Introduction: Is Multiple Sclerosis Really an Autoimmune Disease?

For years, multiple sclerosis (MS) has been labeled an autoimmune disorder—a disease in which the immune system mistakenly attacks healthy nerve tissue. But a growing body of research suggests that MS is actually be an infectious disease triggered by parasites that disrupt brain chemistry and damage nerve cells.

A key player is the vital brain chemical called glutamate, which can be dysregulated by various parasites.

What Is Glutamate and Why Is It Important in MS?

Glutamate is the brain’s main excitatory neurotransmitter. It helps nerve cells communicate, plays a key role in learning and memory, and keeps your brain functioning properly.

But if it is in excess, glutamate becomes toxic. High levels of glutamate outside of nerve cells cause overstimulation, leading to nerve damage and cell death—a process known as glutamate excitotoxicity.

This type of damage is not just seen in MS, but also in Alzheimer’s, Parkinson’s, ALS, and even stroke. In MS specifically, research has consistently shown:

  • Elevated glutamate in white matter and active brain lesions

  • Higher glutamate levels in cerebrospinal fluid (CSF) during MS relapses

  • A strong link between glutamate concentration and nerve fiber loss and disease progression.

Even more concerning, glutamate also harms oligodendrocytes—the cells that produce myelin, the protective covering around nerves. This means that excess glutamate can drive both neurodegeneration and demyelination in MS.

Parasites Disrupt Glutamate Balance in the Brain

So, what causes glutamate levels to rise in MS?

Research points to parasites—particularly Toxoplasma gondii—as a major factor. This common brain parasite infects up to one-third of the global population, often without symptoms. But it can infect and and create chaos in the brain.

How Toxoplasma gondii Triggers Glutamate Toxicity:

  • It damages astrocytes, the brain’s support cells that regulate glutamate.

  • It suppresses GLT-1, a key transporter that normally removes excess glutamate.

  • This leads to glutamate buildup, brain inflammation, and nerve damage—exactly what we see in MS.

In mouse studies, treating infected brains with the antibiotic ceftriaxone restored GLT-1, lowered glutamate levels, and even reversed neuronal damage. This offers strong evidence that glutamate toxicity can be reversed—if the infection is treated.

Toxoplasma isn’t the only parasite involved. Other parasites can invade the central nervous system and cause similar damage.

Is MS Caused by Chronic Parasitic Infections?

The traditional view of MS as an autoimmune disease is being challenged by this new evidence. In fact, researchers have found that:

  • Immune cells in MS lesions overproduce glutamate

  • Damaged axons express glutamate receptors, making them even more vulnerable.

All of this suggests that parasites enter the brain, disrupt glutamate balance, trigger inflammation, and damage nerves.

Instead of the immune system attacking the body by mistake, it may be reacting to real infections.

The Vicious Cycle: Glutamate, Inflammation and MS Progression

Here’s what this cycle looks like:

  1. Parasites infects the brain

  2. Astrocyte function is disrupted

  3. Glutamate builds up

  4. Neurons and myelin are damaged

  5. Immune system reacts, but fails to clear the infection

  6. Inflammation increases, glutamate continues to rise

  7. MS symptoms worsen and progression accelerates.

This is why MS relapses and progression may not be random—they may reflect the activity of underlying infections and their effect on brain chemistry.

The Hope: A New Path to Recovery in MS

If parasites are driving glutamate toxicity and MS progression, then treating the infections could be the missing key to recovery.

Several case studies and patient success stories show that targeted parasite treatment, combined with a supportive healing plan, can lead to reduced symptoms, improved function, and even recovery.

This shifts the MS conversation from “immune suppression” to “infection resolution and nerve repair.”

Final Thoughts: Time to Rethink MS

The link between glutamate dysregulation and parasitic infections offers a groundbreaking new perspective on multiple sclerosis.

Rather than being a random autoimmune attack, MS may be the chronic result of infections hijacking brain chemistry. With this understanding, we can finally begin to focus on real root causes—and offer real hope for healing.

There are real solutions to recover from parasites today!

To restore health, we must focus on treating the cause of inflammation, which are parasites. First, identify the enemy (parasites), then support the body and treat the parasites while following a holistic approach. When parasitic infections are treated effectively, we can overcome inflammation or disease.

If you’re frustrated with the fact that our standard of care STILL doesn’t offer a real solution for treating MS and other diseases, then click on the link below to watch Pam Bartha’s free masterclass training and discover REAL solutions that have allowed Pam and many others to live free from MS and other diseases.

CLICK Here to watch Pam’s masterclass training

References:

The Relationship between Glutamate and Multiple Sclerosis

In Vivo Evidence of Glutamate Toxicity in Multiple Sclerosis

The Role of Glutamate in the Pathogenesis of Multiple Sclerosis

Memory in multiple sclerosis is linked to glutamate concentration in grey matter regions

Multiple sclerosis: altered glutamate homeostasis in lesions correlates with oligodendrocyte and axonal damage.

Glutamate excitotoxicity–a mechanism for axonal damage and oligodendrocyte death in Multiple Sclerosis?

Increased Concentrations of Glutamate and Glutamine in Normal-Appearing White Matter of Patients with Multiple Sclerosis and Normal MR Imaging Brain Scans

Altered expression patterns of group I and II metabotropic glutamate receptors in multiple sclerosis

Glutamate, T cells and multiple sclerosis 

Evidence of elevated glutamate in multiple sclerosis using magnetic resonance spectroscopy at 3 T

Glutamate receptor expression in multiple sclerosis lesions.

GLT-1-Dependent Disruption of CNS Glutamate Homeostasis and Neuronal Function by the Protozoan Parasite Toxoplasma gondii

Increased levels of glutamate in the central nervous system are associated with behavioral symptoms in experimental malaria

Scientists unpack how Toxoplasma infection is linked to neurodegenerative disease

Neurotransmitters and T. gondii

 

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