Have you ever noticed it takes you a couple of days to recover from a stressful event or over-exertion? A 48-hour recovery period is something you commonly hear about from people with fibromyalgia and chronic fatigue syndrome.
We don’t yet know why we need a couple of days to recover from … well, just about anything, but a lot of chronic fatigue syndrome research is focusing on post-exertional malaise—the intensified fatigue and flare of other symptoms following exercise.
Several research groups have identified genetic and blood abnormalities in the following exercise and have documented participants’ inability to perform as well on the second day.
What we do know about this recovery period is that we’re stuck with it. For many of us, it means taking it really easy for a couple of days after anything big, such as a holiday, a vacation, or an unexpected stressful event.
It can be a real problem for people who work or go to school full time. Just getting through a day can drain you enough to need recovery time, yet you have to get up the next morning and do it all over again. So while you may feel pretty decent on Monday, especially if you rested the whole weekend, Tuesday will be a little hard, Wednesday a little harder still. By Friday? It’s not pretty.
When your routine is enough to drag you down, you don’t have the reserves to deal with anything else on top of it. Who hasn’t been there?
Halfway through the week, you have to deal with some kind of crisis that gets your adrenaline pumping. Now you have more to recover from.
It’s likely not realistic for you to just go to bed for two days after every workday, or every stressful event in your personal life.
What we can do, though, is recognize what circumstances are likely to trigger a need for recovery and plan accordingly. For instance, don’t do anything for the two days after Christmas. When possible, schedule time off after big events you know are coming.
If you have some flexibility in your work schedule, you might want to consider a day off in the middle of the week so you can do some recovering before jumping back in. Taking more breaks may also prevent you from needing as much recovery time.
When you can’t schedule an actual recovery period or rearrange your life around your chronic illness, make sure to pare down as much as you can. Order groceries online rather than trying to shop near the end of your workweek. Can someone else get your kids to soccer? Can your kids help more around the house? What jobs can you delegate to someone else? Call in the reinforcements!
You may also benefit from getting extra rest before a big event. That could help your body get through whatever is coming a little better, which might speed up your recovery time.
Life doesn’t always work out how we want. You’ll probably have to go to work or school with a symptom flare or try to get laundry done on your days off instead of resting, because when else are you going to do it, right? When that’s your reality, it becomes all about pacing yourself so you can keep moving forward.
Also, learn to be patient with yourself. At times, you’re like a car that runs out of gas but keeps going anyway. Don’t be too hard on yourself when it’s difficult to keep push, or when you have to take some time off in order to feel better and be a better employee or student.
Be sure to talk to your doctor about this symptom, especially if it’s becoming a big part of your life.
He/she may have ideas about treatments or lifestyle changes that might be able to help you.
You may also benefit, in general, and when it comes to recovering if you build better habits when it comes to sleep and your diet.
Chronic pain is increasingly rampant today. However, chronic pain and chronic diseases are often invisible. In many cases, there are no plasters, visible rashes, or nasal discharge involved. Those who suffer from chronic pain often appear “normal”, perhaps a little more fragile or sad than average. I suffered from chronic headaches for four and a half years and chronic hip pain for two and a half years. He often seemed depressed, disinterested and angry, when I was simply in pain. There were many days that I could not get out of bed. After a conversation, it became difficult at times. I lost a job because of my pain. I canceled plans and ignored friends. I felt misunderstood and alone. I was suffering. I know the answer was there and finally, I cured myself. However, at the moment I wanted to scream from the top of my lungs all the things that all chronic pain sufferers want me to know: 1. Just because you can not see it, does not mean that I am not in pain. 2. It’s not all in my head. 3. It’s not just the flu. It will not disappear in a week. 4. Please, never say, “Just do not think about it.” Being in constant pain is impossible. 5. Hugs can do magic. So they are good messages. I need to know you’re here for me. 6. Thank you for sharing the “magic cure” you have read online. Trust me, I’ve heard about it, and if it was relevant, I’ve tried it.
