Tag: Fibromyalgia

An in-depth guide on Fibromyalgia, covering its symptoms, causes, treatments, and tips for managing this chronic condition effectively.

  • Do you know back in the 1800s fibromyalgia is a psychiatric ailment condition?

    Do you know back in the 1800s fibromyalgia is a psychiatric ailment condition?

    Fibromyalgia was first described in the early 1800s. It was considered a psychiatric ailment for decades. It wasn’t until a study done in 1980 that doctors were able to identify it scientifically. I got sick with it in 1989, a very stressful time in my life.

    The problem was that even though the year 2000 many, if not most, doctors continued to refer their patients to a mental health professional. Doctors refused to believe it was real. In the 1990s internationally known and respected rheumatologists (thankfully I have forgotten his name) continued to claim that FM did not exist.

    He wrote about his opinion and addressed numerous medical conferences to tell the doctors attending to not let what their patients were saying sway their understanding that this “condition” was basically all in their mind, and to continue to refer them to mental health facilities.

    Could this (especially in the 19th century and early 20th century) be because 98% of those patients were women? Who knows.

    The idea that fibromyalgia may be the symptom of inactivity deserves an answer. If you do not have FM or live with someone who does, it is virtually impossible for someone with FM to explain. My way of explaining it is that it is a circle or cycle of pain.

    So, I wake up in the morning in pain. It doesn’t matter how well I did, or did not, sleep. The pain comes from all over my body. Some of it is a dull ache but for me, most of my pain feels like a bruise. It is very easy to elicit pain in a specific area simply by pressing on it. I feel like someone with a ball-peen hammer (the hammer with a round ball on one end) spent the night hitting me with it all over my arms, neck, back, and legs.

    When I get out of bed, I’m dizzy and the pain is bad. But as I go through my day, and my muscles loosen up the pain level drops. I have a few good hours on most days from 10 am to about 2 pm. By the time it gets to 3 pm, the fibro fog has descended and I can’t think clearly.

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    Trying to have a conversation with fibro fog is impossible. I can see somebody’s lips move but what they are saying doesn’t make sense. I can start to answer them but somewhere along the way I forget what I was saying and fall silent. I often say something but the words don’t go together. I am aware of this difficulty, but I am powerless to fix it.

    During this time I am overwhelmed by fatigue. Often I can actually feel my energy drain out of my body. The need to sleep is strong.

    I remember one time when my husband and I were going to go to a nice hotel for the night while my parents watched our two teenagers. We spent the morning packing and taking care of things. We finally got in the car about 1:30. We hadn’t eaten, so we stopped at a restaurant we liked about four miles from our house.

    As we were finishing our meal, I could feel my energy drain away. I decided to ignore it. I wouldn’t tell my husband. We had a three-hour drive ahead of us and I thought I could just nap in the car.

    When we walked back to the car I started crying and told my husband what had happened. He was very used to this. He asked if I wanted to go on or return home. I told him how sorry I was but I needed to go back home. When we got there I went straight upstairs and went to bed, still crying. Eventually, the tears stopped and I fell asleep.

    Now that I’m older, that need to sleep in the afternoon is even worse. I plan my day around it. Doctor appointments have to be finished by 1:00 or my husband has to take me.

    As the afternoon and evening progress, the pain begins to ramp up. I am powerless to get on top of it. By the time I go up to the bed, I am drained. My pain is bad, but my fatigue barely lets me brush my teeth. I fall into bed and as my body relaxes, my mind, which has been sleeping most of the day, wakes up.

    I know I desperately need sleep but my mind is wide awake. Thoughts run through it for hours keeping me awake. I think about my day, about where we should go for our anniversary, I sing songs. Often a bit of a song runs through my thoughts in a continuous loop.

    Three hours later, about 1:30 am, I get up and go to the bathroom. Then I take two Tylenol and go back to bed. I am finally able to sleep until about 8 am.

    And the cycle continues.

    Here’s the thing about exercise. Some days are a little better than others. On those days I may run an errand and come back completely worn out. On those days, if the weather is nice, I may decide to walk half a block. I return worn out.

    On the days when I’m feeling especially good, I might take my three-year-old grandson to the park. It is a significant walk but I love walking with him. By the time we get back home, I can’t move. I go to bed and can’t get out of it in the morning.

    If I really have an active day, sometimes I have to spend the next day in bed. I’ve had severe FM for 30 years and I still can’t figure out how much activity is right for that particular day. It’s constantly changing.

    Doctors who don’t fully understand FM advise their patients to get outside and work up to walking a mile, go swimming, take up a sport. They simply do not understand the pain and fatigue cycle of FM. I have a primary care doctor and a pain specialist.

    Too much exercise causes great setbacks in FM. We have a good exercise bike and I decided to get on it and build up my endurance. The first day I pushed myself and felt horrible that afternoon. I haven’t ridden it since. The amount of time I rode the bike? Two minutes. I think that says it all.

    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

  • Fibromyalgia: Do you think that Fibro Patients are imagined to live without pain?

    Fibromyalgia: Do you think that Fibro Patients are imagined to live without pain?

    I would think that would qualify as an oxymoron, calling Fibromyalgia a “comfort zone”! Since I noticed the first pains, it seems as though I haven’t been comfortable again.

    I know you mean more on a mental/emotional level, however. I would still be inclined to think not. From what I’ve read, the people I’ve talked to a majority of people with Fibromyalgia were “type A” personalities. Meaning, they were movers, shakers, doers, overachievers, survivalists– we were always moving, cleaning, hustling, being as efficient with time, so to do as much as possible, with the least amount of time.

    Plus, we did it right, we did it without asking for help, and we did it for everyone but ourselves. I’ve said, although I’m stuck with FM now, I can still say I lived one heck of life before. And, even since.

    So, when FM hit us, it not only took away our ability to move, it took away who we were at our core. The way we always functioned was yanked away, and after all the Dr’s, tests, and fear before our diagnoses were gone, we were left with that same energy running laps in our brains. Some of us were predisposed to mental illness, some not, perhaps. But, I know a lot of people get depressed. Who wouldn’t? Fibromyalgia is a beast of mythical power.

    It attacks you at your senses-sight, smell, sound, touch, taste, temperature- everything is affected. Sound tones (dog barking), feel like knitting needles to your ears. Sunlight is blinding, phone lights give me headaches. And, smells! I get nauseous walking to the store from car exhaust, cigarette smoke on people walking by, detergents used by the store, (not to mention the detergent aisle-my eyes water & burn &my lungs close), 20 different people with 20 different smells from cologne, perfume, lotion, bath soap, everything.

