Category: Fibromyalgia Conditions

Explore the conditions associated with Fibromyalgia, their symptoms, and how to manage them for improved well-being.

  • Fibromyalgia Life may be tough, but so are you

    Life with one or more chronic illnesses is tough.

    Life with chronic pain is tough.

    Life, whether you are chronically ill or not, is tough.

    But I have news for you! You are tougher!!!!

    Yes, that is right.  I know that there are times when you don’t feel tough.  I also know that there are days when you truly lack physical strength, but that doesn’t mean that you aren’t tough.

    As long as you are fighting for your life, looking for ways to improve it, finding joy in every day, and not giving up, YOU ARE TOUGHER THAN YOUR ILLNESS OR CHRONIC PAIN!

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    I know that taking a nap may feel like your illness has won, but it isn’t true.  You win when you acknowledge that your body needs to rest.  It takes guts to do what your body demands of you, instead of forcing your body to follow your desires.  It takes immense strength to go to physical therapy, to keep trying new treatments, change your lifestyle, make healthier choices, and most importantly accept that all these things must be done in order for you to remain strong enough to survive.

    Here are three examples to help you build and maintain the emotional strength that is necessary for living with a chronic illness or pain.

    Number One: Spend more time with people who lift you up and less with those who bring you down.

    Those who constantly remind you of your limitations or are always bringing up your shortcomings, are only going to weaken you. 

    People who point out your strengths, help you find alternative ways to do things, or just cheer you on when you try something new will build your confidence. 

    Who are you spending most of your time talking to?

    My life isn’t filled with people who understood how difficult living with fibromyalgia, psoriatic arthritis, psoriasis, endometriosis, and its fallout, degenerative disc disease, and coccydynia is. 

    The difference between my life then and now is that I choose not to spend much time with those whose favorite word is CAN’T.  Tweet

    The more I hear that I can’t do something, the more I believe that I can’t do anything. 

    I may not be able to do everything the way I used to, but I CAN find new ways to do what I want.

    Number Two: Seek counseling

    I am not talking about joining a social media support group.  Those are okay to meet other people who “get” it but not for truly dealing with your fears and life choices.  Nor is it fair to expect your family or spouse to be the ones to counsel you.  There are many options available for counseling depending upon your needs.

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     If You Need A Crisis Hotline
    The National Suicide Prevention Lifeline – 1-800-273-8255
    SAMHSA (Substance Abuse and Mental Health Services Administration) – 1-800-662-4357
    RAINN (Rape, Abuse, and Incest National Network) – 1-800-656-4673

    Lifeline Crisis Chat
    Veterans Crisis Line – 1-800-273-8255 (Press Option #1)
    National Domestic Violence Hotline – 1-800-799-7233
    MentalHelp.net (An American Addiction Centers Resource) – 1-866-308-2184
    NAMI Helpline (National Alliance on Mental Illness) – 1-800-950-6264

    And for those wanting regular therapy with a licensed therapist, but either have crappy healthcare coverage or none and have either transportation issues or are just in too much pain to travel one or more days a week, Online-Therapy.com offers therapy when and where you want it.

    Number Three: Start envisioning your future WITH your chronic illness.

    I know that you are hoping and praying for a cure. I am too. But the reality is that our chronic illnesses are most likely going to be with us for the rest of our lives, especially for those of us over 50.

    If your chronic illness isn’t included in all of your future dreams and plans, your future will be filled with disappointment. Not only that, but you will be unprepared for the hard times that await you.

    Sorry to sound like a Debbie downer, but living with your head in the clouds waiting for life to magically be transformed will only lead to more heartbreak.

    When you envision a future that includes your chronic illness, you aren’t giving up, you’re getting real!!!

    Instead, you will grow stronger because your mind will be focused on figuring out what you will be able to do, making alternative plans, or finding a different way to do what you had originally planned for.

    Will things go wrong? Of course, they will! Do you know anyone who hasn’t had anything goes wrong in their life? I don’t! The difference is that you will be better prepared.

    I know you are tough because if you weren’t you wouldn’t be reading this blog post. If you are feeling like you are stuck in your life, take a deep breath, assess your situation, make plans to move forward, and never forget that you are a warrior!

    https://fibromyalgia-6.creator-spring.com/
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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Posture Pump Gets to the Source of Fibromyalgia Neck Pain

    The pain in fibromyalgia often first shows up as chronic upper back and neck pain. In fact, recent studies have shown that the majority of fibromyalgia patients have lost the natural curve in the cervical spine. In this post, I am going to tell you how a device called the Posture Pump® Cervical Disc Hydrator can be an effective home therapy for neck and upper back pain.

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    Fibromyalgia Neck Abnormalities

    One of the possible causes for fibromyalgia discovered by researchers is cervical stenosis. Cervical stenosis is a narrowing of the spinal canal in the neck area or upper part of the spine. This narrowing places pressure on the spinal cord resulting in nerve compression which can affect the entire nervous system.

    Another area of interest is the straight neck abnormality that in itself can cause spinal cord compression. In one study, cervical spine x-rays of 138 fibromyalgia patients were analyzed. Turns out that 88% of the FM patients in the study had a straight neck based on measuring the Cobb angle and 90% had a straight neck by visualizing the lateral view of cervical spine x-rays.