7. I am trying very hard to live a normal life. 8. I try my damned best not to cancel plans and never cancel plans if I had a choice. 9. I can not get out of it. 10. Some days are better, some days are worse. Some days I can even feel close to normal, other days I can not even get out of bed. 11. I worry about you. I want to know about your life and dreams. I want you to be happy and healthy. 12. My chronic pain is different from other people’s chronic pain. All diseases and pain symptoms are unique. Our experiences may differ, but we are all in pain and can relate to each other. 13. Please do not try to convince me to drink and “live a little”. All I want is to live a little, in fact, live a lot. A drink, however, is the last thing on my mind. 14. If I look depressed or bored, it means that I am really in tremendous pain and doing everything possible to look happy and normal. 15. I can not explain how chronic pain feels. However, I can not say, “You will know once you have it” because I would never want someone to feel so much suffering. 16. I need a lot of sleep. But sleep can be difficult with so much pain and often it still leaves me exhausted. 17. Just because I have chronic pain does not mean that I know how to handle it or live with it. 18. Sometimes I feel like I’m in a prison, living someone else’s life. 19. I still have interests, passions, goals, and dreams. 20. I do not want you to forget me. I do not want you to give up on me. 21. I have not given up on healing yet. Deep down I know there is (or will be) an answer out there.
Anger is a very common emotion, particularly for people suffering from fibromyalgia. It is a natural, human reaction and yet it doesn’t get an awful lot of attention as a side effect to chronic pain.
It’s one thing to accept our anger, but it’s another to let that anger consume us and let it impact our lives and the lives of others. It can be difficult to draw that line when you feel enraged by what you have lost and what has emerged in its place; you’ve been given a life that you didn’t plan and wouldn’t choose.
But, there are things you can do to keep your anger at bay and prevent it from encroaching on your life.
A friend of mine once told me I was the angriest person he knew. It became a bit of a running joke – we would meet up for drinks and before long I was ranting and he was mocking my anger. It was just the way it was.
A year later I was talking to a psychiatrist after yet another unsuccessful referral following a fibro flare–up, and I told him about my anger. He asked me to give him some examples of what made me angry.
As I went through the list he quietly listened, then asked: “What makes you think this is anger? You sound like an intelligent girl who’s ranting about the things that are important to her. What’s wrong with that?”
I suddenly felt like a weight had been lifted off my shoulders. I wasn’t weird and angry, I was normal and healthy. I’m sharing this story because there is a big difference between feeling angry and being an angry person. Don’t let the label consume you; recognize that you’re allowed a good rant from time to time. It’s necessary.
This might seem quite simple at first, but I think it’s important to get a good understanding of what makes you angry in the first place so that you can look at ways to control or avoid it in the future.
I’m not a doctor, but experience has taught me that there are often small triggers that can cause you to feel more angry than usual, and identifying these triggers can be a key step to overcoming negative emotions.
You can start by making notes or lists whenever you feel your anger developing, which will help you find patterns in your behavior. For example, you might think your anger stems from something broad, like having fibromyalgia, but as you start to take notes you will start to see the smaller triggers.
Perhaps it’s the patronizing way your partner talks to you when what you really need is strength and support, or perhaps it’s the fact telemarketers call you three times a day and you just can’t cope with another phone call. These small occurrences are part of a bigger issue, but they’re still a valid contributor to the anger you feel.
I’m a firm believer that if you don’t like something the way it is, you should make a change. Obviously, this has restrictions; I don’t like the fact I have fibromyalgia but I can’t change it. However, what I can change is the way I think about it and the way I choose to cope with it.
Having made notes and identified the things that trigger your anger, it’s time to start finding ways to address and avoid it. Taking the examples from above, if your partner’s behavior is causing your anger then you should tell them how you prefer to feel supported.
Taking control over your triggers can be a way of reducing the amount of anger you feel or the frequency with which you feel it.
As a person who is prone to ranting and raving, I don’t find it easy to connect to my inner calm. However, I know that it’s an essential coping strategy for fibromyalgia patients because it doesn’t just ease anger; it eases anxiety and depression and often reduces the frequency of flare-ups too.
The trick here is to make sure you find YOUR inner calm, not the calm that works for someone else. Annoyingly, this takes time and it means you have to put in some work, but it’s totally worth it. I spent a long time thinking that my inner calm could be found at the back of a meditation class or in the depths of a yoga retreat.
After three yoga classes and two attempts at meditation, I realized they were frustratingly slow and making me angry. Oh, the irony! I am sarcastic and impatient so meditation – try as I might – was just not for me. Some find their calm in a bath with relaxing candles, but I’m really more a shower girl so that didn’t work for me either.
