Author: dearfibromyalgia

  • 12 ‘ Harmless ‘ comments that people with fibromyalgia actually hurt

    12 ‘ Harmless ‘ comments that people with fibromyalgia actually hurt

    By: Dr Alexa James

    Fibromyalgia has changed me in many different ways, most often, I don’t feel like my own age and some people think that I either don’t look like my own age, but what a fakes smile or some make-up can do surprises me, that can make you seem like an ordinary, happy and healthy person, but it’s not the way I feel.

    Fibromyalgia is an ill-understood disease. Missing understanding and support almost everybody here face a major problem. You hear such harmless comments, which have actually shattered the heart and drive your spirits down, when you are living with fibro or another chronic illness.

    “Hurtful remarks are not always obvious. We asked a question. What’s “unharmful” about the fibromyalgia that somebody told you? “to our Facebook group” why fibromyalgia “and asked them to share their sentiments and experiences regarding this question with us. You shared your feeling with us, and we compiled a list of your comments below.

    Most of us have heard all of it lose weight because of its weight, and you will be all right. People don’t trust them and say that they lie and apologize for their work. All in your head. Everything in your head. You have never had chemo or radiation, so you can’t count what you’ve had cancer (the FYI is). Are you just silly or psychologically? You should be in a hospital if you have so many mental illnesses. Why do you not eat and exercise if this fat is yours. Your only 26, how are you that sick? (I have multiple diseases that prevent me from doing it.) You’re faking because you want to be careful? And many more. So much more.

    You definitely heard these at some point. It is not clear to people that this ridiculous situation is just as frustrating for the ones of us. Just one morning, what I would not be giving to wake up, only one morning, and not pain.

    Here is what the community share with us:

    1st is You’re Always Sick

    • ALWAYS you’re sick!
    • Just get up and begin to move around. You will feel better!
    • You’ve always got a headache
    • Don’t you hurt anything?

    2nd is You are Not trying hard

    • Stop using it as an excuse. You need to push yourself, the more you exert the easier it will get
    • I know exactly how you feel but really have a job.
    • All you have to do is practice more.
    • People suggest I move more, go to other places to get my MS, etc.

    Click here to Get these Products or Visit Fibromyalgia Store

    3rd is to Lose some weight

    • If you’d lost the weight you placed on you don’t like this, my husband tells me. Your body doesn’t use it all to carry. He never sympathizes with my sorrow. I had him read the other day, finally, about fibro. His answer, doctors say it isn’t real in your head. It’s not true. And I cry with pain. I cry with pain.
    • I am depressed with comments regarding my weight gain (which comes from medicines). Normally I can’t work, and even no longer recognize myself. Thanks for pointing out the apparent!
    • Essentially, I am told that I don’t have fibromyalgia that same family member recently told me to “save” me. It wasn’t my weight.

    4th is It’s a Mental Thing

    • This is a mind. You’re not hurting your body, it’s just your brain lying to you.
    • You won’t get any more in pain if it’s sorted out, and this was said by my own.
    • You thought you were looking for a mental physician.
    • It’s in the head.
    • I was said to be a hypochondria to care for my health and if I could take part in the summers.

    5th is Doesn’t everyone feel tired?

    • “I’ve also been hurt. My 59yr-old dad’s suck it up.
    • The sooner you can solve anything your problem is, the better, my rheumatologist said that. I’m 24
    • people are more conditioned than you and they get up to work. We all got aches and pains, because we’re old.

    6th is Do Exercise

    • I’ve got RA and Fibro. I’ve got RA. There are people who suggest I go out and walk like I’m going to… 2 miles per day, 6 days a week for 20-2 years. Because of RA, I need new knees and a back surgery… I can only begin walking again.
    • Train more, get into normal sleep

    7th is “You’re so young! “

    • You are younger than that! No,
    • you’re going to grow out of it. Out of it I’m not going to grow. But thank you.
    • You’re young enough to be in this great pain–from the numerous physicians
    • You’re always in pains. If it bothers you so much, why do you not give up work?

    8th is It’s not that bad

    • It’s not so bad you’re supposed to try working so many hours a day. All I could say to them was that I wasn’t able to stay on my feet for three hours without my pain being so bad that I was barely able to walk to take a break when time came.
    • The only thing in pain you’re not. Oh, I’m on handicap. Recall?
    • We all get up and deal with pain. “Everybody has pain.
    • Get over it I’m paining constantly and I go to work still you need to be stronger and put the pain at the back of your mind! You are being lazy
    • Everyone has aches and pains”

    9th is You’re Lying.

    • “These people are mankind’s garbage, trying to steal money of people who work.”
    • I told my sister that an interview was going poorly because of my fibroid fog.
    • “While they are not working, I can tell you how to walk, so you’re lying.” She told me she didn’t think “this is one thing,”

    Click here to Get these Products or Visit Fibromyalgia Store

    10th is “At least it’s not cancer”

    • Not cancer, at least,
    • Comparing people to another disease, essentially if you’re not dying, it disregards the fact that a chronic syndrome without treatment does not affect your entire life.
    • I had someone tell me the other day that my fibromyalgia showed that I couldn’t have bad omg. I told that she needed her ignorant self to educate that woman.
    • I have that from my ex-wife, it’s not the worst then cancer!
    • “Is not autism alone?

    11th is Who told you?

    • My last appointment as a doctor, my doctor told me who you told me that you were fibromyalgia? would he stab me in my heart so well?? Certain docs just don’t think until they open their mouths…. Set me really back
    • I was treated just like I was insane. Some don’t believe Fibro to be real. I had it a couple of times. Hope you never have a right condition for pain

    12th is Eye Roll -Making us feel Guilty

    • My6-year-old daughter told me that she couldn’t play her friend because she had to look after her sick mom.
    • My 12-year-old daughter asking if we could go any place, and first of all I would like you to be better so that we can do more things” “DONT WORRY MOM THERE ARE LOTS OF PLACES TO SIT……
    • “You have to be gladder”
    • “I don’t have anything to say about it, but I’ve got plenty of eye-rolls, sounds like” we go here again ”
    • I’m guilty of being ill.
    • Get your pain under control anyway, “my brother after having missed another family,”
    • The worst thing ex told me I was just a burden for him.
    • He’ll get your pain under control somehow. He never wanted to take care of me. When I spent years looking after him, I took him to surgical doctors and knew what he should do. But the cake was taken. For him, I’ve been a burden.
    • They’re not making that pill?