    When you lose the normal neck curve, the weight of the head is no longer balanced by the opposing curve in the upper back. This can cause significant pain for the neck muscles, headaches, reduced range of motion, premature disc degeneration, disc herniation, numbness, tingling, or weakness in the arms. It can also lead to a loss of bladder control, loss of balance, gait disturbances, and dizziness.

    This is where Posture Pump® comes into the picture.

    The Posture Pump® Cervical Disc Hydrator

    Posture Pump® is a spinal health product recommended by doctors to thousands of patients throughout the USA and other countries. Not only it is recommended by doctors, but the Posture Pump® was also created by a doctor with over 30 years of experience treating the neck or back.

    Normal spinal curves allow nutrients to flow into the joints. Loss of postural curves causes disc compression and blocks the flow of nutrients. This forces the head forward. Every inch your head is moved forward an extra 10 pounds of weight is added to your neck. As a result, forward head posture leads to chronic pain, numbness in the arms and hands, improper breathing, and pinched nerves.

    The Posture Pump® Cervical Disc Hydrator shapes and restores the cervical curve hydrates the joints of the neck and back and helps decompress the joints to increase your range of motion.

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    The Posture Pump® Cervical Disc Hydrator (Model 1400-D) comes fully assembled and easy to follow operating instructions. All you have to do is adjust the head strap until it feels comfortable and secure. Then you use a hand pump to pump up the air cells to your level of comfort. Wait 10 seconds and release the air out. You repeat filling and deflating the air cell 10 to 15 times.

    Next, inflate the unit and relax 1 to 5 minutes the first time and gradually work up to 15 minutes before deflating the air cells. There is a warm-up routine that acclimates the neck muscles. Do this before and after using the Posture Pump®.

    The first time I used the Posture Pump® Cervical Disc Hydrator the muscles on both sides of my neck got so tight I could barely move my head. I found out it is normal to be sore the first week. I was only sore the first time. After that, I feel a warmth in my neck muscles as though I can feel the blood circulating through my neck.

    I’ve had neck and shoulder pain since my teens. X-rays at that time showed that my neck had lost its natural curve. The Posture Pump® Cervical Disc Hydrator is made to restore the natural neck curvature. It definitely brings immediate relief to the pain in my neck, shoulders, and upper back. So far, the relief is temporary but with fibromyalgia ANY relief is good. I am going to continue using the Posture Pump and see what happens.

    Key benefits of The Posture Pump® Cervical Disc Hydrator:

    • Relieves Painful Neck and Upper Back Stiffness, Headaches and Fatigue
    • Shapes & Restores the Proper Neck Curve
    • Decompresses & Hydrates Compressed Discs
    • Decreases Disc Bulging
    • Reduces and Corrects Forward Head, Neck and Upper Back (Hump) Posture
    • Applies Reversing Pressure to Upper Back Humps
    • Improves Flexibility and Ranges of Motion
    • Lightweight, Easy to Operate & Travel With
    • Made in the USA & Built to Last
    • 60-day money-back guarantee

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Fibro Flare: Pain is such a barrier

    Obviously trying to do anything with a migraine is stupid, necessary, but stupid. However, struggling to get through the day with that sort of pain makes me rather forget how painful the fibromyalgia pain can be. Today was an extra special pain day where I got both. The migraine was consistent but not bad enough to seriously disrupt my thinking. Some would find that statement hard to believe knowing what a migraine is… but you get used to what you have to get used to. Such is the life, eh? Put that on your resume…’ superhuman pain tolerance’, ‘won’t call in sick for severe pain or run of the mill illness, only for mind-blowing scary-ass nasty pain’… but don’t mention how often that occurs or you’ll never land a job!

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    The FMS pain had to be triggered by the storm we had, but who knows? Sometimes a flare is just a flare, with no reason to be named for it. It started mid-morning with an ache in my knees and a sort of stiffness in my legs. Like zombified. Call me lurch. That sort of level of pain is normal. FMS pain shifts around to different muscles and ranges from mild to moderate on a daily bases, excluding days when I do my intense workout (12 minutes of yoga). It got significantly worse until my knees and ankles were in severe pain and my legs felt like the current running between them. Now it is at that level where it is hard to walk and it damn well hurts enough without moving. Seriously, it is insane how intensely FMS pain can hit for no reason. I get that if I walk too far, do exercise, or whatnot I can expect there to be consequences, but man does it suck when it just comes out of the blue like that. There is just something about spring and early summer that my body loathes and so I get more FMS flares and migraines as a result. Seriously is there somewhere in the world where the temperate is always moderate with lows are -10 and highs are +20 and it is always cloudy? Let me know. I was to move there.

    But sometimes I wonder about the normal baseline FMS pain. I think to myself I live a sedentary lifestyle and weak muscles will hurt. So maybe some level of pain is just normal. That is until I have a chat with someone and realize, nope, so not normal. A co-worker of mine is on this diet which is doing wonders for her and she routinely exercises as well. I joke about my yoga efforts and my pathetic limits and muscle pain. She said she had bad muscle pain after a workout (of good cardio by the way, as if I could do that!) but that she was told to stretch before and after the work out which eliminated that pain. I did not say anything about my FMS situation because why bother when it would take too long to explain and make me sound more of a cripple than my chronic migraines do.