    It’s unpleasant, at best. Worst case, I get headaches, nausea, I “taste” the smells, I get dizzy. It’s not great. I break out into a sweat several times a day, for no apparent reason. Some people are constantly cold, like my icy feet & hands. I constantly have every symptom of a bad kidney infection, which is a gift from FM called Interstitial Cystitis.

    FM is different for everyone, except in that it’s typically different for each of us every day. I often say it would be easier to draw what my body feels like. My skin would be lumpy with huge knots, black and blue, and on fire from the waist up. My eyes, nose, ears & throat would have fire coming from them, as well. My bones would all be broken to some degree.

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    The worst would be my pelvic/hip/tail bone, and my feet would be mutilated, full of broken glass, and look like ice. My hands would also be swollen, black and blue, full of broken bones and glass, with rubber bands wrapped tightly around them. Sharp blades that cut into my wrists, would go down the insides of my wrist, into the bend of my elbows.

    I would have various bugs biting me, making me itchy, and I would have stickers poking my skin. There would be people around me, stabbing me with knives, randomly. I would have twisted metal for my neck/upper spine. Thick, strong cables would be my tendons, and invisible powers will pull them in the wrong directions, at inopportune times, making it easy for a knee/hip/arm to “give out”. A sick marionette doll, of sorts.

    I definitely don’t count nausea as comforting, either. Unable to take meds because of stomach pains/nausea, or getting nauseous from said medications. Feeling your head swim when you’re trying to figure out what to do, or say, because of fibro fog.

    The headaches, body aches, pain all the time take a toll on your mind, body & spirit. Your friends don’t understand or want to hear about it. Your family doesn’t believe you, and why would they? DOCTORS don’t believe you, half the time!

    So, you question your own sanity. You become depressed, isolated, withdrawn. You stop getting invitations because they assume you’ll say no, again. You lose respect from & for others, because you have nothing but time on your hands, and Fibromyalgia WILL be in your thoughts- like it or not. You simply cannot live a “normal life“.

    In my case, I can’t stick to a schedule if my life depended on it. I’ve had FMS for fifteen years, and I get disability, subsidized housing, free rides to dr appointments, and in-home services-someone who comes to help me with cooking, cleaning, etc. I don’t HAVE to do anything, except collect my services, and be “COMFORTABLE”. Yet, I’m constantly trying to do BETTER.

    I’m a double Psych major at the local college, and it will take me longer than most, to finish with my degrees. I’ve gone to Heald college twice for a Business degree. Each time, I have to “fix” my financial aid mess caused from the last time my health stopped me from completing school.

    Each time, I’m older, my abilities are less, and my confidence wavers, when my cognitive abilities are slower, and I’m scared to death I’ll fail. So, why bother, if Fibromyalgia can be a “comfort zone“? Why try to be anything more than who I am TODAY?

    Because I AM NOT FIBROMYALGIA! I HAVE Fibromyalgia! But, I REFUSE to stop moving, stop trying, stop living. Even if I can only move, try 1 day of the week, I’ll take it. And, I won’t feel bad the other 6 days, because ignorant, (read: uneducated, have never felt how I feel, so can’t possibly fathom what it’s like), people often think I’m lazy, I’m lying, I’m scamming the system, or I’m simply comfortable with this horrible condition with which I’ve been afflicted.

    I hope this answers your question. I’m hoping you can answer one for me? Most people don’t know about Fibromyalgia, much less what it does to someone. What would drive you to ask this question, and in the way you asked? With FMS being a pain condition, why would you suggest anyone could/would find any comfort in having Fibro? What is your experience, if any, with Fibromyalgia?

    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 is daily life like for people living with fibromyalgia pain?

    What is daily life like for people living with fibromyalgia pain?

    On a scale of 1-10, my average daily pain level is a 6 or a 7. All-day. Every single day of my life. It’s always there, and cannot be ignored no matter how engrossed in something I may be.

    Being in constant pain is exhausting. Fatigue is a huge issue in my life. Unrefreshing sleep is one of the hallmarks of this disease. I sleep about ten hours per night and still wake feeling like I used to in college when I pulled an all-nighter studying. That’s on my good days.

    Bad days are more like staying up for three days while having the worst flu of your life. Fibromyalgia has what are called “flares” where the disease is more active than usual. For me, these can last for weeks, and during a flare, I’m almost completely bedridden, sleeping up to 20 hours a day. Literally too exhausted to leave the house, sometimes even to shower or fix myself a meal. Careful management of my energy levels helps limit these to just a couple a year.

    Even on good days, energy is in very short supply. I’ve had to learn to plan not just my day, but my entire week carefully. A three-hour grocery shopping trip requires me to build a day in before it to rest up for the activity, and a day afterward to recover.

    Cognitive dysfunction is pervasive, especially on days when the fatigue is severe. Putting together a coherent sentence or following a simple conversation becomes a struggle. My favorite TV shows may as well be in Swahili as far as my understanding of what’s happening. Handling money, paying bills, filling out forms, reading Quora questions correctly, all become simply too difficult when I’m tired.

    Words desert me. My family has become remarkably good at deciphering what I mean when I ask them to go get me the “thing for the thing” (usually accompanied by a vague hand gesture). I lose track of where the thought is going before I finish a sentence when talking. “Sweetie, can you run upstairs and get…” Get what? I have no idea.

    I’ve had to teach my family that a blank stare and a “huh?” means start over with whatever you just said to me. From the beginning. Repeating just the last few words will do no good, and please don’t raise your voice (see below). Slow down. Speak clearly. Watch my face to see if I’m following.

    My memory is completely shot. Yesterday I was going into the next room to tell my husband something. I completely forgot what it was before I can completely stand up from my desk. How I wish I were exaggerating for dramatic effect. I rely heavily on routines and reminders. My smartphone is a lifeline. I have so many alarms and reminders programmed in it’s ridiculous. If I had a dollar for every time I showed up for an appointment on a wrong day, I’d have a fistful of cash.

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    There’s a hidden silver lining, though. I can read a book (on a good day) or watch a movie repeatedly, and it’s new to me each time. Usually, I’ll get about three-quarters of the way through and turn to my husband to ask him if I’ve seen it before because it starts to seem familiar somehow. He finds this amusing. I prefer to watch movies at home because sitting still for two hours is very painful. It helps to be able to get up and stretch from time to time. We do have a wonderful theater with cushy recliners a couple of hours away now, so that helps.

