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What Is Chronic Fatigue Syndrome Like

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You Have A Flu That Wont Go Away

What Is Chronic Fatigue Syndrome?

Despite the absence of research evidence linking CFS/ME to a specific viral or bacterial infection, many people with the condition report initially feeling as if they had a serious case of influenza or mononucleosis. They report being stricken with a high fever and generally feeling unwell. The problem is these people never recover. The fever may go away, but the feelings of fatigue, muscle aches and other flu-like symptoms linger for years.

How Chronic Fatigue Syndrome Is Helping Doctors Understand Long Covid

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Since the outbreak of the pandemic, scientists have learned a lot about COVID.

Long COVID remains a big mystery.

Long COVID is destroying lives. It is actively destroying lives. And right now, there is no known cure for long COVID, Dr. David Putrino says.

Meanwhile, researchers whove spent decades studying Chronic Fatigue Syndrome also known as ME/CFS, are saying, We can help.

There is a lot to be learned from ME/CFS research and it would facilitate whats happening in long COVID research and move it along a lot more quickly, if there was better coordination, Dr. Lucinda Bateman says.

Today, On Point: How doctors studying a condition that many in the medical community have long been skeptical about, could help reveal the mysteries of long COVID.

Guests

Dr. David Putrino, director of rehabilitation innovation for Mount Sinai Health System.

Dr. Lucinda Bateman, founder and medical director of the Bateman Horne Resource Center.

Also Featured

Hanna Tripp, director of operations for the Afghan Medical Professionals Association of America.

Related Reading

Recover COVID Study: RECOVER COVID The National Institutes of Health created the RECOVER Initiative to learn about the long-term effects of COVID.

This article was originally published on WBUR.org.

Copyright 2022 NPR. To see more, visit https://www.npr.org.

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Postprandial fatigue is a state of drowsiness that occurs after a meal. Typically, post-meal sleepiness hits 30 minutes to an hour after eating and can endure for several hours. However, the fatigue may also occur with a host of other symptoms, including: Brain fog and cognitive impairment. Nausea. Flaxseed. Flaxseed can be found in many different types of foods such as crackers, waffles, oatmeal, and many others. It can improve chronic fatigue, and it is generally very good for your body. It contains a high amount of fibers which can improve your digestion and make you feel full after a meal. This will stop you from binge eating. Add Some Spice to Your Life. Certain spices are particularly beneficial when it comes to minimizing inflammation and boosting your body’s healthy immune response. Super-flavorful options include ginger, cayenne pepper, cloves, garlic, cinnamon, and turmeric. Turmeric, in particular, is a powerful anti-inflammatory.

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Tips For Exercising Safely With Me/cfs

If you feel you can tolerate some exercise, be guided by your doctor or specialist, but general suggestions include:

  • Experiment to find the type of exercise that works best for you. Choose from a range of gentle activities such as stretching, yoga, tai chi, walking and light weight training. Often, people find exercises lying down use less energy.
  • Keep an activity diary so you have a long-term picture of your performance levels and factors that might impact on your symptoms. Some people with ME/CFS find they feel good straight after exercise, but then crash later on, so make sure you monitor how you feel, hours to days after exercise.
  • Stop the physical activity well before you feel any symptom flare. Pacing yourself is very important.
  • Remember that the amount of exercise you can do will change from one day to the next.
  • Listen to your body if you dont feel up to exercising on a particular day, dont.
  • Find out as much as you can about your ME/CFS. Make sure you consult with health professionals who fully understand ME/CFS as a biomedical disease

What Can I Do To Cope With Me/cfs

Chronic Fatigue Syndrome: Symptoms and Complications

Talking about your feelings with a friend or family member can help. Sometimes it also helps to talk with people who are going through the same thing. Consider joining an ME/CFS support group. See the “ME/CFS Organizations” section at the end of this fact sheet for a list of organizations that offer additional information on ME/CFS and can help you find ME/CFS support groups.