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    But it made me think about what I do and the level of pain. I know FMS makes it so my body has a low threshold to feel pain, with more intensity and for longer durations… but what she is able to do (and seriously I am impressed with her willpower and determination) is nothing compared to what I can do and I really feel the consequences. But exercise is something I know will cause pain and I do a minimal amount when I can just because I think I should. Not enough that I can shed the weight I gained. Not enough to give me any more muscle endurance. So pain is a barrier to creating a routine in that aspect, but I don’t let it be a barrier to stop me from trying.

    Nonetheless, realizing how crippled I am today, body pain is just as much of a barrier as migraine pain but in a different way. Body pain when it gets severe limits my mobility, and my ability to be comfortable, and sleep and is also a distraction. While I can push through work, and mental stuff, with a nasty ass migraine I cannot force my body to do anything when in an FMS flare. The pain just explodes in intensity when I do. Of course, this is why I knew at a very young age I was destined for a desk job. I have had flares that made a ten-minute walk to school take a very long forty minutes. I vividly remember most of those worst ones. I do not remember much about the situation, all that is vague and hazy, but I remember the single-mindedness of needing to get through what obstacle was directly in front of me so that I could get home. I remember that intense focus of ‘just a little farther. Just a little longer Then there were times when the pain gets so insane your body simply says nope, no further, and gives out. That happened sometimes when I had summer jobs where I stood for eight hours, the moment I would sit down I was screwed because my legs would not let me stand after. This is also by the way why I prefer not to hold babies… I’m just saying, my arms can’t hold much weight either before they tremble, ache and then just give out. And dropping babies is never a good idea. So ‘just muscle pain’ does not quite define how nasty FMS can be. In some ways it might be less invisible than migraine pain because while I can mask both quite well when FMS gets to the crippling point I cannot walk well at all, just shuffle very slowly (I need a scooter or an old lady walker). Can’t hide that and damned hard to find a reason for those not in the know.

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • How to find meaning again when fibromyalgia and chronic illness upends your life

    You’re sitting in the doctor’s office, being told you have an incurable illness. Maybe you have to leave your career, or pull back on your workload, with set accommodations. You can’t live up to being the involved wife, parent, sister, or daughter you planned on being. Travel becomes difficult, athletic ability falls off, and favorite hobbies or pastimes become more challenging. But mostly you just don’t feel like you. A period of grief ensues over your previous life, and it crashes over you in waves.

    Eventually, you start asking the big questions. Can you live a good life despite pain? How do you find meaning again amidst all the change?

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    I don’t have THE answer, but I did find some answers. I had to understand what I’d found meaningful in life Before Fibro (B.F.). And then I had to find the meaning behind the meaning- why is something sustaining, nourishing, enjoyable? Finding meaning is epitomized by the quote “A life well lived is a life fully experienced.”

    I was a very career-focused B.F., finding satisfaction in the field of global health (HIV/AIDS prevention and treatment). Once all that stopped, I felt stuck and lost. The one thing I had been certain of, my “calling”, was gone. Making a difference throughout my career had given me a sense of purpose.

    Travelling was my favorite activity. I came to realize that experiencing different cultures and ways of life was important to me because it had made my own worldview expand. Broadening my horizons made me feel vital and alive.

    How to replicate that feeling from my couch at home? An answer came surprisingly from the podcasts and audiobooks I listened to during my enforced rests. I found I enjoyed learning about history, as a way to travel from my armchair. Learning feels like time well spent, whether it’s listening to a historical mystery or an episode of a podcast on ancient Egypt. After all, curiosity keeps your brain healthy and young. What do you geek out about? It can be anything, from an academic subject to a hobby, to DIY project techniques. Intentionally find ways to learn about things you find interesting, from online classes, podcasts, audiobooks, or just connecting with interesting people online and asking them questions. The time that feels spent on rewarding things makes meaning.

    Over time I came to see that there is a lot of life to live here, in ordinary life, without globetrotting or being career-driven. I never appreciated that B.F., assuming everyday life was boring and humdrum. But in learning to be mindful and still, I’ve found how much I missed before, and how much being present enriches my life. Being on autopilot, or always looking ahead, meant I whizzed past sunsets, birdsong, long hugs, savored meals, belly laughs and so many other moments. Connecting to the beauty and wonder all around us via our senses is possible, even while in pain, even at home. Finding ways to feel that makes life more worthwhile. Mindfulness as a practice, or just realizing the need to be present, means showing up for moments big, and small. Choose to stay with an experience instead of reaching for a distraction.

    And the difficult experiences of chronic pain, surviving the limitations, still mean that you are living fully. I’ve grown in strength, resilience, compassion, self-confidence, and patience in ways I never would have before my illness. After all, what else really is the point of life other than to become a better, wiser version of ourselves on this journey? This is another way to have a purpose in life. I’ve come to value growing as a person as one of my most important accomplishments, instead of getting promotions, keeping up with the Joneses, or any of the other markers we are taught to measure our success by. Without fibro, I would have let external factors determine my self-worth. It’s not that I’m grateful for fibromyalgia, or that I’m glad I have it, but I have found a way to make meaning out of it, and find a silver lining. I’m developing as I go; it’s a work in progress, but a worthwhile one.