It takes time to work out where to find your inner calm, but it’s a journey well worth taking because when you start to recognize the signs of anger you need to know there is somewhere you can go.
This is yet another common coping strategy for fibromyalgia sufferers in general, but it’s really important when it comes to managing your anger.
Often, when we get angry, we shout and become aggressive and intimidating. People stop listening to the words and just see the rage, so you need to make sure that you explain what makes you angry and what you’re doing to overcome it. This could be as easy as talking to your family, but if you really struggle to control your emotions then it may be helpful for you to seek professional help.
This could mean talking to your doctor or attending anger management classes, but there are also a number of mental health support groups and online forums that might give you the outlet you need to talk about your anger.
The important thing is to address your anger. Don’t push it away; the rage monster will lurk in the background and come back twice as angry.
“Widespread” means that it is all over the body. However, many people with fibromyalgia feel their pain in specific areas of their body, such as the lower back, neck, and shoulders.
“Tenderness” means that even a small amount of pressure can cause a lot of pain.
FMS affects more than 5 million people in the United States. That’s nearly 1 in every 60 Americans. Around 80-90% of those affected with FMS are women. These women are primarily between the ages of 35 and 55.
Research has shown that disordered sleep is a very prominent symptom in patients who have FMS. Around 75% of patients with FMS complain about their sleep. Studies show that treatment of sleep disturbances has had a positive effect on their FMS pain and symptoms during the day.
Even though sleep recording is not part of the routine evaluation, polysomnography may disclose primary sleep disorders in patients with FMS including insomnia, obstructive sleep apnea, and restless leg syndrome.
Insomnia is defined as the inability to get enough sleep to feel rested. Lack of sleep produces more pain and increased pain contributes to lack of sleep. FMS pain can make it difficult to go to sleep at night, cause frequent awakenings from sleep during the night, or make a person wake earlier than planned without being able to return to sleep. In this regard, the pain has both an effect on the quantity of sleep as well as the quality.
People experiencing pain are also much more sensitive to stress, which is another major perpetrator of sleep loss.
People in pain are also more likely to worry about getting enough sleep. They feel like they have less control over the amount and quality of sleep they get each night.
Sleep apnea is a potentially deadly sleep disorder in which breathing repeatedly stops and starts.
The incidence of sleep apnea in FMS patients was found to be 61% in men and 32% in women, according to a 2013 study published in Clinical and Experimental Rheumatology. A particular variant of sleep apnea called upper airway resistance syndrome is very common in women with fibromyalgia. Treating sleep-disordered breathing improves both pain and fatigue in fibromyalgia patients.
Restless leg syndrome is a neurological disorder characterized by throbbing, pulling, creeping, or other unpleasant sensations in the legs and an uncontrollable, and sometimes overwhelming, urge to move them.
The incidence of restless leg syndrome has been found to be in excess of 50% of those with FMS, as opposed to 7% of the general population. FMS patients experience improvement in their symptoms of fatigue and sleepiness when restless leg syndrome is treated.
If you believe that you may be suffering from FMS and have sleep-related issues, discuss your symptoms with your primary care provider or contact a sleep clinic for a sleep study.
At the Alaska Sleep Clinic, we help diagnose and treat hundreds of Alaskans every year with sleep disorders. Regular, quality sleep is one of the most important aspects of leading a healthy and happy life. Having an untreated sleep disorder such as insomnia, restless leg syndrome, or sleep apnea can not only hamper the quality of your daily life, it can worsen your FMS pain over time.
If you live in Alaska and want to receive a free sleep assessment from one of our certified sleep educators, click the link below and get on your way to sleeping restfully through the night.
Having IC alone can impose a lot of restrictions on your lifestyle and, like fibromyalgia (FMS) and chronic fatigue syndrome (CFS or ME/CFS), it’s linked to depression. Also, like FMS and ME/CFS, IC can be difficult to diagnose, treat and manage.
Some people have good luck with basic treatments and dietary changes, while others may need more intensive treatments or even surgery.
