Author: dearfibromyalgia

  • How do you sleep with fibromyalgia?

    How do you sleep with fibromyalgia?

    Researchers defines sleep as: The natural periodic suspension of conscience, during which the power of the body is restored, sleep as: a time you lay in bed uncomfortably, completely exhausted but unable to rest and restore Sleep is defined as: sleep

    The funny (fine, cruel and ironic) thing is Fibromyalgia. You’re always tired of it. Totally, incredibly tired. Mental, emotional and physical. Somebody with fibromyalgia would assume that you sleep constantly, but you know what, right?

    For someone with fibro, sleep is difficult, frustrating, and most often non-existent. For more than an hour, I personally don’t sleep at a time, and if I have a total of 4 hours a day, that’s a good night. Usually, sleep is just a few hours from time to time.

    You need sleep, you want it as a fibro-sick person. But you can’t find a convenient position with so much pain. You try various mattresses, pillows, couch, floor… You try to read, watch TV, and totally obscure silence. You’re trying melatonin, relaxing muscles, sleeping aids. Bombs and lotions of lavender bath. Marijuana. Marijuana. Different CBD and versions. You try everything. You try everything.

    And what, suppose? You can’t sleep anyway.

    The physical pain that affects sleep is not the only thing. Depression and anxiety occur with fibro. (Fibro again is a cruel thing.) When you lay there, you begin to become so overwhelmed with how awful it is, and you pray for anything you believe in for only a little sleep.

    Then you do what everybody says you shouldn’t do. You check the time. You check the time. “All right, in XX hours my alarm goes off.” Then fear comes in. How will I do it by working? Do I have enough concealer to hide under my eyes the giant (permanent) bags? Today, I hope I’m not an all-to-all giant. Just let me falsify it, please, until I do.

    I relate sleep to the five stages of grief:

    1. Denial–You’re tired of sleeping. There’s really no way you can have a restless night…. Okay?
    2. Anger–I believe this is quite self-explainable. This is so unfair and frustrating. Life has dumped you on this awful sickness, and won’t even give you a bit of sleep and a bone?
    3. Bargaining–all right. Give me two hours and I’m going to be taking a bad day of pain. In fact, I’m going to choose pain only to be able to sleep a little. Food Good.
    4. Depression–this has already been covered by us. But, yes. But, yes. It’s sweating.
    5. Acceptance–well, that’s it. Sleep is yet another night. Now that’s my life. 

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    7 phases of grief in sufferers of Fibromyalgia

    There’s no way through these stages and many will fight to get through them with the “how.” I certainly don’t have the right replies, and I’m not sure I have passed successfully any phase if you really want to know the truth. How does one navigate these stages, then, if we have crossed them, how do we know?

    I’ll share a very personal article to everyone because, as a friend of mine, I said,’ I share in transparency. I share some very individual things with each other. The hard stuff is too often hidden. Maybe that’s a way for me to go through some stages of grief.

    So, what is the process of a person’s grief?

    As I have, when people experience grief or stages of grief, you may find that you can walk through every stage and experience some common senses. However, what does each stage really mean?

    Acceptance is the final stage of grief, but it may be one step or the end of each stage. And if you can take part in each stage, perhaps you will “reach it” successfully. Maybe this is the end of your sorrow, and you’re continuing and your life is progressing and learning to live what will become your “new” life.

    But this complaint process can never end for many of us. It can be like a song repeatedly, we tap into every stage, experience the feeling of each stage and go to the next stage, but with no real resolution. Alternatively, you move on and return to an earlier phase or start again in stage one. There is no timeline or arbitrary time spent climbing or moving from left to right like a book, to a new level or even if you look at these steps, you don’t have a timeline to proceed.

    Let’s start at the first stage and work through it. I don’t say you will pass through all these stages successfully, but I’ll share my journey through all these stages as I have experienced them, and as you will see, I may not have passed every stage successfully, I just “live” each stage.

    1. Shock

    So, first stage; SHOCK!!!! Well, I believe I can safely say that this is a phase of grief that we have not really been shocked by. Many, if not all of us, knew what our doctors/specialists would say on the day we got the diagnosis, which is probably an easy stage of sorrow to be undertaken as many of us are going to skip right through. We don’t know what news we’re going to hear.

    But we will fight the diagnosis because those with this disease know that there are limited options for treatment. In fact, like many of you, we suspected or knew what was going on, we couldn’t find a doctor who took our concerns seriously enough to investigate them. I know that we were not at all shocked at this diagnosis. You have had some success with the available treatments, good pain and symptom management in some of those facing Fibro or chronic pain.

    So either you jump to Stage2, or you go on to Stage 2, or you don’t have to experience the remainder of your grief. We can all do this in a perfect world. But this is not a perfect world as we all know. We are therefore now trying to proceed to Stage Two.

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    2. Denial

    And the second phase is, negation. Now this is a stage we’ve all passed but we can fight with it or can’t. Like with the “shock” stage, denial is also a very popular feeling. While we were deeply aware of what was happening, we try to negate what is and hope that there’s a more “rational” explanation. This is probably because we all know that fibromyalgia is a stigma.

    Perhaps this is a diagnosis of “catch all” given by doctors who can find no more causes. Or it’s all in the lead as many of us have heard, or if you’re trying to get some weight and exercise, you’d feel better. And perhaps some of us are going quite easily through the denial stage, finding we know what is coming, well, it is a foregone conclusion that we are dealing with and we have gone on to “acceptance,” because we knew that this diagnosis was coming, why deny what we knew. No shock, no denial, but perhaps we have an overwhelming sense of endurance!

    Finally, somebody tells us what we suspected. Whether weeks, months or years have passed, anyone has “HEARD” what we say at last. It is a rather satisfying feeling to have a feeling of finality, to finally hear what we say and acknowledge what we feel. However, this is some sort of subjective phase of grief.

    Many people are willing to miss the denial phase because it is an unnecessary phase. It was a diagnosis which has long been underway. Why would we deny a diagnosis we knew, we knew our lives were being destructed? Well, maybe the denial is because we want to reject the fact that our body has turned on us this way, whatever we knew. We want to deny that the life that we once enjoyed is not the same now? We would like to deny that this beast has come into our lives, causing the path of life to change, changing from what we “think” our way to the future. We are faced with a refusal of life now.

    3. Anger

    Stage 3 is anger. This is a stage that I know, as most of us certainly do. It was a very hard phase of “acceptance,” for most of us, if not all of us, in the complaints process. Anger is a very real part of the grieving process if someone who has Fibro knows it. Because of our condition, we are angry at what our lives have become.

    We’re angry that there are limited options for those who were unable to find any kind of relief from any treatment scheme. We were trying “this” for a time, if that didn’t work, try “that,” and so on. We’re upset that there aren’t limited treatments.

    Anger seizes us, why did this happen to us, why should we live in pain, Why do all we do with pain in life? “Why,” particularly when your life is family-orientated, is most difficult to address. You have to be with them, you want to spend time with them, but why are you going to be like that now, to choose between your family or your body, and miss so many plans?

    If you can still work, you are angry that you have to deal with pain and tiredness while you try to keep your physical ability to do a good job, or because you are struggling in pain mentally and physically each and every day. You push yourself to the limits, therefore. You get so upset that your life is not as planned.

    There’s so much that you’re angry about because of this condition, all of them are so difficult to note and we’re all angry at various things. I’m going to be the first to admit that I probably won’t get completely through this stage. It ALWAYS will be something that will make me angry with this condition. If it means that I never pass all the stages of sorrow successfully, I’m willing to accept this because of the fact that I’m stolen from who I am, and how I live my life, I cannot give up my wrath. I’ve got to live the way I do, I’m angry.