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    I’ve written before about the critical importance of our happiness of selfexpression and contributing to something greater than ourselves. We are often taught that the only way to do this is to work and be a “productive citizen.” However, there are so many other ways to find connections, such as sharing your story and finding online relationships, to learn from and support others. Writing on my blog and now writing as a freelancer, has transformed my life. Volunteering, supporting others online, teaching, mentoring, and sharing your experience are all ways to contribute, big and small.

    Fiction writing has engaged me again in a new way through imagination. (I’m writing a historical mystery set in Niagara Falls during the American civil war when the area was a hotbed of spies and intrigue). Creativity can be a form of salvation, as a craft, art, music, or interior decoration, in the kitchen, the garden, on the page, or anywhere else. We shift into an active mode, not passenger mode when creating. Yet we also refrain from intellectualizing, analyzing, number crunching, or any other left-brain thinking. Creativity is about engaging intuitively, emotionally, and symbolically with the world, through self-expression, using the right brain. It’s good for your heart; it’s good for your soul. Don’t disparage it as “unproductive” or unimportant, because it is a meaningful source of intrinsic pleasure. It’s meaningful because it’s a way of being open and engaging with the world around you (sensing a theme yet?), via your senses and interpretations, from your own unique perspective.

    We find meaning in our relationships, in our faith, and in our philosophies. But we have to be present, open, and engaged to really benefit from these resources. That doesn’t happen overnight! But tuning in to our senses, our inner strengths, our creativity, our intrinsic interests and sources of pleasure allows us to connect to the world in ways that create and cultivate meaning in our lives. This is a form of strengths-based healing – leveraging your inner resources to create a life fully experienced, and well lived – in spite of adversity.

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • The Emotional Effects of Fibromyalgia

    Living with fibromyalgia can affect you physically and emotionally. Fibromyalgia is stressful. The pain and stress of fibromyalgia raise your body’s level of cortisol, a stress hormone. Adjusting to the disease and finding treatments that work can be frustrating. This fits with the fact that about 20% of people with fibromyalgia report feeling anxious or depressed

    Don’t let fibromyalgia bring you down. Instead, do what you can to reduce the psychic toll of the illness. Integrating various coping strategies can affect how your body responds to the disease and give you the tools you need to feel better emotionally and physically:

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    Daily Time Outs

    Set aside time each day for meditating or deep breathing exercises. These calming techniques can help you manage the stress hormones that make fibromyalgia symptoms worse. You might also try guided imagery, biofeedback, or progression relaxation. You can learn these mindfulness techniques from a trained practitioner, classes, books, and DVDs or audiotapes. Get into the habit of regularly practicing them on your own. 

    Yoga

    A recent study in the Journal of Pain Research found that women with fibromyalgia who practiced Hatha yoga (a gentle form of exercise) for 75 minutes twice weekly for eight weeks felt less pain and stress. Their bodies also produced less cortisol. Overall, the women were more accepting of their disease. 

    Another study revealed physical activity helps reduce depression in people with fibromyalgia.  Whichever form of yoga you try, be sure to modify the poses in response to pain. For instance, don’t hold the pose as long, or use a yoga block for support

    Positive Self-Talk

    If you have fibromyalgia, you may find it easy to put yourself down for not being able to do as much as you used to, for depending more on others or even blaming yourself for the disease. But negative self-talk is not helpful. Keep your self-talk as positive as possible. Tell yourself, “Fibromyalgia isn’t my fault,” and “I’m going to do all I can to control the disease.” Focus your self-talk on what you need to do to get better, not on what might have possibly caused your illness

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    Therapy

    If you are overwhelmed by the illness, consider seeing a therapist who practices cognitive-behavioral therapy (CBT). This type of therapy can be helpful for people with fibromyalgia. It focuses on helping you think positively and redefining your beliefs about illness, to help you feel more hopeful.

    Music

    In one study involving 22 fibromyalgia patients, those who listened to the music of their choice were able to function better physically than patients who didn’t. The study found that music can boost mood enough to overcome the perception of pain, especially before doing something physically taxing. If you don’t have one already, invest in a portable device so you can listen to your favorites at home and on the go.  

    Support Groups

    Getting feedback from others with fibromyalgia can give you the inspiration you need to manage your illness better. Blogs and message boards can be safe places for you to get ideas and talk openly with others in the same situation. What are they doing to cope that you might try? How are they managing to get tasks done? What are they doing to thrive despite their condition

    Ask your doctor if there are support groups in your community that you can visit. You can also search for a support group online. The right support can give you the tips and encouragement you need to focus on feeling better.

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • 4 Conditions That Can Mimic Fibromyalgia

    If you have symptoms that point to fibromyalgia but haven’t been diagnosed, you are not alone. Many people spend years working with doctors to rule out other diseases. That’s because a number of other conditions share fibromyalgia’s primary symptoms—chronic pain and fatigue.

    Ruling Out Similar Conditions

    Wouldn’t it be a relief if there was a simple lab test that could identify fibromyalgia? Unfortunately, there are no tests or X-rays available to diagnose the condition. As a result, doctors often look at conditions that share the same symptoms. Learn what other conditions can be mistaken for fibromyalgia and why finding a clear diagnosis is so important.

