Tag: Chronic Disease

Understand chronic diseases, their causes, common symptoms, and effective management strategies to improve long-term health and quality of life.

  • 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

  • To the person who does not believe in my illness

    To the person who does not believe in my illness

    By: Dr Alexa James

    I just feel you. I feel you. I look okay, I’m okay. I live an active life, which is relatively normal. I’m walking, I’m driving, I’m climbing stairs. Visibly, I’m not disabled. I have no limp, no cane or wheelchair or walkers. I have no limp. I’m working a job of complete time. I’m living alone. I live alone. I take care of myself. I take care of myself. I’m cooking, I’m cleaning, I’m going to the ground to make a linen. I’m a grocery store and believe in all the bags on a journey to the house. I am laughing, I am crying, I am joking about it. Life, I’m glad and excited. I’ve got great days, and I’ve got awful days. I’m on holiday. I’m hiking, I’m bathing, I’m skydiving. I date, I go to the bars and dinner.

    However, my disease is invisible. It’s the constant dull, burning muscles that you do not see. You don’t feel my full weariness and frustration that I can’t get a good sleep during the night. You see that I don’t twist and turn all night, hoping and praying that I will be sleeping for at least an hour. For times I am so defeated you are not there that I cry, sometimes for hours. You are not there. From my depression, you do not hear the negative self-talk in my mind because my body and mind are under constant strain.

    It doesn’t make it any less real because you can’t see my disease. You can’t see the air, but it’s right there? (All right, this is an extreme example, but you get where I go). You can’t see IBS, but when you have it, you believe. Somebody’s migraine you cannot see, but you can empathize with it. You can’t see someone’s cancer always, but you know how awful it is for someone who suffers and you want to help them.

    This invisible disease is awful. This wouldn’t be it, if I had to choose a fake disease. Pain, pain, sorrow, flames, shoots, blows, pain. The rigidity every day. Difficulties with daily tasks like hair washing, drying with blow and styling. The cabinet is vacuumed, dusted and cleaned. Remove the trash. The frustration of the time it takes to perform a simple task, usually in minutes.

    It’s impossible to imagine the energy it needs to counteract this disease day after day. It would take a great deal of time to come up with these specific pain points and sentiments just to keep up with the disease. There are so many specific, random and non-fibromyalgic symptoms and chronic pain conditions. The problems of the inner stomach are so unpredictable. For no reason, the dry skin. Sleeplessness. The fatigue. And fibro fog, the memory and focus are lacking. It might certainly be a good excuse, but it’s one of the most frustrating pieces of fibromyalgia. It is terrible to constantly forget and be distracted.

    Do not assume that you see someone parked in a handicapped car park and they appear “fine.” Don’t judge and ridicule them. Do not judge them. It can sometimes be unimaginable the pain and energy to even reach the car and drive to the shop. Any steps that are saved are pain and energy. Energy to try and get the essential elements through the shopping trip, then fight back to the car, get home and be done during the day. This is sometimes the equivalent of a “normal” marathon runner.

    It’s not real to the person who stuffs my disease. Be patient. Be kind. Be friendly. Be comprehensive. Train yourself. Education others.

    Sincerely, 

    An exhausted, frustrated, and hurt fibromyalgia sufferer

    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

  • I’m More than my chronic disease

    I’m More than my chronic disease

    By: Dr Alexa James

    We always look for ways of identifying and distinguishing ourselves. A way to be a single person. The Funny One, the Smart One, the Beautiful. The fan, the creative, the athletic. The “fan of sport,” One way I don’t want to do that is to “be a fibromyalgic girl.” “The painful girl, the painful girl” or “the tired girl.” “The painless girl,”

    I’m more than my pain.

    Ask me to camp. Ask me to camp. That’s the way to go. Please ask me to go shopping for a day. Suggest that we walk the city. Don’t be afraid to hug me or to joke in a joke with the jab in my arm. Call me, your house, to parties. We’ve been dreaming of this picnic. Holidays? Let’s just do it. Let’s do it. So let’s get tickets and tailgate. I want to go to that baseball and soccer game. I’m not sorry, I enjoy Chronic Disease

    I’ve got a lot of interests. I love cooking (read 36 fibro patient cooking hacks) and baking. My air fryer obsesses me. I love learning about various people and cultures. Overall, I love to learn. Something teach me. Animals, especially dogs, cats, alpacas, narwhals and dinosaurs. (Let’s read more about pet health.) I am obsessed with animals. It’s black, my preferred color. That is how I take my coffee. I love that black color. Pizza, wings, beer, I love them. I love to check out various breweries. We’re going to hop the bar. Let’s make brunch. Let’s make brunch. Make it a day. Let’s do it a day.

    I’m training. My body allows me to do what I do. I work with my body. I work with my body. I do yoga, I walk, I weigh lightly. In home workouts, I do TRX and randomly. My body works although it feels like my body works some days against me.

    I am far more than just my chronic disease.

    I am clever. I am being driven. – I’m determined. I was somewhat crazy and got out even more forcefully than I knew. I’m impervious. I am just funny. I’m being caring. I am empathetic. I am being creative. I’m just laid back. I’m just organized. I am a do-er. I’m a thinking thinker. I am an introvert. I am a cat mother.

    A sister, a sister, an aunt, mother and a cousin. I’m a daughter. I am a friend. I am a friend. I’m as much as I can to my friends and family. The times are good and the times are bad. I’m leaning on a shoulder. I make jokes. I make jokes. I give you advice. I give advice. I am a sports fan. I am a sports fan. I shout on the TV when it’s a bad call during a football game. I’m staying far too late to watch football on a Sunday or Monday night. On a sunny afternoon, I catch a baseball game.

    I’m working. I work. I work very hard. I go to meetings. I believe. I learn. I don’t. I succeed that. I succeed. I’ve been working for a career that I still work for.

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    My chronic disease, I am not. I’m a human living with a chronic disease.

