Long, and transparent post alert! (in other words, get comfy)
Do you ever wish you could go back in time & smack yourself? I do. Why? June of 2010.
To spare you all the reasons that led me to it... I stupidly got breast implants in June of 2010. I have to admit, my research on the implants themselves, was minimal. All I had on my brain was that I wanted them, and that was it. My husband had an upcoming deployment, and the plastic surgeon had an opening that she made for us, so he’d be able to help with my recovery. Together, we chose the implants - Mentor smooth silicone, 300 cc's. It was all very quick, and of course, I didn’t think much about it. The day of surgery, the plastic surgeon said “Y’know, so many women wish they’d gone bigger… are you sure you don’t want to go with a bigger size?” I was so stupid. So, I chose a bigger size (350 cc’s), because “she wouldn’t NOT have my best interest, right?”. Wrong.
I woke up from surgery and felt like I had an elephant sitting on my chest. Everything hurt & my skin was stretching. I had immediate buyers remorse. It took me a few days to be able to function. But then, it was like a new “me”. Suddenly, I had confidence. <insert face palm> — whyyyyy did I think a bigger chest would make things better??! Helloooooo, insecurity! Life was good. Until it wasn’t.
About 6 months after getting my implants, I started having a lot of pain in my body. My General Practitioner sent me to physical therapy & prescribed anti-inflammatories & muscle relaxers that didn't work. This pain was so excruciating, that I went from physical therapy, to seeing a pain management doctor & having live X-ray cortisone injections in a matter of months. I went from running half marathons prior to getting implants, to being down on the couch for days. My running days had basically ended.
Within a year, the pain spread all over my body. The cortisone injections were no longer working. My pain management doctor said he couldn’t do anything for me anymore, and referred me to a spinal surgeon. After determining that I didn’t need spinal surgery, the spinal surgeon referred me to a neurologist. After waiting to get in to see a neurologist, he ran me through a gamut of testing… to rule out MS, Lupus, Lyme, or anything else. Everything came back in the “normal” range.
In 2012, after the gamut of testing done by the neurologist, I was given the diagnosis of Severe Fibromyalgia, and was given medication. At least we had an answer. I was all but a shell of my former self. I couldn’t function. I was in pain all the time. My family was having to pick up the slack where I was failing. The first medication helped, but made me feel stoned (I’ve never actually been stoned, but if I could imagine what it would feel like, this was it) 24/7. I couldn’t string 3 words together, slept all the time, and didn’t trust myself to drive. It made me swell up horribly. Then came the second medication… which did all of these things + made me swell even worse. So, then came the third medication. This one gave me relief, hallelujah! After this medication, I was able to function somewhat again. And for that, we were all grateful.
After about a year of being on this medication, I realized a lot of my symptoms were getting worse. Y’know when you hear a commercial for a drug, and they list all of the possible side effects? I was having just about every side effect possible for this drug. To counteract some of these, my neurologist was writing me more prescriptions. Now, if you know me, you KNOW I’m not a fan of taking pills if I don’t need to. My meds list was getting ridiculous. I was only 40, but had the meds list of someone in their 80’s. This medication I was on made my hair fall out, gave me permanent memory loss, and exacerbated my symptoms. On a daily basis, my pain level was excruciating and my skin hurt to the touch. The only way I can fully describe my skin hurting is if you rolled around naked on fiberglass insulation & had the flu on top of it. Hugging became something I hated (and I’m a hugger!), just because it hurt.
In 2014, I went to my neurologist and said that I was feeling worse taking these meds than I ever did before taking them. He suggested we try a different medication. I told him that I wanted to get OFF of the meds, clear everything from my system, and then reassess before we started anything new. He begrudgingly agreed, but as he walked out of the exam room, he said “you’ll be back and BEGGING me for a new prescription”. Challenge accepted, Dr. Jerkface. I never went back to him. He was a pill-pusher, and I’m not interested in someone that won’t at least listen to my concerns/wants/needs.
With the help of my General Practitioner, we found more natural ways to combat my pain and symptoms. I learned to take supplements, learn my limits, and listen to my body. While this was helpful, the pain was too much somedays. Depression & anxiety were prominent, and I kind of became a hermit for a while.