Interstitial cystitis (IC) is abdominal or pelvic pain related to your bladder getting full, often accompanied by other urinary symptoms, but with no infection or other obvious diseases. The cause of IC is unknown. Frequently, doctors misdiagnose it as a urinary tract infection, and most people have IC for about 4 years before they’re diagnosed correctly.
You’re most likely to develop IC in your 30s or 40s, but it’s also possible to get it earlier or later.
Why the overlap? Good question! Problem is, we don’t have an answer. Researchers are still trying to puzzle out the causes and underlying mechanisms of all these conditions, and until they can, we probably won’t understand why they overlap.
IC is diagnosed primarily based on symptoms. Before diagnosing IC, your doctor will need to rule out other possible causes of your symptoms. Tests include:
Urine cytology (for detecting cancer and inflammatory diseases in the urinary tract)
Video urodynamics (which shows how much urine it takes for you to feel the need to urinate)
To confirm an IC diagnosis, your doctor may perform a hydrodistention, in which your bladder is filled with water. That helps your doctor view your bladder walls for possible hemorrhages common in people with IC.
IC isn’t well recognized or easily diagnosed, so if you think you have it, mention it to your doctor.
There’s no cure for IC, and treatment needs to be tailored to the individual. It can take a lot of trial and error before you find the right combination of therapies and lifestyle changes.
Your doctor may prescribe one of the several medications for IC:
If you’re being treated for IC and FMS or ME/CFS, you should talk to your doctor and pharmacist about any possible drug interactions.
For instance, you shouldn’t take SSRI/SNRI-type antidepressants, which are common treatments for FMS and ME/CFS, with tricyclic antidepressants used for IC. Also, the FMS treatment Lyrica (pregabalin) doesn’t mix well with prescription pain medicines.
However, the tricyclic antidepressants prescribed for IC work well for some people with FMS or ME/CFS, and other IC treatments such as physical therapy and biofeedback may provide a cross-over benefit. You may also have food sensitivities that exacerbate more than one condition, so an elimination diet could really help you.
Because pain from other conditions can make FMS symptoms worse, you’ll really benefit from finding a good treatment regimen for IC.
Any one of these conditions is hard to live with, so when you have them in combination it can take a big toll on your life. Limitations imposed on your life by pain, fatigue, and urinating possibly dozens of times a day often can lead to depression, loss of social life, unemployment, and other problems.
It’s important to find and follow a treatment regimen that works for you, and to seek out support either from people in your life or support groups, online or in your community.
Here are more resources to help you learn about, manage, and live with IC:
Interstitial Cystitis Basics: Symptoms, Diagnosis & Treatment from Mary Kugler, R.N., Verywell.com Expert on Rare Diseases.
Interstitial Cystitis: Questions & Answers from Verywell.com Expert on Women’s Health, Tracee Cornforth
Breaking the Cycle of Appointment Fatigue in Chronic Pain Management
Living with chronic pain means navigating a constant balancing act—managing symptoms, medications, work, relationships, and self-care. At the core of this juggling act lies an unspoken burden many patients face: appointment fatigue. This term refers to the emotional, mental, and physical exhaustion that comes from attending endless medical appointments, undergoing tests, meeting new specialists, and often, repeating the same explanations of symptoms without seeing long-term improvement.
For individuals dealing with persistent pain, medical visits become a routine, yet their frequency can slowly wear down one’s motivation and hope. What begins as a path to healing may transform into a cycle of burnout, disillusionment, and disengagement from healthcare altogether.
This article dives deep into the phenomenon of appointment fatigue, what causes it, how it impacts chronic pain sufferers, and how patients can reclaim their autonomy in the face of healthcare overload.
Understanding Appointment Fatigue in the Context of Chronic Pain
Chronic pain is not simply a lingering ache. It is a long-term condition that can stem from various sources including autoimmune diseases, nerve damage, past injuries, fibromyalgia, and musculoskeletal disorders. Unlike acute pain that resolves with treatment, chronic pain persists beyond the typical healing window and often requires ongoing care from multiple providers.
As a result, patients may attend appointments with:
Primary care physicians
Pain specialists
Physical therapists
Psychologists
Rheumatologists
Occupational therapists
Each of these visits involves waiting times, transportation planning, paperwork, billing concerns, and sometimes disappointing news. The repetitive nature of these experiences, coupled with limited improvements or inconsistent care, builds up over time. This accumulation can give rise to a deep sense of frustration, helplessness, and a strong desire to simply stop showing up.