    I think those comments follow almost everybody with a “hidden” disease, some of whom also have no hidden disease. In your comments, tell us if you heard one or two of them … tell your friends and family to let them know that they’re hurting us.

    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

  • EBV The potential cause of Fibromyalgia, research says

    EBV The potential cause of Fibromyalgia, research says

    By: Dr Alexa James

    It is expected that 9 out of 10 adults were somewhere in their lives infected with the Epstein-Barr virus. The virus causes no severe symptoms for most people. It is good that you actually didn’t know at the time, if you were infected with it at some point.

    However, some people may experience the virus significantly more severe and have repeated symptoms for years. People with fibromyalgia are particularly vulnerable to the virus and it can explain some of the odd symptoms people often report.

    The virus causing mononucleosis is Epstein-bar. You could use the nickname “mono” to better know this disease. It is also referred to as a “kissing illness,” because you can spread it one way to another. Even if Epstein-Barr (EBV) is not a household name, without your knowledge you’re probably infected. Many people are carrying the virus, but they’re not getting sick.

    Research in the Neurology and Neuroscience Journal says that EBV is the potential cause of fibromyalgia.

    EBV’s an awkward bug. It is most commonly known as mono, or ‘ kissing illness, ‘ as the cause of infectious mononucleosis.

    Mono recovery has long been known, and repetitions are characterized by extreme tiredness.

    Abstract of Research:

    “Fibromyalgia (FM) is marked by chronically wide-spread and mechanically pressured pain lasting for at least three months in at least 11 out of 18 points of tenderness. Unknown is the reason for fibromyalgia. Several hypotheses including’ central sensitization’ have been developed. This theory suggests that patients with fibromyalgia have a lower pain threshold because painsensitive neurons have increased reactivity in the spinal cord or brain.

    Some investigators assumed the pathophysiology of Fibromyalgiaassociated symptoms could be involved in various Neuro-sender (serotonin, catecholamine). It has been proposed that FM be linked to various viral infections. Because of symptoms similitudes, Epstein Barr virus (EBV) has not yet been demonstrated. The association was considered as a possible cause of FM.

    The purpose of this study was to determine the prevalence of IgM and IgG antibodies to EBV and the presence in the FM group of patients of viral infections. We also analyzed the association between the titer and various clinical symptoms of antiviral antibodies (serotonin, noradrenaline and adrenaline). The results show that high EBV IgG levels correlate with the intensity of pain and associated clinical symptoms in serums for FM patients.

    Click here to Get these Products or Visit Fibromyalgia Store

    This is in line with the fact that FM is associated with the immune reaction of some infectious agents (e.g. EBV, CMV), “published in the Neurology and Neuroscience Journal.

    A large percentage of FM patients are caused / causing by the Epstein Barr virus. As previously noted, although IgM antibodies are missing the presence of active infections correlate with a higher IgG antibody. In general, this infection is not an acute but an intracellular reactivation of the old disease; an increase in IgM antibodies is generally not seen when EBV is active.

    Fatigue is also a common symptom of FM and viral infections. So it is not surprising to find evidence of infection with pathogens like EBV among these patients in both early studiation of FM and the associated syndrome of chronic fatigue.

    One observation made by Moldofsky is the effect of acute viral infection on the development of FM pregnant sleep disorders. The capacity of the EBV encoded protein for early non-structural dysregulation and the instigation of clinical symptoms like fatigue have been discussed in recent publications.

    Connection of Fibromyalgia with Infectious Mononucleosis

    An acute Epstein-Barr virus infection is infected with infectious mononucleosis. This condition involves an increase in splenomegaly, widespread lymphadenopathy and hepatitis-associated white mononuclear blood cells. Kissing disease is also called glandular fever. In childhood Epstein Barr can cause infection that later leads to glandular fever. EBV contagion. EBV infection. It can be passed through the mucus and saliva from person to person during kissing, coughing and sneezing.

    Symptoms of fibromyalgia associated with glandular fever

    You will not waste your time, if you experience jaundice, discomfort, nausea, etc. Get your treatment done immediately. Your hips, shoulders and neck will achor every time you’re exhausted. You are going to lose appetite and have trouble sleeping. 

    Swelling and loss of appetite around your eyes must show signs. It is a symptom that your fibromyalgia flares up if your muscles are bad. Heart problems, depression, and anxiety are other evidence that glandular fever is associated with fibromyalgia.

    Management

    After some bed, doctors are recommended to progressively return to normal daily life activities. Stay moisturized. Stay moisturized. After every two hours, drink water or juices to avoid dehydration. Avoid exercises such as jumping, running and swimming. Stay with aspirin since aspirin can result in rye syndrome. Gargle for sore throat every day. Every time you feel low close your eyes and breathe deeply. Slowly breathe in and exhale.

    This will exhale all of your concerns, and you will soon have no pain. The consumption of sugar should be reduced as the lymphocyte activity can be reduced. For you, soup is best, but without preservatives. Have small foods in place of heavy foods. Zinc-and vitamin C fruit and vegetables work best for you.

    Instead of sugar, raw sweet should be used. Stay away from the person with Glandular Fiber Fibromyalgia to protect yourself. Before using them again, useful vault should be washed. Better than cure is prevention. Medicines that are antiviral may also be used.

    Other Diseases Caused by EBV

    EBV is best known to cause mononucleosis but can lead to other diseases less frequently, including:

    • Infections of the ears and childhood diarrhea.
    • Guillain-Barre syndrome
    • Some cancers, including Burkitt Lymphoma and Nose and Hore Cancers
    • Study also show a link between EBV and MS but further research is needed to determine whether the virus can lead to MS.