2018, I started having burning & pain in my breasts quite often. My mom had mentioned an article that mentioned something called “Breast Implant Illness”. I read it, but didn’t put a lot of thought into it. It was also time for a yearly check-up with my plastic surgeon. I mentioned that I was having a lot of breast pain, and wondered if this breast implant illness could be a factor. She literally laughed in my face, and quickly said “NO”. But then proceeded to quickly send me for a MRI to make sure the implants hadn’t ruptured. (they hadn’t)
2019, with every symptom getting worse, I was researching Breast Implant Illness more. Without sounding dramatic, I literally felt like I was dying. The more research I did, the more articles I found. It was everything I’d felt in the past almost 10 years. Pain, being sent for lab work… only for everything to come back in the “normal range”, and every single symptom I’d been having:
Brain fog/memory loss/cognition problems
Muscle pain & weakness
Joint pain in my neck/shoulders/back/hips/knees/hands/feet
Hair loss
Weight problems
Inflammation
Insomnia & poor sleep
Dry eyes
Diminishing hormones/early menopause
Slow healing/easy bruising
Slow recovery after exercise
Vertigo
Headaches/migraines
Throat clearing/cough/difficulty swallowing/choking
Reflux
Nausea/gastritis/leaky gut
Fevers/Night Sweats/Heat Intolerance
Persistent bacterial/viral infections
UTI/Interstitial Cystitis
Ear ringing
Sudden new food/chemical intolerances/allergies
Heart palpitations/heart pain/chest discomfort/shortness of breath
Swollen & tender lymph nodes of breast & underarm
Numbness & tingling in limbs
Cold & discolored hands/feet
Depression/anxiety/panic attacks
Pain throughout my body
Skin pain
Blurred vision
Constant rash on my chest, which worsened in the sun
The feeling of my implants burning me from the inside out
I came across a Facebook group called “Breast Implant Illness and Healing by Nicole” and joined to see what it was all about. HOLY. MOLY. Hundreds of thousands of women, all with the same symptoms as me. I finally felt validated, and no longer like a hypochondriac! I had a group of people who understood! I spent days just reading everyone’s stories. Through all of these ladies, they found surgeons in each state that fully believed in Breast Implant Illness (or better known as BII). There were several in Indiana. I made a consultation appointment with someone near me. She was AMAZING. During my 90-minute consultation, this surgeon explained everything in detail & made sure I understood. She’s doing a study on BII with another doctor. While she still does implants, she fully educates everyone, and is doing more explants these days than implants. After listening to my story and all of my symptoms, she assured me that I would have relief. I made my surgery appointment, and literally COULD. NOT. WAIT. for these toxic bags to come out of my body.
October 6, 2020 — I was able to get my implants removed with a full enbloc & capsulectomy (fancy terms for full removal of the capsules that surrounded my implants). My left implant had become attached to my ribcage & intertwined in my muscle, thus contributing to the pain I was having. She had to scrape to get it all, but she got it. I woke up from surgery, and the first thing I noticed was that I could take a deep breath. For the past 10 years, I had roughly 3 pounds of implants sitting on top of my lungs, and my breathing, unbeknownst to me, had become shallow. For the first time in 10 years, my shoulders didn’t hurt. This was all in the first few minutes of waking up!
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My sweet friend sent me these socks & I wore them to the surgery center! |
I had my surgeon send the capsules surrounding my implants to pathology. The results were interesting. They tested positive for 2 kinds of bacteria: Cutibacterium acnes, and Staph. No WONDER I was always sick! The recovery was not an easy one, and it took time. The amount of detoxing your body does after having something toxic in it for a decade is astounding. It took me a solid month before I felt good. But wow, did I ever feel GOOD! I hadn’t felt like that in a decade. However, I got Covid (horribly) a week later. So, my recovery took a bit longer than some, just because my immune system kept taking hits.
It’s been one year since I explanted, and I have not regretted that decision for even one second. I’d say about 85% of my symptoms are gone, and even those that are remaining, aren’t constant.
In a year’s time, not once have I been relegated to my bed because of pain. Not once have I had a “fibromyalgia flare”. (I’m not saying I don’t have fibromyalgia - because I do still have some pain, but it’s definitely not severe, and it no longer leaves me bed-ridden.) Not once have I had a mysterious low-grade fever, and continuously felt like I have the flu. Not once have I had to take a nap daily. Not once, have I missed out on family fun because of my pain level. Not once.
Coincidence? I think not.
I was robbed of 10 years of my life because of a really dumb decision on my part. Not everyone has a reaction to implants like I did, and they're lucky. But because so many women are coming forward with their reactions like mine, others are seen & heard. Insurance companies are listening, and now explants are starting to be covered, which is HUGE.
Please, if you are considering getting implants, DO YOUR RESEARCH. There is no “safe” type of implant. Even saline implants are made of silicone - they’re just injected with saline solution internally. Please join the Facebook group I talked about. Read every story, and then make your decision. If you have implants and are wanting them out, feel free to DM me. Join the Facebook group. Little did I know, I had several friends in there… and one of them, whom was already a dear friend, went a day before me with her explant. We virtually held each others hands throughout the entire process, and for that, I will be eternally grateful. You will have hundreds & thousands of women in your corner… who understand you, who support your decision.
I’ve been through hell & back, fighting for the woman I am now. Sadly, it took all of this to see myself the way my creator sees me, and has always seen me… Psalm 139:14 “I praise you because I am fearfully and wonderfully made; your works are wonderful, I know that full well.” How sad that insecurity and society made me doubt that.
In the past year, my energy has returned. My smile has returned. Jenni has returned. And I couldn’t be happier! My body is still healing, and that’ll be on it’s own timeframe. It’s different for everyone, and I’m embracing that.
It took me a year to be brave enough to share this — mainly because I was so embarrassed that I felt that I needed implants to begin with. More so, that this process also robbed me of 10 years of my health, family, friendships, and so many missed “things”. It’s been a year of forgiving myself, and asking forgiveness from my family… who had to pick up the slack for the past decade.
I’m hoping that my journey through all of this may help someone, or someone you know. I’m not sharing this in hopes of gaining attention (quite the opposite, actually, because this is SUPER personal), but that it educates someone. That it makes someone feel seen & heard. That it gives someone a hand to hold while going though it themselves.
Peace, love, and health to you all,
Jenni