Common Signs That Indicate Appointment Fatigue
Recognizing appointment fatigue early can prevent further deterioration in one’s healthcare engagement. Some common signs include:
Canceling or rescheduling appointments frequently, even when not sick or physically unable
Feeling dread, anxiety, or anger when thinking about medical visits
Becoming emotionally numb or indifferent during consultations
Not following through with referrals, tests, or treatment plans
Avoiding contact with healthcare providers or clinics altogether
Declining in health due to untreated symptoms or complications
It’s important to understand that appointment fatigue is not laziness or irresponsibility. It is a valid response to an overextended emotional bandwidth in an already stressful healthcare experience.
The Emotional Toll of Navigating a Fragmented Healthcare System
For chronic pain sufferers, the road to diagnosis and treatment is rarely straightforward. Often, it involves seeing multiple specialists who may offer conflicting advice. Patients may be forced to re-explain their pain journey at every appointment, recount failed treatments, or defend their need for pain management, especially amid growing stigma around opioid use.
All of this contributes to a feeling of being unheard, unvalidated, and overly medicalized. Instead of feeling supported, patients may feel reduced to a list of symptoms on a chart. This emotional toll erodes trust and contributes to appointment fatigue.
Financial and Logistical Strains Amplify the Burden
The cost of chronic pain management is another contributor. Even with insurance, copays, transportation costs, unpaid time off work, and prescription expenses add up quickly. If appointments don’t deliver tangible results, the perceived cost-benefit ratio becomes unfavorable. Patients begin to question, is this really worth it?
Logistical hurdles like coordinating care between specialists, scheduling appointments months in advance, and finding available practitioners who truly listen can become overwhelming. These tasks consume energy that patients would rather use for daily life or symptom management.
Healthcare Inequities Worsen the Experience for Some
Those from marginalized communities may experience even deeper levels of fatigue due to systemic barriers. Language differences, implicit bias from healthcare providers, lack of nearby specialists, or financial instability can all lead to fewer options and worse experiences. Appointment fatigue for these individuals often includes an additional layer of distrust or previous medical trauma, further discouraging engagement.
How to Cope and Break Free from Appointment Fatigue
While appointment fatigue is real and challenging, it doesn’t have to become a permanent obstacle. There are steps chronic pain patients can take to regain control over their healthcare experience.
Prioritize Appointments Based on Value
Not every follow-up is essential. Patients can work with a trusted provider to identify which appointments are crucial and which can be delayed, reduced in frequency, or combined. Prioritizing value over volume gives patients more control over their time and energy.
Set Clear Goals for Each Visit
Approaching appointments with a purpose can help reduce frustration. Write down specific questions, concerns, or goals beforehand. If possible, share these in advance with your provider to focus the conversation and avoid wasted time.
Use Telehealth When Available
Virtual appointments eliminate travel time, reduce scheduling stress, and may be more manageable on bad pain days. While not ideal for every visit, they are a helpful tool for routine check-ins or medication management.
Track Symptoms and Share Concisely
Using pain journals or digital symptom trackers can streamline communication during visits. When providers see patterns and progress laid out clearly, appointments tend to be more productive and less repetitive.
Build a Core Care Team You Trust
Rather than relying on multiple specialists, try to work closely with a few key providers who understand your history and goals. A coordinated team reduces duplication and provides more personalized care.
Take Mental Health Seriously
Psychological support is vital. Seeing a therapist familiar with chronic illness can help process the emotional exhaustion that feeds appointment fatigue. Therapy can also provide strategies for setting boundaries and communicating more effectively with medical professionals.
Chronic pain does not just impact the body; it infiltrates every aspect of a person’s life. When medical care starts feeling more like a burden than a support system, it’s a sign that the balance needs to be restored. Patients have every right to advocate for themselves, to ask for care that meets their needs, and to opt out of what is not serving them.
This might mean switching providers, taking breaks between appointments, or even re-evaluating which symptoms need professional management versus home care. The most important thing is for patients to feel like active participants, not just subjects of an endless medical routine.
Frequently Asked Questions
1. What is appointment fatigue? Appointment fatigue refers to the mental and emotional exhaustion experienced from attending frequent medical appointments, particularly when managing chronic illnesses like chronic pain.