    Instead of letting my pain control my life, I’ve learned to listen to my body and work with pain. I’m studying equilibrium. I know that it differs from good pain to bad pain. I know I can continue to push a bit further. When I have to take a break, I also know. Yes, sometimes because of my illness, I can’t show up. Yes, I’m going to say no sometimes. But don’t stop inviting me, please. Do not let one “no” stop the “normal” person from seeing me. Not only my illness, learn about me. Let’s speak about family, hobby and interest. Let’s speak to our family. Let’s speak of what we’re enthusiastic about. Tell me your best father joke and jokes. Tell me. What’s the most awkward thing you’ve ever experienced? If you want my fibromyalgia to learn. I would love to speak too, but don’t forget, please, that is so much more for me.

    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

  • Things I found help me handle my Fibromyalgia.

    Things I found help me handle my Fibromyalgia.

    By: Dr Alexa James

    Living with Fibromyalgia is challenging.

    We do need to find out how Fibro works and how best to treat the symptoms, and we really need scientists to get it and to make this weakening condition, based on several factors, attention, and time. Doctors have only treated the symptoms that are enough to control the condition, but it does not work long term.

    In the past, the medical community tend to consider Fibromyalgia as an explanation for people who have sleep, pain and other problems. We seem to be reaching a point when some researchers are prepared to say “wait, there’s more,” than they thought before. As a result, currently living with Fibromyalgia are obligated, for pain relief, emotional turmoil and other symptoms that we experience, to go to communities full of people dealing with the same symptoms and problems as we.

    The following list shows the things I’ve discovered that help me deal with my fibromyalgia every day. It is a battle, and it can be very solitary. I hope they can help anyone else who lives with this condition. People don’t understand how it affects us, but they just don’t get it even when we try to explain.

    You can’t imagine how you feel, yet you still work, so you don’t think this should be so bad. That’s it. It’s pretty horrible, and it is very confusing, since you can’t control how physically you feel. If you feel like I’m doing every day, please take advantage and use these tips to at least handle Fibromyalgia in some way.

    For this condition, there is no cure-all. These techniques are not designed to help me say anything close to “Do these and you’ll find it.” These techniques will not fix you, but they can only help you to cope with what you’re dealing with.

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    1. That’s easier said than done, I understand, but truly try. As we often struggle against the sense of meaninglessness and feel like a burden, this could be one of the hardest things to do for us. Knowing when to give up and seek assistance can have a substantial impact on how we feel. Don’t care what people think, your emotional stress will also lessen. You are a combatant. You’re fighting against a condition that people can’t understand, or even imagine. They don’t think any more because they don’t know how it looks like.
    2. Assign a value to each event based on the effort you need to achieve and the time it takes before and after the recovery. Use this chart to help you figure out the next tip and also to help you understand how each activity is affecting you. (I started using a5-point system, 5-point system.
    3. It’s not a good day, not a bad day, but one of the days that most of us spend our time between. Once you know that, you can better measure what activities you can do before you stop, or better predict what you can fit in a given time frame.
    4. I’ve actually gone so far as to take a scheduling calendar before and after, to help me see how I need to take care of oneself. My body is not like that, and sometimes I find it difficult to remember and accept that fact.
    5. It is just as important to recover as to prepare. It takes time, and less activity takes place during the day, so many of us have to do it hard, but it is necessary. We hurt ourselves more if we don’t take the time to do these things, and we can do even less. The preparation and recovery aspect of a calendar like the calendar I mentioned before can help. Sometimes it’s easier to accept when you can see how much time your body needs to recover.
    6. Make a list of foods which you believe could affect you and begin to get rid of, one by one. Tell any changes you notice from the latest food eliminated every day during your daily routine. My own investigations have convinced me that food can have an impact on our feelings absolutely. I systematically removed food from my diet for a solid couple of years. It was more difficult to tell at the beginning which foods caused which symptoms, but the more I eliminated it was easier to know exactly what effects every product caused. For myself, it is necessary for me to avoid all the milks of dairy, many strong spices, and caffeine and to drink anything that is unclear (due to my kidneys.) I stick with lean grilled meat, veggies and not too hard for me fruits. Many books and websites on anti-inflammatory diets are available. I suggest that you look for an idea what foods are going to be eliminated.
    7. It must be very simple on your body but it still helps to move your muscles so that atrophy does not cause damage. In times you can’t get out and do things, that matters even more. That is why you want it to be sufficiently light, whether you have a good or a bad day. In 5-10 minutes, 2 or 3 times a day, this is easiest for me. I’m stretching lightly, walking in and a few 2.5 lb weight arm lifts. This is not so much, but in moderation it is movement, and motion DOES help. In our cases, excess can hurt us seriously, so it is difficult to exercise. I regard movement and practice as two different worlds. I have not the energy or the power to resist pain, but I have the ability and the strength to create energy, to move at least a little daily, because the effects of being only sedentary can be far worse.
    8. There may be several things to this. You want, of course, to physically care for yourself. This includes stretching, medication, noticing new symptoms, etc, which are elsewhere covered, but it also includes mental care. It is even more important to ensure that your anxiety is relieved and managed when you have anxiety or other mental illness. Stress can have an important physical impact on your body, particularly if you have chronic conditions. Develop a routine for everyday stress or anxiety management, which can be included in your everyday self-care.
    9. Someone who said it could be a new treatment or a symptom you didn’t know had something to do with Fibro. The more you know about it, the better you can understand what is going on with your doctor and about what you need to discuss. Make sure you don’t take and focus only on one-off situations. Do not allow it to send you into paranoid mode when you are looking for stuff. It’s not sound. Make sure you also look for others in the same field, if you read a personal experience, in order to get a more varied perspective on the matter. You would at least like to ensure that the author has experience with this subject or is from an officially certified source when reading informative articles. Reading articles with outlying headlines on Fibromyalgia adds to confusion and can overwhelm you with fear without further exploration of where the information is from. Please ensure that the proof can be supported on what you read.
    10. Many of you may have tried to, but if you don’t, or you may not, you ought to try. When maintained at constant, consistent levels, most medicinal products work best. That means that they can really be taken in a timetable. When you learn about fibromyalgia every day, you should also investigate your medications. Knowing what side effects can actually contribute to making them less severe in some people and also helps you to know when your medications are causing something.