    It’s not just nerves endings that are oversensitive. Bright lights, too much noise, fast motion, slightly rough fabrics, strong smells or flavors. Everything causes pain and distress. If someone raises their voice at me, I can’t understand what they are saying, because the sound overwhelms my senses. They start to sound like Charlie Brown’s parents. “Whaaaw whaaw whaaw.”

    Talking on the telephone is stressful. I avoid it as much as possible. My hearing is perfect. I just can’t process spoken words well anymore. Without facial expressions and non-verbal cues, I have a really hard time understanding what people are saying. It’s really embarrassing to ask people to repeat themselves, especially when I often don’t catch it the second time either.

    I much prefer communicating in writing. Then I can take as much time as I need. I’ve been working on this answer for about an hour now (and am writing this sentence after the five paragraphs below). On a good day, I can dash off an answer in ten minutes. Today is not a good day, but not so bad I’ve lost the ability to read yet. It’s still early, though.

    Fibromyalgia wreaks havoc in other ways besides pain and fatigue. Bowels and bladder are irritable and unpredictable. I make sure I know where the nearest bathroom is at all times when I have to go out. Clean panties and wipes in my purse at all times.

    I’ve lost the ability to regulate my body temperature. It feels a lot like having a fever and chills. I can be burning up and shivery at the same time. Any temperature above 75 or below 60 is debilitating. Today it’s 70 degrees here in this room I’m sitting in. I’m wearing a sweater, drinking hot tea, and using a heating pad right now, and I’m still chilled through.

    All of this is complicated by the fact that it’s an invisible disease. I look normal, and like most fibro patients, I have developed a good game face. People judge. If I let the pain show, I’m judged as a whiner. If I hide it, I’m judged as a faker when I say I can’t do something. I can sympathize with peoples’ impatience/skepticism. It does seem unbelievable if you haven’t experienced it for yourself.

    A lot of people feel I should just “suck it up and push through”. They don’t realize the amount of mental fortitude it takes to resist my own impulse to do just that. I’ve learned the hard way that the price for doing is just too high. If I “soldier on” and mop the floor today after I do the dishes and laundry, I’ll be bedridden for the next three days, and fall behind on everything. But the temptation to do so is always there. It takes a lot of discipline to pace yourself during simple activities you used to do with ease.

    The worst part isn’t the physical difficulties. It’s the loss of self-esteem, of self-confidence, of my health. I grieve for the person I used to be. Twenty years in and that loss hasn’t become any easier to accept.

    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 Fibromyalgia Suffer can start Strength Training?

    How Fibromyalgia Suffer can start Strength Training?

    Exercise helps break the chronic pain cycle associated with fibromyalgia syndrome (FMS) by improving fitness and functional levels, relieving physical and emotional stress, and boosting one’s confidence and self-esteem. While you probably have heard a lot about the benefits of aerobic exercise, you may be wondering about strength training. Women at risk of osteoporosis commonly hear about including strength training activities in an exercise program.

    Should a person with fibromyalgia perform strength training activities? Is it safe? Will this type of exercise hurt you? In the following article, we will answer these commonly asked questions and describe how you can include basic strength training activities in your exercise regimen.

    First Steps

    There are three important steps to take before beginning an exercise program.

    First, let your doctor and other health care providers know about any change in what you are doing to manage your health—including exercise. While exercise has many physical, emotional, and social benefits, there may be health issues you need to address before starting an exercise program, such as unresolved foot pain or back pain. You may be directed to stay away from certain forms of exercise because of other health issues.

    Second, an exercise program is most effective when you do it consistently. Decide on what you are going to do for exercise and where you will do it. If your exercise is not enjoyable or convenient, you probably will not do it regularly. Follow a basic program, like the one at the end of this article, or get the help of a knowledgeable professional—exercise physiologist, physical therapist, doctor, nurse—to formulate your exercise program.

    Does it make sense for you to be outside or inside at this time of year? Do you like to exercise alone or with others? You can exercise at home, in a community center, or in a commercial fitness center. Once you decide what to do and where to do it, make a commitment to yourself to make time in your schedule to exercise. The more hectic your schedule, the more important it is to review your other commitments and plan your weekly exercise schedule. Consider the times of day and days of the week that works best for you.

    Click here to Get this or Visit Fibromyalgia Store

    Finally, anticipate that you may be a bit sore or uncomfortable at first, especially if you have not been physically active in recent months. You should not be in severe pain, however. If you experience severe pain, then you probably have done too much and started too fast. Listen to your body—learn to know the difference between your chronic fibromyalgia pain, the pain of overused muscles, and the acute pain of an injury; they are different.

    One way to help judge your level of pain when exercising is to utilize a 0-10 numerical scale with zero signifying no pain, 5 moderate pain, and 10 the worst possible pain. In general, if your pain is 1-4, exercise as you planned; if the pain rates 5-7, cut back on the amount and intensity of exercise you do that day; if your pain is an 8 or 9, don’t do your regular exercise routine, but you may still be able to perform some gentle stretching and maybe go for a short walk, and if you are experiencing pain that is a 10 it is best if you do not exercise that day.

    While fibromyalgia can be extremely painful, it is important to remember that you are not damaging your muscles and joints when you exercise appropriately. Making good judgments about how much to exercise takes time to learn, but is essential to your successful self-management. With practice, you can become your own exercise expert.

    Adding Strength Training to Your Exercise Program

    Recent research has demonstrated that strength training exercises, when done appropriately, can be safe and beneficial for individuals with FMS. Strength training exercises increase your muscle strength and can make daily activities, such as climbing stairs and carrying laundry, easier. 

    Stronger muscles use less effort to do work than weaker muscles. Some think that by using less effort, your muscles do not get as fatigued. For many years, when FMS was thought to be a disorder of the muscles, people believed that you might damage muscle if you exercised it too hard. Therefore, people with FMS were discouraged from doing strength training type exercises. Today, research demonstrates the safety and benefit of this important type of exercise for the person with FMS.

    Strength training activities can be incorporated into your exercise regimen regardless of your level of experience or fitness. The strength training part of a program ideally should include one exercise for each of the major body areas (legs, chest, shoulders, back, arms, and abdominals). Strength training exercises should be done 2-3 times per week with at least one day of rest between workouts to allow muscles time to rest and recover.