2. Is appointment fatigue common among chronic pain patients? Yes. Many people with chronic conditions report feeling overwhelmed by the frequency and burden of medical visits, especially when results are minimal or progress is slow.
3. Can appointment fatigue lead to worse health outcomes? Avoiding or skipping appointments can result in missed diagnoses, unmanaged symptoms, or complications, potentially worsening a patient’s condition over time.
4. How can I talk to my doctor about appointment fatigue? Be honest and specific. Explain how the frequency of visits impacts your life and ask whether some appointments can be spaced out or handled differently, such as via telehealth.
5. Are there ways to manage my care with fewer appointments? Yes. Coordinating care through a central provider, using digital symptom logs, and setting clear health goals can reduce the need for frequent appointments.
6. Should I feel guilty for needing a break from medical visits? Absolutely not. Taking a step back to recover emotionally and mentally is valid and may ultimately improve your engagement and outcomes in the long term.
Conclusion
Appointment fatigue is a real and often overlooked side effect of managing chronic pain. It affects motivation, emotional well-being, and the overall healthcare journey. Understanding this phenomenon allows patients to take proactive steps toward regaining control, creating more meaningful medical interactions, and protecting their energy for healing. Empowerment begins when patients recognize they are not just their symptoms—they are people who deserve respect, rest, and choices in how they pursue wellness.
Fibromyalgia and myofascial pain syndrome often go together. Because of the frequent overlap and some similar symptoms, they’re often mistaken for the same condition and, as a result, people with both are sometimes only diagnosed with and treated for one.
In MPS, muscles and connective tissues (which make up the fascia) develop what’s called a trigger point (TrP). These are not the same as FMS tender points.
A trigger point is a small, hard knot that you can sometimes feel under your skin. The knot itself can be painful, especially when poked, but it often causes pain in another area, which is called referred pain.
Trigger points typically form as a result of trauma to the tissue. Experts don’t know why damage that heals normally in most people causes TrPs in others. However, studies suggest that muscle injury in some people leads to abnormalities where the nerve cells connect to muscle cells. This suggests MPS is a neuromuscular disease.
Why people with MPS frequently develop FMS isn’t yet clear, but a growing body of evidence shows that, in some people, chronic pain can make changes to the central nervous system, resulting in central sensitization. If theories are correct, early treatment of MPS may help prevent FMS.
Referred pain makes MPS especially hard to diagnose and treat. Typically, a doctor says, “Where does it hurt?” and then looks where you point. To treat MPS, you and your doctor need to examine your symptoms and figure out where your trigger points are.
Your doctor can find trigger points by feel or based on symptoms.
Tests such as magnetic resonance elastography and tissue biopsy may show abnormalities in TrPs, but their roles in diagnosing MPS still aren’t clear.
By contrast, no test or scan reveals abnormalities in the tissues where people with FMS experience pain.
Trigger-Point Injections: The doctor inserts a needle directly into a TrP or in several places around it to loosen up the taut bands. The doctor may inject a pain-relieving medication, such as corticosteroids or lidocaine. (Note: some doctors believe corticosteroids can exacerbate fibromyalgia symptoms.) When no medication is used, it’s called dry needling.
Acupuncture:Acupuncture is an ancient Chinese practice similar to dry needling. While studies of its use in MPS are limited they are promising, and many patients and practitioners report good results.
Physical Therapy: A special kind of therapy called spray-and-stretch is common for treating MPS. A physical therapist guides you through stretching exercises while spraying a numbing substance on your muscle. The therapist may also use certain massage techniques to loosen your muscles and TrPs. In addition, a therapist can work with you on factors such as poor posture that may contribute to MPS.
Medications: Common drugs for MPS include nonsteroidal anti-inflammatory drugs (NSAIDs) such as Aleve (naproxen) or ibuprofen-based drugs like Advil and Motrin, and tricyclic antidepressants such as amitriptyline, doxepin, and nortriptyline.
With significant differences in their symptoms, diagnostics, and treatment, it’s clear that fibromyalgia and myofascial pain syndrome are not the same conditions. However, it can be extremely difficult to determine which condition is causing which pain when a person has both of them.