    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 live on a solitary journey with fibromyalgia

    To live on a solitary journey with fibromyalgia

    By: Dr Alexa James

    A Life Not Fully Lived

    A lonely journey can be fibromyalgia and chronic pain. Although it is a lonely journey even if you are surrounded by many people. It’s warm and inviting when you’re “your people.” But yet, you try your best not to give your discomfort and pain away. You feel your pain and struggle when you are alone and you know that you are always going to live it. If you feel’ ok, ‘ even if you don’t know you should push your limits.

    You feel the pain and the fight and you don’t know what to do if you feel bad. You have never seen anyone before when you meet yourself, your heart runs joyfully but in panic. You’re glad to see them, but, “How are you? You get the question. “The correct words to say can’t be found. “Where are you working? where are you working? “Or,” How are you working? “Words fail you once more.

    You don’t want to give your hand a tip, you won’t admit it’s not all right. Naturally, they want to know why if you tell someone you don’t work. However, without a long explanation request, how can you answer that? And without further questions, answers?! How do you make anybody realize that? I want to work, but I don’t agree with my body. My body doesn’t say it!

    But, tomorrow, the deeper problem is, I could feel “OK” enough to try to take part in life. My life could be manageable tomorrow. So, on manageable days, what do I do? I might try to “catch it up” on those rare occasions. I’ll try to catch up with things I’ve put on the back burner, because my body said nothing! But tomorrow will catch up with me when I “catch up.” For at least a few days, I’ll inevitably’ pay’ for it.  I want to live my life! I want to live my life! I want to work! I want to work! My life and my family I want to enjoy!

    But it’s affecting my life and my family. You are suffering from pain, you are suffering from fatigue and your physical limitations are affected. Fibromyalgia and chronic pain affect them. This condition, which nobody has the answer, is now my life. My life is all about tiredness and pain. Now my life is about my physical limitations. In every day, I will try to find simple joys.

    I’ll keep trying to celebrate the small victories which everyone else may think are small. The fight I can’t win will continue. I will. The purest, most honest and most hardcore person I can be, I will continue to try to be myself. Perhaps my body will abandon but God will never give up my spirit!

    Life as you know suddenly takes a new turn when you are diagnosed with a chronic disease. You fight to accept it first and then try to learn how to live with it. So many things will change in your life, things that you once did without a second thought require you to draw energy from a pool that doesn’t exist.

    Plans now “depend on the day” and how you feel. Now you have to wait for anything you have every intention to do. Your body will never be the same, and your mental health will certainly be affected. You will enter and leave depressed mental conditions, guilt and sense of meaninglessness.

    There are five stages of grievance, most of us have some or all of these stages of chronic pain. One day my therapist informed me of the possibility of a person being diagnosed with a condition such as this, and hence also the stages of grief.

    But I’m going to address that in another article. But what about a person who has a chronic disease, could they learn anything? Here are a number of things that can teach us about chronic disease or chronic pain.

    Click here to Get these Products or Visit Fibromyalgia Store

    Patience:

    From the day we suspected that something was wrong physically with us, we had to start looking for a physician that we could trust to help us find answers. This is not an easy task, as we all know and experienced. Many times, chronic doctors will see several doctors before finding a doctor who takes us seriously and will help us get some answers, or at least a direction to get started.

    There is a virtue of patience,” well, that is not truth. We all know well that this is not going to happen, as much as we want immediate answers. We therefore need to learn the lesson from the Tortoise and the Hare, the race will win slowly and steadily, well, perhaps it won’t win anything other than that. Patience will lead to a better understanding and understanding of what life will be like now for us and those we love. We must be patient with ourselves, most importantly.

    Understanding:

    Once we know this chronic condition, we can begin to understand how it affects our lives. Things in our lives will change and what our limitations are now to learn and understand. We have to understand how this affects our families and those we are close to, and not just us. It is important to understand a broader view of what lies ahead.

    And above all, it will be different to understand that life as we knew, and we need to understand that it is “New Normal” and we need to find out what life will be and learn to live this “New Normal.”

    Acceptance:

    When finally diagnosed we are full of fear, sadness, anger, and many other emotions, including relief. Finally, somebody gave us a reply as to why we feel how we do it. Once we learn to accept this and learn how to adjust to this new life, we will learn how to adapt.

    There is no time to learn this acceptance piece, but once we have reached it, we can start to move on and learn how this new life goes, accept our’ new normal’ and start again.

    Appreciation:

    It was a good day every day. Well, there are few good days and far from it. If / when they come, we really have to enjoy the “good days” and appreciate little things that make us smile every day. However, consider “understanding” part of this is that, because it will cost you afterward, you don’t want to overdo anything on a good day.

    It is priceless to appreciate the time you can spend with your family and enjoy all the activities you can do. Enjoy your hobbies and activities to keep your mind from your pain. You can still. Enjoy what you have against what you have lost.

    Love:

    It is not because those of us with chronic pain, chronic condition, don’t know or feel any kind of love before this diagnosis, but now, or should I say, we have a different level of love. You have the profundity of love and caring, because it’s said with no judgment, if someone you really love and care about, can look into your eyes, if your worst is, and say “I understand and wish I could help you.”

    There is not a certain number of things that someone can learn during this “new life,” but we can continue to look for good or positive things. It’s much easier said than done, and it’s sure a process, and trust me, I still try every day to find it. Some days are certainly easier for me to find peace or positiveness, but if I find it, I will continue to search for it and enjoy.

    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

  • Recommendation 22 Lingerie Brands Women with Fibromyalgia

    Recommendation 22 Lingerie Brands Women with Fibromyalgia

    By: Dr Alexa James

    The last thing you might want to do is put on a bra when dealing with your skin’s sensitivities and extensive fibromyalgia pain. You can feel totally comfortable when at home, in several layers or with a small chest, and skip a bra entirely! But there are times when a bra feels essential for many women.

    Maybe you feel uncomfortable physically and unbearable without it or need to run commands and feel self-aware. Many people go for tops that have cami built, but a jersey panel with some elastic won’t incise if you need or want to have more. Sports bras, the trendy “anti-bra” throng proposal would also not be a strong choice since the bra’s tautness can cause a lot of discomforts.

