Medical Misfit
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This is the journal of a 20 year medical mystery healing from traumatic brain injury, toxic mold exposure, Lyme & co., chronic fatigue syndrome and breast implant illness.
07/10/2026
Complex chronic illness is one hell of a ride. If there's one thing two decades of being a mystery patient have shown me, it's that lab results can never arrive fast enough. It's an odd feeling to want them to come back positive for a particular condition or disease. But answers are answers, and an answer usually means treatment, meaning that I'll eventually start feeling better.
I remember when I learned I had Lyme disease. It came to me after years of treatment and medical nightmares that never seemed to end, endless gaslighting, and frequent dismissals by medical professionals. I lost count of how many providers told me to go to therapy. No matter what I did, what treatments I tried, the number of therapists I saw, or how many lifestyle changes I made, I wouldn't get better. I thought it was in my head; maybe if I just tried a little harder, summoned more willpower, or improved my attitude, I would get better. But I never did. Positive thinking doesn't cure this disease. When I learned I had Lyme, I was excited, thinking that a simple round of antibiotics would be my hero, but I quickly learned that it was so much bigger than that.
The issues with Lyme disease are deeply systemic, and I honestly couldn't have come up with a better analogy to explain the flaws within our medical system; it's not any one individual or practice, it's in the systems that educate and pay, it's in the corrupted science that ignores evidence that doesn't serve particular motives, it's our government agencies who go to bat for for profit entities, it's everywhere all the time and all consuming.
The medical system failed millions of people affected by environmental health issues like Lyme disease. Have you experienced something like this in your healthcare journey?
When I was in alternative medical care and noticed the drastic differences between what they considered healthy and conventional standards, I often wondered why conventional medical professionals didn't use optimal lab ranges in their care. Doing so would call for a sweeping switch from sick care standards to optimal care, but what challenges exist in making this transition?
In this part one interview clip with Dr. Aimee Duffy ( ), we discuss the first hurdle this switch would need to clear: time. Doctors live busy lives; between juggling patient load, charting, appointments, and personal demands, they have very little time and bandwidth to learn new things like optimal lab standards. In addition, most doctors are so overbooked that they are unable to spend enough time with their patients to ask questions, leading them to the heart of the issue. Interestingly, many of the medical professionals who work with optimal lab standards either went through health challenges themselves or had patients that they were unable to help with the conventional SOP. It shouldn't be this way, and it's not their fault; that lies within the system.
Our medical professionals deserve to live happy, balanced lives. The overworking of our medical professionals is something that is widely known, accepted, and, for some, seems like a rite of passage, but ultimately it is a symptom of a broken system. I don't know about you, but I want the medical professionals who are holding my life in their hands to be well-rested and happy. How can we improve our healthcare if our heroes are too exhausted to keep up with the science?
U.S. Department of Health and Human Services Secretary Kennedy
Contact Dr. Aimee Duffy: https://carolinaintegrativemedicine.com/ or https://www.aimeeduffymd.com/
If you'd like to see the entire interview called Optimal vs. Conventional Lab Standards, where Dr. Duffy discusses this topic in further detail with more examples and explanation, please visit my channel at: https://tinyurl.com/MedicalMisfit1
07/08/2026
I can’t believe I’m saying this, but on July 25th, Monsanto won in the Durnell v. Monsanto case. The Supreme Court's landmark 7-2 ruling protects the manufacturer of Roundup from state-level "failure-to-warn" lawsuits. The justices decided that federal law overrides state laws, meaning companies cannot be penalized for failing to add cancer warnings to product labels if the U.S. Environmental Protection Agency (EPA) does not require them.
This ruling doesn’t prevent people from suing Bayer completely; they just won’t be able to sue for failure to warn at the state level. Most lawsuits involve multiple cases, but it is a ruling in favor of a company that knowingly harms us for profit. There have been thousands of cases against Bayer for damages like cancer from Roundup that have been ruled in favor of the individual and paid out by Bayer.
This ruling really made me think about the larger picture: who decides on labels anyway, and why does this matter? Currently, at the state level, manufacturers must warn about potential adverse health effects from products like Roundup. However, that is not the case on the federal level. Under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), manufacturers are legally required to sell products with EPA-approved labels, who doesn't currently require warning labels on Roundup.
According to the EPA, they have repeatedly and consistently reviewed glyphosate and determined that it does not pose a cancer risk when used as directed, so it does not mandate a cancer warning on product labels. As I was reading more into this, I learned that the reviews and research done by the EPA utilized studies that were ghostwritten by none other than Bayer, and even though the EPA knew these studies were compromised, it continued to use them to legitimize the safety of Roundup.
Read further here: https://tinyurl.com/Durnell
The illness box the sick care system tries to put us in misses the mark in many ways, leaving people with unresolved and unexplained symptoms, many of which indicate forming dysfunction that is the precursor to more serious health issues. As many with chronic illness will tell you, not everyone fits in that box.
