Thursday, May 29, 2025

More Than Just Pain: Exploring the Link Between Fibromyalgia and Autoimmune Diseases

So many people that have been diagnosed are actually seronegative for some other Autoimmune disease. I know there are plenty of us out there that only have that Fibromyalgia diagnoses, and we KNOW that there is more wrong. I am just writing this to let you all know you have to Advocate for yourself. Make yourself heard, don't be gaslit! 

Fibromyalgia is a chronic condition characterized by widespread musculoskeletal pain accompanied by fatigue, sleep disturbances, and cognitive difficulties (often referred to as "fibro fog"). While the exact cause remains elusive, there is growing evidence suggesting a link between fibromyalgia and autoimmune disorders. This post delves into this fascinating connection and its implications for those living with these conditions.

What are Autoimmune Diseases?
In autoimmune diseases, the body's immune system mistakenly attacks healthy cells and tissues, causing inflammation and a variety of symptoms. Examples include rheumatoid arthritis, lupus, and multiple sclerosis.
The Overlap: Shared Symptoms and Risk Factors
Fibromyalgia and autoimmune diseases often share common symptoms like fatigue, widespread pain, and sleep disturbances. This overlap can sometimes make diagnosis challenging, and it's not uncommon for individuals to experience both conditions.
Evidence of the Connection:
While fibromyalgia is not currently classified as an autoimmune disease, there's compelling evidence for a link:
  • Shared Genetic Factors: Research suggests that individuals with a family history of autoimmune diseases may have a higher risk of developing fibromyalgia. This points to a potential shared genetic predisposition.
  • Immune System Dysregulation: Some studies have found evidence of immune system abnormalities and elevated levels of certain inflammatory markers in individuals with fibromyalgia.
  • Co-occurrence of Conditions: People with fibromyalgia are more likely to have other autoimmune diseases like lupus, rheumatoid arthritis, and Sjogren's syndrome. This raises the possibility of an underlying immune system dysfunction that predisposes individuals to both conditions.
  • Emerging Research on Autoantibodies: Newer research has explored the possibility of specific autoantibodies being present in some fibromyalgia patients. However, more research is needed to confirm these findings.
Why is This Important?
Understanding the link between fibromyalgia and autoimmune diseases is crucial for:
  • Diagnosis: Recognizing potential overlapping conditions can lead to more accurate and timely diagnoses.
  • Treatment: A deeper understanding of the underlying mechanisms might pave the way for more effective and targeted therapies.
  • Patient Care: Individuals with fibromyalgia and autoimmune conditions can benefit from a multidisciplinary approach to care that addresses both aspects of their health.
Living with Fibromyalgia and Autoimmune Diseases:
Managing fibromyalgia and autoimmune diseases can be challenging but is absolutely possible. Important strategies include:
  • Finding the right healthcare team: It's important to work with a team of doctors (including specialists) to develop a tailored care plan.
  • Prioritizing self-care: This includes managing stress, getting enough rest, following a healthy diet, and engaging in gentle exercise.
  • Joining a support group: Connecting with others who understand what you're going through can be a powerful source of support and information.
Conclusion:
The relationship between fibromyalgia and autoimmune diseases is complex and requires further research. However, the growing evidence suggests that there is a connection, and this connection can have a significant impact on the lives of those affected. Increased awareness and research efforts are essential to improve diagnosis, treatment, and overall quality of life for individuals living with these conditions.
Note: This blog post is for informational purposes only and should not be taken as medical advice. Always consult with a qualified healthcare professional for diagnosis and treatment of any health conditions.

Wednesday, May 28, 2025

What Is Gaslighting and How Does It Affect Chronic Pain sufferers


Sadly, Gaslighting is a term that’s become increasingly common in conversations about emotional and psychological health. But what does it actually mean—and why is it so damaging, especially when it happens in places we should feel safe, like the doctor’s office?

What Is Gaslighting?

At its core, gaslighting is a psychological manipulation tactic where someone causes another person to doubt their own perceptions, memories, or understanding of events. The term comes from the classic play and film "Gaslight," where a husband manipulates his wife into believing she’s losing her mind.

How Does Gaslighting Happen—Especially in Healthcare?

While gaslighting can happen in any relationship, it’s especially harmful when it comes from people in positions of authority, like doctors. In a medical context, being gaslit by doctors means having your symptoms, concerns, or experiences dismissed, minimized, or doubted. Sometimes, this goes so far that you begin to question your own reality or sanity.