    Exercises can be performed with free weights, machines, stretchy bands, household items (e.g., soup cans), or the resistance of your own body. Exercises can use one or more of the above methods to provide resistance. There is no magic about how you provide resistance. The key is to perform the exercises correctly and regularly, so convenience should be considered when making your decision of what you will use for resistance.

    When beginning a strength-training program for fibromyalgia, you should first learn and master the proper techniques for all exercises. You can learn proper techniques from a book, an introductory session with trained health or fitness professional, or by participating in a class where an instructor will keep a watchful eye on you while you learn with others. More guidance from a knowledgeable professional usually translates into faster learning.

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    A repetition of “rep” is the performance of an exercise one time, and a “set” is a sequence of repetitions of an exercise performed without prolonged rest. The number of repetitions and sets and the amount of resistance is how strength training exercise is quantified or measured. Begin with a level of resistance that allows you to perform eight repetitions “fairly easily.”

    If you can comfortably lift the weight eight times (8 reps), it is safe to progress to 10 reps the next time you exercise. After you are comfortable with 10 reps, you can try to perform a set of 12 reps. When you can perform 12 reps of an exercise for two sessions in a row, you are ready to increase the weight/resistance slightly. When you increase the resistance, remember to reduce the number of reps to eight and repeat the process of gradually increasing the number of repetitions with the new resistance.

    There are several important keys to remember while performing strength training exercises. Always use proper exercise techniques. Avoid “guarding” sore muscles when you perform an exercise. Contracting muscles around an aching body part leads to more tension and poor posture. Poor posture puts unnecessary stress on other body areas. Exercising with good body posture and technique will work the muscles in a balanced manner and reduce the chance of injury.

    Breathing during the exercise is very important for keeping muscles relaxed, comfortable while exercising, and supplied with oxygen to do the work. To breathe properly during an exercise, inhale and exhale slowly as you perform the part of the movement that requires the greatest effort. As you return to the starting position of the movement, breathe in slowly and smoothly. An easy way to remember this is to “exhale on exertion,” and inhale on the less strenuous part of the movement. Remember, you should never hold your breath while performing an exercise.

    Speed or the pace of a movement is also extremely important to your strength training program. In most strength training exercises there are two parts to each repetition. The first is the concentric or “positive” phase. The concentric phase is when the muscle you are exercising shortens while performing the exercise movement. An example is the biceps muscle, on the front of the upper arm, when you move your hand from your thigh to your shoulder.

    The second part is the eccentric or “negative” phase of the movement where the muscle you are exercising lengthens while you return to the starting position of the exercise. The biceps muscle lengthens when the hand moves from the shoulder to the thigh. Strength training exercises should be performed to a count of two seconds for each of the concentric and eccentric parts of the exercise.

    Our work over the past several years with the SELF-study (Self-management and Exercise for Living with Fibromyalgia) has shown that shortening the eccentric phase can help decrease muscle soreness in people with FMS when beginning a strength training program.

    Strength training exercise has many health benefits for people of all ages. While people with FMS have often been discouraged from performing strength training exercises in the past, evidence today suggests that when performed appropriately, strength training can be an enjoyable and beneficial part of a balanced exercise program. As with any new type of physical activity, it is important to start and progress slowly to allow your body time to learn the exercise and safely adapt to the level of effort.

    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 much Stressful Experience will Face by Fibromyalgia due to their Illness? Tips to face their Disease

    How much Stressful Experience will Face by Fibromyalgia due to their Illness? Tips to face their Disease

    Tips for the Warrior

    Caring for someone with CFS or FM can be a stressful experience. You may take on extra responsibilities, experience financial strain, feel frustrated and resentful at times, lose companionship, face uncertainty about the future, and experience both reduced socializing and sexual difficulties.

    Even with all the challenges brought by serious illness, there are many ways to take care of yourself. Here are nine to consider.

    Maintain Your Health

    This is the number 1 recommendation of experts on warriors. To serve your loved one well and to avoid resentment and burnout, take time to get adequate rest, to eat well, and to exercise.

    Accept Help

    When people offer to help, accept the offer and suggest specific things that they can do. If your finances allow, consider paying for help in such areas as meals, house cleaning, and transportation.

    Take Time for Yourself

    Get a respite from caregiving by spending time away from the person who is ill, for example by pursuing a hobby. Give yourself an opportunity for leisure and enjoyment, a way to recharge your batteries.

    Click here to Get this or Visit Fibromyalgia Store

    Educate Yourself

    Seek information about CFS or FM, especially strategies for reducing symptoms and improving quality of life. One source is the articles on our website. See the article “Educate Yourself” for a list of patient organizations, other websites, and books about the two conditions.

    Stay Connected

    Avoid isolation and reduce stress by maintaining relationships with extended family and friends. This may mean getting together regularly for exercise or outings with friends, spending time with children, or any other kind of socializing that keeps you connected with others.

    Consider Counseling

    Be sensitive to signs of stress and consider seeing a counselor if you detect them. Signs that counseling might be appropriate include feeling exhausted, depressed, or burned out, or over-reacting, such as by angry outbursts.

    Counseling can be helpful for gaining perspective on your situation or exploring communication problems. You might get help in individual sessions or in joint sessions with the person who is ill.

    Grieve Your Losses

    Just as people with CFS and FM experience many losses, so do those around them. They are deprived of part of the companionship the patient used to provide, as well as her work around the house and, in many cases, financial contribution.

    And, just as the person who is ill has lost the future she hoped for, so do you have to adjust your dreams for the future. Like the person in your life with CFS and FM, you, too, need to grieve your losses.

    Create New Shared Activities

    Serious illness may make it impossible for you to spend time with the person who is ill in the same way as before, but you can develop new shared activities to do together.

    One couple told us they took up the study of music using courses on DVD. The husband in another couple said that once he realized his wife’s new limits, they shifted from camping and hiking to dinner and a movie.

    The point is to create occasions for shared pleasure so that the relationship is strengthened and both ill and healthy members of the family don’t come to see their relationships as just about illness and deprivation.

    Seek Support from Other Warriors

    Fellow warriors can offer strength, support, inspiration, and models of successful adaptation. You might meet such people through patient support groups.