By working both on your own and with your doctor and/or physical therapist, you may be able to figure out where you have trigger points and how best to treat them without exacerbating your fibromyalgia. Relieving the myofascial pain is likely to quiet your fibromyalgia symptoms, so you could well see a double benefit.
“I deal with everything on a day-to-day basis,” says Stephanie Parker of Dover, Del., who believes her symptoms are consistent with fibromyalgia but has not yet been formally diagnosed. The symptoms keep her from participating in daily family activities, such as watching her kids’ ballgames in the afternoons.
Tina Pringle, who was diagnosed 16 years ago with fibromyalgia, says that her fibromyalgia symptoms have been overwhelming at times. “The symptoms all merge together, and because of the fatigue and brain fog, everything becomes a maze of sheer confusion,” explains Pringle.
The United Kingdom resident says her eye doctor identified her light sensitivity, but it’s her sensitivity to sound that’s most troubling. “Loud bangs, a child crying, loud music, shouting, dogs barking, and my worst annoyance, whistling, are all an issue,” she says. “The noises resound in my head like a clanging cymbal and cause my whole body to tense up.”
As her tension grows, so does her fibromyalgia pain, and she has to retreat to a darkened room to relax. Her reaction is particularly problematic at home, where her teenage daughter often loves to play loud music and behave in typically boisterous adolescent fashion.
Noise is just the beginning of the sensory anguish that might be contributing to your fibromyalgia pain. People living with fibromyalgia report:
This heightened sensitivity may be difficult for you to understand, much less explain to friends and family members who see no outward problem. The uncomfortable and painful sensations of fibromyalgia may be part of your brain’s unusual way of processing pain, suggests fibromyalgia researcher Benjamin Natelson, MD, a neurology professor at the Albert Einstein College of Medicine in New York City and author of Your Symptoms Are Real: What to Do When Your Doctor Says Nothing Is Wrong.
Another study, published in the journal Pain Research and Treatment, suggests that changes in brain chemistry among people with fibromyalgia may be linked to sensitivity to stimuli such as sound and smell. Imaging studies have provided visual depictions of this altered response to sensations. In some respects, the brains of people with fibromyalgia may be hyper-responsive to even the possibility of pain or discomfort, Dr. Natelson says.
Researchers have also tested tissue samples and found elevated levels of inflammatory markers in the skin of people with fibromyalgia — which may be linked to hypersensitivity to touch. Touch sensitivity is real for people like Pringle, who says that there are times when even holding hands with her partner is too painful to bear. Clothes that are too tight, massages, and even light touches all ratchet up her pain and stress. To make matters worse, Pringle says she occasionally even flinches involuntarily when touched by others, which can be hurtful to those around her.
How can you address a problem that might stem from your brain’s wiring? Here are some practical steps you can take to manage these sensory symptoms:
Work with a supportive doctor. “If your doctor doesn’t believe you have fibromyalgia, get a new one,” stresses Natelson. Pain treatment will be most effective, he says, when you and your doctor are on the same team. Three prescription medications have been approved for treating fibromyalgia and could help you manage your fibromyalgia pain and reduce your hypersensitivity.
Be active. A review of exercise as part of fibromyalgia treatment, published in the journal Rheumatology International, showed that aerobic exercise may offset pain and minimize tender point sensitivity. Natelson advises gentle physical conditioning. His prescription: “Walk for 30 minutes every other day at about 1.5 to 2 miles per hour.” This increases blood flow to the muscles and tissues. Very gradually, increase your pace to about 3.6 mph. This level of activity “seems to downregulate pain perception,” Natelson explains. Walking outside is ideal, but if you’re sensitive to temperature changes, light, smells, and other sensations, start a walking program inside your home or at the gym.
Take care of your skin and reduce irritation by using gentle products and avoiding temperature extremes, such as very hot or very cold water.
Wear loose-fitting clothes and dress in light layers that you can remove if the weight of your clothes starts to irritate your skin.
Set boundaries. When her sensitivity to light is especially intense, Pringle simply explains to family members that she can’t watch TV with them right at that moment.
Create a retreat. On particularly difficult days, a comfortable, cool, darkened room might be a soothing place to relax and recharge.
Wear sunglasses. Inside or out, if you feel sensitive to light or certain patterns, put on some shades and give your eyes a break.