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    Taking time to do these things can actually help your quality of life when you are suffering from a chronic disease. If you develop and adhere to a routine to manage your diseases on a daily basis, it’s more likely to help you control your disease–at least to the degree to which it is controlled.

    Nothing will improve everything–that’s why this is a chronic disease–but we can take some control and give ourselves the best chance to feel as good as we can. I hope that my fibromyalgia management can also help you to get as much control over them 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

  • I’m not going to excuse myself for “OK” days

    I’m not going to excuse myself for “OK” days

    By: Dr Alexa James

    Our days are dictated by pain, tight muscles, fatigue and many other factors and symptoms for the patient who suffers from fibromyalgia or Chronic Pain. Sometimes we have to go so far as to plan a relaxing day, as far as our plans are concerned. What people who don’t have difficulties to understand with these conditions is how we can be productive some days, take part, enjoy fun activities, but some days we can do nothing, and getting out of bed or showering might be the greatest achievement for the day.

    Some people don’t realize that we live a daily life but, sometimes, hour by hour. However, this is our lives, it is not guaranteed what happens from day to day, things may not always be planned and the days are always uncertain. Nevertheless, regardless of what, if it’s an “ok” day, I will try to enjoy it and if I can apologize for it, I will be damned.

    This may sound a bit harsh, but our “new existence” is a reality not understandable by all. There are some days where the major challenge we face is living with fibroid and chronic pain. We’re full of pain and sleeplessness our day and nights, lost plans, friends who don’t exist anymore or who can’t work and just the simple disinformation, the lack of understanding and ignorance from medical professionals.

    But there are days when we can actually tolerate the magic pain scale, even though we may not be completely restful, and the door opens with the opportunity of living, if for at least one day or for some hours. There are many days in which we can take part.

    We need to do that just when we have a day, or days, that we can possibly enjoy family or friends, much necessary and pleasant activities or even go on holiday. We must spend the days in which we can take part in life. But now the inevitable feelings of guilt and physical sorrow come, that are always there if we push ourself too hard, with those days of actually taking part in life and trying to get the most out of a tolerable day.

    We sometimes feel guilty that we can now enjoy living for a day or two for as much as we have lost. Today, for example, I had to miss a family because I couldn’t handle it physically or mentally. I might be seeing myself having lunch with friends tomorrow or having a holiday with my family, but I feel guilty and guilty that yesterday I had to say no, but I can say yes today.

    There is absolutely nothing to predict if there is one thing that can be certain about fibromyalgia and chronic pain. We cannot always plan or commit ourselves to anything in advance, so that’s why we have to take advantage of the days. We can communicate these achievements and joys by touching a button with the age of the social media. People can see and participate in the things we could enjoy.

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    We want to share the joy we had because we had an all right day. But we feel the judgment, the voices behind our back and what we actually feel in this life of fibrous and chronic pain because someone only saw us, smiled, lived and enjoyed this moment. They won’t walk in heating pads or ice bags tomorrow when they do not see the tears, if we have to get up and go up on the stairs and do not see us suffering. They’re going to see the tears on our faces tomorrow. But let us still feel guilty because people were happy to see us and today, we had to say no to another family.

    We feel like we’re in the mountain of guilt because all can see that we could have fun, we must remember, it’s a picture. It is only a small part of our life that people see and enjoy from us, a picture that shows we were OK, if just for a while. A snapshot of an opportunity to enjoy our family activity. A snapshot of the fact that we could exist as closely as we would ever be for a little bit of time.

    An opportunity to have a good time with our families or loved ones, for an activity or at least. What this picture doesn’t show is the sorrow we experience every day, the pain which keeps us couched, the tiredness that has wiped over us and stamped out every opportunity for something to happen. We don’t want people to see these parts of our lives. We don’t share the times, we don’t post our struggles on social media.

    For as limited a life as we can live, we really need to enjoy and enjoy the times we can live. So why are we guilty of having enjoyed this time? It’s a difficult question to answer because we found that we can’t work anymore for some of us with chronic pain and fibromyalgia, and that we can’t help our family. This is a fight in itself, and by feeling that we do not have the right to go out with family or friends, or the right to enjoy ourselves when we feel like we are human beings, we do not need to add to my mental sufferings.

    We DO have the right to live as much as possible without apologizing or guilty that we may not get out of bed yesterday. We suffer from physical or mind pain every day, fighting that nobody can see, feeling just about us, so why should we not be able to enjoy activities, holidays, nights with friends, dinners without being guilty of it? We have to take advantage of these unique opportunities, and we can’t think about our pain and struggles in every minute. Enjoy the days when even if the pain doesn’t go away, we can smile at a level without force.

    Take every chance to forget what your New Existence is, just for a little while. Whenever we can have a good day, we must stop feeling the fault we experience won’t keep apologizing for having some “ok” days, because I’m sure I fight on the other days! These are things and feelings that anyone with fibromyalgia or chronic pain cannot ever understand. And how would they really be since they were never in our shoes? The condition that we say, “I would never wish this to my worst enemy” is that we mean fibromyalgia!

    We don’t seek sympathy or mercy, we just want to understand a bit that our lives differ, because we have chronic pain to live “always.” We must enjoy things as they come and live on the days when we can truly live them.

    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

  • Tried to be a mother in a chronic condition

    Tried to be a mother in a chronic condition

    By: Dr Alexa James

    At least by the standards of society, I won’t lie. I succeed in being a mother. Not because I don’t love my kids because, above and beyond anything I could ever have imagined, I do it. No, my body makes me spend more time, energy, and money on ensuring I survive and work than I can on my children, I suck being a mother. It was very difficult to accept that I could not give them all I deserved. I’ve been severely depressed for years and beat myself.