    4. Bargaining

    The next step is to negotiate. This is not a stage of complaint which, I believe, is completely relevant to chronic pain. If negotiation means a lot of’ what ifs,’ I don’t think about it. There is no cause for fibromyalgia or chronic pain, so hours can be spent thinking, “If I did, maybe I wouldn’t be here” or “If I didn’t, maybe I wouldn’t suffer.”

    But for me personally, it’s like any other chronic disease, nobody can predict that we’d end up with it, it’s just happened. As I often say, that’s what it is, and even though it doesn’t happen, at least in my less terrible days, I have to take it every day and deal with things as they come.

    5. Depression

    Depression is the fifth phase. This is a stage, as many of us can attest, which I do not expect to complete ever. Medicines can help with symptoms of depression, but not a magic pill that removes all of those sensations. I won’t go into all the medical nuances of depression because there are many reasons and effects and it’s also a symptom of so many things, depression is a very complicated thing.

    However, depression could also be a sign of chronic pain or fibromyalgia as we find it hard to look at how our lives have changed and are going to change as a result of suffering and fatigue and other signs that hinder our pleasure in life. Depression can also be a sign of depression. What we’ve lost or will lose depresses us.

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    We find ourselves in depression because we have to miss this family gathering for the “hundredth” time, this family vacation, our evening with friends or something simple like going to a film. Nothing can substitute for our feelings, because we must miss life again. As our family goes away without us having fun, we’re going to shed countless tears while we don’t get out of bed or out of a sofa. Depression is between mild and severe.

    Some are looking for therapy and others are going to rely on medications. Don’t be afraid or ashamed that you will seek help with this. I did both treatments and I continue to treat my depression with medications. Some days are certainly better than others, and I will admit again that I still struggle with it.

    I struggle on those days when my pain and fatigue are high. In that day, I struggle to find happiness and find the silver lining. I fight to smile and fight to hide my pain and discomfort. I fight to smile. In the day I only want to “do” that day or that I can’t do those days, my family is usually good at picking up. I can plaster on the smile other days and say, “I’m all right.” Other days.

    My best recommendation is, don’t always do it. Don’t put the fake smile on and try to be all right through the day. It’s all right to give in as you feel, as your body reacts. It’s all right to keep you in bed and settle the world. However, it is very important not to allow your life to become so. Care for yourself includes the mental health care of yourself.

    So, can anybody who has a chronic condition ever pass the depression stage? I’ll admit that if depression didn’t touch a section of your ongoing life, I would be very surprised. However, please, seek assistance if it gets too bad!

    6. Testing

    Phase 6 is “testing.” This phase is usually not linked with stages of grief, so it’s a stage where I don’t know how much I have to talk about.  The only way I can try to connect it myself and my limits would be to “test.” Probably for fibro patients, this is not uncommon.

    ALWAYS are going to get things done. Laundry is not going to pull itself up; the house isn’t going to clean itself; the dishes won’t make themselves and so forth. But to get to know our limits, we need to test ourselves. Learn how far we can move towards minimizing our next day’s pain.

    Try to ask for help when we have to stop and rest and learn most of the things we have to do to take care of ourselves. Easy to say, hard to listen to! As often as I should I admit, I don’t ask for help. I can do stuff slowly but I still do it without requesting help as I can’t do it myself, maybe asking for help. I think we can all relate to this at some point on this journey.

    7. Acceptance

    Finally, acceptability exists. I’m probably never going to be able to complete this at another stage. I was taught a concept called radical acceptance when I was in therapy. You know your future, and you must find a way to accept it and live accordingly, the easiest way to explain this concept is.

    This is probably not the best way to explain this concept, but it will be accepted in the final stage of grief. I’m pretty sure that there’ll never be a time in my life when I can accept fully that my life is that. I live every day, I do whatever I can, I stop, and I’ll ask for help when I need it, though unwillingly.

    But these actions don’t mean I’ve accepted in any way that my life is now. Yeah, I “know” that this is my life, and I try to do the best I can every day. However, I’m not sure I can ever accept this, accept my restrictions, accept that my life revolves around suffering, accept that I’m not who I have been for a few years.

    I can say with complete certainty that I can’t accept that my life will be that condition. I’m going to do my best not to let this define me and I realize that acceptance doesn’t mean it goes away. The fear of acceptance, I believe, is the ultimate purpose. I am sure it won’t be cured, no matter what type of treatment I try, I won’t be relieved, I won’t be cured.

    But if I don’t accept this condition, is there hope that perhaps I will find a better way of life, a way of alleviating my suffering? I’m not an expert at all, I don’t know. Will I continue with treatments for research? Will I keep trying to change my lifestyle like I already did? Of course, nobody wants to accept this life, but maybe I accept it to some extent, because I know that it won’t change. I know I will continue to suffer unless a miracle treatment is found.

    Maybe I’ve passed this stage and didn’t realize it. However, I don’t want to accept this again, in order to be fully transparent, and always hate what my life has made. However, I’m not going to leave. I will not stop trying every day to find even a sliver of happiness, remember my luck, love my family and the gifts I have. I will not stop trying to find I’m not going to stop trying to “start freshly” with lifestyle choices, to do what I can to try to live as well as I can.

    So, I’m not sure if anyone can go beyond who they once were, complain of what their life was, complain of what they missed. I know that my complaint about what my life is will never be solved. But perhaps we don’t have to, as long as that sorrow doesn’t overcome who we are and keep us from living as much as possible.

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    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

  • For Fibromyalgia Pain and Muscular Aches We have CBD Bath Bomb

    For Fibromyalgia Pain and Muscular Aches We have CBD Bath Bomb

    Science and people at large are exploring new ways to experience this with the continuing presence of the medical marijuana industry in the medical field. In the medical marijuana industries, cannabidiol or CBD has been put on the spot with a highly respected form of alternatives.

    CBD is a cannabis compound that many claims have but are highly beneficial. Actually, the psych activity of THC can be counteractive. For people who want to take advantage of its healing properties without getting stoned or using conventional pain drugs, it makes it a valuable alternative to address issues such as inflammation, anxiety, seizures, arthritis, PTSD, epilepsy, and more.

    Their anti-cancer properties are even being explored. Furthermore, the fact that science has suggested that even at high doses CBD can be taken safely adds to its credibility.

    Nobody can deny that a luxury tub with warmth and blisters can be a great way to relax whether you’re a bath-man or you prefer a more time efficient shower.

    What are Cannabinoids??

    Cannabinoids are the great class of cannabis plant chemicals. More than 113 cannabinoids have been identified in the marijuana plant by scientists. Everyone interacts in different ways with the endocannabinoid system. Cannabinoids interact with the CB1 and CB2 receptors in the endocannabinoid system.

    This affects the body’s cell functions to create a variety of effects. A key mediator of homeostasis or balance in the body is the endocannabinoid system. The majority of marijuana cannabinoids are non-psychoactive. This means that euphoric consumption does not produce a high level. THC is one of the few plant cannabinoids that cause a high level of cannabinoids.

    What are CBD Bath Bombs?

    Did you ever want a spa at home? CBD bath bombs are your solution for everyday rest and relief, accompanied by a colorful explosion of aromatic fizziness. The CBD bombs are a complete solution. If you never saw bathing bombs before, they are small bombs which plunge into a fizziness scene when dropped into water. They often include essential oils and other agents that provide an endless body-pampering experience and many advantages.

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    What is the Type of CBD in These Bath Bombs?

    One of the two best-known cannabinoids found inside the cannabis plant is cannabidiol, also known as CBD. CBD does not produce this famous high that is so often associated with the smoking weeds, as opposed to Tetrahydrocannabinol (THC). Unlike THC, CBD is legal in America and is unbelievably sought after as a potent medicinal substance that can ease many symptoms!