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    Rheumatoid Arthritis

    Rheumatoid arthritis may seem similar to fibromyalgia because pain is a primary symptom of this disease. But there are a lot of differences. Unlike fibromyalgia, rheumatoid arthritis causes inflammation in the body. And some symptoms of rheumatoid arthritis are visible. For example, people with the condition may have swollen or deformed joints. 

    Doctors diagnose rheumatoid arthritis by a physical exam, blood tests that look specifically for rheumatoid factors and signs of inflammation, and X-rays to look for joint damage.

    Lupus

    Lupus, a chronic disease that also causes fatigue and painful joints, can be difficult to diagnose because there is no specific test for it. But certain factors make it possible to differentiate it from fibromyalgia. For example, unlike fibromyalgia, lupus causes inflammation, arthritis, skin rashes, and damage to tissue and organs. 

    Doctors make a lupus diagnosis by taking into account your symptoms, medical history, and a series of lab tests. 

    Chronic Fatigue Syndrome 

    Chronic fatigue syndrome is a complex disorder that some medical experts believe is closely related to fibromyalgia. People with chronic fatigue syndrome have many of the same symptoms as those with fibromyalgia, including pain, fatigue, brain fog, difficulty sleeping, headaches, and more. 

    The main difference is that severe and overwhelming fatigue is the primary symptom of chronic fatigue syndrome, while pain is the dominant symptom of fibromyalgia

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    Hypothyroidism 

    Hypothyroidism occurs when the thyroid gland does not produce enough of the hormones the body needs to regulate metabolism and other functions. An underactive thyroid can cause a number of symptoms similar to fibromyalgia. These include fatigue, joint pain, and more. However, unlike fibromyalgia, hypothyroidism can be confirmed with a blood test and treated with thyroid hormone.

    When Conditions Overlap 

    Although it can be frustrating to take the time to rule out other conditions, it’s very important to do so. Not only is having a correct diagnosis vital to getting the right treatment, but it may also shed light on a bigger health picture. That’s because fibromyalgia not only mimics other conditions, it tends to overlap them. This means you may have fibromyalgia as well as another condition, like rheumatoid arthritis. In fact, you are at higher risk for fibromyalgia if you have a rheumatic disease—one that affects the joints, muscles, and bones. 

    Getting the Best Treatment

    Once you have a clear diagnosis, you can work with your doctor to develop a treatment plan. If you have more than one condition, treating fibromyalgia can affect how you and your doctor manage your other conditions. And the treatment of other conditions can affect the pain of fibromyalgia. Understanding all your medical needs can lead to the best treatment possible.

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • What People With Fibromyalgia Wish They Could Tell You

    Fibromyalgia affects about 5 to 6 million people in the United States, mostly women. Yet, so little is known about the condition and people with fibromyalgia often feel misunderstood. Here, three women share their thoughts about living with fibromyalgia.

    1. The pain and fatigue are real.

    People understand pain and fatigue if they can see the cause, like a broken bone or an incision from an operation. Fibromyalgia is an invisible illness though, making it harder to understand. But, “That pain is real. That pain is debilitating, affecting every part of your life,” says Sharon Gates, a retired nurse from Montreal, Canada.

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    2. Fibromyalgia has been around for centuries.

    Fibromyalgia isn’t a new illness. It’s existed for centuries under different names, such as rheumatism. Historical records about Florence Nightingale, the founder of modern nursing, show she probably had fibromyalgia.

    “It’s a real medical condition, backed up by decades of work and many, many studies,” says Susanne Gilliam, a recent law school graduate in Massachusetts. But because there are so many unknowns, there are people who don’t believe it exists.

    3. It can be a relief to finally be diagnosed.

    Illnesses like cancer or diabetes have tests to diagnose them. There are no tests for fibromyalgia and it can take an average of about five years to get a diagnosis. For some people, it takes much longer. Gilliam thinks she’s had it for about 18 years. In the meantime, it’s easy for people to begin wondering what is going on–because so many tests are coming back as normal.

    Having a diagnosis is important. “When you get a diagnosis of something, it’s not always a positive thing, but at least you know you’re not crazy,” Gates says. “You make changes and you try to manage the best you can.”

    4. Fibromyalgia doesn’t go away.

    Fibromyalgia is a chronic illness and, while people may have periods with few symptoms, it doesn’t go away. This can make it hard to talk about the illness because no one wants to seem like they’re always complaining. “People lose patience with chronic illnesses,” points out Randi Kreger, an author from Wisconsin. “They’re more attuned to short-term things that get better. They don’t really realize that not everything is curable and that some things just don’t get better.”

    5. Fibromyalgia can make you extra sensitive to the sensations around you.

    When people have fibromyalgia, it’s as if their sensitivity dials are turned up too high. Lights can be too bright, smells can be too strong, and noises can be too loud. These sensitivities can make it hard for them to get out and be an active part of the community.

    “I went to a book club that met in a coffee shop,” Randi says. “They were roasting and grinding coffee. The noise was really too much and I asked if we could go to a place where it was just not that noisy.” But the others in the group refused to move. They didn’t find the place particularly noisy and couldn’t relate to Randi’s discomfort.