    I hated myself for some time because of my guilt and shame. When I was healthier, it was a big problem for me to feel as close as I can to the perfect, so much so that I became insane trying to make every small aspect of my life micromanage able and often the lives of people around me. It was both good and bad, trying to be as close as possible to perfection.

    It meant that I could do things that the average person couldn’t (at the time) but that I was also extremely obsessed with every detail. I’d be obsessed with things that didn’t really matter but could ruin the whole thing for me. It was devastating for me to finally realize that I would not be a “super mother.”

    So much so, I still have tears in my eyes, although I write about it now-I am better off accepting my limitations. It wasn’t at all easy to accept, but it was necessary to stop feeling so guilty. The guilt was detrimental to my own mental, emotional, and relationships. Time contributed partly to this acceptance. It was much harder for me to think I could not do anything when I was younger.

    I had to accept it to find out how to be’ ABLE‘ –not the best I can be compared to healthy people. So I don’t have to find unconventional ways to be a “good mum” for my children as physically as the average person. Fortunately, I’ve got a supporting family who did the things I couldn’t do for them. My children have never been lacking in love and have never starved or met their needs.

    I am so blessed and unbelievably appreciative that my parents care for it. I know everyone isn’t able to step in and help in this way. I don’t accept that it wasn’t me who could 100 percent provide them with this stability even when I know how good they were in a lifetime. I wished desperately, but every effort to fix something wrong with my body was foiled by an emergency operation or procedure.

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    I finally gave up trying to work a real job almost three years ago. The last time was an eight-month long period, and at the end there was a 19 day torturous urethra stent experience. It’s never impossible for something like that to happen at a time when I can get enough income to stabilize or finally get to an objective that I’ve been working toward. I learned that I can keep the major medical events, which require hospitalization or bedriding, from taking place so often if I do not work, limit my activities, care about what I put in my body, and take time to recover between activities.

    Easy, eh? See, stress aggravates every condition I have. (The Sarcasm Please take note.) It lowers my immune system and makes me generally more susceptible to flares due to my fibromyalgia and any viruses or bacteria with which I come into contact. I come into contact with all kinds of germs when I have to go to an office every day to work. Because my immune system is crappy above all else, I am sick and it is likely to get much worse than that if I meet somebody with a cold-and it will lead to worse things. I can’t stay away from it until I remain home. It’s a vicious cycle.

    This also applies to almost all. Don’t work doesn’t mean I can spend with my children all the time I want to, and do anything. My children attend public school and are exposed to all the diseases I have brought in, so I also have to be very careful when I have close contact with them sometimes. I just look and feel too bad other times to let them see me like that. It caused him stress and nightmares when my oldest was very young to watch me sick. I chose to allow them to live permanently in my home while maintaining a place in the neighborhood.

    When I looked / felt good enough not to scare them I spent as much time as possible with them, and just telephoned when I was so sick to be around. It was not perfect, but I had to decide that it would be better to be alive and to function partly than to work to death. Some of you might consider it egoistic of me to do something like that, but I feel that when I had the option of relieving some of that, it would have been egoistic for me to put them through fear and stress.

    Now I am 18 years old and may not have been allowed to ask a more responsible, caring, knowledgeable, compassionate and well-adjusted man. He leaves his way and tells me that I have done the best I can through them. Nothing can take it away whilst it helps guilt somebody. Although I feel guilt and anguish, I still have two wonderful children who are very well adapted and honestly can say that they are loved.

    My point is-we are not so much as long as we love the kids and take decisions which are the best for them as we cannot get our bodies to work like they are supposed to do, as long as we do not succumb to the feelings of not being good enough or the pressure of society to function beyond our physical ability and put it potentially in.

    These sensations can get into our heads and make us feel more comfortable with our parenthood. This could lead us to make our bodies feel better than better, or to take decisions based on the things we shouldn’t do. At the time, it doesn’t feel like that. It seems that we try to do what is best when we are the perfect parent. I’d love to keep my kids full time like a normal family in my home.

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    It would make ME feel like a better mother, but it was not better for them. Sometimes being a good parent means knowing when you can’t say you can do anything and ask people you trust for assistance. I’m not suggesting that every person who is chronically ill runs out to find someone to take their children. I’ll just say that based on your specific circumstances and the general picture you should evaluate your situation. Try to reflect on these questions when evaluating:

    • Does this activity cause additional injury to my body? When compared to the advantages of doing this, compare that additional damage. For example, it is not best to put yourself in a hospital to participate in a game or recital if someone else can support your child.
    • Is this an activity needed, or can I do something easier on my body instead? One example of something easier is a virtual presence, rather than having a physical presence or perhaps having a private dinner together rather than a large party.
    • Is there more chances of doing this in the future? Or something I was to before?
    • How much does my child care for my presence in this particular activity?

    Please apply all of these questions. Even small, worldly activities, because you can figure out how to lighten your load without having a real impact on your children. You must weigh options if you are chronically ill. Instead of attending, it sometimes means to have someone log the game or recital because attending causes your condition to worsen.

    It is more important than keeping “appearances” alive and able to interact with your kids or that other people don’t think that you are doing enough. You know what can handle your body, and what it can not handle. You can’t do all you can to care about yourself and your children for as long as you can, but as a parent with chronic disease, you can only fail, so long as you’ve done what you can do to help them.

    Healthy parents are luxurious that if they choose to be there for all. We’re not, so to be there is more important than to get into the ground trying to do whatever we think a healthy parent wants to do. If you are lucky enough to have a support system, ask for help. Taking care of yourself, allow them to do what you need to provide your children with stability. It is neither disgusting nor egotistic— it’s clever.

    Yeah, I’m still guilty. It will probably never go away completely because I’m a mother who loves her kids and wishes to “do” them. I wish I was able, but life had other plans and I had to adapt. I wanted to do all the things’ supermum I certainly know that the best thing for their well-being was my decision.