    How Do CBD Bath Bombs Work?

    Backing bicarbonate, citric acid, Epsom salts and natural, organically colored soda are the iconic fizziness that bubbles produce. The natural coloring process is characterized by the iconic bombs. Bath bombs are typically made up of additives such as essential oils, which double as aromatherapies, and nutrients working on the skin directly.

    For bombs containing CBD, one of the additives placed in the product is non-psychoactive cannabidiol (CBD). CBD has outstanding healing properties, ranging from anxiety to pain relief.

    The new way in which bath bombs are used to ingest CBD is to absorb the bath by opened pores. This enables CBD to reach the blood flow more quickly and penetrate more importantly throughout the body rather than a small area than topical applications. In order to induce some of the resilient effects internally produced by cannabinoids (so called endocannabinoids), CBD interacts lightly with the system.

    CBD interacts also with many other neural systems, for example:

    The all-round actions of the CBD bath bomb will lead to the following advantages:

    1. CBD Salt Work Together: Epsom remove harmful toxins from your body and restore equilibrium.
    2. Relaxation: CBD is a powerful inducer of relaxation and relief.
    3. Environmental spa-like
    4. Glow: hot water process and salt from Epsom increase blood flow and open pores, leading to distinctive physical luminosity.
    5. Smooth Body Aches CBD Benefits
    6. Dampness: The warm mist is favorable to the throat and lung and moisture is also used as a medium for the direct transportation of essential oils and CBDs into the body. This helps with aromatherapy.
    7. High Care: It helps with various skin conditions like anti-aging, worsening of wrinkles, antioxidant effects, treatment of eczema, psoriasis, Acne and blackhead.
    8. Core Oils and CBD Each Other Compliment

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    How to make for your own CBD bath bombs

    The CBD bombs you have if you have CBD isolates are often less costly and offer more flexibility. You will need the following ingredients and supplies to make CBD bombs yourself:

    • 1 cup of soda
    • half cup of citric
    • half cup of Epsom salt
    • 1 cup of tsp essentials oil
    • 10-50 mg of CBD
    • 3 dc. Food coloring
    • jar
    • mold
    • bowl and whisk
    • Food Collector

    Mix them all for twenty minutes and let them dry.

    Instructions: Fill the bath with hot water, drop in and enjoy your bath! Allow yourself to enjoy the full effects of CBD and essential oil at least 30 minutes to achieve the best results.

    What is CBN?

    Cannabinol is one of the least talked about marijuana cannabinoids. It’s an important part of the plant, however. In contrast to THC, CBC generates psychoactive effects, if any, very minor.  CBN molecules are not well-adapted to the CB1 receptor in the brain. It also has problems binding to CB2, but it binds better to CB2 than to CB1. There has recently been a lot of buzz about the use of CBD oil products in our fibromyalgia community.

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    We have researched extensively and asked for feedback from members of our community. We saw two things: 1-feedback from those who tried CBD oil was overwhelmingly positive, and there is still a lot of misinformation and confusion about the product.

    Below are 5 key facts on CBD oils that we felt were useful and informative for our audience.

    Fact#1:

    CBD (Cannabidiol Short) is one of 85 chemical compounds commonly found in a cannabis plant known as cannabinoid. CBD may be extracted from either marijuana or hemp in oil form, both of which are cannabis. In many of the countries where it is a schedule, I drug, marijuana CBD oil remains legal. On the other hand, CBD hemp oil is currently legalized in all 50 countries because hemp and not marijuana is extracted.

    Fact#2:

    You’re not going to get high CBD products. THC is an ingredient that produces psychoactive effects, such as a “high” feeling, a feeling of anxiety or paranoid. CBD is not psychoactive, so you will not get high and studies have shown that CBD actually counteracts the anxiousness or paranoid caused by THC. Since the products containing CBD-Hemp-oil are without or trace amount of THC, a person testing them for THC in a standard drug-test is unlikely (but not impossible.)

    Fact#3:

    CBD products come in various forms, including drops, capsules, steam oils, rubber and topical creams. Based on the feedback from the community, the drops have been the second most popular form for personal use with capsules.

    Fact#4:

    U.S. FDA standards have not proved scientifically that CBD is a treatment option for disease and medical conditions. The FDA currently does not regulate CBC products as well. We hope that CBC will be researched and scientifically studied in the near future as there will be more and more people using these products.

    Fact#5:

    CBC hemp products for online sales can be of different quality. If you are interested in trying CBD products, you should make sure they are purchasing them from a reputable company because of scams. The FDA has sent warning letters in each of the last two years to some firms that have misled the marketing of their CBC products, selling products with few or no real CBD.

    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 and Stress

    Fibromyalgia and Stress

    Around 77 percent of people are under regular physical symptoms of stress, according to the American Stress Institute. 73% of people say that they experience stress-related psychological symptoms regularly. This can be manageable for a “normal” person. However, our bodies always have to be constantly stressed for a person who has fibromyalgia, so anything else can be weakened.

    Sometimes a little hip can cause a bit of stress during the day, but you can brush it off and move on easily. Somebody dealing with fibro has already dealt constantly with stress symptoms, and it’s sometimes not that easy (literally or figuratively) to pin your shoulders on. He’s on my shoulder like Devil.

    Some symptoms are low energy, headaches, stomach upheaval, pains, stiff muscles, insomnia, shaky hands and feet. Anyone who reads this knows that I have just described an ordinary day. The pain goes from 5 to 10, and 4 sleeping hours to 1 or 2, when a fibropatient has added to the stress. Emotional signs of stress are also present. Some are overwhelmed, like losing control or having to take control, relief difficulty, low self-esteem, depression, isolation.

    There is also a constant concern about oblivion, lack of focus and pessimism (including the “fibro fog.”) Now, these symptoms are not ideal for a “normal” person but they can be managed for a short time. But these symptoms are again a daily symptom for a fibro patient, and a lifestyle. Patients with fibromyalgia are often affected both physically and mentally by stress. Without any additional work problems, schools, families, relationships, money etc.

    Much stress is a wicked circle, physical stress increases psychological stress, and psychological stress increases physical stress and soreness. 48% of people reported lying awake because of stress at night. Again, this is normal for a fibromyalgia patient. Fibromyalgia causes constant tiredness but sleep is extremely uncommon to a fibrosick person due to pain and anxiety. If you add a strain to a relation, to money problems, to the stress of a project at work, that adds to the serious already sleep shortage of a fibroid patient (or who is not).

    Many different medicines are available to assist in fibromyalgia’s emotional and physical pain, and there are different sleep-help options but no cure. Just as no cure is available in life for stress (if anyone is aware of it, please share it for fibrous or stress).

    Over the years I tried to relieve and manage my stress by trying countless options. I’ve worked, tried yoga and even worked (I will run horizontally next time). I’ll do this. Newspapers, puzzles and treatment. While I have no relief from some of these options temporarily (again, if someone has suggestions, please share them).

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    Much of the sufferers with fibromyalgia struggle to explain to someone what “the day” actually means. How do you explain someone’s invisible illness? The last time they’re really stressed, one good way is to ask them. Work, school, finance.

    Finances. A battle with a family member, best friend or other important person. Ask them to remember their physical pain, sleeplessness, racing ideas. It all feels like fibromyalgia, day by day. All this.

    How does fibromyalgia and PTSD connect??

    Now that you understand what PTSD is and the symptoms, most people wonder how fibromyalgia is diagnosed. The main idea is that if you have such stress in your PTSD systems, your serotonin levels drop in the brain. This results in an increase in the P substance in patients with fibromyalgia. People with PTSD may also find that they begin to experience signs of fibromyalgia in addition to the symptoms of PTSD.