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Things No One Tells You About Chronic Fatigue Syndrome

Imagine feeling too exhausted to get out of bed, let alone go to work or spend time with your family. Now combine that kind of physical exhaustion with severe stomach pain, aching joints, and brain fog that makes it impossible to read a book or sustain a thought. Finally, imagine telling a doctor how you feel, and having him roll his eyes.

This is reality for many of those who suffer from the disease most know as “chronic fatigue syndrome.” There’s often little help or support available to them from the medical community or from friends and family.

“When you tell people how you feel, they say, ‘Well, I’m tired, too,'” says Carol Head, a recovered CFS sufferer and president of the Solve ME/CFS Initiativea charitable organization that funds medical research in pursuit of a cure for chronic fatigue.

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Part of the problem, Head says, is that non-sufferers hear “fatigue” and think they understand what a CFS sufferer is going through. But they really don’t. “People who have endured both chemotherapy and ME/CFS say ME/CFS is even more debilitating, so ‘fatigue’ is not a good word for it,” she says.

The “ME” in ME/CFS stands for myalgic encephalomyelitisan alternate name Head and other sufferers prefer to chronic fatigue syndrome. “CFS is such a lightweight name,” she says. “The term ‘myalgic encephalomyelitis’ has actually been around longer, and it has the advantage of sounding like the serious, real disease that this is.”

It’s often debilitating.

What Are The Risk Factors Of Cfs

There are a number of risk factors that may increase your chances of developing CFS, including:

  • Age: CFS is most common in adults between the ages of 40 and 60. However, it can occur in people of any age, including children and adolescents.
  • Gender: Women are more likely to develop CFS than men.
  • Infection: People who have had certain infections, such as Epstein-Barr virus CFS.
  • Stress: Stressful life events, such as the death of a loved one, divorce, or job loss, may increase your risk for CFS.
  • Genetics: You may be more likely to develop CFS if you have a family member with the condition.

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How Does It Happen

Doctors don’t know what causes ME/CFS, but they have identified different underlying abnormalities in people with the condition.

Immune system problems: Several parts of the immune system are different in people with ME/CFS. Some research indicates that these abnormalities may cause the symptoms of the illness. Fortunately, people with ME/CFS don’t have a defective immune system in the way that people with HIV/AIDS do.

Energy production: In you have ME/CFS, the cells in your body have trouble making enough energy.

Brain abnormalities: Abnormalities show up in pictures of the brain , in levels of brain hormones, and in the brain’s electrical system . These abnormalities can come and go, and aren’t necessarily permanent.

Blood pressure and pulse issues: When you stand, you blood pressure could drop and your heart might start to beat faster. You might feel faint or pass out if your blood pressure drops too low.

Genes: Some studies have found abnormalities in the structure of certain genes. Others point to abnormalities in the way certain genes are turned on and off inside your cells. Studies of identical and non-identical twins indicate that some people inherit a genetic likelihood for getting the illness.

Serotonin and cortisol: Several studies indicate that serotonin, a major brain chemical, plays an important role in ME/CFS symptoms. People with the illness have low levels of cortisol, a hormone the body releases in response to stress.

How Can Parents Help

Chronic Fatigue Syndrome | Triggers, Symptoms, Diagnosis, Treatment

To help your child cope with the emotional symptoms of chronic fatigue syndrome:

  • Encourage your child to keep a daily diary to identify times when they have the most energy and help plan activities for these times.
  • Help your child to recognize and express feelings, such as sadness, anger, and frustration. It’s OK to grieve the loss of energy.
  • Get support from family and friends because emotional health is important when coping with a chronic health problem.
  • Allow more time for your child to do things, or break down activities into smaller steps, especially activities that take concentration or physical effort.
  • Work with your childs teachers and school administrators to adjust their workload so that it fits within the limits of what your child can tolerate.