    The evidence shows how well it is adjusted at my 18-year-old. Don’t beat what you can’t do to beat yourself. Put all the energy and concentrate on what you can do and use it to show your concern. Try to be there through videos and images, and for the time before and after when you can’t be physical. Be always emotionally available to them. If you can’t physically do anything for them, find someone you can. There are so many ways to show your love that we normally don’t think about. Look for and do these things at all times. Whatever you do, don’t feel bad enough that you can’t. You, or somebody else, don’t help.

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  • Ways to Aid someone with Chronic Disease

    Ways to Aid someone with Chronic Disease

    By: Dr Alexa James

    It can be frustrating if we need help, but don’t want to accept it, or even harder, that we don’t want to burden anybody else. Fortunately, as someone living with chronic conditions that make it harder to do normal business, I can say that there are people who really want to help others.

    Some people have the best of intentions but don’t know exactly what to offer, or maybe just want to do something else. When you offer support, the choice of words can really determine how comfortable we feel to accept your offer. I would like to note that this doesn’t mean that anyone is ready to help us at all.

    Perhaps the appreciation we feel when people help us can’t be imagined. You probably also could not imagine how difficult it would be when we were in the middle of the pain of our conditions or overwhelmed by the kindness of yours, or when we felt embarrassed that we needed your help.

    If you live with an invisible and unpredictable disease, emotions can be strong. One of us wants to be the last thing that a person cares for, and if, by offering, we feel like you are uncomfortable, or just to be cute, then we’ll probably thank you, but say that you don’t have to.

    Although we fall into daily tasks such as washing and dishes. In my case, I would rather harm myself to do what I need every day instead of having somebody who doesn’t want to help me, or be given “help,” which really doesn’t help me. I’d really like if you didn’t offer people just to be cute or to say something, because I can’t tell it is very rare.

    That is why it is very important to offer your assistance. Things to do can help someone with a chronic illness. The following are ideas. I also have a way of asking everyone to make it easier for the recipient to accept your offer, for the wording will make them feel like you want to assist them.

    Offer to clean them without any assessment or expectations.

    Rather than saying, “I’ll come and clean you up,” “Do you want me clean up?” Try to say: “On Thursday, Thursday, or Friday, I come to cleanse FOR you, whatever day works best for you. You just have to point me into a room, tell me some special instructions, and then relax.”

    That means we’ll need to work when you are coming, and it can really be hard to know when that is possible so usually, we’ll say something like, “Oh, I want it to work,” or “Oh, thank you so much for this offer, but it isn’t needed.” We’ll do the same often if you start your offer with, “You want it to work,” or “Oh, thank you so much for it.”

    We’re not ungrateful, nor do we think the worst of you. This is because we have to live with feelings we don’t do enough, and the culpability that accompanies this leads us all the time to feel like we burden those we love. We just try to avoid such sentiments and are actually a burden.

    I suggest using the phrase I mentioned previously, or saying, “Hey, I’m coming for whatever task you do,” to which many will answer, “Oh, you don’t have to,” and then, that you may tell them flat-out, to which you WILL, that you really wish to help someone without making them feel you are just being polite.

    Sometimes, you come into someone who does not really want any help, and you should fulfill their wishes in those cases. You can at least know that you’ve done all your best to make them feel comfortable accepting your assistance if you offer to use the same word that I suggested. The key is to make sure that your words imply that you WILL be helpful, not just polite.

    Go for them to the shop. It may be hard for us to perform on a bad day and it will prevent us from carrying out several other tasks so we can prevent it from being great at any time.

    Try to use sentences like: “I head to the shop later, thought I’d see if I could collect anything while I was there? “Or:’ On Thursdays I go shopping. If you list anything you need, I can pick it all. “Both of these examples are helpful in making sure that we accept the offer because: a) it allows us to recall some time in every scenario; b) you make it clear that it’s not just a journey for us. If you’re going there anyhow, we don’t feel so bad to let you help.

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    Trust the person you are trying to assist that the number of items is not an issue if you let them know that you are shopping throughout the store. I would leave things outside a list sometimes because I didn’t want a person to go back to the shop. Find a way to let them know you’re ready to get everything they need, and this isn’t a big problem.

    For this particular task, storage-specific applications can be extremely helpful. A number of them now have all the items, prices, sales and coupons listed in the app. You can use the app when you draw up your list, so it almost sounds as if you can see the items in person.

    Pay a bill or give you a prepaid gift card, that can be used wherever it is required.

    If you suffer from a chronic disease, this at least means medical bills. It could also mean that you can’t work so that finances can get tight. Even if you have great money and you do everything you can to earn income, medical expenses can keep you broken. When you can and want to really help, it can be one of the most useful things to do to relieve some of the financial strain.

    Some people might not want your money, but if you know they need help there are ways to do so. Much money stuff can be treated anonymously. Some companies used to have programs that allow you to pay on a bill without the information of your account.

    Many places have changed that because of privacy policies but checking for any company for which you want to pay is at least worthwhile. If you cannot find a way anonymously to do this via the company, slip cash into an envelope or a prepaid card, and make sure that they will only receive it anywhere else. It will alleviate some of their stress unless they are rich.

    Watch your children so that they can relax regularly.

    Many people with kids may have this very well in its wording. You are more likely to offer some sort of assistance, if you have been that fatigued parent to see another parent. For chronically ill parents, it’s both common that we feel like we aren’t doing enough for our kids or that we are riddled with it all. We will not want to accept assistance, but the fact is that a chronic disease will never go away when we feel like we “pawn them” at someone.

    Some of us are in pain and exhausted daily, regardless of how sleepy we are. Daily self-care can be very helpful in our management, but we often lack the time, especially when we are parents. The best way to do so is to talk about children as much as possible or a routine. “Annabeth needs to socialize more, why don’t I go to Isabel every Thursday to get together? “or:” You are on my school journey right now, and children need to make friends, how can I get them every day?

    Adjust these suggestions according to how long you can / would like to devote yourself to helping. If you can’t do things regularly, providing some help can still alleviate some stress every once in a while. Therefore, don’t let the suggestions lift you away from proposing a few hours ‘ free time to play random playdates.