    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

  • Fibromyalgia Couples make Good Communication Difficult due to their Illness

    Fibromyalgia Couples make Good Communication Difficult due to their Illness

    Improving Communication

    The stresses brought by serious illness can make good communication difficult. To complicate matters, CFS and FM create the additional challenge of cognitive problems. Here are seven ideas for how to improve communication if you or your partner have CFS or FM.

    Pick a Good Time and Setting

    If you have something important to discuss with a significant person in your life, select a time when both of you will be at your best. It should be a time when both of you can give good attention and you will not be distracted by pain or brain fog, preferably during your best hours of the day. Choose a place that minimizes distractions and interruptions.

    Practice Good Listening Skills

    Good communication is based on each person understanding the other person’s views. Understanding begins with listening, which means focusing your attention on what is being said, with the goal of understanding the speaker’s point of view.

    Listening works best if it occurs without interruption. After the person is finished speaking, respond by acknowledging having heard them. You might say something as simple as, “I understand.” If you are not clear, you can respond by asking for clarification or more information. You might say something like, “I’m not sure I understand. Can you say something more?”

    From time to time, check whether you have understood the other person’s position by restating it in your own words. You could say, “Let me try to summarize what I’ve heard and you can tell me if I’m understanding you.”

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    Focus on One Thing at a Time and Be Specific

    Focus on one issue at a time. If you are requesting that the other person change, be specific in your request. Avoid making general requests such as, “I need help with the housework.”

    The person being asked may wonder what would be involved in responding to the request. Instead, say something like, “Can you do a load of laundry today?” or “Can you do the grocery shopping?”

    If you are the one being asked to do something, it’s reasonable to defer giving a yes or no answer until you are confident you understand what is expected of you. You can ask, “What specifically would you like me to do?” Even if you decide to decline, you can still acknowledge the importance of the request to the person asking for help.

    Aim for Solutions

    Have as your goal finding solutions, not blaming one another or finding fault. The idea is to be able to discuss problems in a constructive rather than a confrontational way. Treat each other with respect, acknowledging his or her support and effort. Avoid demeaning comments, sarcasm, and blaming. Acknowledge your part in shared problems and express appreciation for the other’s efforts.

    Use Problem Solving

    Use problem-solving to find solutions. Begin by brainstorming, which means thinking of a variety of possible ways to solve a problem. In brainstorming, the goal is to generate as many ideas as possible, without evaluating them.

    For example, if your problem is how to do household chores when one member of the family is ill, alternatives might include dividing up the chores differently among members of the family, hiring occasional or regular assistance, simplifying tasks (for example, having simpler meals or cleaning less frequently), and moving to a smaller home that is easier to maintain.

    Second, you evaluate each proposed solution, decide which ones are most promising, and try one or two of them. Third, after giving each solution a fair try, evaluate the results. Some potential remedies may not work, so you may need to have further discussions and try other solutions. The final solution may be a combination of several approaches. If several strategies are unsuccessful, you may decide that a problem may not be solvable or not solvable at the present time.

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    Consider Getting Help

    In many cases, you will be able to solve your problems yourself, but at times you may want to get help, either in understanding the causes of your problem or in finding solutions. So it may help to ask what resources are available to you. For example, to get a fresh perspective on your situation, you might ask other families how they have solved a similar problem or you might ask what community resources (church and public groups) are available.

    Also, if conversations about your problems are not productive, you can consider getting professional help. A counselor can facilitate a solution to particular problems and also help you practice good problem-solving skills.

    Have Regular Relationship Discussions

    Finally, here’s a technique that one couple in our program uses to nurture their relationship and to solve problems in their lives: having regular discussions of their relationship. They set aside Sunday evenings as a time to discuss any issue that is on their minds, calling it their “talk night.”

    Having regular discussions means that both husband and wife know that they have a forum in which to state problems and frustrations, and a means for finding solutions. Also, because the talks are frequent, they can refine their communication skills through regular practice.

    The husband explains that “Anything either of us sees as a problem or causing stress is a likely topic. Even very minor things are OK.” Topics include an issue one has with the other, problems with friends or children, or problems around the house.

    “A rule is we each openly listen to the other without being defensive. We problem-solve together to come up with a resolution for each issue. After doing talk night we start each week refreshed and with the feeling that comes from having dealt with whatever problems were there.”

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    Official Fibromyalgia Blogs

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  • Evidence shows that Fibromyalgia and CFS put Couples under Stress

    Evidence shows that Fibromyalgia and CFS put Couples under Stress

    Fibromyalgia and CFS put couples under stress. This chapter offers strategies for addressing three problems faced by couples: sexual difficulties, strained communication, and caregiver burnout.

    Improving Intimacy

    When CFS or fibromyalgia enters a marriage, one casualty can be intimacy between the partners. Pain, reduced energy, reduced interest, health problems of the partner, and increased responsibilities for the healthy spouse can all affect a couple’s sex life, but, like other aspects of long-term illness, intimacy problems can be addressed as well.

    When we asked people in our program to describe the effects of their illness on their sexuality, all those who responded said that illness had reduced their sexual activity.

    Many people mentioned having a much lower level of sexual desire than before, due to factors like ongoing fatigue and pain, and the side effects of medications. Other causes of sexual problems included the effects of menopause, relationship strains, and the medical problems and/or impotence of their partner.

    Even though people said that they had either reduced their sexual expression or given up sex, most also reported using a variety of strategies that have either enabled them to adapt their sexual life to their illness or to connect with their partner in other ways. Here are six of the most common adaptations.

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    Talking

    Several people reported that their relationship with their partner improved after they talked openly about their reduced interest in sex.

    As one said, “I explained that I still loved him and felt the same (or more strongly) about him, but I just couldn’t show that through initiating sex…I have no desire for self-pleasure either. Explaining that sure made a difference to his acceptance of my state!”

    Others reported that they benefited from open communication in bed. One said, “I let him know if a certain position hurts and we change positions.”

    Alternative Activities

    Another very common theme was adapting to illness by focusing on alternatives to conventional sex. One person wrote, “The times I am not up to having intercourse, he knows I am usually up for some cuddling and happy to satisfy him another way.”

    Others wrote of alternatives to intercourse, for those who think that appropriate. “You don’t have to have intercourse to be sexually connected…You can be satisfied by manual stimulation and also oral sex.”

    Others have found other ways to express their affection: through hugging, kissing, and holding hands, through words of appreciation and thoughtful acts, and through shared activities like going out for dinner together, watching a favorite TV program, or giving one another a massage. One said, “We still hug, kiss, and say ‘I love you lots. I feel we have a very strong and healthy relationship.”