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What Are The Signs & Symptoms Of Chronic Fatigue Syndrome

Someone with chronic fatigue syndrome can have many possible symptoms. The most common ones include:

  • severe fatigue, which can make it hard to get out of bed and do normal daily activities
  • sleep problems, such as trouble falling or staying asleep, or not having a refreshing sleep
  • symptoms getting worse after physical or mental effort
  • symptoms or dizziness that get worse after standing up or sitting upright from a lying down position
  • problems with concentration and memory
  • headaches and stomachaches

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Diagnostic Criteria For Me/cfs Using The National Academy Of Medicine Clinical Criteria

For a diagnosis of ME/CFS, the person must have the following three symptoms:

  • Substantial reduction in functioning and persistent and profound fatigue for at least 6 months. The person is unable to undertake the same level of activity before they became ill. Their fatigue is not the result of significant exertion and is not substantially alleviated by rest.
  • Post-exertional malaise.
  • Diagnosis also requires at least one of the following two symptoms:

  • Cognitive impairment .
  • Orthostatic intolerance .
  • It is important to note that these are not the only symptoms of ME/CFS, just the minimum needed to meet the diagnostic criteria.

    While diagnosis requires that a person has had symptoms continually for six months, early intervention with pacing and rest can help reduce symptoms, improve quality of life and reduce the risk of exacerbating the disease. Research suggests that patients who are able to pace their activity and not push themselves tend to do better in the long term. Pacing and rest can start even prior to an official diagnosis.

    While there is currently no cure and no evidence-based treatments, it is important to find a doctor who is not only sympathetic to ME/CFS, but can work with you to help manage your symptoms.

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    The cognitive impairment that can accompany CFS/ME often reaches debilitating levels. People who formerly were able to concentrate at a high level may find themselves unable to write a simple sentence after being stricken with chronic fatigue syndrome. Memory can become unreliable with CFS/ME, and many people have to stop working because they simply do not have the cognitive ability to focus on completing mental tasks.

    Is There Any Treatment

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    There is currently no cure for CFS. The therapies for this disorder are directed at symptom relief. It is important to maintain good health by eating a balanced diet and getting adequate rest, exercising regularly without causing more fatigue, and pacing oneself because too much stress can aggravate the symptoms of CFS. Working with a physician to develop a program that provides the greatest benefits also will help in reducing frustration with the illness.

    Non-pharmacological therapies include acupuncture, aquatic therapy, chiropractic, cranial-sacral, light exercise, massage, self-hypnosis, stretching, tai chi, therapeutic touch and yoga. Certain psychotherapies such as cognitive behavioral therapy also have shown promise for facilitating patient coping and for alleviating some of the distress associated with CFS.

    In pharmacological therapy there is a variety of medications that can relieve specific symptoms. It is important to begin with low doses and to escalate the dosage gradually as necessary.

    Some CFS patients may also find it therapeutic to meet with other people who have this illness, and this can be accomplished by joining a local CFS support group. Support groups are not appropriate for everyone, and may actually add to their stress rather than relieving it.

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    Diagnosis Of Chronic Fatigue Syndrome

    • Laboratory tests to exclude other causes of symptoms

    At least one of the following manifestations is also required:

    • Difficulty thinking

    • Feeling of light-headedness or dizziness when standing up that is relieved by lying down

    The frequency and severity of the symptoms should be assessed by a doctor. If people do not have these symptoms at least half of the time with moderate, substantial, or severe intensity, doctors reconsider the diagnosis of chronic fatigue syndrome .

    Criteria for diagnosis are important mainly because they help doctors communicate clearly with each other when they study a problem. However, when treating a specific individual, doctors focus more on that person’s symptoms rather than the criteria.

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    Pacing Activity For People With Me/cfs

    Pacing, or keeping within your available energy, is a self-management strategy to help people with ME/CFS make sure that they dont overdo activity or exercise. It reduces the likelihood of triggering PEM and can help reduce symptoms. Pacing is not a cure for ME/CFS and does not treat the underlying, physical cause of the disease.