    Another thing to consider when providing childcare-if they are really going to use downtimes, they should do their best to make arrangements for all their children. People often forget children who are not close to their own age in their home, because they may not know them so well. If your objective is to help people really, try to involve everyone, so that their feelings are not hurt.

    Offer emotional support to those who appear to have everything covered. Sometimes we only need someone who can listen and truly understand.

    Some people are physically covered or helpful, or even financially, by themselves or other. You may appear to be in control of everything. In such cases, I offer at least to be someone they can’t compete with, or say they can be fixed easily or anything. You only have to vent sometimes. I have experienced this many times myself, so I offer to be there for others who may need it.

    Many times, if I try simply to let them vent, I’ll let them speak about anything they want, without offering much.

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    Only if they say something that they really need or want to know, will I offer you information. I usually say something like, to offer emotional support: “I know what it is like that someone does not judge, does not participate in, and does not. Sometimes, I’m adding, that I have experienced similar or detailed experiences that make them know, I’m going to understand and not be judge-full, like: “My children are 12 and 18, if you ever want to speak. I’m going to be here. I know that teenage years can be frustrating times, “or anything that is relevant to what they appear to experience. All five of these things provide you with the best opportunity to offer your assistance to someone you are interested in helping.

    Remember, there are the rarity people who just don’t want to get bothered and it is sometimes difficult for us to accept that because people want to help others. We must also respect these people, because it can also create more stress if we continue to let them help us. It can be a difficult situation to measure but you only know it can happen. Providing the wrong type of assistance can significantly increase our stress level. We always deal with people who just don’t try hard enough to fight our conditions. We always deal with people.

    Unless we have a discussion (and it is clear that we do not know something that exists, it is not appropriate or helpful to suggest practice more, yoga, meditation, diet or other similar things.

    If you have met a recent article in our condition on a new development, that is great information and helpful. Alternatively, there may be a book that you know about our situation, which can be useful, but only provide suggestions. Try not to tell us that it’s going to heal us. CHRONIC are the chronic conditions. There is no cure, only symptoms are managed.

    You should not make a comparison of the pain and the symptoms with your own when offering help (unless you have the same condition, even then, all bodies can be different).

    “Oh, when my muscles hurt, I just stretch out and take a hot bath and they feel so much better.” We wouldn’t fight so badly if it were. Without being very new to pain and diagnosis, we have tried every normal remedy, and we tend to become exasperated when people continue to put forward simple stuff.

    Together with the other examples of how not to offer combined with how to help in ways we feel comfortable with acceptance, both of these examples should certainly provide guidance if you really want to help someone. When done in the right way, your support is needed and appreciated. We will certainly try to ensure that we do not burden you for the majority of people with invisible diseases, but that your help is so needed.

    Thank you for your readiness to offer your assistance in the best way possible. More people are needed who really want to help. Some people in their lives are not ready to do so with chronic conditions. Seek them, and all of your loved ones who are struggling with your health and do whatever you can to facilitate your lives.

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  • What or Who I Am the Invisible Intruder – Chronic illness Awareness

    What or Who I Am the Invisible Intruder – Chronic illness Awareness

    By: Dr Alexa James

    I was something that was wanted to deny the health community once. You told me I was just in your head, I didn’t exist, you felt like freaks who have lost their minds. Something different than what their practice has been teaching them could not believe. Oh, but I’ve demonstrated I’m so real, and now they know that. I am not in your head as a figment of a psychological or overactive imagining.

    I’m a nightmare you’re worst. I have always been a mystery through the decades — a haunting mystery that no cure exists. Medications may mask a symptom if you have sufficient medication but there is no cure. I’m going to rob your family and friends away, because they don’t understand why you are as…

    May I describe one day of your life–maybe they’ll know a little about you. If they are to look at me in your midst, they might see shining red and blue flames, struck in the midst of every muscle you have. I’d be the scream of a Banshee in order to hear me. They would feel the sand and the fire on their skin to feel you from within.

    In severe cases, you cry and cry to touch something, for it’s like the hottest fire you can imagine, the sand piercing on the skin and reaching every nerve within you…. even the softest of fabrics is wounded and you are burnt when you try to use them, bedding sheets are untenable and sleep evades you. You want to rip off your skin. They will find that it is like a bass-guitar played far beyond what is regarded as “normal,” to enter your realm, and the vibrations are insupportable.

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    Every day or night, I’ll rob yourselves of sleep, sleep is uncommon. I will command your mind and body to feel less than human so long as you cannot escape into any other realm. I tear up your life and ask you to be my 24/7 slave for suffering and pain. Yes, the level of mental, emotional and physical pain you suffer doesn’t understand.

    Some say they understand, but they don’t believe them, because they walk in shoes different from you. Some suffer a similar “me,” however, at all levels and extremes, each of you suffers. Forever and a day, I shall remain a mystery. I’m not the kind of nice thing because, once in a while, I’ll tear apart your heart and soul, and I’m going to fear those you care and want to love.

    You’ll suffer, lie down for days if you’ve had that luxury, and cry out for help just to find empty arms… If you’re lucky, you may find someone that tries to stay near you! If they are lucky, you can find somebody who tries to stay close. But I usually frighten them. The time is turned into hours, the hours are turned into days, the days turn into months, the months turn into years without a cure–all that’s “Me’s pain” within you.

    Remember, I live in all of your nerves and your muscle–there’s no escape. I’m the unseen intruder. There’s no drug, no pharmacist, no wondrous drug or herb that takes me off from you… no sleeping pill or narcotic that can get me from your body… there’s no separation from “me,” I can’t live and not kill. You can never escape me when I have you inside of my grasp.

    But the biggest thing is that your torment flourishes in my favor because you don’t understand the suffering that you are suffering; just as you can’t live a life without pain you, you can’t understand who you don’t know, or want others to have time to understand, you just don’t understand. However, they often go away, if the pain that you feel is expressed, which is not really possible… There are really no words to express what each of you feels or masks. When you work with people you are forced to wear an a’ mask.’ When you come home, you cry out because of the terrible pain.