    On these occasions you will need an applied bra that is soft, not too tight and not add to the pain that you feel when facing sensitivity and generalized fibromyalgia pain. As anyone with fibromyalgia who has been a shopping bra knows that many bra and brands are not going to do their job, people with fibromyalgia can be seen as painful in light touch. That’s what allodynia is called.

    The result should be that clothes are loosely fit, lightweight, and not limiting. “Tight clothing is the enemy, in other words. It is not surprising that bras are high on the list of clothing, with all the straps and cables not to mention their close proximity to the skin, causing chronic pains among fibromyalgia females. Many women with fibromyalgia do not actually get on their arms due to the painful feeling.

    To ensure that arm and underwear help instead of damage, choose loosely fitting styles that are not restrictive and easy to pull on and off.

    We ask the Community of “why fibromyalgia” a question: “If you are having chronic pain, what kind of lingerie are you finding comfortable? What do you find in our community?”. Many Members have answered and have spoken to us. Bra is painful to your ribs and back. Most people prefer not to wear bra or underwear, as bra causes more pain and spasms for them. Most also like wearing camisoles.

    Click here to Get these Products or Visit Fibromyalgia Store

    Note: Initial names are used for confidentiality. We don’t promote bra brands, we just share what other fibro women do.

    Here is what the community share with us:

    1. The only bras I found I can wear are Sainsbury. Sometimes, they only stretch but also have soft touches for normal bras. they do also make a soft touch.
    2. “LACE BRALATTE SHEAR RHONDA I wear” I wear. No hooks, no seams. Seams. I need not fight. I don’t need to fight. Cotton night shirts as far as sleep is concerned. I appear to have a sensory problem with materials, particularly recycled materials.
    3. SOMA makes for me the softest underwear I’ve been trying to make. They’re skin sensitivity friendly to their bras, slips and pyjamas.
    4. The most comfortable thing to me is “Curvy Kate,” and it gives me the best support. In the bust area I’m not small never had a hard time wearing an unwired bra.
    5. I like Victoria’s little secret for me. Makes me look sexy and luxurious even if I don’t feel it.
    6. The Bryant Cacique brand is the most comfortable and stylish one. Moreover, without the wire in them, it is difficult to find bras. -M.C-M.C.
    7. Panties of 100% cotton grannies. When I was pregnant with my oldest child, I discovered how comfortable they were. I’m wearing the good old grandmother’s slippers. The new super-thin super-soft type are the night gowns. They’re long t-shirts, however. And they’re in Walmart. Unless I’ve got a firm or go somewhere, I rarely get dresses. And I’ll go back in the second. In the nightgown, I am back. I’m back.
    8. “Fruit of the Loom” makes great sports bras!! And purchase your underwear a size or two larger, so that it isn’t tightly tightened by the bandage too.
    9. It’s “Women’s wear Hanes,” to me anything that’s comfortable with Haynes brand.
    10. Non-underwire bras and cotton (heathers) fruit of Warner’s loom.
    11. Sloggi is certainly the comfiest!
    12. Target nightgowns for Gilligan and Omalley Modal. They have an adjustable bra, which is really uncomfortable and soft, and provides decent support. OR 1 of my marriage crew sweatshirts + sports bra + lularoe leggings over large hanes. 
    13. My bra is Glamorise through Amazon, I’m very heavy and I tend to wear big t-shirts for nightgowns and my daily robes, so they’re comfortable. L.–H.
    14. No shop or brand in particular. Have a super sweet George brand nightie with broader straps a few years ago, loose from Walmart. One of my preferred ones. Any loose jackets that fall down in the middle of the thigh.
    15. I found coobies a few years ago. Love love love them. Love love love you love them. Bra and shorts for sports and boys.
    16. Stoffe from bamboo is incredible.
    17. JOCKEY FOR HER, French… all cotton
    18. Boy shorts, tanks built in in bras & only a small, light, satin slip for’ night’ time. Soft, convenient and straightforward. Like the mark.. Super soft or natural anything. Anything. Shorts Cotton boy. It’s comfortable and adorable! They can be found in many colors and patterns. I don’t wear a bra or Yummie one.
    19. I really find the complete Primark briefs comfortable! Cotton! Cotton!
    20. Comfort bras for Marks and Spencers. Or a plant top if it hurts.
    21. Hanes briefs only with cotton.
    22. At La Senza & la vie en rose, I buy seamless arms and panties. You must be washed in unscented tide & no tissue softeners. In the evening I like to remove my bra and get into my stretching cotton, la vie en rose pjs!

    Click here to Get these Products or Visit Fibromyalgia Store

    Few tips on shopping Bra

    1st Tip is Cotton only

    Stay ahead of synthetic textiles. They are not well respiration and can cause humidity to build up, which makes it uncomfortable to wear. Airflow is promoted by natural resources. A microfiber blend will be your best gamble if you have to deal with a material that is less than normal because of financial constraints.

    2nd Tip is Front closures

    For many people with fibromyalgia, this is an important point. They often have problems reaching around to close and open their bras with joint pain and increased sensitivity. Hanging them on the front and turning them can lead to pain in responding bodies already. Rather, it provides an easy alternative to a bra with a foreclosure. The advantage is that these braces ‘ backs are often much lighter than conventional.

    3rd Tip is Getting your exact size

    This is the problem for many people. It is essential to make sure your bra is well fit. Some pain problems can be solved by simply fitting a bra rather than adivinating the wardrobe professionally. While one-size-fits-all answers (or bras) are not provided, a few options are possible. Couples that have no braces or any kind of band, but are not a permanent solution, can offer support. Some people have also found easy’ invisible back’ arms and freedom / revival bras.

    The important thing is to find something for your body that works and not to “fix the least of two evils. And I’d recommend trying Wacoal red carpet strapless, Wacoal’s t-shirt bra, Spanx bra-leluya or the post-surgery bra of Amoena available from Nordstrom. Many women also note that looking for the perfect, painless bra is quite costly.

    Some women have used bra-less, but this has caused their own difficulties. For many, the solution is to fit a bra personally. Making sure your bra fits well is a great way to minimize the chance that your Fibromyalgia will get worse.

