Category: Chronic Fatigue Syndrome

A detailed guide to Chronic Fatigue Syndrome (CFS), including its symptoms, causes, and effective treatment strategies to improve energy and well-being.

  • College Student With Fibromyalgia? Here Is How To Stay Organized.

    College Student With Fibromyalgia? Here Is How To Stay Organized.

    At the age of thirty-nine I decided to go back to college and finish my degree that I had started over 20 years prior. If I thought college was hard at eighteen, I had no idea what was in store for me. At this time, I was married with three kids and a full-time job. I wondered how I was going to fulfill all my responsibilities. I didn’t know at first what my end goal was going to be other than just getting my AA. It wasn’t until a couple years in that I finally decided on Psychology.

    Not Your Everyday Challenges

    About a year into taking 2 classes per semester and working full-time I was diagnosed with fibromyalgia. I always ran myself ragged as an adult, so I was used to feeling tired all the time. This time though the tired came with pain, a lot of pain. My first reaction was that I wasn’t going to let anything stop me, not even fibromyalgia. I pretty much didn’t until 2018. This was the year that fibromyalgia stopped my whole life. I had to take time off from work and school for a few months. Even when I went back to both I still wasn’t at full capacity.

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    I seemed to have developed a tenacity in my old age though and I still wasn’t going to quit. I kept on taking 2 classes per semester and working full-time. Let’s not forget still raising a family at the same time. This has not been easy, but nothing worth doing is.

    Staying Organized

    I often hear, “I don’t know how you do it” from people. I always tell people my two secrets are that (1) I have a planner that I use for everything and (2) my house is a mess (don’t judge). When you are working towards a goal sometimes sacrifices have to be made. Sadly, what I sacrificed a lot of was taking better care of myself (see above flare). The other part that has been hard is the fact that I am a Virgo and I LOVE organization. But loving being organized and having the energy to clean and organize your house are separate. I can’t do it all, so I have to choose.

    This is exactly how I organize my college career down to the semester level. I do not claim that what has worked for me will work for you. The key is you have to take your own life circumstances into account and do what is best for you.

    It helps if you define your goal completely. This means knowing what you are working towards and how to get there. If you were like me and couldn’t see that far ahead then I broke down my goals.

    1. Finish my AA
      1. Use your college advisor to help determine what classes you need.
    2. Find my passion and/or interests while working on my AA
      1. Take classes that sound interesting, not just requirements. If it meets both even better!
    3. Decided major is psychology
      1. Map out the reality of what it will take to choose that major and what jobs are available with each progressive degree.
    4. Transferred to University to complete my BA
      1. Make sure the university you choose has proper accreditation (regional, etc)
    5. Choose what to do with BA                                             
    6. PhD or Masters?
    7. Decided on Masters….choose graduate school/program

    I’m still working on this, but this is my basic guide on decisions I need to make and breaking the big goal down to smaller ones.

    Semester Goals

    The first step I take at the beginning of each semester is to map out my semester. I am addicted to Erin Condren planners, but you can use any that you want. I write out each week’s readings and assignments, making special note of bigger projects or exams. This really helps me plan out my energy to make sure I complete everything when I have the most energy. I recommend planners and even wall calendars so you can easily visualize what is to come. You can even use technology and utilize apps on your phone for assignment reminders.

    Speaking of technology if you are using Word or Google Drive make sure to break down courses into corresponding folders to keep all your documents organized and easy to find.

    Each week I look at what is expected of me in my classes and then I fill in other responsibilities outside of school. Each Sunday, I review the week ahead and see where I can fit each item in the best. I have learned to give myself plenty of leeway for those days I don’t feel well. This has served me well over the last seven years. Granted there have been times I had to really struggle and push through pain and exhaustion, but that is also just part of living with fibromyalgia.

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    More Tips and Tricks

    1. When I was working on my AA, I had to take classes at the college physically. This was a challenge since I worked all day. My secret to getting through these days was to not just pack lunch for work, but dinner as well. I went straight to school after work and sat in my car. This was my free time and I could either eat my dinner and do some homework or take a nap (which I often did). I recommend only a 20-minute nap at the most, otherwise you will feel too tired to go on with your night.
    2. Since enrolling in Penn State World Campus all my classes have been online. Still I feel drained after work and so I often lay down for a quick nap before starting any homework. Sometimes this ends up that I cannot function the rest of the night. This is where the planning and allowing leeway from above comes in. This is why I plan for earlier deadlines to give myself more time if I need it.
    3. Join clubs! You are not too old, and this is a great way to establish social support. In addition, if you do want to go to graduate school having some extra-curricular activities is good for your application.
    4. Wellness is so important to maintain while completing college. This is the one area I struggle with the most and need this reminder myself.

    Ways to maintain wellness

    • Find nutritious snacks to keep at your desk while you study.
    • Read while on the treadmill or bike.
    • Get enough sleep.
    • Drink plenty of water.
    • Use meditation to clear your mind.
    • Sometimes you have to just put it all down and go for a walk outside!