Examples of Medical Gaslighting:

  • A patient with chronic pain is told, “You’re just anxious,” with no further evaluation.

  • Someone with unexplained fatigue is told, “You’re just getting older,” despite being much younger than average for such symptoms.

  • A woman reporting heart attack symptoms is told, “It’s probably just indigestion,” without appropriate testing.

Why Does Medical Gaslighting Happen?

Medical gaslighting is especially common with chronic illnesses that lack clear diagnostic tests—like fibromyalgia, endometriosis, or chronic fatigue syndrome. These conditions are often misunderstood, and patients (especially women and people of color) face higher rates of dismissal and skepticism from healthcare providers.

The Emotional Impact of Gaslighting

Being gaslit—especially by someone you’re supposed to trust—can have profound, long-lasting effects on your emotional well-being:

1. Self-Doubt and Confusion:
You may start questioning your own perceptions and experiences, making it harder to trust yourself—not just about your health, but in other areas of life.

2. Heightened Anxiety and Stress:
Not being believed can lead to persistent anxiety about your symptoms and your future, and worry that something serious is being missed.

3. Depression and Hopelessness:
Repeated invalidation can fuel feelings of helplessness, sadness, and despair. You may feel isolated, misunderstood, or like you’re “going crazy.”

4. Loss of Trust in Healthcare Providers:
Being gaslit erodes your trust in doctors and the healthcare system. You might become reluctant to seek care, fearing further dismissal or judgment.

5. Social Withdrawal and Isolation:
If friends, family, or coworkers echo the dismissive attitudes of doctors, you may withdraw socially, deepening your loneliness.

6. Lower Self-Esteem:
Constantly being told your experience isn’t real or important can chip away at your confidence and self-worth.

7. Worsening Physical Symptoms:
Emotional distress can actually exacerbate physical symptoms, especially in conditions like fibromyalgia, where stress is a known trigger for flare-ups.

Why Does Gaslighting Lead to Emotional Exhaustion and Depression?

Gaslighting forces you into a constant state of self-doubt and emotional hypervigilance. The ongoing mental labor of second-guessing your thoughts, memories, and feelings drains your emotional energy and leaves you feeling worn out. Over time, this can trigger symptoms of depression—hopelessness, sadness, loss of motivation, and emotional numbness. The cycle of invalidation and self-doubt can make you feel isolated and disconnected, deepening emotional exhaustion and depressive feelings.

How Does Gaslighting Compare to Other Emotional Abuse?

While all emotional abuse is harmful, gaslighting is particularly insidious because it targets your fundamental sense of reality and self. Other forms of emotional abuse may involve direct criticism, shaming, or control, but gaslighting adds a layer of psychological manipulation that can make victims feel as if they cannot trust their own minds—a uniquely disorienting and isolating experience.

What Can You Do If You’re Being Gaslit?

  • Acknowledge Your Feelings: Your emotions are valid and a natural response to being dismissed.

  • Seek Support: Reach out to trusted friends, family, or support groups who understand your experience.

  • Consider Therapy: A mental health professional can help you process your experiences and rebuild your confidence.

  • Advocate for Yourself: Document your symptoms and bring an advocate to appointments if possible.

  • Find a Supportive Provider: Don’t hesitate to seek a second opinion or switch doctors if you feel consistently dismissed.


In summary:
Gaslighting is a severe form of emotional abuse that can have deep and lasting effects on your mental and physical health. Recognizing the signs and seeking support can help you protect your well-being and advocate for the care and respect you deserve.


If you or someone you know is experiencing gaslighting—especially in a healthcare setting—know that you’re not alone, and your experiences are real. Trust yourself, seek support, and don’t give up on finding the care you need.

Thursday, May 22, 2025

The Hidden Connection Between Fibromyalgia and Post-Nasal Drip: What You Need to Know

 As anyone who lives with fibromyalgia knows, it’s more than just widespread pain. It’s a complex condition that affects every aspect of your life, from energy levels to sleep quality to overall immune function. But here’s the thing—I never really put the two together myself. I never made the connection between my fibromyalgia and the ongoing issue of post-nasal drip until recently. However, once I started digging into it, it totally made sense. And now, after learning more, I can’t help but think that this is something that may be affecting far more fibromyalgia sufferers than we realize.

