doctor, I decided to return to the bioidentical hormone replacement doctor who had given me my initial diagnosis in April 2018. Although he doesn’t see or acknowledge the correlation between Depo and the mass destruction it had on my mental, emotional, and physical health, I know the person I was before that day, and I know, without any doubt in my mind, that Depo Provera tried its hardest to tear me down.

Almost exactly three years to the date of my one and only Depo Provera injection, yes, that’s all it takes, I still deal with some lingering effects. Depo affected me on a cellular level by depleting my serotonin, dopamine, and GABA neurotransmitters, and ultimately caused me to develop a panic disorder, not to mention a thyroid disorder, which requires me to take medication for the rest of my life. I’d be remiss not to mention that Depo completely destroyed my oral health. Over the course of a year and a half, I had countless, and very painful, dental procedures costing thousands, and still counting.

What the Depo Experience Taught Me

The fact is, this experience changed me, but it certainly did not defeat me. It is true that I am not the same person I was three years ago. Throughout my experience, including my sister’s death, I was taught some major life lessons and am much wiser, and more cautious now. I use the word “taught,” and not learned, because this was definitely something I never expected to happen and certainly wasn’t prepared for. The first lesson is summed up in the saying,

“Every tragedy that happens in our life is not intended to defeat us but to make us stronger.”

For those going through the same thing, although you may feel like giving up like you will never again be the same, know that you have more strength than you realize, and more importantly, that you can get through this!!  Hold onto that hope and keep moving forward, even if it’s only small steps at first.

Second, please understand that KNOWLEDGE IS POWER. I attribute a lot of how far I have come to empower myself with knowledge. This allowed me to advocate for myself and my health, even when so many others told me differently. Remember, you are your biggest cheerleader and only you know yourself better than anyone else. Don’t ever question that.

And last, but certainly not least, the biggest lesson I was taught is to NEVER, EVER TAKE HEALTH FOR GRANTED because it can be gone in an instant. Sometimes that is all it takes. I thank God every day for these lessons and for making me stronger than I ever imagined. I dedicate my story to my sister, Christy, my guardian angel, whose memory gave me the will to keep on fighting and the spirit to never give up.

Unfortunately, the negligent, unethical, and blameless medical practices continue to take place, while the number of unsuspecting victims rises. Arm yourself with knowledge! For more information on how birth control affects the endocrine system, please join our Facebook group, “Depo-Provera Endocrine Disorders Support Group.”  Thank you.

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Image by Jan Mallander from Pixabay.

This article was published originally on January 5, 2020.