Can We Finally Ask the Questions?
- clicks4acause
- Dec 1
- 4 min read
Why “Incurable Diseases” in America Deserve Transparency, Truth, and Accountability
By Wendy Jean — Functional Genomics Practitioner (FGP), Certified Functional Nutrition (FN), Holistic Health Coach (HHC), and Global Lyme Advocate
When Your Body Knows Before the System Does
My digging started in 2017 —but my symptoms started long before that.
Back in 2013–2014, I felt the first signs of something deeply wrong:
the bone-crushing fatigue
the strange neurological fire
the hormonal chaos that wasn’t “just hormones”
the shortness of breath
the migrating pain
the cognitive fog
the anxiety that didn’t match my life
the sensitivity to chemicals, foods, and environments
I went to doctors. I trusted the process.
I believed someone would recognize what was happening.
Instead, I faced the most common epidemic women silently suffer under: medical gaslighting.
I was told:
“You’re a mom, you’re just exhausted.”
“It’s stress.”
“It’s your hormones.”
“You’re doing too much.”
“Your labs are normal.”
Everything I said was minimized, excused, or blamed on my life instead of my biology.
But I knew something was collapsing inside of me.
By 2017, the decline was undeniable. I was bedridden, debilitated, losing functionality, and desperate for answers. That was the year I started digging for myself — because nobody else would.
The digging is what saved my life.
The digging is what built my career.
The digging is what made me an advocate.
The digging is why I speak out today.
Why Are We Discouraged From Asking Where Diseases Come From?
When illnesses become chronic, confusing, and expensive, an uncomfortable truth emerges:
People aren’t encouraged to heal…They’re encouraged to stop asking questions.
You’re told:
it’s anxiety
it’s stress
it’s “just hormones”
it’s aging
it’s lifestyle
it’s all in your head
But diseases don’t become “incurable” because they cannot be healed. They become incurable when the systems around them refuse to investigate their origins.
Origin determines:
accountability
research priority
medical education
treatment access
disability policies
long-term public health strategy
And when origins threaten political, financial, or institutional power?
They’re buried.
The Controversial Claims: HIV & Lyme Origins Back in the Spotlight
Recent interviews — including those from FDA Commissioner Dr. Marty Makary — have reopened debates around the origins of certain modern diseases.
HIV/AID
Claims suggest:
Cold War primate labs in Central Africa
U.S.-funded research on simian viruses
Early clusters near research hubs, not remote villages
The scientific consensus still supports a natural spillover, but the public has the right to transparency and archived data.
Lyme Disease
This is where the story hits home.
Claims connect:
the sudden recognition of Lyme in 1975
to the Plum Island Animal Disease Center
its Cold War tick research
and the involvement of scientists moved under Operation Paperclip
What we can confirm:
Lyme as a bacteria is ancient
Ticks have always carried pathogens
Cold War insect-vector programs are documented
Some labs experienced containment failures
No federal agency has ever done a full origin audit
For patients like me, who suffer real infections with real consequences, this isn't a conspiracy theory — it's a call for transparency.
What if Lyme is a virus?
What about the FAILED Lyme Vaccine - Lymerix?
What about the new Vaccine coming to market?
What about the Doctors silenced for treating Lyme?
The Real Crisis: Chronic Illness Is Treated Like an Inconvenience
Lyme is now one of the fastest-growing infectious diseases in America.
And yet:
insurance doesn’t cover chronic treatment
disability is routinely denied
doctors are punished for treating beyond 28 days
women are dismissed the most frequently
children are misdiagnosed for years
environmental factors are ignored
When I applied for disability in Pennsylvania, the state recognized my chemical sensitivity — yet refused to recognize Lyme disease as disabling.
I was told I could work a tollbooth that didn’t even exist anymore.
People aren’t failing the system.
The system is failing the people.
But there are voices speaking TRUTH!
What My Research Showed Me: Genes Don’t Lie
When no one would help me, I became the researcher I needed.
I studied:
functional genomics
detox pathways
methylation
immune regulation
mitochondrial health
epigenetics
toxin accumulation
trauma biology
And what I found was simple, powerful, and consistent:
Lyme patients share predictable genetic vulnerabilities:
methylation impairment (MTHFR, MTRR, BHMT)
detox bottlenecks (GST, CYP, COMT)
inflammation misregulation
mitochondrial fragility
heightened sensitivity to environmental toxins
This is why:
certain people collapse
certain people stay chronically ill
certain people develop neurological symptoms
certain people never bounce back
Our genes reveal the “why.”
Our environment reveals the “how.”
Our untreated infections reveal the “what now.”
From Bedridden to Global Lyme Advocate
I didn’t choose this path.
Lyme forced me into it.
Gaslighting hardened me.
Research transformed me.
Faith carried me.
And now I carry others.
Today I am:
Functional Genomics Practitioner (FGP)
Certified Functional Nutrition (FN)
Holistic Health Coach (HHC)
Global Lyme & Environmental Health Advocate
A voice for the disabled, dismissed, and misunderstood
I advocate in:
Pennsylvania
Washington, D.C.
Center for Lyme Action
global webinars
women’s groups
community wellness events
His Place and healing circles
I became who I needed in 2014.
I became who others need in 2024.
So… Can We Ask the Questions Now?
Not from fear.
Not from politics.
Not from conspiracy.
But because the public deserves:
truth
transparency
research
competent care
disability recognition
coverage for chronic illness
genetic-informed treatment
environmental detox education
People are suffering.People are dying.People are being dismissed while their bodies fall apart.
It is not radical to ask,
“Where did these diseases come from?”
It is responsible.
It is not radical to ask,
“Why are certain diseases not recognized?”
It is necessary.
It is not radical to say,
“I deserve answers.”
It is human.
If You’re Sick, Searching, or Silenced — You’re Not Alone.
If you need:
genetic insight
detox guidance
Lyme support
trauma-informed health strategies
envir
onmental and toxin education
a coach who has lived this
community
faith-filled support
I’m here.
You deserve answers.
You deserve healing.
You deserve truth.
Join me FREE and let's make a plan of ACTION
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