    Lyrica, Cymbalta and other medications, such as pain relief and muscle relaxing medications, just add to my control, and until they work, you don’t even know–if they work at all.

    Who am I? I’m the Invisible Intruder, and I’ve got many siblings, usually living in you as well, my name is Fibromyalgia. Welcome to my world and perhaps to the world of your friend. “The Invisible Intruder” is my name, yes. There are no escapes, because there’s no cure, I live in you, around and through, and in every aspect of your life. –by McKimson Holly

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  • My Body negotiations: Someone with Chronic Diseases Negotiations

    My Body negotiations: Someone with Chronic Diseases Negotiations

    By: Dr. Alexa James

    I spend a lot of time negotiating with my body as someone with multiple chronic illnesses. I feel I can’t go for days and I’m determined to never give up for days. The emotional range is wide. I was through all of them and I have a great deal of coping mechanisms. My inner dialog is one of them. It could be my enemy or my friend. I have a large number of approaches because I really like them. The day depends on which one I use and how much they torture me. Some examples are as follows:

    Approach Tough Love:

    “It’s true? Can’t you work as an ordinary body?!?! I know before that you did it! Halfway you were willing to do that. Why can’t you just do what I need to do rather than be so hard? I know how.” I know your know-how.

    Approach to Nice:

    “They’re hard, I know. It felt like nothing would want to survive, but this is something you can do. We had a rough week. Simply put one foot before the other. Come on.”

    Approach to Negotiation:

    “Come on, get up, take the shower, get it over. Then, for a few minutes, you can relax. Manage one small thing and I’m going to break you.

    Bitter Approach:

    “It is true? Can’t a shower just? You once could do TWO work, AND go to school, manage a social life, and don’t even have a little shower? What have you become?”

    Empowering Approach:

    “This you have! You’ve had a worse time. That shower you can take. Just get up and move forward! Every day, woman, you fight pain. Compared with operations and other things you have experienced, this is nothing. Give it a grip!! Get into that shower! Get into that shower!”

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    The Approach I have Given up:

    “You are pathetic. you are pathetic. That’s a DOWN JUST. Can’t wash, you couldn’t. How difficult is it? Aren’t you really trying to be meaningless? I don’t know why I bother but go into the shower, even if you’re now lame and weak. “I’m going through these negotiations, and more, on a very everyday basis. The latter is not something I really control. When I have all I can do to encourage myself, and feel like I have failed, that voice comes out.

    It’s frustrating and emotional, so all these various scenarios continue in my head. I do my best to stay positive, but nobody can always be positive realistically. Many of the people with whom we interact daily can forget that chronic diseases are challenging. We fight with our bodies while trying to maintain the apparitions we cope with when we don’t.

    It’s uncomfortable that we spend a good deal of time trying to determine whether it’s worth living so we try to hide it. We hide our tears of suffering, despair, anger, and frustration in order to make all the others all right. In my head, there is a constant internal dialog. It’s usually about trying to talk about how my body functions or trying to convince me that despite my feeling I’m not worthless. It sometimes persuades me that somebody deserves my patience and understanding. It’s an ever-changing ripple of emotions.

    A typical day can go something like this:

    At 3 am, when waking up, there seems to be no reason for ridiculous pain:

    ME: (eyes opening through my body when pain shoots) “OW. Oh yes? That’s so, now, huh? BODY: “It’s safe. Well, good luck with that. “ME,” You’ve just been stuffing my hips with a big knife like someone? At 3 a.m. when I am just LAYING DOWN is this necessary? Can’t you just be glad to rest? “BODY:” Simply wait until you really feel it and just sit up there. Will be an enjoyable one. Muahahaha “ME:” Super. Much more. Thank you. Thank you. Enjoy this.

    20 Minutes Later

    BODY: “Now you are completely awake……” The room will now begin to spin. BODY:”……….” ME:’ Nothing? Fabulous.’ Do not comedies snarky? “BODY: Wait. I:” Ah, I see. Wait for it. Heat and severe nausea flashes. You’re finished yet? BODY: “Don’t really do. You haven’t learned I’m never finished yet? “I had been hopeful that we could only quickly get it over so I could move on.” BODY: “Pffft.” Hang it up for a while. Nope.-Nope. What’s the fun there? “It would certainly be more fun for ME to get through it quickly. BODY:’ Well………..’ ME:’……….’ I want to feel halfway normal rather than tortured.’

    45 Minutes Later

    BODY: “Hey. Hey. ‘ My goodbye? ‘” I: Oh, oh, oh? Have we now changed? BODY: “How cute. About Time.” You believe this change is going to like you. Oh, oh, oh!

    Uncontrollable shaking while lying under four heavy blankets after at least 30 minutes non-stop:

    BODY: “You’re having fun? BODY:” Hahahahaha. “Go away, I know.” I’m going to stop here. For the time being. “Too weak, too weak. Enjoy the aftermath.” Later I’m going to talk to you.

    About an hour after passing out:

    ME: “Is waking up still safe? BODY:” Perhaps. Perhaps not. Not perhaps. I: “You’re so precious. Try it and see.” Well, that knows? “I know. I know. BODY:” Normal pain so far. Will a catch be there? “BODY:” All right. ME: “Argh.” We’re going to see.

    A few hours later when I have to get up and be productive:

    BODY: “Whoa, whoa. What do you believe you’re doing?” Me: “I can’t go to the kitchen downstairs?” BODY: “Good, no. There was still nobody telling you to move. ME:” Hrmph. BODY: “Too bad.” I’ve got things I need to do.

    An hour later:

    ME: “I’m still able to move? It should be enough for three hours of rest. BODY: “I think it was all I did. But don’t get too excited. Don’t get too excited. “Oh well, thank you so much for your goodness.” BODY: “Would you like absolutely nothing to do today? You want nothing to do today at all? MY:”…….” Keep it up.