    These symptoms are

    • They often report that they feel as if they are living in a fog.
    • They are always feeling sick and tired.
    • Memory problems.
    • Sleeping problems.
    • Stomach problems that cause even more discomfort.

    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

  • 13 tips to make your Fibromyalgia comfort and helps you sleep better

    13 tips to make your Fibromyalgia comfort and helps you sleep better

    Sleep is defined as: a length of time you lay awkwardly in bed and totally exhausted but unable to rest and re-establish Fibromyalgia is funny (all right, cruel and ironic).

    Sleep is a fibromyalgia sufferer. You always get tired of it. Completely, incredibly tired. In physical, mental and emotional terms. One assumes that someone sleeps all the time with fibromyalgia, but you know what, right?

    For a person with fibrous, sleep is hard, frustrating and often non-existent. I don’t sleep more than an hour, and if I’m going to get a total of 4 hours of sleep, it’s a good night. Usually sleep is only a few hours away.

    You need sleep as a fibro patient, you want it. But you can’t find a convenient position in so much pain. You try various mattresses, pillows, couch, floor, everyplace. You attempt to read, watch TV, complete silence and obscurity. You try melatonin, soothing muscles, sleeping aids. Bombs and lotions for the lavender bath. Marriage. Marriage. Different CBD products and versions. You try everything. You try everything.

    And what, suppose? You can’t sleep anymore.

    Unrefreshing sleep

    One of the main symptoms of fibromyalgia is uncooling sleep. Regardless of how much we sleep, we still get tired of waking up. Multiple studies confirmed our sleep disorder. In the deeper, restored phases we do not spend enough time, and studies have also shown that we have so-called wakefulness-associated alpha wave intrusions during deeper phases of sleep.

    Explanation for trouble sleeping in fibromyalgia

    One reason for sleeping problems is that the normal order of brain waves is disturbed when fibromyalgia is present. Brain waves that show wakefulness are interrupted by deep-sleep patterns, so that you never really sleep well. So, what can you do to get your rest? With the consequences of little or no sleep, you should not suffer. Here are the hints you absolutely need to get the snooze time.

    Set the Right Environment

    You want to ensure that you don’t fall asleep or wake you up as soon as you drift. This means that the room’s lights or sounds are minimized. Shut down your television and make sure mobile devices are set to silent mode. Even a telephone that vibrates at a bedside table can prevent you from entering deeper sleep.

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    Soothing Sounds

    Music can improve sleep before bed. The sound and how long they heard could be changed by people with fibro in their 4-week study and replayed when they waked up in the night. Everyone listened to the same mix, for their special beats “Music to promote sleep” on the Sonic Aid label.

    Keep a gratitude journal

    Thanks, are on the reverse side of the coin! It is difficult to live with chronic pain, no question. But it can be emotionally calm and even distracted from physical pain to express gratitude. There’s something to be thanked for every day, whether it’s a fibro-friendly dinner or pet cuddles. Focusing on these small joys can help your mind and body to calm.

    Avoid stimulants & alcohol late in the day

    Coffee, tea, chocolate, and lots of sodas contain caffeine, which is the last thing you need to sleep late in the afternoon. You may also consider how much coffee you drink in the first part of the day. Alcohol is a depressant, on the other hand, but sleep can easily interfere. You could sleep easier, but in the morning you probably won’t feel restless.

    Keep a consistent sleep schedule

    “It is essential to maintain regular sleeping times for Fibro patients,” said Doghramji. “I emphasize more regularly, when they get up in the morning and not so much when they go to bed in the evening. The moment you get up in the morning, you can determine your next 24-hour circadian rhythm, including when the person is likely to sleep on the next evening. This is also true for weekends and weekdays and holidays.

    Consider getting a sleep study

    You must discuss these symptoms with a sleep doctor or a sleep specialist if you have frequent sleep interruptions, daily sleepiness, unusual sleep motions, snoring or breathing pauses and/or difficulty falling and sleeping that you believe is not only due to your fibromyalgia, “stated Dr. Clete Kushida, Medical Director of Stanford Sleep Medicine Center All common comorbidities in fibromyalgia patients are sleep apnea, restless leg syndrome and periodic limb movement disorder. Sleep can improve by diagnosing and treating such conditions.

    Try to skip daytime naps

    Try skip naps during the day that can hurt your sleep at night. If necessary, snooze for only 60 minutes and move when you wake up.

    Click here to Get these Products or Visit Fibromyalgia Store

    Keep Cool

    Actually, when the sleep begins, your body temperature decreases, so why not help it? Before going to bed, try lowering the room temperature to 60-70 degrees Fahrenheit. Watch how you sleep at a cooler temperature for a week. You might need to experiment somewhat to find your own personal “perfect room temperature,” but in general people are better placed to sleep in cooler environments.

    Sleep in a dark, quiet room

    Make sure you are looking for refuge at night, in a dark and comfortable place. Sleeping in a cooler room has demonstrated a lot of warmth from blankets and has helped achieve a deeper sleep. Machines for white noise can help to clear subtle sound distractions. Some people can help induce sleep by listening to soothing music or a book.

    Essential Oils

    Some swear that certain fragrances make sleeping easier. Lavender, bergamot, ylang-ylang, sage and chamomile are among the most popular choices. Talk with your healthcare provider if you choose this option and ensure that you avoid anything you are allergic to.

    Upper Cervical Chiropractic

    When the atlas is out of line (C1), the brain stem can be pressurized and the blood flow to the brain can be inhibited. Correcting the misalignment can help reduce symptoms, including pain, which can make it easier to get and sleep. Contact a senior cervical doctor near you to learn more.

    Take a bath or shower before bed

    We are certainly more susceptible to cool temperatures with fibromyalgia. You can take a hot bath or shower right before bed in winter so your muscles are comfortable and relaxed. In contrast, a cooler bath or shower could help you to feel more comfortable during the summer heat. The objective is to calm your muscles and relax them. Tucking between your necks and your pillow can also help if you put an ice pack (or a hot pack).

    Put down the mobile devices, turn off the TV and dim the lights

    “It’s a few hours before sleep to try to eliminate as much light as possible,” Doghramji said. “To make your environment as dim as possible for a few hours before you sleep, the light has a way to disturb the circadian rhythms by decreasing your melatonin levels.”

    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

  • Do not stop yourself from fighting with Fibromyalgia

    Do not stop yourself from fighting with Fibromyalgia

    It doesn’t make me literally explode in tears often, but today. It’s not often something. I’ve been catching all things on a TV series, yes a TV series. I wasn’t reacting emotionally this time because of the treatment of the person. This was due to the actress ‘ very real despair when she was told her character could not find anything wrong. She was so emotional that I had felt personally that for a moment it overwhelmed me.

    Such desperation felt so many of us with Fibromyalgia and other invisible diseases. It’s a terrible, solitary sense. You are so nuts because tests come back with no meaningful results for your pain and all your other symptoms. Or, they find things, they treat them, and yet you feel awful. It’s disappointing, furious and humiliating. Some of us had to go to a doctor and find somebody who even listens. Particularly when we are young.

    People do not like to believe that if you’re over 50, you have serious medical problems. The older I get, the more obvious it is because, without my history and without an argument, doctors are more willing to hear and test each year. These days I don’t have to argue much because I have so much surgery and diagnosis once they see my medical history. In dealing with doctors who do not know my history and with people who are untrained or misinformed, I still must deal with ignorance.