    Planning

    A third common adaptation is planning for sex. Several people mentioned taking extra rest or reducing their activity level on days they anticipated having sex. Also, a number said they and their partners plan “dates.”

    One said, “What my husband and I have learned is that we need to schedule a ‘date’. I actually put it on my calendar.” Another said, “The ‘date’ planning has worked for me because I tend to do less of the things that I know will cause me residual pain.”

    Others mentioned being mindful of the time of day. Pain and other symptoms may be lower during certain hours of the day. By timing intimacy for those times, couples minimize discomfort and increase enjoyment.

    Another couple reported increasing the frequency of sex through making a commitment to having sex once a week. The wife reported that more frequent encounters made sex less painful and her husband “is much more cheerful and doing more around the house.”

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    Flexibility and Experimentation

    Given the often-unpredictable course of CFS and FM, it can help to be flexible about when sex occurs and what positions and activities are involved. One person said, “We’ve experimented with timing (morning is best), position (I seem to do best on my side), and lubricants.”

    Others use observation as a basis for experimentation. One person wrote, “I noticed that in the summer I had more desire and realized it had to do with the heat, so we started to shower together.”

    Addressing Pain and Hormone Problems

    Some people said that their sex lives improved after treatment of pain and hormone problems. They reported treating pain by the use of pain pills, topical ointments, massage, and heat, and by adapting how intimacy occurs.

    There are several factors involved in the use of medication. One solution is for the person who is ill to time the taking of pain medication so that it will be at peak effectiveness when sex is planned to occur. The type of pain medication is also important.

    The person with pain may want to avoid narcotic pain medications and tranquilizers, which dull the senses as well as reduce pain. Other means of pain reduction include taking a bath before sex, stretching, and massage.

    Pain can be reduced by using positions that are comfortable, by changing positions periodically during intimacy, and by alternating activity and rest. Another pain control approach is the combination of distraction and meditation.

    Distraction means reducing pain by placing attention elsewhere, focusing on sensations, both those given and those received. Also, concentrating on mental images of making love keeps the mind focused on pleasure, distracting attention from pain.

    Several people in our groups also commented on how their interest in sex had improved with hormone treatment, either estrogen, testosterone, or both. One said that testing showed that both her estrogen and testosterone levels were low. Treatment of the latter “not only helped libido but my energy level as well.” Hormone problems can also affect men.

    Emphasis on Caring

    A number of people distinguished between intimacy and sex and said they and their partners focused on closeness and mutual caring. One wrote, “Sex is important in a relationship, but I don’t feel that it is the most important. I think all of the little everyday things that we do for each other and being supportive of each other is what really makes a marriage.”

    Another said, “My husband and I have found we don’t NEED to express our affection sexually…For us, sex does not compare to the kind of fulfillment which is a beautiful thing when shared between two people who are filled with warm, tender, loving feelings toward each other.” She wrote of expressing affection through sharing time together, touching, caressing, and cuddling.

    CFS or fibromyalgia do not have to mean the end of sex. Using flexibility, experimentation, and good communication, couples can continue to enjoy sex and may be able to strengthen their relationship. For those who decide that sex will no longer be a part of their relationship, a focus on other aspects of the relationship can foster closeness.

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    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

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  • Why was I Hiding Fibromyalgia the Person I have Become?

    Why was I Hiding Fibromyalgia the Person I have Become?

    Story of Fibromyalgia Warrior

    Recently I was looking at my social media accounts I came across accounts that I had chosen to hide either my content from. As I looked down the list I realized that many of those people were people that I knew for a significant amount of time in my life.

    Most were people I had either worked with somewhere along the line since Nursing School Graduation, or I went to high school or college with. These were people who were a significant part of my life at one point or another. Not people who were trolls or people from my past that I didn’t want to think about again.

    But as I sat and thought about it I couldn’t find a reason that any of them would have been on the hidden list. The more I thought about it I came to the realization that I must have hidden my posts because I didn’t want them to see my life or my journey.

    But why? I spent a LOT of time thinking about this the next couple of days and the more I thought about it I realized that I had done it because I was embarrassed by what my life had become.

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    The people who knew me 10 or 15 years ago probably don’t know that I am no longer working in my chosen field. That my marriage didn’t work out, that is a whole story for a different day. Or that I am not living my best life with kids, a husband, and my dream job.

    While I know most people are living their exact ideal life. Sometimes I still struggle with the path my life has taken. I know there are always going to be things that we want to change. But my life is FAR from what I ever imagined.

    That being said, this is NO REASON to be embarrassed though. The things that have made such a change were nothing I did. Or bad decisions I made, for the most part anyway. A person can’t change their genetics. Or honestly in many cases like mine the hand they were dealt. So, what? I may not be at a patient’s bedside twelve hours a day.

    Or working to teach future nurses.  But I am still making a difference. I may not be calling Drs or drawing blood. But I am still touching people’s lives. Is it the way that I planned? Hell NO! But I have adjusted and found ways to share my knowledge and provide support in other ways.

    Disability has a way of changing a person and their outlook on life. The things that once seemed so important no longer rank in the top five of the things we worry about.  That isn’t a bad thing though. The version of me that was once embarrassed to let people from my past knew the person who I have become doesn’t exist anymore.

    That person has learned to hold her head up high and be proud of the things she has accomplished. To be proud of the life she has built despite the truly crappy hand she has been dealt. In the end, it really doesn’t matter what any of those people think of me. Whether they knew the person I once was or the person that I am now. The only thing that really matters is how I feel about myself.

    That is what should matter the most to all of us. The opinion of the eyes looking out. Not the eyes looking in. Paths change and so do people, and that’s okay. But we never should be ashamed or embarrassed about the person we became because of an illness.

    Fibromyalgia takes so much away, but it shouldn’t take that. It changes our paths, our hopes, and our dreams. It changes how we look at life as a whole. But it should never change the way we look at ourselves. We all deserve to hold our heads up HIGH and be proud of the badass WARRIORS we have become.

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    For More Information Related to Fibromyalgia Visit below sites:

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    Fibromyalgia Contact Us Directly

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    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

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  • Does Fibromyalgia Cause Back Pain or any other Health is the Reason for it?

    Does Fibromyalgia Cause Back Pain or any other Health is the Reason for it?

    Fibromyalgia a disorder that causes widespread chronic pain and tenderness affects 2 to 4 percent of women and men in the United States (women ages 20 to 50 are the most affected) and impacts patients in many different ways.