Fibromyalgia symptoms can mask the presence ofchronicinflammatory disease affecting the joints of the pelvis and spine, according to new research.
The study, titled “Prevalence of Axial Spondyloarthritis Among Patients With Fibromyalgia: A Magnetic Resonance Imaging Study With Application of the Assessment of SpondyloArthritis International Society Classification Criteria,” was published in the journal Arthritis Care & Research.It highlights the importance of vigilant management of fibromyalgia symptoms by doctors and patients, taking into account the possible underlying presence of inflammatory disorders.
Unlike other rheumatologic diseases, fibromyalgia is non-inflammatory in nature, and recent reports suggest that it is caused by uncontrolled hyper-activation of the pain-associated nervous response.
Fibromyalgia patients can present a broad spectrum of symptoms, including chronic nocturnal back pain, morning stiffness, and disturbed sleep. However, these are also symptoms of an inflammatory condition called axial spondyloarthritis (SpA).
The spA is a chronic inflammatory condition involving the spine, pelvis, and surrounding joints. Although SpA and fibromyalgia are very different diseases, they can overlap and share similar symptoms.
Aiming to determine the incidence of SpA among fibromyalgia patients, a total of 99 patients with fibromyalgia underwent magnetic resonance imaging (MRI) evaluation for the identification of structural alterations common in SpA chronic inflammation1, such as bone erosion and spine deformations (sclerosis).
About 8% of patients presented symptoms of inflammation in pelvic joints, while 17% and 25% presented bone erosion and sclerosis, respectively. Despite the frequency of these symptoms, only 10% of fibromyalgia patients were positively SpA diagnosed,accordingto the Assessment of SpondyloArthritis International Society classification criteria.
“When approaching the clinical conundrum of differentiating between ‘pure’ fibromyalgia and those cases with an unsuspected underlying inflammatory disease, the physician must attempt to rely[on] onclinical judgment and on available diagnostictools,” the study’s authors, from medical centers in Tel Aviv, Israel, wrote.
Through blood tests that evaluate levels of a protein associated with inflammation, known as CRP, the authors found that the diagnosis of SpA was positively associated with increased CRP levels and physical function limitation. This result suggests that CRP could be used as a diagnostic tool for SpA among fibromyalgia patients.
“These results underscore the importance of recognizing the overlap between inflammatory and centralized pain in each patient and call for increased clinical vigilance in the process of differential diagnosis,” the authors concluded.
According to a study titled “Lengthened Cutaneous Silent Period in Fibromyalgia Suggesting Central Sensitization as a Pathogenesis” and published in the journal PLOS One, dysfunction in spinal cord processing may be responsible for pain in fibromyalgia (FM) patients.
Among other side effects, Fibromyalgia is portrayed by chronic widespread pain, but the root cause that is responsible for chronic pain in FM is still vague. A recent study has shown that for fibromyalgia pathogenesis, central pain amplification is key, FM pathogenesis also known as “central sensitization” is a process that is characterized by augmented pain and sensory processing in the spinal cord and brain.
The cutaneous silent period (CSP), a spinal reflex interceded by A-delta cutaneous afferents that are used to evaluate pain processing in both the central and peripheral nervous systems, between FM patients and normal healthy controls were compared by the researchers. The amount of people that were analyzed was 24 fibromyalgia patients (diagnosed according the 1990 American College of Rheumatology classification system) and 24 healthy controls of same age and sex. CSP was checked from the abductor pollicis brevis muscle which is present in the hand between the wrist and the base of the thumb by using standard electro diagnostic equipment, along with patients’ parameters in which statistic information, number of tender points, visual analog scale and fibromyalgia affects surveys scores were included.
These findings suggest that in the central nervous system, fibromyalgia is linked with pain modulation mechanisms dys-functioning. Also, according to researchers study, there was no correlation between CSP and clinical parameters like VAS score, K-FIQ score, age, and height, which postures questions in the matter of whether to utilize CSP to survey ailment seriousness. As a matter of fact, researchers emphasize that extra reviews are required to additionally assess the relationship between CSP parameters and clinical information.
The authors write in their report, “In conclusion, dysfunction of supraspinal control may be responsible for pain in FM, giving additional proof that central sensitization underlies the pathogenesis of the disease,”