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    6. Fibromyalgia makes you forgetful.

    Most people have memory lapses from time to time. They forget where they put their keys or to show up for a doctor’s appointment. But for those with fibromyalgia, it’s worse. “Fibro fog” makes thinking fuzzy and remembering difficult. It can also make it hard to follow conversations.

    7. There can be good days.

    The confusing thing about fibromyalgia is that for many people, the pain, fatigue, fibro fog, and other symptoms aren’t always there. One day, they may be able to go on a hike with their children and then out to a movie with a friend, but the next day, they may not be able to get out of bed. Nothing is constant.

    8. It can be hard to plan ahead.

    Because people with fibromyalgia have both good and bad days, it’s next to impossible to plan ahead. It’s no fun to make plans only to have to cancel them. It’s disappointing, but they can’t know what they’re going to be feeling like a month from now, a week from now, or even a day from now. “I just do the best I can,” Gates says.

    9. Medications help some people with fibromyalgia.

    There are medicines that are effective for some people’s symptoms. Gilliam experienced a complete turnaround when she and her doctors found the right drug combination for her. “Every day it was like crossing the finish line at the end of a marathon,” she says. There was something new each day that she could do, like carrying her laundry up the stairs, going to the pharmacy alone, and even going back to school to study law. “But this isn’t the standard outcome,” Susanne points out. “It isn’t even a common outcome, but it does happen.”

    10. But the medicines don’t help everyone.

    Unfortunately, the medicines do not help everyone with fibromyalgia and for others, the medicines cause serious side effects, such as depression, weight gain, or dizziness.

    Patient listening and helping hands mean a lot to people with fibromyalgia. It can be discouraging to live with a chronic illness, but the understanding of friends and family goes a long way and can make all the difference, perhaps turning a bad day into a good one.

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • How to Face the Day During a Fibromyalgia Flare

    When you wake up in a fibromyalgia flare—with that feeling that you can’t move, as if a 500-pound weight has been dropped on you in your sleep—you can’t help but wonder how you can possibly face the day.

    On mornings like this, the best thing you can do is limit your activity and rest. Still, even as your body takes the downtime it needs, feelings of guilt or other negative emotions can make days like this even more challenging. However, making a few positive shifts in perspective as you start the day can make a difference in how you end it.

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    Accept the flare.

    When you wake up in a fibromyalgia flare, you can either get mad and allow negative thoughts and emotions to make you feel worse, or you can accept what is and take steps to change it. 

    On any journey, you can’t make the correct turns to reach your destination without first understanding and accepting your starting point. When you wake up in a fibromyalgia flare, accept that that is how you are starting the day, then encourage yourself to build your energy as the day goes on. Remind yourself that ending the day with more energy than you started with may require a few changes to your daily routine, then take that first small step toward feeling better.

    Focus on self-care.

    Your focus should be on self-care from the moment you wake up before you even attempt to get out of bed. Keep a bottle of water by your bed and drink it before you start trying to move. Follow that with some light stretches in bed. Avoid physical exertion that may use your energy and leave you feeling more fatigued. Light stretching should feel good and warm up your muscles without making you more tired.

    After you are feeling a little more awake, spend some time meditating to focus your attention for the day. Clear your mind of all the things you had planned for the day, of all things that weigh you down and make you feel stressed. Instead, focus your attention on wellness and feeling energized.

    Other ways to practice self-care during a fibromyalgia flare include:

    By giving yourself the time to rest—both mentally and physically—you can begin restoring your energy bit by bit.

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    Start small and avoid overwhelming tasks.

    There is nothing as overwhelming as waking up in a fibromyalgia flare only to see a huge to-do list staring at you from your phone. The best thing to do when fatigue takes over is to wipe that list clean. Move everything that’s not essential to another day.

    Cleaning the house will wait. If you have children to care for, do what you must, but enlist their help as well. The only task that should take top priority is caring for yourself. This way, you can have more energy to accomplish your tasks later and be better able to take care of others.

    Motivate yourself with small tasks you can complete without effort, and commend yourself for what you are able to do. This may be as simple as just getting out of bed and getting something to eat. Take the day slowly, focusing only on one simple task at a time.

    Skip the mental gymnastics.

    Don’t allow your thinking to get stuck in a loop, ruminating on what you should be doing or what you wish you were doing. Those mental gymnastics will only make you feel more stressed and fatigued. Give yourself grace and patience and remember that your illness is frustrating, but it is not your fault. You are taking control of your symptoms by taking care of yourself.

    When you spend your time focused on how uncomfortable you are, you will stay uncomfortable. Focus your attention on the outcome you want to achieve—feeling better—and take small steps to achieve your goal.

    You can’t control your body. You don’t pick and choose when fibromyalgia flares hit, but you can make choices that will help limit the pain and fatigue. By pausing and practicing mindfulness about the flare and how to fight it, you can end the day feeling better than you started, allowing you to start tomorrow with renewed energy.

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Hypersensitivity to non-painful events and Fibromyalgia

    Hypersensitivity to non-painful events and Fibromyalgia

    I am printing this study because it is pretty basic to the understanding of fibromyalgia. We feel pain when there shouldn’t be a pain. It is interesting, in particular, to look at the areas of the brain that are activated when we do though.