    These are just some of the ways I have gotten through college as an adult-student with fibromyalgia. I think being a college student with fibromyalgia is possible and I hope these tips help you! Feel free to reach out if you are in the same situation. I would love to hear any tips and tricks you may have as well.

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  • The ‘legalization of cannabis in the UK’ for chronic illness

    The ‘legalization of cannabis in the UK’ for chronic illness

    By: Dr. Alexa James

    The cross-party MPs had predicted on a Canadian exploratory expedition that cannabis use would be fully legalized in the UK within five or ten years. In 2018, Canada is the first to allow the recreation of drugs from a group of seven countries. One of the group’s three politicians has changed its outlook greatly.

    Labor David Lammy is now opposed to his party’s position on legalizing drugs and in support of them. The documentary on Radio 1 is called Legalizing Weed: The History of Canada and all three of Mr. Lammy, Jonathan Djanogly from the Conservatives, and Sir Norman Lamb from the Liberal Democratic Party were on the way to the documentary.

    Cannabis is classified as a Class B drug in the UK and can end up in prison for up to five years if you have it. However, the approach to medical cannabis products has changed which some patients are now legally prescribed. Certain modifications were made as patients may be prescribed certain medical cannabis products if necessary. Many have suggested that its medical use precedes the recreational use of cannabis.

    When MP David Lammy returned from Toronto, he said that “I want the market legalized, regulated and removed from the criminal gangs.” “To not criminalize young people with use and educate them properly.” “I want the strength of the material in this country to be reduced, labeled, and organized properly.”

    The Liberal Democrat Party supports the idea of legalizing cannabis in the UK already. Many people now say cannabis is all right. For example. For example. The head of the policy decision was Sir Norman Lamb Parliament member for North Norfolk. Whilst wanted to use cannabis oil legally in Canada for sleeping disorders. However, he was very aware of the illegal nature of such a product in the UK. He is the only parliamentarian in the United Kingdom to use Cannabis made on camera.

    “I will take it before bed and before my flight home if I just sleep in order to relax. Cannabis oil is difficult to find legally in the UK because it poisons the user and contains THC.

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    “I was very worried because I chaired the committee on technologies and science, I went back over the night and thought it will be a challenge if I get back without sleep.” He said it helped him sleep but did not poison his mind. “I was so anxious. “I have unbelievingly slept well.” “I have taken drops and have slept very well on my plane home.

    A campaign group from Great Britain, Volte-Face, who wants Great Britain to legalize the drug, has organized a tour. The campaign group is sponsored by a part of North American cannabis company MPX. Newsbeat’s suggested that British politicians had money on them.

    Boyes, the MPX CEO, said “We are shifting it to a legitimate trade industry from organized crime,” We had many UK investors investing in our company and moving to six countries.” Much of the money we raised has come from the UK, so I think it’s not impeding other people’s policies and many expenses were born on their own.”

    Their own flights and accommodation have received funding from Sir Norman Lamb and David Lammy. MPs are aware of some problems with Canada’s experience. Piper Courtenay told us that illegal “gray” cannabis suppliers flourish in a documentary whose title is a weekly newspaper cannabis editor. If the cannabis products are restricted but licensed, then that means they would continue to exist. She also said that “it’s sure better than the legal product I’ve tried up to now because they really care about good cannabis production.”

    The MPs on the journey believed that in the UK as it is in Canada in the 10-year period, cannabis would be legalized. But his partisan name, the most conservative in his predictions, was given Jonathan Djanogly. That’s what he said.

    “I believe we have a lot to learn before legalizing recreational cannabis, which I think will happen sometime,” “I think we are in the cycle of ten to fifteen years, which will reflect what happened in Canada.”

    Some believe it would also be legalized in the 5 or earlier period. It is also the government’s view that the law on the legalization of cannabis use would not be modified.

    “The legalization of such substances would not eliminate the crime of illicit trade or address the harm that could be caused to the families and society by the harm of drug dependency and misery,” said a spokesperson for the home office.

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  • Check These 9 Possible Causes of Dizziness and Fatigue

    Check These 9 Possible Causes of Dizziness and Fatigue

    Understanding Dizziness and Fatigue

    Dizziness is a word describing the sensation of spinning while off-balance. You can use these more specific terms to explain to your doctor exactly how you feel:

    • Imbalance is when you feel shaky
    • Lightheaded means you feel tired and woozy
    • Vertigo is a feeling of spinning when you are not moving

    You can feel dizzy and exhausted in many different conditions. Such signs are transient at times, or they may come and go. If you often feel dizzy or exhausted, have a consultation with your doctor. Untreated dizziness and tiredness can lead to a fall. It can also increase your risk as you drive into an accident.

    1st Cause is Low Blood Sugar

    Your body needs energy for sugar, also called glucose. You can get dizzy, shaky, and exhausted if your blood sugar level drops.

    Low blood sugar is often a side effect of diabetes treatment with insulin and other drugs. Such medications lower blood sugar, but the blood sugar could drop too much if the dosage is not right.