    Thus, fibromyalgia remains mysterious, and questions still linger like why are more women affected by fibromyalgia than men? And why is fibromyalgia so hard to diagnose and treat? Why do some patients with fibromyalgia have more back pain than others?

    “What causes fibromyalgia has puzzled many scientists for a long time,” says Elena Schiopu, MD, a rheumatologist and internist at Michigan Medicine in Ann Arbor. While the exact cause of fibromyalgia isn’t certain, doctors do know that the disorder can be triggered by an injury, surgery, infection, psychological trauma (like an extremely stressful period), or even just from an accumulation of symptoms that lead to the eventual classification of fibromyalgia.

    The reason for the heightened pain? Fibromyalgia may affect the way your brain interprets pain signals. “Fibromyalgia is basically a miscommunication between the central, peripheral, and autonomic [vegetative] nervous system, which results in abnormal or amplified sensations,” says Dr. Schiopu. This is known as central pain sensitization. It causes your nervous system to become “wound up” and in a constant state of hyperactivity, which creates a lower threshold for experiencing pain.

    When you poke someone without fibromyalgia, for example, it might be no big deal, but for someone with fibro, that same level of touch can cause significant pain or discomfort.

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    The Nature of Pain in Fibromyalgia

    Unlike arthritis, in which pain occurs in specific joints, the pain that fibro patients experience is more in the muscles. It’s widespread pain, which means you feel pain all over your body. According to the latest diagnostic criteria for fibromyalgia, patients must experience pain in four out of five general regions of the body. These include left upper, right upper, left lower, right lower, and low back.

    What Causes Back Pain in Fibromyalgia?

    People with fibromyalgia may experience long-term back pain along with a number of other symptoms. “Back pain that’s patient-reported and physician-observed — called paraspinal lumbar tenderness — is very common,” says Dr. Schiopu. “All the areas of the body that are being ‘used’ on a regular basis could hurt, like your hands, neck, or upper or lower back.”

    “The back is a common area to have pain in fibromyalgia because muscles, in general, are often painful in fibromyalgia, and the human back has a large number of muscle fibers to support posture,” says Amanda Sammut, MD, a rheumatologist and assistant clinical professor of medicine at Columbia University Medical Center in New York City.

    Also, says Dr. Schiopu, patients with fibromyalgia could have a degree of wear-and-tear arthritis of the lumbar spine, which is amplified by fibro. In fact, it’s common to have fibro at the same time as other diseases, such as inflammatory arthritis or osteoarthritis.

    Back Pain in Fibromyalgia: Could It Be Something Else?

    Lower back pain is an extremely common medical complaint — some 80 percent of Americans experience it at some point in their lives. So, if you have lower back pain, how do you know if it could be from fibromyalgia or something else?

    The answer is complicated. If you’re experiencing back pain as well as other symptoms, it’s possible you could have a different health problem entirely — or a health problem plus fibromyalgia at the same time.

    Misdiagnoses are common with fibromyalgia — both in terms of not being diagnosed with fibro when you really have it, or in terms of being diagnosed with fibro when you actually have a different health problem.

    Fibromyalgia is technically an exclusion diagnosis,” says Dr. Schiopu. This means you shouldn’t be diagnosed with fibromyalgia until a doctor has fully ruled out the possibility of having other diseases.

    That’s why a thorough visit with a rheumatologist is critical. If you’ve already been diagnosed with fibromyalgia but find that your current treatment plan isn’t helping your back pain, you could have a different or additional diagnosis, such as one of the following:

    A muscle or ligament strain

    Maybe you lifted a heavy box, strained to reach something in a high cabinet, or picked up your child or grandchild, which could have triggered a back muscle strain. A sudden movement can cause a strain, as well as constant use of your back (like doing repetitive motions), especially if you’re not in good physical shape.

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    Axial spondyloarthritis

    If you have lower back pain as well as pain in other places — say, your knees, jaw, neck, or shoulders — it could be from the widespread aches of fibromyalgia, or it could be another condition you may not be familiar with: axial spondyloarthritis (AxSpA), which is an inflammatory type of arthritis in your spine and the area where your spine meets the pelvis (sacroiliac joints). Back pain is a primary symptom of AxSpA, though it can also affect other joints and areas around your body.

    AxSpA is often divided into two categories. Radiographic AxSpA (which is often called ankylosing spondylitis), means that evidence of joint damage is visible on X-rays. Non-radiographic AxSpA (nr-AxSpA) is essentially the same condition, but without joint damage is visible on X-rays.

    Fibromyalgia and axial spondyloarthritis are caused by very different things (AxSpA is inflammatory and due to an overactive immune system that’s attacking the joints) and thus have very different treatments. It’s important to get the right diagnosis so you can get on the right treatment and start feeling better.

    Scoliosis

    You may have never realized it, but your spine could curve to the side, a condition known as scoliosis. The physical changes of scoliosis often start in childhood but the condition might not start causing back pain until middle age.

    Bulging discs

    The cushiony discs between your vertebrae may bulge or rupture, which can then put pressure on a nerve in your spine. While some people may not feel any pain when this happens, others may find it excruciating.

    Osteoporosis

    A frustrating part about aging: The vertebrae in your spine may develop compression fractures if your bones become too brittle (a condition known as osteoporosis). These fractures can then lead to back pain.

    Common Fibromyalgia Symptoms Aside from Pain

    While you may experience back pain if you have fibromyalgia if you’re experiencing back pain alone, and not other fibromyalgia symptoms, then your pain is likely, not due to fibromyalgia, says Dr. Schiopu.

    Sleep problems

    In addition to pain, sleep problems are a big part of patients’ experience with fibromyalgia. Even if fibro patients sleep for hours, they still may wake up feeling unrefreshed. That could be due to pain waking people up at night, or they may experience other sleep issues, like restless leg syndrome or sleep apnea. This troubled sleep, in turn, can contribute to debilitating daytime fatigue.

    Fibro fog

    Many patients with fibromyalgia complain of fibro fog, in which people feel like they can’t concentrate, hold conversations, or even remember certain things, like plans or where they placed objects. One reason for the fibro fog could be a lack of sleep. Another explanation is that there is potentially something happening in the brain that’s unique to people with fibromyalgia.