    The leading brands for fibrous women are:

    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/
    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’s Best Exercises and Workshops

    Fibromyalgia’s Best Exercises and Workshops

    By: Dr Alexa James

    Chronic body pain causes fibromyalgia. Continuous tissue and muscle sensitivity can cause problems with sleep. The painful regions can include the neck, the back, the elbows and the knees, which are sometimes quite severe. Their bones are also called “tender points.” Fitness can help to soothe your fibroid pain and help you cope.

    It seems counterintuitive to strap on your running shoes and go for a jog when you’re struggling with fibromyalgia. In the past, doctors have recommended rest when pain erupts, but new investigations have shown that fibromyalgia exercises are helpful during fibromyalgia and can actually be helpful in preventing it.

    Less Pain, More Energy

    Don’t let fibromyalgia’s muscle pain and tiredness sideline you. You could and ought to move. A few simple exercise tweaks can improve your energy, ease pain and rigidity, increase your mood, and enhance your sleep. Before you start, check with your physician.

    Get active

    As the first course of fibromyalgia treatment, many doctors recommend a fitness and exercise program. This is before any medication is considered. It is important to remain active, even if your doctor prescribes medication for your condition. Movement should be a key element in your treatment plan as a whole.

    Research shows that 12 weeks of moderate aerobic training combined with strength training can improve pain and well-being in general. According to the Cochrane Library. According to the national arthritis institute, regular exercise is one of the best ways to treat Fibromyalgia.

    Walking

    It is an excellent type of light aerobic practice that lists the healing benefits: it provides your muscles with oxygen and nutrition to maintain their health, helps them rebuild resilience, boosts energy and reduces pain and stiffness. In fact, an overall review of research found that the most effective way to improve FMS symptoms is to use low-impact aerobics.

    Click here to Get these Products or Visit Fibromyalgia Store

    Replacement movement, or back-and-forth movement, helps relax” adds Iversen, who is also Chairman of the Department of Physical Therapy at the Bouve College of health studies at the University of Northeastern Bouve. The swimming and water in the hot pool (warmwater relaxes muscles, the water flourishes helps movement, while cold water can make muscles tense) and use the elliptical trainer (which is less impact than a bandwidth) are other effective types of aerobic exercise.

    Strength training

    Aching muscles may be balky at first, but force is an important component of physical fitness overall. It can be a good way to start working with a strength training video, and don’t forget to modify where you need to start. If you don’t have stupidity or want to start with lighter weights, take some canned goods and start!

    Biking

    A ride on a bicycle is an excellent way to practice low impacts without taxing the lower body. Muscles and articulations start warming and smoother when you ride. To start with, take a paved road and start with shorter routes and build progressively on longer trips.

    Low-Impact Aerobic Activities

    Aerobic activities such as walking, cycling and swimming can be started. You don’t even have to go to a fitness center to practice. You can just walk across the park or swim at your country club. Just say that for at least 10 minutes a day we are engaged in this physical activity.

    Household Chores

    Household tasks may not classify as a workout if you want to lose weight, but they can help considerably if you just try to stay active and fit. Don’t cut homework because of your condition but try to do those things that are right for you and can help you. Gardening, mopping, mowing the lawn and taking out or playing with your children are just some fewer challenging activities which will always keep you active.

    Bodyweight exercise

    Fibromyalgia bodyweight exercises are easy and convenient because your own equipment is the only thing you need. Seek videos or classes to adapt the exercises at your own pace and make it easier for you to start and more difficult to get going. Fibromyalgia exercises have certain special considerations, particularly if you have a comorbid state. Before starting any new exercise program, it is important to talk to your doctor.

    Turn up the Heat

    Swimming and water sports are a form of mild aerobics, and by swimming in a heated pool you can improve the results of this exercise. Many studies have demonstrated the potential for significant fibromyalgia relief by exercising in a pool with warmed water. This is perhaps one of the best fibromyalgia exercises and within a few weeks you will notice results.

    Stretching

    Do that at least once a day to improve flexibility, loosen tight, rigid muscles and increase the range of motion that will facilitate daily movements, such as watching over your shoulder or reaching a ladle on the top shelf. Extending during workouts can also help you tolerate better training.

    Click here to Get these Products or Visit Fibromyalgia Store

    Balance Training

    Chronic pain not only affects joint mobility, but also affects your balance and restricts activities. It also affects your balance. With a poor balance, there is a great risk that you will fall, which can become even harder if you have chronic pain. Balancing training activities can help you considerably to address these problems and also improve the functionality of other activities.

    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 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.

    Click here to Get these Products or Visit Fibromyalgia Store

    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

  • I’m searching for the pain relief, not for the pain. Oh, I’m searching for bread administration, not a miracle!

    I’m searching for the pain relief, not for the pain. Oh, I’m searching for bread administration, not a miracle!

    By: Dr Alexa James

    The chronic pain of such a hot button is pain relief, pain medication, and the treatment of pain. People believe that people who are suffering from chronic pain or seek pain medicines can not go beyond the truth. Individuals with chronic pain and chronic pain seek one thing alone, pain relief or pain control. Unfortunately, many pain conditions are widely misunderstood, especially fibromyalgia. Fibromyalgia, therapy and management of this condition are very little understood. In some instances, fibromyalgia is the most painful misunderstanding and how to handle it in all aspects, especially the pain.

    We suffer from other conditions that also cause pain for most people with fibromyalgia. Autoimmune conditions, arthritis, degenerative disk conditions, spinal problems, etc. On top of fibromyalgia, all of these conditions cause pain, daily pain, relentless pain, uncontroverted pain! So, what do we want from life, pain management and pain management, but above all, understanding of our pain! So why can’t we get so desperately needed pain relief???

    The best solution is, right now, the current epidemic of opioids. I’m not here to begin a discussion about this but simply to debate how it has an impact on people like us. People like me who suffer every day, people who want to have better than bad days, people who want to have a sharp edge removed from what we feel every day.  First and foremost, we are trying to find a little relief for people suffering from chronic pain and pain. When we tell an average person that they will have pain from now on every single day, not just headache or joint pain.