    Fibromyalgia is a chronic syndrome defined by widespread muscle pain, fatigue, sleep dysfunction, and cognitive dysfunction. Fibromyalgia pain dysfunction involves increased sensitivity to pain known as hyperalgesia. A recent study published in Arthritis & Rheumatology, a journal of the American College of Rheumatology (ACR) shows that people with fibromyalgia have hypersensitivity even if events are non-painful based on Functional magnetic resonance imaging (fMRI) imaging of the brain.

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    Brain imaging reveals reduced activation in primary sensory regions and increased activation in sensory integration regions. These responses to a non-painful stimulus may be the cause of problems with tactile, visual, and auditory stimulation. Patients often do report reduced tolerance to environmental and sensory stimuli in addition to the pain.

    The small study included 35 women with fibromyalgia and 25 controls. Patients had an average disease duration of seven years and a mean age of 47. Functional magnetic resonance imaging (fMRI) was used to analyze the brain’s response to visual, tactile-motor, and auditory stimulation. Patients reported increased subjective sensitivity or unpleasantness in response to this multisensory stimulation in daily life. The results of the fMRI showed patients had reduced “task-evoked activation in primary/secondary visual and auditory areas and augmented responses in the insula and anterior lingual gyrus. Reduced responses in visual and auditory areas were correlated with subjective sensory hyper-sensitivity and clinical severity measures.” (ACR)

    The study concluded there was a strong “attenuation of brain responses to non-painful events in early sensory cortices, accompanied by an amplified response at later stages of sensory integration in the insula,” and these abnormalities are associated with the main FM symptoms suggesting this maybe be linked to the pathology of the syndrome. Dr. Marina López-Solà from the University of Colorado Boulder stated, “Our study provides new evidence that fibromyalgia patients display altered central processing in response to multisensory stimulation, which is linked to core fibromyalgia symptoms and may be part of the disease pathology. The finding of reduced cortical activation in the visual and auditory brain areas that were associated with patient pain complaints may offer novel targets for neurostimulation treatments in fibromyalgia patients.”

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Cognitive Dysfunction and fibromyalgia

    When we are talking about the poor cognitive function we have to be precise and not confuse it with just being absentminded but studies have shown there are real cognitive dysfunctions occurring with fibromyalgia. What is the cause of the cognitive dysfunction seen in the syndrome though? Is the brain aging faster? Is it due to depression or anxiety? Or is it correlated to pain or lack of sleep?

    There are many areas where people with fibromyalgia can point to there being a problem but not all of them have been specifically studied. There is what is called Fibrofog the term used to refer to poor concentration. Often people have problems with their short-term memory, their long-term memory, and their working memory. They have trouble remembering the names of objects, and people and have problems with facial recognition. When they speak the wrong words come out or they forget what they say in the middle or they cannot comprehend what the other person is saying. When they are writing they use the wrong words, mix up their letters, make odd grammar mistakes and forget how to spell a word altogether. It is the same with numbers; they transpose them and cannot copy them from one page to another without mistakes. They forget how to do simple routine tasks or forget the order to do them. It is scary and confusing when you do not know what is going on with your brain and what is to blame.

    There have been more than a few studies looking into the fundamental aspects of cognition to figure out exactly where the cognitive dysfunctions are and how they compare to others of the same age. This helps determine whether the cause is brain aging or if the cause lies elsewhere.

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    Areas fibromyalgia patients perform lower than age control subjects

    Free recall- such as having a list of words to remember at a later time.

    Working memory- Working memory is quite important for everyday functionality. It is the ability to take information, hold it in your mind and use it in some mental process.

    Vocabulary tests- Often people with fibromyalgia have problems accessing their vocabulary, not that they do not, in fact, have one. A test could ask a subject to come up with a list of words that start with the letter B quickly and accessing that knowledge would be problematic compared to age-controlled subjects.

    Cognitive Functioning in Fibromyalgia Patients: ARTHRITIS & RHEUMATISM

    The ‘Cognitive functioning in fibromyalgia patients’ study published in the journal of Arthritis & Rheumatism compared 23 FM patients with 23 healthy age-matched controls and 22 older control adults. The older control subjects were to compare the cognitive dysfunction reported in FM patients to the natural decline we have seen over time as we age. They measured “speed of information processing, working memory function, free recall, recognition memory, verbal fluency, and vocabulary. We correlated performance on cognitive tasks with FM symptoms, including depression, anxiety, pain, and fatigue. We also determined if memory complaints were correlated with cognitive performance.”

    According to the study, the FM patients performed more poorly than their age counterparts on all aspects of the study such as working memory, free recall, recognition memory, verbal fluency, and vocabulary with the sole exception of information processing. The FM patients performed more like the older controls in the study except they had better information processing and poorer vocabulary. It also is suggested within this study that poor cognitive performance was correlated to pain and not depression or anxiety. The fact that “speed of processing was intact in FM patients suggests that the most basic and global information processing ability—how fast we process new information—is not a problem for FM patients. Our findings do indicate that FM patients have more limited working memory and long-term memory than do age-matched controls. The cognitive symptoms described by these patients are likely to be related to difficulties in these domains.”