In this part-two interview clip with Dr. Aimee Duffy( ), she continues the discussion on how the one-size-fits-all approach to convention lab standards limits patient care, and touches upon two issues I know intimately: liver function and blood sugar regulation.
If you're reading this, you've probably been exposed to a lot of toxins; it's inescapable in today's world. When I was dealing with liver issues, the fatigue and sick feeling were blatant, yet my labs would come back within normal range, leaving me sick and untreated. It wasn't until I completed a program for liver congestion independent of my traditional doctor and saw a drop in my liver enzymes that I started to feel better. I experienced the same situation with my fasting glucose, which, as Dr. Duffy discusses, was consistently coming back right under 100, indicating metabolic issues that went unaddressed by my conventional doctor.
I think the biggest takeaway from this clip is that many of the ranges the conventional medical system considers normal are the beginning stages of disease. The only lab ranges we should be using are optimal. We will never become healthy otherwise.
U.S. Department of Health and Human Services
Contact Dr. Aimee Duffy: https://carolinaintegrativemedicine.com/ or https://www.aimeeduffymd.com/
If you'd like to see the entire interview called Optimal vs. Conventional Lab Standards, where she discusses this topic in further detail with more examples and explanation, please visit my channel at: https://tinyurl.com/MedicalMisfit1
07/06/2026
Why insurance companies won’t cover compounding pharmacies is something I have frequently wondered about. There was a time period when I didn’t have health insurance because all of the care I received was considered alternative. The ironic part was that for me, this care was essential to saving my life; there was nothing “alternative” about it. During that time, I paid for all of my care and medications out of pocket, leaving me unable to afford medical insurance in addition to my medical needs. Many of my medications came from compounding pharmacies because the drugs were either cheaper, safer, or unavailable in traditional medicine. This is especially true for peptides and bioidentical hormones.
When I looked into why compounding pharmacies weren’t covered, I learned that insurance will only cover drugs that have been FDA approved, even if they are the same drug. To add another layer of complication, compounding pharmacies are typically regulated by state pharmacy boards, not the FDA, which to me feels like an intentional disconnect that further supports the interests of both insurance companies and Big Pharma. These three entities have held hands for far too long regardless of what's best for the patient.
I know what I’m suggesting is a broad, sweeping change to the pharmaceutical and regulatory systems, but maybe that’s exactly what we need. If my doctor says I need it, I need it, and it should be covered by health insurance.
07/04/2026
Happy 250th birthday, 'Merica! Hope everyone has a good Fourth of July this year and bought enough snakes and sparklers to go round. Who's watching fireworks tonight?
I think a lot of people with chronic illness can relate to the feeling that you don't fit into the box the medical system wants to put you in. I know I didn't fit, and when my health was in the worst shape, and my labs read normal, even though my providers could see my health slipping away just by looking at me, they didn't know what to do with me. But this is not just a lab standard issue.
In this interview clip with Dr. Aimee Duffy ( ), I ask her how the one-size-fits-all approach in conventional lab standards may limit patient care. She touches on a topic that I think most chronic illness patients can relate to: symptoms are ignored due to numbers falling within range, but there's another layer to this issue. Traditional medicine is also driven by what your insurance will cover, so even if a doctor wants to order extra labs, they may be unable to because the insurance company will deny extra testing if related labs come back within range, passing the extra cost on to the patient. What's frustrating about this is that the lab ranges used in traditional medicine are usually not optimal to begin with, causing a stacking of unhealthy ranges. An example of this is thyroid testing, which is spoken about at length in the full interview on my YouTube channel.
Insurance companies should not be deciding our healthcare for us.
U.S. Department of Health and Human Services Secretary Kennedy
Contact Dr. Aimee Duffy: https://carolinaintegrativemedicine.com/ or https://www.aimeeduffymd.com/
If you'd like to see the entire interview called Optimal vs. Conventional Lab Standards, where she discusses this topic in further detail with more examples and explanation, please visit my YouTube channel at: https://tinyurl.com/MedicalMisfit1
07/02/2026
With Carolina Integrative Medicine – I just got recognized as one of their top fans! 🎉
07/02/2026
Scary how accurate this is 😱😨
Don’t be this person 😆 Also this is AI - not real CRED to @jakegtv and @denny_dure for the video
07/01/2026
Last week, I earned a new chronic illness trading card for my collection: Epstein-Barr Virus or EBV. My labs show a previous infection, and not necessarily an active one as the marker that would indicate that came back as equivocal, but I am symptomatic. So, my functional medicine doctor has recommended that I start a round of treatment soon that will also address parasites, Lyme, and mold. It's going to be a rough ride. Hopefully, I will start perking up a bit because I am beyond exhausted.
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