    I used to be confused and confused about what the people said to me. Sometimes it devastated me and asked me for a while. So, all the treatments I had and I followed all the advice I had received from those people. I heard all their theories about weight loss, my diet changing and more exercise. They have used all of their medicines and have all their procedures carried out. I allowed the doctors to do anything they suggested, thinking that with all their education and training they knew best. For months, I finally passed over a ridiculous number of renal stones along with kidney infections, urethral stents, and lithotripsies. I also lost my gallbladder, became more cysts on my ovaries and I suffered pancreatitis as well as a ton of drugs that were not drug-free and drug-free.

    It was terrible, and I was finished one day. Everybody else I was done listening. I decided it was time to get up for myself. I decided. I fired, got new doctors and changed the whole point of view and the whole approach. It was my best choice ever. No, I have not solved all my problems and healed my symptoms, but I have improved my emotional and mental condition. Neither did I accept any new physician. Indeed, I still want a very good medical team, but that’s because I’m not going to settle down. I go to an appointment and measure their response to my circumstances. I move on, if they’re not my favorite. I will only work with doctors who know about Fibromyalgia up to date because they are the least investigated and important information of my condition.

    If they seem not well-informed, I will even print out accurate information that they cannot deny from a credential source. They are immediately rejected when they have a negative attitude. See, my point of view has changed so much that I’ve decided I don’t have the energy, or time, to get doctors to learn. It is their job to treat their patients correctly and know the latest ways. I don’t want them to do anything if they don’t perform the most essential function of their job.

    Click here to Get these Products or Visit Fibromyalgia Store

    I’m not wasting my breath again to try to persuade people that want to stay uninformed. I am going to raise awareness, but after seeing the factual information, I will not try to persuade. Between these two things there is a huge difference. I’m going to walk off. If people don’t want to see and try to understand the valid research available then they can’t understand my life. Why in my life should I want them? I decided that I did not, and it liberated me from the many awful feelings that I experienced earlier.

    I live this. It is true, abnormal, and painful, I know. I know that the ordinary person would be on MY pain scale at the hospital begging for pain medicines. I know I have been conditioned not to make the average person lose his or her consciousness out of pain and nausea and stay calm and focused when other people are hysterical. I have all this to learn and my body has to deal with because it is not acceptable as an alternative. I don’t need anybody else’s validation. Because someone MUST, I’ll advocate for myself. Everything you need, too. With your medical team, I do not propose to be arrogant and uncooperative. It is important to ask questions and to do research; however, you must recognize your medical knowledge’s limitations and know when to listen to the professionals.

    When you go to a new doctor, ask your doctor or whatever your condition is about fibromyalgia. Either educate or move forward if you don’t like their answer. Don’t waste your time if you don’t say 100% that your condition is valid and requires up-to-date research for proper treatment. The doctor you need WILL can admit that the research remains underway and is ready to try new ways of managing it unless the older / average methods improve you’re living. You deserve to be treated by a doctor who is willing to do anything to really help your patient.

    It is unfortunate that it has to do this, but we really need to take an active part in finding and managing our health. Right doctor. In certain areas, finding a good physician is even harder. At these times, doctors choose to keep a close eye on new research against their beliefs or to be present in an area seriously influenced by the opiate crisis, so that all their attention is focused on curbing the epidemic rather than learning how to recognize and treat invisible diseases.

    Some people may be able to find a doctor in their local area who has developed their understanding of less well-understood diseases. It is worth to visit me to find a physician who is informed and willing to listen. In some cases, only major appointments may be required in person and the rest can be practically done. You can even have the option of long-distance care if you’re fortunate enough to have good insurance. Take a look at your policy’s fine print to see the options.

    When you do not have the option of traveling, I suggest looking for new doctors from an institution with accurate information in the curriculum. You can also join local support groups and seek guidelines. You might know somebody who is good in the area. You want mainly a primary doctor and a rheumatologist. Multiple websites rate physicians’ online. Read the reviews to have an idea about the character of the doctors. It can be a very long process, but it cannot settle for a doctor who doesn’t evaluate and treat you correctly.

    Click here to Get these Products or Visit Fibromyalgia Store

    You need to remain active in the management of your health even once you find a doctor and treatment plan. It’s also a must have a backbone. In our arsenal our intestine can be a very significant, potent tool. If something’s not right, your brain knows. It’s connected to your body and knows if something is wrong. It knows exactly what is going on and where we just do not know how to interpret the information correctly. Our intestine will only tell us something’s wrong. Listing to the feeling.

    You want to listen to your intestines, of course; but if you persist, that something is not right–bring it to your doctor. You want to be reasonable and logical. Previously, I told you when I fired and changed my doctors. I couldn’t be here today if I didn’t. I was injecting a drug with a variety of side effects. Three injections, each one week apart, were scheduled for me, but somewhat told me to cancel the second. The day after the planned trials re-appeared showing that the pancreatitis caused my gallbladder had to be removed. The medicine caused it. When I have received the second round, it’s not clear if my pancreas could have been saved. You can’t live without one-listen to and protect your instincts.

    We do have a strong healthcare team, but we are the number one instrument in our arsenal. Support yourself. Advocate. Squash your disgraceful feelings as it’s true. Your pain is real. Your pain is real. Every symptom and complication you fight is real. You deserve love, knowledge, good care and compassion. They call us warriors because we have to fight for ourselves and our own bodiesRegardless how weak you feel on your worst day, on your best you are stronger than many.

    Raise awareness and inform untrained people, but don’t waste skeptics ‘ energy. They are worth it not, and you have to focus on the best that your body can make you live and be there for those who want to have you around. Love yourself. Love yourself. Take care of yourself and try not to live up to society’s expectations. Take a break, it’s all right to pause. You’re different, but all you do is make you better because you’re probably more aware of things than others. Use it.

    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

  • Daily routine development for the relief of fibromyalgia

    Daily routine development for the relief of fibromyalgia

    By: Dr Alexa James

    Living with Fibromyalgia is challenging.

    We really need researchers to get on with this weak condition, which appears to be advancing on the basis of several factors, attention and time, and to fully find out how Fibro works and the best way to treat symptoms. Doctors have just treated the symptoms and thought that it would be enough to control it, but it doesn’t work long-term.

    In the past, fibromyalgia tended to be considered by the medical community as something people who had pain, sleep problems and other problems for whom they could not find an explanation. We appear to be just reaching the point when some researchers are ready to say, “Wait, there’s more to this,” than they thought before. As a result, the people with Fibromyalgia now have to turn to the communities that have the symptoms and problems we face in order to find any kind of alleviation of the pain, emotional turbulence and other symptoms that we experience.

    The below list includes the things I’ve discovered that can help me manage my fibromyalgia every day. I’m looking forward to helping someone else with this condition because it’s a fight and because it can be very lonely. People don’t understand how it affects us. They just don’t get it even when we try to explain it.

    You can’t imagine how you feel, yet it still works, so you don’t think it should be that bad. That’s it. It’s quite horrific and confusing because you have very little control over the physical feeling. If you feel as if I do, take a favor and implement these tips to manage the Fibromyalgia to extent at least

    For this condition, there is no cure-all. These techniques are not meant to tell me “Do these and it’s going to be fixed.” They’re not going to fix you, but they can help you cope with what you’re dealing with and any relief is better than anyone if you live as we do.

    1. Let somebody help you and don’t stress it.

    That’s easier to say than done, I understand, but actually try. Since we often have to fight against sensations of evaluability and feel like a burden, this can be one of the most difficult things we can do for us. Knowing when to give in and ask for help can have a major impact on how we generally feel. Do not worry about what others think, your emotional stress will also decrease. You are a combatant. You’re a combatant. You’re fighting against a condition people don’t understand and can’t even imagine. They don’t really think because they don’t know how it feels.