    Co-existing health problems

    Fibromyalgia often co-exists with other ailments, like irritable bowel syndrome, migraine, interstitial cystitis (a painful bladder syndrome), and TMJ (a jaw disorder). “That’s all followed by a slew of hypersensitivity to cold, light, noises, smells,” adds Dr. Schiopu. Thus, it can seem like fibromyalgia patients have a laundry list of health woes, which can be incredibly frustrating.

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  • My Fibro Fog is Diagnose with Mental Illness

    My Fibro Fog is Diagnose with Mental Illness

    Experiencing Fibro fog can make you feel like you’re lost in a maze. You might feel confused, alone, frustrated, disoriented, bewildered, unclear, and adrift. Fibro fog can also affect your emotional well-being. Being unable to think clearly may make you feel powerless, irritable, and downcast.

    Constantly feeling this way can put a damper on your mental health. Having a mental illness can trigger Fibro fog, as can other conditions. Understanding Fibro fog, its causes, and how it relates to mental illness can help you better understand the relationship between Fibro health, mental capacity, and emotional well-being.

    What Is Fibro Fog?

    Fibro fog isn’t a specific medical condition. Instead, Fibro fog is an “extremely common term used to describe changes that have occurred in the Fibro function over a period of time,” Dr. Christopher Calapai explained. “A decrease in focus, concentration, memory, alertness and word retrieval are all part of the description of ‘Fibro fog.’” Basically, Fibro fog happens when your Fibro doesn’t serve you as well as it can.

    Also known as “mental fatigue,” Fibro fog is a symptom of cognitive dysfunction. The type of cognitive decline caused by Fibro fog can vary from person to person, but typically, Fibro fog causes one or more of the following challenges:

    • Memory problems
    • Lack of mental clarity
    • Poor concentration
    • Inability to focus

    Other symptoms of Fibro fog can include:

    • Headaches
    • Forgetfulness
    • Anxiety
    • Confusion
    • Low energy
    • Insomnia or trouble sleeping
    • Emotional detachment or an inability to connect with others emotionally

    More often than not, these challenges can interfere with your daily life.

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    Despite what you may think, there isn’t a connection between Fibro fog and age. Teens, adolescents, and young adults can experience Fibro fog while healthy elderly adults can have strong cognitive ability and sharp thinking. When your Fibro is healthy, you can age with your cognitive functionality intact. Even though the Fibro does age, well-nourished Fibro’s can avoid most signs of cognitive decline. Malnourished Fibro’s, on the other hand, experience mental fatigue.

    Common Causes of Fibro Fog

    The causes of Fibro fog can be as diverse as the symptoms. But luckily, many of the causes of Fibro fog can be reduced with lifestyle changes, medication, or professional counseling.

    Some of the most common causes of Fibro fog include:

    • Sleep deprivation. When you don’t get enough sleep, you may feel a little bewildered and have trouble concentrating. Poor sleep can also make the Fibro tired, which can make thinking clearly difficult.
    • Stress. Like poor quality sleep, prolonged stress can also exhaust the Fibro. When your mind is tired, thinking, reasoning, and focusing become difficult. Additionally, chronic stress can increase blood pressure, weaken your immune system, and trigger depression.
    • Hormonal changes. Hormonal changes can have a significant impact on your memory and ability to think clearly. When estrogen and progesterone increase during pregnancy, many women experience “pregnancy Fibro,” which can make remembering details, focusing on tasks, and concentrating hard to do. Menopause, which causes estrogen levels to drop, can also cause forgetfulness, poor concentration, and cloudy thinking.
    • Diet. The Fibro needs energy, proper nutrition, iron, and vitamin B-12 to function optimally. A poor diet and low B-12 levels can cause memory loss and hazy thoughts.
    • Physical inactivity. The Fibro and body work together. When your physical activity slows, activity in the Fibro also slows, which can lead to symptoms associated with Fibro fog.
    • Medication and certain medical conditions. Occasionally, medication can cause Fibro fog as a side effect. If you suspect this, talk with your doctor. They may be able to lower your dosage or switch out your medication. Medical conditions that cause inflammation, fatigue, or changes in blood glucose levels can also cause mental fatigue. Some of these conditions include anemia, depression, fibromyalgia, diabetes, lupus, multiple sclerosis, Alzheimer’s, migraines, arthritis, hypothyroidism, and diabetes.

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    Scientists have also discovered a few connections between mental illness and Fibro fog.

    Fibro Fog and Mental Illness

    How you feel and think are intricately connected to the health of your Fibro. As such, mental illness can increase your risk of Fibro fog. Similarly, living with cloudy thoughts and an inability to focus and concentrate can also increase your risk of depression, anxiety, mood disorders, bipolar disorder, PTSD, and other mental health conditions. Scientists continue to study the links between Fibro fog and mental illness, but they have discovered that:

    Mental Illness Can Interfere with Fibro Functionality

    By definition, mental illness is any condition that affects your mood, thinking, and behavior. One of the main symptoms of Fibro fog is an inability to think clearly. As mental health conditions develop, Fibro function changes. These changes prevent the Fibro from working as well as it should, which often leads to Fibro fog. In fact, depression, anxiety, bipolar disorder, PTSD, and schizophrenia can affect the brain in ways that lead to Fibro fog.

    Mental Illness and Fibro Fog Can Have Similar Causes

    Mental illness and Fibro fog can be triggered by some of the same causes: lack of sleep, poor diet, unregulated stress, and hormonal and biochemical imbalances. Some scientists believe these similar causes may demonstrate a link between Fibro fog and mental illness.

    Mental Illness and Fibro Fog Are Associated with Brain Inflammation

    Fibro inflammation is a common thread in both mental illness and Fibro fog. In most cases, Fibro states that produce mental illness also tend to activate inflammation. Likewise, inflammatory responses in the Fibro can cause depression, anxiety, fatigue, and social withdrawal. Ironically, the same inflammatory responses typically manifest in the Fibro as Fibro fog. Inflammation in the Fibro hinders the production of neurons, making neural communication difficult. This is what causes the Fibro to slow down which triggers forgetfulness, lack of concentration, and dull thinking.

    Healthy Brain Equal Healthy Lives

    Here at Stoneridge Centers, we believe that healthy Fibro’s help us live thriving, healthy lives. Our comprehensive treatment plans can help restore your fibro brain to health. Let us help you get there. Contact us today if you’re ready to overcome Fibro fog and live a healthy, happy, thriving, and purpose-filled life.

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    References:

    Fibromyalgia Contact Us Directly

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    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store