    Pain which will continually disrupt their lives, pain that makes it nearly impossible to perform “daily” tasks, pain which makes good sleep difficult, pain that makes it impossible to work, pain in your social life, pain in your family, your day-to-day life, pain that makes life easier to enjoy, well, impossible! Well, I don’t think masses would be silent if we told the average person that this is their life from now on!

    Those of us who suffer the way we do want nothing but hope and a little relief. Some people could “work the system” to get pain medications, therefore there is abuse of pain medicines, pain med addiction and opioid drugs. Unfortunately, some of those suffering from addiction and abuse simply sought treatment for pain. The healthcare system was left rolling due to these problems!

    The sufferers left unfortunately are the ones who benefit from pain medicinal products and need them for a life that is somewhat’ tolerable.’ This is so wide-ranging topic that you will try in one article to address so many avenues and a controversial subject. But rest assured, chronically painful people want to listen, we want a voice, we want to say a saying, we want a choice. And the headline on local news speaks of excessive deaths as I write this. We fight to make our voices heard, no wonder!

    Click here to Get these Products or Visit Fibromyalgia Store

    Now please understand that I don’t want to promote the use of pain medicines in an unnecessary way, nor do I try to normalize the use of pain medicines. I hope that there will be more options. More options for pain alleviation that will ultimately make pain patients feel like a ‘ drug seeker. ‘

    A handful of medicines can be used to treat pain related to fibromyalgia that cannot be discarded, although many individuals with fibromyalgia can also be diagnosed with a slew of additional pain and fibromyalgia, and some of the treatments for fibromyalgia do not exist where our options and access to appropriate pain management are very limited. And some of us have serious reactions to the drugs that are out there, or they just do not work for us.

    We want a treatment plan to help relieve some of our pain, medication, therapy. Many of us have taken the path of uncertainty and unsuccessful treatment. Medicines and therapies work for everyone differently, I’ve spoken it over and over, and what works for one person can not work for another. The side effects of one person are very different from the effects of another. Nobody has the same body chemistry as anybody else. It is difficult to treat pain that what works for one person, can work for another or cannot, does not all people react to a certain medication or treatment in the same way.

    It is a way of hope that we have to find. Hopeful and hopeful abundant, the “alternative” therapies will improve and broaden our options for relief from pain. It is hoped that we will not feel like a drug addict if we need pain relief. We also hope that a physician who will assist us can finish without doubting us. With fibromyalgia, we struggle to get people to know our daily business even remotely, let alone to question our doctors about the validity of our pain and suffering.

    Unfortunately, now we are in a time of immediate dismissal or judgment if we have any type of pain. It must be stopped. The health care professional must be able to achieve the knowledge they really need on PERSON and PATIENT. The use of pain medicines may or cannot be included. But the more the patient AND the person understands the more hope they will see the whole image and not just a screenshot and can work with the patient to find a solution or to develop a plan. It’s time for you to find a new one, which I am finding at the moment, if you’re not in contact with your doctor or health care provider.

    Sometimes, especially when it comes to chronic pain conditions it is difficult to advocate for oneself. But we cannot give up! We must continue to fight for the United States! We need to struggle and hopefully find a common ground or a decent treatment plan. Nobody with chronic pain expects to live entirely without pain; we know that this is a totally unrealistic objective.

    But what can we hope to find is a treatment plan that addresses the most, if not all, of our needs and a plan is provided to attempt to achieve them and, most importantly, we want a healthcare provider who understands our struggles and is ready to listen not only to our needs but is ready to help us try, regardless of what the treatment plan involves, to achieve a pain management goal.

    We’re all looking for the same outcome, whether it’s tomorrow, next week, next month or years away. Those who are suffering from chronic pain simply want to see what we are suffering and to find options so we can “live the best of our life! “We do not need to seek the pain medication, we want the control of pain, we don’t need the pain medicine, we want the treatment of pain. We want to understand and support, however, most of all!

    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

  • 25 “Fibro Fog” Unforeseen side effects

    25 “Fibro Fog” Unforeseen side effects

    By: Dr Alexa James

    Is there a fiber fog? It feels that you’re dazzled by the simplest things, you can’t remember. You have a loss of memory and can’t speak the words you want to say. You find it difficult to concentrate, you can forget little information and even plan. You may feel confused, just as you can’t understand what is being said to you. The concentration and even a lack of vigilance and energies have decreased. It can be deceptive and depressing. This is one of the major challenges that we face every day. It can range from mild questions, such as forgetting the word hairbrush, to serious problems, such as the sense of confusion about why you are in the room first.

    Fibro fog. Current cognitive problems with fibromyalgia. Fibro-fog, what is that?

    You feel that you can’t remember the simplest things. You can’t remember. You have a loss of memory and may not speak the words. You find it difficult to concentrate, you can forget little details and even plans. You may be confused, just like you can’t understand what you’re told. Concentrations have decreased and even energy has been lacking.

    It can be frustrating and depriving, even. This is one of the most important problems that we face every day. It can range from mild issues, such as the forgetfulness of the word hairbrush, to the seriousness of the confusion of why you’re in the room. I will speak, have a word on my tongue, I’ll have a simple word, like hairbrush, and can’t say that word in my life! I’ll be talking! Rather, I walked through my room and dressed for the day to finish looking through a book of photos and then proceed out of the room. I watched a picture book and then a book of photos. That’d disturb me to the point of tears, and sometimes still. Time to admit to my psychiatric department. I feel like I go nuts.

    Here’s where we share community resources:

    1. Three times I’ve left my garden pants, because after watering outside animals I’ve forgotten to turn them off, and they’ve spent 24 more hours. After all the set of washers, if you forget about starting washing, come back to put the dryer in later. Think it’s not done, I’ve returned a call or sent an email. Forget about what I say… it’s so outrageous!!! –haggy

    2. I ask my husband to take me something high in the cupboards, for example, by replacing a word for another, but I say the name of that other object while pointing at what I want, if I have a glimpse of another object before asking him. I often ask him the “chair” in my kitchen cupboard that’s high up.