Post-nasal drip, the sensation of mucus dripping down the back of the throat, is often associated with conditions like allergies, sinus infections, or colds. However, recent research and personal accounts are starting to suggest a connection between fibromyalgia and chronic post-nasal drip that may be more common than we think.

A Chronic Inflammation Link

Fibromyalgia is often characterized by chronic inflammation and immune system dysfunction, which are thought to play a key role in its symptoms. Interestingly, conditions like sinusitis, allergies, and post-nasal drip are also driven by inflammation. This means that people with fibromyalgia might be more vulnerable to developing other inflammatory conditions, including those that affect the sinuses and respiratory system.

Research has shown that immune dysregulation in fibromyalgia can lead to an overactive immune response, increasing the likelihood of allergic reactions or sinus problems, both of which can cause post-nasal drip. According to a study in Clinical Rheumatology (2017), chronic pain conditions like fibromyalgia often coexist with inflammatory diseases that affect the sinuses.

The Role of Sensitivity

Another crucial factor in the fibromyalgia-post-nasal drip link is central sensitization. In fibromyalgia, the central nervous system becomes hypersensitive to pain and other stimuli. This means that environmental irritants, such as allergens or pollutants that might cause mild sinus congestion or post-nasal drip in the general population, may be much more bothersome for someone with fibromyalgia. A 2013 study published in The Journal of Pain highlighted how individuals with fibromyalgia often experience an exaggerated response to sensory inputs, making them more prone to developing symptoms like post-nasal drip.

Sleep and Gastrointestinal Issues

People with fibromyalgia also often struggle with sleep disturbances and gastrointestinal problems, which can contribute to or exacerbate post-nasal drip. For instance, GERD (gastroesophageal reflux disease), common in fibromyalgia patients, can lead to laryngeal reflux, where stomach acid irritates the throat and causes excess mucus production. This feeling of mucus in the throat can mimic or trigger post-nasal drip symptoms.

Moreover, fibromyalgia’s sleep disruptions might worsen other conditions, including sinus congestion, making the cycle of discomfort even harder to break.

The Impact of Medication

Many medications used to treat fibromyalgia, such as antidepressants, muscle relaxants, or pain relievers, can also have side effects that impact the sinuses and throat. For example, some of these medications can cause dry mouth and throat irritation, which could make post-nasal drip feel more uncomfortable.

Should You Be Concerned?

If you're living with fibromyalgia and experiencing post-nasal drip, you're not alone. It's important to recognize that these symptoms could be connected, and understanding the link could help you find better ways to manage both.

Managing Fibromyalgia and Post-Nasal Drip Together

Managing both fibromyalgia and post-nasal drip might involve addressing common triggers, like stress, sleep hygiene, and environmental allergens. Keeping your immune system balanced and reducing inflammation through diet, exercise, and stress management techniques can make a big difference. Additionally, working with your healthcare provider to find a treatment plan that minimizes the impact of both conditions can improve your quality of life.

Conclusion

Fibromyalgia is a multi-faceted condition that affects far more than just your muscles and joints. The connection between fibromyalgia and post-nasal drip may be an important piece of the puzzle that many sufferers haven’t yet recognized. By understanding this link and addressing both conditions holistically, we can work toward a more effective management plan—one that leads to less discomfort and a better quality of life.


Thursday, May 15, 2025

From Myofascial Pain Syndrome to Fibromyalgia: The Overlooked Connection

 It was one of those pivotal "aha" moments—the realization that my fibromyalgia didn’t just appear out of nowhere. For years, I had battled persistent muscle pain, dismissed as tension, stress, or minor injuries. What nobody recognized, and what I had failed to connect at the time, was that my journey likely started with myofascial pain syndrome (MPS). The deep knots, the unexplained trigger points, the frustration of being told it was "just in my head"—all of it added up. But because MPS wasn’t properly acknowledged or treated, my condition evolved into something much more complex: fibromyalgia. This realization reframed everything I thought I knew about my own health.

The Overlapping Symptoms: MPS vs. Fibromyalgia

Both MPS and fibromyalgia cause chronic pain, but their mechanisms differ. MPS is localized, characterized by tight trigger points in muscles that cause referred pain, while fibromyalgia involves widespread musculoskeletal pain, fatigue, and cognitive challenges. Despite these distinctions, their interaction is increasingly recognized, particularly in cases where unresolved MPS symptoms seem to contribute to fibromyalgia’s onset.