    After it was placed in the kitchen and half the dishes were done:

    BODY: “HOLDING!! This is sufficient of it. You’re trying to murder me?!?”I:” Thanks. A sink filled with dishes, I did like. This isn’t about killing you. BODY: “It’s, yes. That’s essentially nothing.” I’m no longer able to cooperate. The next dish you touch, I’m breaking. You know I’m going to do that. “ME:” Okay. BODY: “Shut up. Spaz.” BODY: “Lay down.” BODY: “Well, it would help if you would make stairs easier to get up.” BODY: “Ha! I’m tired.” You want the world! You want the world! Get over it! Get over it! I would say “Grrr” to Crawl if you must.

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    Upstairs after the restoration to sleep:

    BODY: “I don’t want to lay on that side.” ME: “I just might have said that instead of sending my left side piercing pain.” Me: * Eye roll * Funnier this way.

    20 minutes later:

    BODY: “There’s no longer I want to lay down.” Will you let me sit up and get sick? “BODY:” Now, you know that all that I can’t be. ME: “With whom exactly is the reputation? BODY: “So? You are living in my head. “It happened to you, what happened to me?’ You were only moderately hard. In your old age, you got so bitter? “I’m bitter, BODY:” Yes. Very bitter. -Very bitter. Now pay. ME: “Great.” Now pay for it.

    About an hour later:

    BODY: “Too long I left you alone! This is some more love. I: “No thanks. I don’t know. I’m all right that I’m neglected. Doesn’t need AAAAAA!! Are you?!? Do you want to move Right now a kidney stone? From nowhere?? I said: “Oh, you thought that I needed no rest since you gave me soo much sleep last night? I’m so bored and you looked like you were too peaceful!” I said. “BODY:” You could handle it, Nah. BODY: “Love you,”* a huge smile*, “I don’t like you.”

    Four hours later (the kidney stone was fighting all the time):

    ME: “Hey, what’s the pain up? BODY: “Well, the stone was a little stuck. It’s out of control.” All the tissue of the scar, you know. You will do something about it. “ME:” You kidding me? You guys kidding me? You began this, how did you deal with it?”I’d like to do more things than me.” BODY: “I’ve got better things to do.”

    After a lot of water drinking & moving, two hours later:’ME:

    BODY: “Oh, you got it taken care of at last?” “Finally.”I:” I do. I: BODY: “I don’t know about you, but I’m getting pretty tired. I don’t know about you. “Think it is time to get to bed. I think this is time to go to bed.” It’s just 6 pm and all day you gave me a tough time. I’m not going to sleep now anyway. BODY: “Sleep.” ME: “No.” I need a little time to recover.

    This goes up and down until after fighting to keep my eyes open all the time I finally get into and go to bed. Then we usually start again with a number of medical problems and symptoms. I usually imagine the sarcastic kind of part of my body that has nothing better to do than harass me. It sounds crazy, I know, but, hey, we all have our mechanisms of coping. It’s a constant struggle of different degrees.

    Some days are worse than others, but no days are really what someone used to be healthy would call “the good.” The majority of days are as described above, or I spend the day discussing with myself whether I go slip into bitterness or depression internally. In this series, I’m going into that a little more. Only the first installment. These are the real talks I’ve got in my mind. I decided to put them on paper since I also understand that others are fighting in a variety of ways with their internal dialogues.

    https://fibromyalgia-6.creator-spring.com/
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  • Fibromyalgia Weeping for the Suffers Before have a Chronic Disease

    Fibromyalgia Weeping for the Suffers Before have a Chronic Disease

    I suddenly sat at the end of my bed, like a ton of bricks I hit my chest. My lips tremble, in my throat I feel a lump and before the tears flow, I must stop.

    I’ve got difficulties putting my socks on and fast I know my life is gone and it won’t be what it was. It took a while for me to mourn my former self’s loss, and even more to understand that I was doing it. The whisper.

    And like suffering, you will never weep regardless of how long you need to cure. I have been losing loved ones over the years, unique individuals for me, and every day I think of it. After years, by remembering them and thinking about them and the lovely memories I shared with them nothing is lost. But I’m not prepared sometimes.

    I will see the favorite treatments of my babysitter in the shop and I will get them, so it’s lightning. My girl doesn’t exist anymore. It hurts the most when you forget about this loss for a second.

    With my situation, this is a comparable method. Now I’ve been struggling with this issue for nearly 10 years, so accepting my boundaries is simpler now, but sometimes I want what I have.

    And it’s when the blow hits my throat and eyes in the throat, because it’s so painful, I forget that I have limitations and when I remember things, I couldn’t do… True and raw I hear the news for the first time, it’s pain, confusion and dismay again.

    Every step is taken rapidly: he refuses his disease, he pushes to the complete limits and then he feels such frustration in difficulty keeping others up and doing straightforward duties.

    Then there are the negotiations: if I’ve got healthier, done more work, eaten less craps, meditated more but your diseases won’t vanish no matter what you do. Awareness about this trigger’s depression, feels poor and helpless until it takes the whole turn to be accepted. It is not good enough. It is helpless and helpless.

    I receive it quicker and lasts longer every time I pass through the cycle. This doesn’t imply I’m glad I’m, it’s good for me. It is now part of me, and I embrace it, in most instances, in the same manner that I managed to embrace it, even though my grandma missed me wholeheartedly.

    When I think of my grandma and how many she misses me, then I believe of my happiness in meeting her, in being loved by her, and in getting beautiful memories, which no one can maintain.

    I’ve got more than I lost. But it didn’t decrease me. My sickness has altered me. It created me empathized with others, strengthened me, made me a fighter, and showed me more than anything how much my family and friends loved me.

    Sometimes I cry out my ancient body, and I could have lived an ordinary and painless life. But mostly, I will take advantage of what I have, that is more than enough if I believe about it.

    https://fibromyalgia-6.creator-spring.com/
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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