    3. My depression is heavily affected by the inability to talk normal. Sometimes I feel like my only meaningful conversations with my 3-year-old granddaughter. -Lisa

    4. I’m anxious to talk to people who don’t know me because my talk is quite choppy. I have a lot to pause and think about words or say the words off the wall that are null and void of what I say. I forget about appointments, talks and questions. However, the part which most disturbs me is that my level of intelligence has fallen dramatically can’t concentrate, like simply discovering issues or puzzles, and sometimes my brain can’t do much work. Occasionally, I drive down the highway and panicked, not knowing where I was for a while. I forget where I go and I’m going. My husband had the checkbook and the accounts to take over. I have messed up paying bills and balanced the checkbook too often when I did it perfectly well for years and years. Jessica

    Click here to Get these Products or Visit Fibromyalgia Store

    5. Once more, I’ll say this too. All of us forget stuff. All of us. Big gap between fibro fog and forgetting. I can easily forget to keep my food list. Like all others, just forgot. Forgetting Fibro Fog has a feeling. A dumb, hazy sensation. A sense of hangover. And I’m beginning to sling out my talk. For the frightening feeling and forgetful thing, I did, I go into panic. My brain tries hard to get to the side of the answer and literally you can feel pressure and hurt. I left the burner last night and decided that Tupperware was a great butter lid on the stove after cooking. -Sammy

    6. I start sweating and my body blows and I try to sit in the middle of grooming my horse. I must lie down, not move, no suffering like floating, for around 15 minutes staring straight ahead. All returns to normal after the fifteen. As normal as we get fibro. Margaret

    7. The worst thing is what we all share: the failure to find words, to blank in mid phrase and to feel stupid. I agree with that. Curiously enough, I write a lot better than I talk, and for decades I have kept newspapers. I’m so happy that I’ve been affected by many of my long-term memory. During flares, I kept a pain newspaper, a dream diary and so on. I must force myself to write a little nowadays but it helps to have a naked soul and not to make it out loud–Terry.

    8. Try to write down things and forget what I write immediately. I’m a cook and have to write on labels what food is and how often I fight to get the food right in front of me. I already write the date several times but forget every time. I have no choice. I’m a cooking assistant. This is so frustrating. So, dumb I feel. – Cory

    9. Go to the airport to pick up my daughter and realize I was going in the wrong direction! Times when I can’t figure out how to get there are thousands of times! Words can’t remember, can’t spell when you talk…. –Alexa

    10. The most frustrating thing for me is that I cannot follow the word. It’s like I hear it, but it doesn’t work in my brain. Words that are wrong and things that are misread are also frustrating, especially because I like to read and write and have always been very good at them. Forgetting about what I’m doing is something else, but without fiber many people do so, so it’s not just as embarrassing to ask someone to reply.

    11. In the second year of the tough doctoral program, my chronic fatigue brain fog first hit me, where I was assumed to have excellent memory and skills. I started asking my professors, and even some of my colleagues, if I was part of the programmed, and felt like an impostor. There was nobody talking about chronic tiredness or brain fog at that point, so I felt I just lost my mind. So, a pity.– Rimse

    12. Losing the mud-thinking phrase, even the middle word. Put the milk into the wardrobe, cereals in the refrigerator, leave oven for 3 hours, use a calendar to keep track of the new medicine. Increase schedule, daily pills had to be purchased because I forgot whether or not I used medicines. Set an alarm 2 times a day to remind you of medication. -Shannon

    13. I could not remember this summer, on holidays at the lake, how to deal with a solitaire game–something I did a thousand times every summer of my life. I had Google. I had it to Google. I sat then crying at the table because I’m new to that symptom and I’m afraid of that. –  Kible

    14. I work in the hospitality and I literally look at the cash register to make a customer change and I can not make a registry because the fibrofog makes me confused and I only forget what I say in the middle of the sentence. Kelly

    15. Oh, I’m just chatting when I need to speak with a repairman, customer service etc. That way, I can’t sound like a jerk on the phone. I could have time to reflect on what I want to say Aimee

    16. Phone number mixing up. Often I have to ask people to write me or put their own phone number, l mix the number sequence up tox inconveniently– Amma

    Click here to Get these Products or Visit Fibromyalgia Store

    17. Because I forget their names, I can’t introduce people. Just like the names of my parents. I forgot my own name. I forgot my own. I had them after flashbacks in particular. It’s awful. It’s awful. My brain goes blank and I forget about talking, saying the simplest phrases or doing things to help me. Things and what’s going on to me, so they could understand, I told my family and good friends. They were awesome, apart from my mother. She is simply not open to it. I’m always not familiar with the date. I’ve got lots of advice. My calendar, my phone notes, lists of things to do. –Cynthia

    18. Cooking! I’m on a budget that is very limited. It makes me want to weep when I burn food, because every bit is precious. I continue to forget that I’ve got food on the stove. But I keep forgetting to set it. I’ve got kitchen time. This way, I have ruined many of my favorite pots.– Eva

    19. When I couldn’t follow discussions at work, I noticed the fibro fog. I wrote legal papers and supported my colleagues, and I was frightened when I began to fail to understand what people were saying to me. What was happening, I didn’t understand. My fiber symptoms have been getting worse and I can do what I need to do now in order to try and cope with my work I have been retired for 35 years and it was a good choice. My friends and family came to expect my forgetful words, names or places. I can laugh about that now, but still very frustrating. I can laugh about that. –Dolly

    20. I think I’ve all had at one time or another. Because of my delayed time of action, I no longer drive. When I stood before my children, I always felt so bad that I could not remember their names completely. Fortunately, now they’re older and they know that Mummy isn’t trying to be funny. At first I thought I was losing my mind literally and went to Doc for Alzheimer’s and Detention to have him check it out (age 45). It wasn’t so bad until then, then it just got worse. I forget what I do when I do. Trying to type this was a frustration exercise and I lose my thoughtfulness and need to continue to figure out what I was speaking about, or write in a word that is not even near the word I want to say. Some days I just want to shout that when I’m with someone, my brain will just go away somewhere. Yes, that’s helpful, when I remember, to know that I’m not alone. Olivia

    21. When I speak, I get my words changed. When I tell my daughter, for example, that she has to remove the trash, it turns out that “you have to waste it.” Failure to drive, too. I suddenly feel lost as I don’t know where I am or where I am going when I drive in a familiar area. Forget what I say in the middle of the phrase. I wonder if I said loudly something I thought. –Pritey  

    22. I find it difficult to follow the easiest directions, for example on the side of a rice box, pasta, etc. I must ask my husband for assistance many times. That never thought, but it did. Sandy

    23. Go through the food shop with a list and then don’t know where I’m going and walk– Simi

    24. Once my son asked why my bag was in the refrigerator. I looked and it was there, sure enough. I was therefore looking where I kept my bag normally and the milk was there. Couldn’t remember what to call an appliance for a kitchen, it was always called the “garage of dirty meals.” My son asked if the dishwasher was meant to me. Oh, yes, I meant that. Twice, I couldn’t find out where I was suddenly while driving. Nothing looked familiar–not road signs or companies. I could figure it out until something finally got my brain in place.