    2. Make a kind of diagram listing common activities in your lifetime.

    Provide every activity with a value based on the amount of effort to achieve and the time it takes for recovery before and after. Use this chart to help you determine your next tip, as well as to help you figure out how each activity impacts you. (I started using a 5-point system.

    Click here to Get these Products or Visit Fibromyalgia Store

    3. Learn what the average day your body is going to handle.

    Not a good day, not a bad day, but one of the intermediate days we spend most of us. Once you know that, you can assess what activities you can handle before you stop, or you can predict what you can fit for a certain period of time.

    4. Prepare to minimize their impact on your body before activities.

    In fact, I have gone so long before and after to take a schedule and shady days to visually help I see how I need to take care of myself. It’s not like my body was, and I sometimes find it difficult to remember and to take this fact.

    5. Allow yourself time to recover from every task or event, based on your body.

    It is as important to reclaim as to prepare. This takes time, that means that fewer activities are to be performed during the day, so for many of us it is difficult, but necessary. We hurt ourselves more and can do even less if we do not take the time to do these things. The preparing and recovery of aspects can be helpful if a calendar like the one I said before is created. It is sometimes easier to accept when you see how much time your body needs to recover.

    6. Begin to systematically identify what foods contribute to the symptoms you experience and track your pain levels or other symptoms (many do with a pain journal already in this last part).

    Make a list of foods that you think may affect you and start eliminating them one by one. Each day write down any changes from the most recent food you have eliminated when you perform your daily routine. I am convinced by my own research that food can absolutely influence how we feel. I systematically removed food from my diet for a good couple of years. It was harder to tell which foods caused symptoms at first, but the more I removed it was easier to see the exact consequences of each food. I have to avoid every milk, a lot of strong spice, caffeine (because of my kidneys) and drink anything not clear I also limit my bread, red meat, grease, red sauces and greens and foods processed. I stick to lean grilled meats, veggies, and fruits that are not too difficult for me. A ton of books and sites on anti-inflammatory diets are available. I suggest that you look for an idea what foods are going to be removed.

    7. Choose a light stretching scheme that you can use every day.

    It must be very easy on your body, but it must still help to move your muscle so that atrophy does not damage it. In times you can’t get out and do things, it matters even more. That is why you want it light enough, regardless of whether you have a good or bad day. For me, this is easier in 5-10 minutes, twice or 3 times daily increments. I stretch lightly, walk in, and have a few 2.5 lb arm lifts. It’s not a lot, but in moderation it’s motion, and movement DOES support. In our cases, too much can hurt us seriously, so it can be difficult to practice. I see movement and practice as two worlds. I have no strength, I don’t have the power to stand pain, but I have the capability, I have the strength, I have the power to create the energy, to move at least a bit every day.

    Click here to Get these Products or Visit Fibromyalgia Store

    8. Every day you have to set aside some time for yourself, just like you want to create a routine and move.

    There may be many things to this. Naturally, you want to physically take care of yourself. This includes stretching, taking medicines, taking note of new symptoms, etc. covered elsewhere, but also mental attention. It is even more important to make certain you include things to ease your stress and manage your anxiety if you have anxiety disorder or any other mental illness.Stress can have a significant effect, especially in chronic circumstances, on your body. Develop a daily stress management routine that can be included in your day-to-day self-care.

    9. Expand your knowledge on fibromyalgia with some new aspects every day.

    Someone who mentioned it might be a new therapy, or a symptom that you didn’t know was Fibro. The more you know, the better you can understand things that happen to you and what things you need to talk to your doctor. Make sure you do not simply take and focus on one-off situations. Don’t let it send you in paranoid mode to fix things when you are researching. This is not healthy. This is not healthy. Please ensure you also look for others on the same topic if you read a personal experience to get a broader view of the matter. You want to at least make sure the author has experience with the subject when reading informative articles, or that it comes from an officially certified source. The reading of articles with odd headlines of Fibromyalgia only increases confusion and can overwhelm you with fear without looking further into the information. Please ensure that evidence supports what you are reading.

    10. Take your medicines every day (unless directed by your doctor otherwise) at the same time exactly every day.

    Probably many of you try to do this already, but if you don’t or perhaps don’t do that, try. When maintained at constant, consistent levels, most medications work best. So, taking them on a schedule is very important. When you learn about Fibromyalgia every day, you should also look for your medicines. Knowing what side affects you can expect may actually help make some people less severe and also help you to know when your medications cause something.

    Taking time to do these things can help with your quality of life if you experience a chronic disease. If you develop a procedure to assist in managing and sticking to your illnesses every day, it is more likely to help you control your disease— at least as much as it can be monitored.

    Nothing will improve everything-that’s why it’s a chronic disease-but we can do some control to get the best chance to feel as good as we are able to. I hope that my Fibromyalgia management of these things will also help you to get control over yours as far as 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

  • It may look like this if your fibromyalgia can text you.

    It may look like this if your fibromyalgia can text you.

    By: Dr Alexa James

    Fibromyalgia cannot, of course, text the people who live with it, but it could look like that if it did. It was thus a hypothetical question that we asked to share what a text conversation with fibromyalgia might look like in our Facebook community. Many people talk and we have compiled a list of few messages for you.

    Here is what community share with us:

    1st Warrior Share Their Fibro Conversation.

    Fibromyalgia: “When bad emotions turn sideways, I’m what happens. I began when you were very young and grew up with you. I found the right time to attack, and I have been staying firmly in your brain and body. And I’ll change you completely regardless of what you do.

    Me: “Yes, this is true of everything. There’s no way you’ve been prevented and not my fault. I can remember a time when you didn’t come across me, and I don’t expect to change that at any time. I’m sorry about it some days ago, and I don’t want to accept it. And then there are days when I just want to kick your ass. But mainly for everything I don’t like about me, I just blame you. I know, however, that I will have to work with you to do anything in this lifetime. Okay, I’m going to do what I have to do, because you are going to paralyze me least. But I do not like it. But I do not like it. And I do not like you.

    2nd Warrior Share Their Fibro Conversation.

    Fibromyalgia: “Hello, I’m here to wrack your life!”

    Me: You can make my hell days but I’m going to survive, “she says.

    Click here to Get these Products or Visit Fibromyalgia Store

    3rd Warrior Share Their Fibro Conversation.

    Fibromyalgia: Is going to say, I am forever changing your life. Your strength, energy and autonomy are gone. You can’t do the things that you like to do. You’re never going to feel pain… and it’s going to get worse if it’s worse. I’m going to make people discuss you, doubt you and leave you. Any money you make will be spent on doctors, medicines, any kind of supplement in your search, if you can manage to keep a job. But you will not. But you will not. And you feel more defeated every day, discouraged and despairing.

    Me: have compassion on me, please.

    4th Warrior Share Their Fibro Conversation.

    Fibromyalgia: “I am sorry to hurt you,”

    Me: “Give me my life back … please”

    5th Warrior Share Their Fibro Conversation.

    Fibromyalgia: Hello …

    Me: Why don’t you leave me alone?

    6th Warrior Share Their Fibro Conversation.

    Me: I’m cold, I think I’m going to curl my blanket up.

    Fibromyalgia: This thing, you mean, that feels like a concrete sheet? Here’s a HOT FLASH, however, to warm and also warm your body.

    Me: Please don’t. Not a hot flash again!

    Fibromyalgia: it’s too late baby, Enjoy. I just showered.

    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

  • Big battles because of chronic pain when little things happen

    Big battles because of chronic pain when little things happen

    By: Dr. Alexa James

    We experience hundreds, thousands and hundreds of tiny movements every day in our everyday lives. We probably don’t even think about most of that. We have natural instincts and reflexes. We have tasks and tasks every day. We’re working, we’re playing, we’re training. We are breathing in, we are exhaling. Even before we get out of bed we wake up in the morning and spend another day facing. In the night (or in the middle of the day, because we sleep wonderfully). We’re dreaming, we are rummaging, we are drooling. As a human being we tend to be very self-evident.