The Progression from MPS to Fibromyalgia

Several studies suggest that untreated or prolonged MPS can lead to central sensitization—a hallmark of fibromyalgia. Chronic trigger point pain may send repeated signals to the nervous system, potentially triggering widespread pain and heightened sensitivity. A scoping review in PLOS One explores how fascia adapts to chronic tension and how sustained myofascial dysfunction might contribute to fibromyalgia’s development.

Other research, such as an article from ePainAssist, discusses the theory that repetitive, untreated pain from MPS may increase brain sensitivity, leading to the systemic pain response characteristic of fibromyalgia.

Challenges in Diagnosis and Treatment

One of the major hurdles for those dealing with both conditions is the diagnostic process. Many healthcare providers focus solely on fibromyalgia’s systemic symptoms while overlooking the muscular dysfunction characteristic of MPS. This gap in recognition often leads to delayed intervention, forcing individuals to struggle with worsening pain and frustration.

Treatment approaches should ideally target both conditions. For MPS, trigger point therapy, physical therapy, and stretching techniques can help alleviate localized pain. For fibromyalgia, a multidisciplinary strategy that includes medication, lifestyle adjustments, and nervous system modulation is key.

Why This Connection Matters

Understanding the relationship between MPS and fibromyalgia could change how patients and healthcare providers approach treatment. If MPS is identified early, interventions might prevent or minimize fibromyalgia’s progression, ultimately improving quality of life. This underscores the importance of medical practitioners taking a holistic view of chronic pain conditions instead of relying on narrowly defined diagnostic categories.


Can Plasmapheresis Help Fibromyalgia? What the Latest Research Says

 Fibromyalgia is a chronic condition that affects millions, causing persistent pain, fatigue, and a host of other symptoms that can be tough to manage. For decades, it’s been considered a disorder rooted in the nervous system-not the immune system. But new research is shaking up that view, suggesting that, at least for some patients, the immune system (and specifically, antibodies) might play a surprising role.

One treatment that’s getting attention is plasmapheresis (also known as plasma exchange). But can this therapy, which is already used for autoimmune diseases, actually help people with fibromyalgia? Let’s dive into the science.

What Is Plasmapheresis?

Plasmapheresis is a medical procedure that removes plasma (the liquid part of your blood) and replaces it with a substitute. This process removes antibodies from the bloodstream-think of it as a “blood wash” that targets potentially harmful immune proteins.

It’s already a proven therapy for autoimmune diseases like myasthenia gravis and Guillain-BarrĂ© syndrome, where the immune system attacks the body’s own tissues.

Why Consider Plasmapheresis for Fibromyalgia?

Here’s where things get interesting:
A landmark 2021 study found that IgG antibodies from fibromyalgia patients could actually induce fibromyalgia-like symptoms in mice. When these antibodies were removed, the mice recovered. This suggests that, for some people with fibromyalgia, their own antibodies might be driving their symptoms.

Since plasmapheresis is so effective at reducing antibody levels (sometimes by as much as 80–90% in other conditions), researchers are asking: Could it work for fibromyalgia, too?

What Does the Evidence Say?

  • Antibody Reduction:
    There’s no doubt that plasmapheresis can quickly and dramatically lower antibody levels in the blood.

  • Animal Studies:
    In mice, removing these antibodies reversed fibromyalgia-like symptoms. That’s a promising sign!

  • Human Studies:
    Here’s the catch: As of now, there are no published clinical trials or case studies showing that plasmapheresis improves fibromyalgia symptoms in people. The evidence is mostly theoretical or comes from animal models.

  • Expert Opinions:
    Many experts are excited about the potential and are calling for clinical trials. But until those studies are done, we can’t say for sure if plasmapheresis is effective for fibromyalgia patients.

The Bottom Line

Plasmapheresis is a powerful tool for lowering antibody levels, and early research hints that it could help some people with fibromyalgia-especially those with an autoimmune component to their illness. But right now, there’s no direct clinical evidence that it works for fibromyalgia. If you’re interested in this therapy, keep an eye out for upcoming clinical trials, and always talk to your healthcare provider before considering new treatments.  

More Than Just Pain: Exploring the Link Between Fibromyalgia and Autoimmune Diseases

So many people that have been diagnosed are actually seronegative for some other Autoimmune disease. I know there are plenty of us out there...