    Over 20 years, I’ve been living in the same city! It frightened me! I’m going to be at my house and just stand because I want to watch TV, but I don’t understand what to do first, and I’m going to want a glass of water. I just got to get to do something, finally. Speak with me loud and concentrate all the time. I often “twist” the words because of “verbal dyslexia” when I speak. For example, knives and forks are turned into knorks and fifes. Fog could turn into foog. I’m using “thingie,” because I can’t remember the word for them, to describe things a lot. I started saying bluntly that I can’t think of the word to the people. So until we get the right one, they’re helpful and say words.

    25. Occasionally I can’t remember if I eat and I just realize I didn’t feel wonky. I’m also forgetting when I’m driving home after doing something which takes concentration, like driving to the shop. I have to trust my car pilot at times like that, but it’s frightening! Lavit

    Well, let me say what I am confronting when this article is compiled. I forget how many comments I have already listed, I forget about the wording of the person who shares his views. I forget that it has already been covered, while reading the comment, so you may also see a few repetitions of some issues in the article. In the image below, a summary. Please inform us in the comment section when you want to add or share your experience in the list. “Chronicillness.com,” because we found the question on their website, would also be appreciated for the issue.

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • The Holding foods for fibromyalgia

    The Holding foods for fibromyalgia

    By: Dr Alexa James

    Fibromyalgia is a condition that causes muscle, joint and tiredness and depression pain. There are certain therapies that your doctor can order, but fibromyalgia consumption foods can help you to control this disease and improve your symptoms noticeably. A person-to-person diet of fibromyalgia should differ because some foods that are typically in a balanced diet might cause allergic and other adverse reactions.

    It is now well recognized that the syndrome is genuine and affects millions of people every year (in the United States only), but it may not be so clear that it has other characteristics.

    For instance, it is still not widely known what causes Fibromyalgia to develop. Naturally, most doctors agree that the disease is neurobiological or functional, and most of them will decide that their development is closely related to the imbalance of the brain’s neurochemical element, which causes the brain to incorrectly process the pain. All else, however, to a certain extent is still vague.

    While a list of clear reasons has yet to be completed, one of the risk factors may lead to the syndrome. Genetics, diet, stress and other psychological factors play an important role in these factors.

    Other symptoms commonly seen in patients with fibromyalgias are headaches, tiredness, sleep disturbances, bowel irritation, weak appendages, tingling and numbing fingers and limbs.

    Since it is not clear why Fibromyalgia is actually present in some patients, there is no real cure for this syndrome. However, their different symptoms may be treated and improved, and a number of things are suggested and recommended by the doctor in these situations.

    Click here to Get these Products or Visit Fibromyalgia Store

    It is most likely to prescribe a combination of drugs, which include pain-releasing, anti-inflammatory and even benzodiazepines and antidepressants.

    Furthermore, most of the doctors are advised to take advantage of natural or alternative medicines: yoga, meditation, acupuncture, tai chi, etc. Basically, it could also be suggested to simply walk or just relax in any other way.

    What causes fibromyalgia?

    However, some studies suggest trauma, stress, nervous abnormalities, and genes may lie behind it. This is still unclear by the research panel. The symptoms you are a candidate include muscle strain, pain, joint pain, abdominal pain, inflammation, fatigue, sleeping difficulty, depression, headaches, digestive problems, rigidity and stubbornness. These symptoms often appear alongside and usually the pain is general, not just an arthritis-like part of the body.

    What are the best foods for fibromyalgia?

    Any foods with gluten should be completely avoided for fibromyalgia patients. In many foods, from white to pastry, gluten can be found. The reason gluten is harmful is because, in most cases, it causes digestive complications such as indigestion, diarrhea, and abdominal pain. Next time you visit the supermarket, make sure you ask and store gluten-free products such as bread and avenue to avoid causing your symptoms.

    Fibromyalgia should include fruits and vegetables among your top food, because they include properties that keep your blood sugar well-adjusted, boost energy and reduce mood shifts. Tomatoes, green potatoes, spinach, kale, broccoli, sweet potatoes, berries, cemetery and tropical fruit, such as mangoes and papayas, are the most suited fruit and veggies in your regular diet.

    Similarly, fibro-myalgia foods are fed fish such as sardines, salmon, cabbage, herring, tropic and mackerel. They offer abundant proteins, fatty acids and can comfort muscle and joint pain. Bake or grill as a substitute for frying to obtain as many nutrients as possible. The amount of protein required to manage muscle-related symptoms is also available in eggs, chicken, pork and turkey.

    In place of trans-or saturated grease from packaged foods and junk food, you should also choose healthy fats in olive oil, nuts, seeds, advocates and butter.

    What are the worst foods for fibromyalgia?

    The food you should avoid depends on the reaction of your body to it. Many claims to have digestive problems and inflammation when they eat cheese, milk, sour cream and other milk-based foods. You can best find out how to keep a food journal in which you can keep a clear list of the food you eat to determine what foods you should not eat.

    In general, eat plants, fresh water fish and healthy fats as many as you can, such as fruits and vegetables. Switch your sweet juices and carbonated drinks to a replacement for fruit. Create a good calorie diet to manage your weight, drink plenty of water, and make a change as soon as you feel 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