    Some people face a much bigger challenge in these small, tiny tasks. People who have chronic pain face daily problems that can be seen as natural and second nature by other people. A simple act like sleeping can be torturous for someone with chronic pain. Sleeplessness, not able to be somewhat comfortable. Furiousness and frustration. The exhaustion of the physics, mind and emotion. It can be life or death for someone suffering from chronic pain the morning that some people find happy and refreshing. Whether it provides temporary relief or throws muscles into a bigger spasm is unknown.

    Simple, necessary tasks are becoming stressful and complicated. For example, you have to shower and wash your hair. This is usually relatively fast and easy. However, due to slow, meticulous movements for other people it can take two or three times as long to try to minimize pain. Slowly shampooing, before taking a break. For women, shaving your legs (or men, this is the year 2019, I don’t judge) can feel like you are an eight-leg shaving pulser instead of 2. Blow drying and hair styling is another daunting job after showering. Sometimes (all right, most of the time) you sit in a towel for one hour on your bed, trying to get the power and the mind to continue. It might just be easier to shave your head some days, honestly.

    We live in a world of shopping online, but there are still grocery stores and orders. Some people love (or love) food shopping (like me). Walk around the shop, check out sales, decide what to eat for the week and, above all, people who watch make Sunday morning fun. Finding unforeseen treatments and surprises. The surprises here are the rapid appearance of pain and the feeling of having a nap on the center of the cereal aisle. You have to take the groceries to your house once shopping is done and you finally make it home.

    Click here to Get these Products or Visit Fibromyalgia Store

    Yikes. As if it wasn’t enough to drag you to the checkout? Some of us were one tripper (and always tried to be). Load your arms like a pack mule and refuse to return to the car for a second time. Well, the smartest idea is not when chronic pain is mediocre at best. One trip, turns into two trips, turns into three trips, turns into “What I want, I’ll just take one after the other out the cans of Seltzer.” (I’m not known for my clever thoughts…).

    Cleaning. Oof. We all need a clean house and enjoy it, right? Clean clothes and clean? I’m living alone myself, so every job and care for my overall well-being is over me. I always enjoy standing up on a Saturday morning, coffeeing a French press, sprinkling music and cleaning my apartment and washing laundry. This is not very pleasant with chronic pain. I have “good” days (a good day is a day when my pain is at 6-8 instead of a constant 10).  Many people with chronic pain are not so fortunate, and none of these days are acknowledged to me. Rather than clean it all in a single day, I do my best to keep my friends or family away. One room, and one object at a time, I do it.

    The bathroom, for instance. Take a break, I’m going to clean the toilet. Take a break, purify the sink. Take a break, clean the shower. Take a nap, Sweep and Swiffer. This goes from one room to another. I barely make it across a room for many days. My poor cat. A simple litter box scoop can destroy my arms and back completely. Poor thing has been dealing with a full box for many days, but bless her little heart never got stuffed on the floor (all of them knocking in the wood now, please. Thank you!).

    It is a PROCESS; my washing room is in the basement. Fill my basket, carry it, bend down to the laundry, return to my apartment. Go back to the cellar and bend down to a dryer and go upstairs. And finally, one last trip back to my apartment to load the basket up and return. Really, all that happens is a load of washing one day. And if you think it will be folded and packed in 10-14 working days you will joke. Other simple stuff that I, and others with chronic pain, fight with cans, and bottles (the day I fought to crack open a cold beer after a long day was a sad, sad day.) Day after day, tying shoes, putting your hair in the middle, I’ll admit it was mid-March and all my festivals, including the artificial tree, are still up. Dinner for cooking is a trip. From planning, preparation, execution to food. It is exhausting to stand, to stir and to pivot. Dishes, if you have no washing machine? Ha. Hey. That same day won’t happen. It’s awkward because it’s frustrating.

    Probably now you can see the trend. Do not be patient or understanding if you don’t suffer from chronic pain. Don’t give up if you have chronic pain. Don’t get on yourself. Don’t get on yourself. You are not alone.

    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 is NOT …” What I Mean!

    “Fibromyalgia is NOT …” What I Mean!

    By: Dr Alexa James

    The main cause, which often circles misunderstanding and myth around the chronic condition causing pain and exhaustion, is experienced by everyone with fibromyalgia syndrome. Education is a key to managing symptoms effectively. Fibromyalgia is a chronic, untreatable condition that can affect between three and six percent of the world’s population, characterized by widespread musculoskeletal pain, chronic exhaustion, brain fog, and sleep disorder.

    Since fibromyalgia was only recognized officially some decades ago, however, many people (even doctors) still do not know how the disease and how it affects the lives of someone. Unfortunately, these doubts can make way for assumptions which are not only mistaken but disturbing. Many still believe that fibro is not a “real” disease and that if it is not possible, those who do need to be just fake and “attention-seeking.” Fibromyalgia can already be a difficult disease among the physical symptoms and emotional impacts of a lifetime condition.

    There may always be misconceptions; it is important to separate truth from fiction. Understanding fibromyalgia information may help the patient understand better his / her condition and help the outer viewer understand friends or friends with fibromyalgia better.

    We asked our community “Healthizes,” to share what fibromyalgia is not in order to address some of the circulating mis concepts. Many members attended the survey and communicated their views to us. The list of them we have compiled for you.

    “Fibromyalgia is NOT …

    1. … Fake”

    • Not fake fibromyalgia. I don’t know how often people say that fibro is not “real,” or that “it’s all in your head,” I don’t know. All day, all the time, I wouldn’t pretend to be in pain. I don’t pretend I’m having problems sleeping. I would not pretend sick. I wouldn’t pretend. I wouldn’t claim to have problems with the stomach. There wouldn’t be mood swings I pretend. I wouldn’t leave school. I’m not going to leave innumerable jobs. All these things, I wouldn’t claim to do. It is true, it sucks, it changes its life. Provide it with the respect it merits.
    • It’s not Fibro in our head.

    2. …Biased”

    • The only illness of a woman.
    • Fibro is not that most people gain weight after fibromyalgia, because, in many cases, even daily activity becomes impossible.
    • Fibro is a weight-created bacterium. Overweight is a co-morbidity with Fibromyalgia, it’s not the cause of Fibromyalgia… Small people are also affected.
    • You can get fibromyalgia at any age not restrictive. Smith’s Amy

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    3. … Something else”

    • Psychiatric or mental illness or depression.
    • Psychosomatic fibromyalgia is not. Real body pain. Real body pain.
    • No pulmonary fibromyalgia.
    • Fibromyalgia does not cause my diabetes damage to the nerves.
    • Hypochondria does not exist.

    4. … for Weak”

    • Not forgiven for fibromyalgia
    • No sissies are fibromyalgia. The symptoms of fibromyalgia are endured by a strong person every day.
    • “To take your life, fight every day, take your strength again.” “Fibromyalgia isn’t …”

    5.  … Easy”. 

    • Not easy fibro. Every second of the day, hell live every second, and there is always something new happening when my friends and husband see parts of the knees and hands and even the pain in my neck dips.
    • The symptoms in all are different and change from day to day. Fibromyalgia is not easy to treat or understand.
    • Fibro is not simple, plus difficult to explain, because everybody is different. We have the same pains but can do it in the various areas of the body.
    • It doesn’t like “in a few days you’re going to get better”
    • I can get over something.

    6. … Made up”

    • Fibromyalgia is not supposed to go away
    • It is not consistent with fibromyalgia. You’re not sure what to expect from day to day.