    The intact speed of processing is quite good news if this study can be validated because it is vital to most cognitive functions. The decline in the speed of processing, in fact, might indicate deterioration of cognitive functions, and “Speed decreases that occur with age have been hypothesized to be related to age-related declines in dopamine receptors, decreased brain weight, increased dendritic branching that leads to circuitous cognitive processing, or decreases in a myelin sheath.” However, functionally, on most other indicators, people with FM are operated cognitively twenty years age advanced and even more poorly indicated on vocabulary standards.

    Cognitive impairment in fibromyalgia syndrome: The impact of cardiovascular regulation, pain, emotional disorders, and medication:

    In the European Journal of Pain, a study was published to look at whether high or low blood pressure could be affecting the cognition of fibromyalgia patients. Indeed some people have speculated the lack of blood flow to certain areas of the brain is responsible for some of these symptoms. The study included 35 FM patients and a control group of 29 healthy people. This study saw the same cognitive impairment patterns seen in the study above.

    One finding was that the study suggested that “pain plays an important role in the genesis of the cognitive deficits in FMS. Clinical pain ratings in terms of the number of words used to describe pain were inversely associated with the number of calculations in the FMS sample. Furthermore, when pain ratings were statistically controlled, the group difference in performance was no longer significant. This is in line with our finding that FMS patients using an analgesic medication, particularly opiates, performed better than patients not using these drugs. These results corroborate numerous studies supporting the interfering effects of pain on cognition. Pain is an attention-demanding condition that activates brain areas associated with cognitive processing such as the cingulate and the prefrontal cortex. One may thus speculate that central nociceptive processing detracts from cognition by requiring enhanced neural resources in the respective brain areas.”

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    In the control group, blood pressure was a factor in cognitive functioning however in the FM group “the inverse association between BP and performance was absent, which may indicate that the affected patients are protected against the negative effects of high BP on cognition. Taking the aforementioned mechanism into account, it may be hypothesized that the CNS inhibition due to baroreceptor stimulation is reduced or absent in FMS. This is in accordance with the observation that the frequently described reduction in pain experience following experimental baroreceptor stimulation did not occur in patients with chronic pain disorders. It has furthermore been shown that pain dampening during experimental baroreceptor stimulation only occurs in individuals with normal to high BP, whereas in those with low BP this procedure may even increase pain.”

    He likewise determined anxiety and depression did not correlate to the cognitive concerns. However, this study shows that blood pressure does not look like it is a factor and that level of pain might very well be an important factor.

    Conclusion

    Clearly, there is a great deal of cognitive dysfunction with fibromyalgia sufferers such that a person is cognitively functioning twenty years older than they are. However many studies have validated that intact speed of processing is not affected which suggests the brain is not in the process of accelerated aging and that is a key difference. Another important thing to note is that these two studies and more have shown that anxiety and depression are not factors in fibromyalgia cognitive issues. The last study suggests that perhaps it is the level of pain experienced that affects cognitive abilities and certainly that does seem like an area that needs to be explored further. However, we are left wanting are we not? There have been other studies showing that pain is an indicator but perhaps because the same area of the brain is activated and it is a distraction. We are left with knowing there are these cognitive impairments but not the specific cause for them or what is going on in the brain with enough clarity to do anything specific about it. Therefore while we have a few options for pain treatment there is really nothing available to assist a person with some very important cognitive concerns. In fact, side effects can make cause mental grogginess anyway. Discovering the relationship between pain and cognition in the fibromyalgia brain is a very important area to delve into. It hardly seems probable the cognitive problems are associated with a cause separate from what we know causes pain to be hyperintense. Although it is rather hard to argue with the theory that pain is distracting, perhaps inherently so, due to its function to grab our attention and focus.

    Helpful tips

    Until then all we can do to help with our cognition is stick to regulated routines, keep regular sleep habits and keep regular eating habits. Routines establish habits that enable us to remember things easier so we are less stressed. We want to keep our stress levels as low as possible. Sleep habits are difficult to maintain but irregular habits and changes cause disruptions that we physically do not handle well and can cause greater stress and fatigue. Regular eating habits of eating throughout the day, and snacking every three hours, will keep our energy levels higher and keep the fibrofog at bay. Using reminders and To-do lists also helps in the organization. If during the day you feel your concentration waning get up and have a stroll about the office or a walk around the block. The break will energize you and help refocus some of that mental energy. Sometimes changing from one task to another can also get your brain going. Distraction seems to be a component of cognitive issues. Pain is one major distraction. Perhaps along with our over-sensitivity to the environment and stimulus to external distractions. Therefore our ability to pace ourselves and take breaks when needed can certainly help if we are overly strained. Another key is to avoid multi-tasking because it naturally segments your attention into different areas and it is easy for interruptions or concentration issues to make you suddenly lose your focus mid-task. Try not to overstimulate your system with loud noises and bright lights; the fewer distractions from your environment the better. There is also a little something to exercise your brain with puzzles or brain games. Finally, double-check with your doctor to ensure the medication is not having a side effect that may be making these symptoms worse if they are troubling you.

    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

    Click Here to Visit the Store and find Much More….

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store