    The goal of pacing is for activity to be sustainable, so that the person can have some stability in their symptoms and what they can do each day. Pacing should be used in conjunction with rest.

    The most challenging aspect of pacing is that PEM is very often delayed by as much as 24-48 hours, which can make it difficult to recognise when youve done too much. Using tools like an activity diary or heart rate monitor help you learn about your body and how much activity you can safely tolerate.

    Suggestions on how to pace yourself include:

    Is There A Cure For Chronic Fatigue Syndrome

    What is Chronic Fatigue Syndrome?

    Unfortunately, no. But there are methods for managing symptoms. As an article in The Atlantic eloquently explained in an interview with David Kaufman, the medical director of the Open Medicine Institute in Mountain View, California:

    Simple diseases work like a chain of dominoes, with a clear cause setting off a series of possible symptoms, which hint at a diagnosis, and, usually, a standard treatment. Click, click, click, youre cured. Chronic fatigue is more like a pile of pick-up sticks: a giant mess in which no one can see a beginning or end. Most patients begin their history by saying something like, I was totally fine, and I got mono at 19 and Ive never been the same since, said Kaufman, who later treated Vastag .I want to find a single, neat, nice packaged cause. Every day I think Im less and less likely to find that.’

    Some people who suffer from CFS are housebound or bedridden, long-term or for short periods of time. The majority of patients, however, are able to remain functional with a regime of different medications, therapies, exercise plans, or other interventions.

    To learn more about what treatment options are available to you, click the link below. There, youll find a doctor who can review your chronic fatigue syndrome symptoms and provide options for finding relief.

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    Facts About Chronic Fatigue Syndrome

    • The CDC estimates up to 2.5 million Americans have ME/CFS.
    • Anyone can get it, including children and teens.
    • Its most common in women in their 40s and 50s.
    • Women are more likely to develop it than men.
    • Most cases are mild or moderate.
    • About 1 in 4 people with the condition have severe symptoms.

    If you have mild ME/CFS, you can probably manage on your own. Moderate symptoms can make it hard for you to move around. For example, you might need to sleep in the afternoons.

    Severe symptoms can impact your quality of life and abilities as badly as if you had lupus, heart disease, or rheumatoid arthritis.

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    10. Red Meat. Red meats tend to be high in saturated fats. The saturated fats in red meats interfere with proper circulation and increase sensitivity to pain. They also contribute to fatigue, making it difficult for fibromyalgia sufferers to get the exercise they need to promote muscle flexibility and range of motion.

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    Foods high in these types of fats are foodstoavoid if you have chronic pain. 3. Milk/dairy. Milk and dairy products contain lactose, a type of sugar that may cause inflammation. Other side effects of milk and dairy consumption include stomach upset and difficulty with digestion. This can cause pain and painful bloating. Theres no. Tips to Prevent Zoom Fatigue. One of the simplest ways to fight Zoom fatigue is to turn on the camera to be more present and engaged. While sometimes this is not an option, being on camera allows everyone to be more involved and on target. Fatigue sets in during long periods of time on video conferencing, and below are ideas to.

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    Impact And Prognosis Of Me/cfs

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    BMC Public Health.J Chronic Fatigue Syndr.

    Br J Occup Ther.

    • Mild: mobile and self-caring may continue working but will have reduced other activities
    • Moderate: reduced mobility, restricted in instrumental activities of daily living, needs frequent periods of rest usually not working
    • Severe: mostly housebound limited to minimal activities of daily living severe cognitive difficulties may be wheelchair dependent
    • Very severe: mostly bedridden unable to independently carry out most activities of daily living often experience extreme sensitivity to light, sound, and other sensory input

    Am J Epidemiol.Chronic Illn.

    Qual Life Res.Disabil Rehabil.Occup Med .

    Rehabil Psychol.Front Pediatr.Fatigue.

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