    7. … The Same”

    • Even minutes by minute from day to day. Month after month, year after year, as well. It also changes according to medications and what you do.
    • Day by day it isn’t the same. For every person, every day will be different. Nor will anybody have exactly the same symptoms.
    • Each patient is the same. Some of them do not have other immune diseases. We have as individual symptoms as we are!

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    8. … Curable”

    • The positive attitude will not improve fibromyalgia through a fresh air!
    • There’s no curable fibromyalgia
    • Fibromyalgia will not ever go out. The pain is so bad that you feel constantly tried to enjoy your days. Most people think you are ok because they can never see their pain. You must pace yourself to get things done. It’s difficult to concentrate all the time in pain. I hope that somebody will find a healing.
    • Fibromyalgia is not cured by weight loss or exercise. I think I’ll cry right there and then if I’ve got another doctor tell me just to get weightless and get on with things.

    9. … Fair”

    • In the medical industry Fibro is not well represented. Many never heard about it. Most physicians cannot fully understand why the treatment is insufficient or inadequate.
    • Fibro is just an undiagnosed symptom. –a catch-all when there is no other diagnosis.

    10. ...Myth”

    • Fibromyalgia in Lyrica commercials is not the way it is depicted.
    • It’s not a myth for fibromyalgia. It’s real, very real. It’s very real.

    Fibromyalgia isn’t something we’re finally going to get “good.” It’s going to be life. We’re going to have good and bad days. Good weeks and bad. Good weeks and bad. Good times and bad times. Good times. And that’s not what we can control. Also–it’s not something to control fibromyalgia. It doesn’t mean just that a therapy worked last time. Don’t press me, therefore, please. The worst thing you can do to me is pressure. Pressure. If I feel stressed, I’m much more likely to get unwell longer.

    Fibromyalgia is like waking up every day to fight a fight you know you’ll lose and get out of bed. It is the daily routine of defeat and every tear, explosion and collapse that follows. It holds its fingers desperately with hope and courage and allows them to take you out of your bed when your body fights for anything. However, you’re going to win the war.

    There were some misconceptions about fibromyalgia that we needed to correct. These stigmas are largely disrupted by promoting general perception and awareness so that ultimately more research and better treatment options can be found for those with the disease.

    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

  • So much more than just pain is Chronic Pain

    So much more than just pain is Chronic Pain

    By: Dr Alexa James

    Very often, people do not understand what Fibromyalgia is like, and other chronic, invisible diseases that cause chronic pain. In their lives they have experienced constant pain, so many have somehow, but they have never had to deal with long-term pain. I tried to search for the “official” pain labels for different pain types I felt but could not find a label with a proper description for them all. I found technical descriptions and patient descriptions sometimes, but nothing entirely correct.

    Chronic pain differs greatly from the average pain. It can vary from mild to severe, but it can be more difficult to treat the mildest chronic pain long term than the severe acute or short-lived pain. It constantly stalks you until you cry, weep and are desperate for relief–making even the simplest task a serious fight. We celebrate some days just getting it from our bed to our couch, because that day is really so difficult to do. The pain probably prevented a relaxing sleep and does not forget all the other symptoms that are accompanied by these diseases.

    The list is long, with extreme fatigue, nausea, cognitive problems, migraines, light sensitivity, sound, smells, contact and motion. The pain is also not a single type of pain. It’d be too easy, I suppose. No, many forms of pain are accepted. Multiple forms are often used simultaneously. It’s a blow… read this with as much sarcasm as you can, because it definitely doesn’t have any fun at all.

    The following kinds of pain seem common to our condition by feeling my own pain and interviews with others with Fibromyalgia:

    Musculoskeletal pain:

    Feeling like a deep, ache and flu-free feelings, sometimes for weeks, or months, at once, crawling through my body.

    Pain of the nerves:

    I wrote it in advance, and the pain of the devil is the nerves again. It’s torturous, so you can feel crazy because your body is on fire, you’ll swear. The worst pain you can imagine is stabbing, itching and burning. Like burning on a red-hot metal piece, but can’t do anything to calm it down. In order to persuade myself to NOT fire, I always look at whatever part of the body it happens. It’s a mental trick of some kind.

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    Pain of pressure:

    my own label, since I still have to find a proper “official” label. Two different forms can be used. You can feel that one man is sitting on a semi-truck all over my body, and then running over for a couple of times. You feel weighed, almost incapable of moving, just like your body is held down. The second type appears randomly, apparently wherever it wants, like a flow pierced you suddenly. It is usually in a round spot of two “-four, “and the pulses are deep, but sharp and stirred pain for 4 to 20 minutes, everywhere. After a while it goes away and leaves behind a strange ache.

    Joint pain:

    This type of pain, whether caused by general aging or arthritis, is already known to many. It may feel like a sharp jab in your joint or a deep ache in the joint bone.

    Inflammation:

    I include it, as it rarely brings pain. It can cause you to swell, to cause another kind of pressure and make you think that your body is exploding. Medications often appear not to be helpful and rigidity becomes harder to walk without feeling like a stick-figure. Pet scan also shows that fibro patients have brain inflammation.

    Surgical procedures/medical treatment pain:

    Oh yeah, the very things that should help me can add to our pain very often, making things even more exhausting! Things that should help us. It is impossible to describe all of them but I will call them “healing pain.” There are so many different pains this can cause, it is impossible.

    TMJ / jaw / face pain:

    This appears to be common to us, too. We may have sharp pain in our faces either because of poor teeth caused by their conditions or medicine to treat them or because of the inflammation of the joint tissues in the jaw. It can be awful, taking all the self-control that I don’t have to cry. All the pain and the long list of other symptoms which constantly bombard us make it much harder for us to do simple daily activities than the average person.

    I have compiled a list of a few normal activities to try to explain the differences really, which virtually everyone has to do at some point. I explained to those of us with chronic pain how it can feel after each activity.

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    1. Just taking a shower — may be that at the end of a very long day we just ran for a few miles and jumped into the shower. When it’s over, we’re exhausted and can hardly move.
    2. Stepping outside in the weather above 75 °–immediately feels like 8 hours of hard work in 100 ° + weather have actually been spent. It is almost impossible to be mindful, because every ounce of energy in seconds is drained by heat.
    3. When the temperature is below 40 ° C–immediately it looks as if we have plunged into an ice bath naked. The pain is heavy, heavy and bone-like.
    4. NO drinking–it feels like we went to a bender for Spring Break and just woken up the first, sober day, following an outing at a club or concert.
    5. Getting an inflammation–feels like a flash.
    6. Two hours a day–may feel that we have been up straight for three days already.
    7. Having a light yard work for an hour usually feels like we’ve been digging holes for 8 hours.
    8. Riding in the vehicle–it feels like in the middle of a storm in a demolition derby race.
    9. As a spectator, it feels like we played it ourselves and it was a sport of contact.
    10. Making some foods–it’s like working as a dish washer an eight-hour shift.

    At least one of these things should give you an idea of how much energy it takes to do things compared to the average person and pain it causes. I can remember a time when it was much easier for me too. Earlier. Before all pain, symptoms, exhaustion, emotional difficulties and relationship problems due to an invisible chronic disease are dealt with. A normal, active life was previously impossible to live.

    We do not choose to make it harder for us to make it easy for others to do, or to try to understand when we are slower, or can’t go out, or cook dinner, or anything else that we might expect. It’s hard for my fellow pain patients. It’s true, not only in your head. It’s tiring and we’re trying to break it, but we’re stronger. Every day we fight. We have courage, value and compassion. Continue to fight. If you feel worthless, find something for yourself. A career doesn’t determine your value, just as it won’t determine your condition unless you allow it.

    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