    If you don’t have diabetes, you can also get hypoglycemia. It can happen if you have not eaten in a while or if you have not eaten alcohol.

    2nd Cause is Low Blood Pressure

    Blood pressure is your blood pressure that pushes against the walls of the blood vessel as it circulates through your body. You may have signs such as dizziness or lightheadedness, and fatigue when your blood pressure drops. Certain symptoms are:

    3rd Cause is Anemia

    Red blood cells carry oxygen to all tissues and organs. The body does not have enough red blood cells when you have anemia, or these cells do not function well enough. You may feel dizzy and exhausted due to a lack of oxygen.

    4th Cause is Migraine Headaches

    Migraines are intense, throbbing headaches that last between a couple of hours and a few days. You may experience symptoms along with the headache that include:

    • vision changes, such as seeing flashing lights and colors
    • nausea, vomiting and fatigue
    • sensitivity to light and sound

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    5th Cause is Medications

    Many medications as side effects can cause dizziness and fatigue.

    6th is Abnormal Heart Rhythms

    Your heart normally beats in a familiar rhythm of “lub-dub.” Your heart beats too slowly or too fast when you have an irregular heartbeat or arrhythmia. It could skip beats as well.

    Other signs of arrhythmia, apart from dizziness and exhaustion, include:

    7th Cause is Chronic Fatigue Syndrome

    Chronic fatigue syndrome (CFS) is an excessive exhaustion disorder, even after you’ve slept well. CFS signs include dizziness and difficulties in keeping the equilibrium.

    You may also have the following symptoms:

    8th Cause is Vestibular Neuronitis

    An infection such as cold or flu can inflame your inner ear’s vestibular nerve. To keep you upright and balanced, this nerve sends sensory signals to your brain. Swelling can cause dizziness and vertigo in the vestibular nerve. You may also feel tired.

    9th Cause is Dehydration

    Dehydration occurs when there is not enough fluid in your body. If you don’t drink enough water, you can get dehydrated. This is particularly true when you are in hot weather or exercise outdoors.

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  • What’s the Causing of My Fatigue and Nausea is Full of List?

    What’s the Causing of My Fatigue and Nausea is Full of List?

    Understanding Fatigue and Nausea

    Fatigue is a condition that is a combined feeling of sleepiness and energy drainage. It can range from chronic to acute. Fatigue can be a long-term occurrence for some people, affecting their ability to perform daily activities.

    Nausea occurs when you feel uncomfortable or queasy in your stomach. You may not vomit, but you may feel as if you were able to. Nausea can be caused by many causes, including fatigue.

    Understanding Fatigue and Nausea Causes

    Vomiting and exhaustion can be caused by many factors, ranging from physiological to lifestyle habits. Examples of lifestyle habits that can lead to tiredness and vomiting include:

    • excessive alcohol use
    • poor eating habits
    • taking medications
    • lack of physical activity
    • jet lag
    • lack of sleep
    • excessive caffeine use
    • too much physical activity

    List of All Factors of Fatigue and Nausea

    • anxiety
    • depression
    • excess stress
    • because of sleep apnea
    • inflammatory bowel disease (IBD)
    • gestational diabetes
    • because grief
    • West Nile virus infection (West Nile fever)
    • so colon cancer
    • H. pylori infection
    • because chronic kidney disease
    • pelvic inflammatory disease (PID)
    • celiac disease (gluten intolerance)
    • however bleeding esophageal varices
    • because of PMS (premenstrual syndrome)
    • so high blood pressure (hypertension)
    • malignant hypertension (arteriolar nephrosclerosis)
    • Burkitt’s lymphoma
    • because epilepsy
    • liver failure
    • marine animal bites or stings
    • because of flu
    • kidney disease
    • however HELLP syndrome
    • so acute infective cystitis
    • amebiasis
    • because of hepatitis
    • E. coli infection
    • because of migraines
    • due to adult brain tumor
    • so concussion
    • multiple sclerosis (MS)
    • because of traumatic brain injury
    • pancreatic cancer
    • pregnancy
    • chronic pain
    • cirrhosis
    • endometriosis
    • chlamydia
    • Ebola virus and disease
    • erysipelas
    • chronic pancreatitis
    • fifth disease
    • malaria
    • polio
    • l medullary cystic disease
    • ischemic cardiomyopathy
    • food allergies and seasonal allergies
    • food poisoning
    • infectious mononucleosis
    • infection
    • hookworm infection
    • therefore Colorado tick fever
    • so dengue fever
    • hyperparathyroidism
    • because of hyperthyroidism
    • hypothyroidism
    • because of hypercalcemia
    • Addisonian crisis (acute adrenal crisis)
    • therefore low blood sodium (hyponatremia)
    • so addison’s disease
    • because of peptic ulcer
    • COPD
    • because of diabetes
    • chronic fatigue syndrome (CSF)

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    Understanding Fatigue and Nausea Treatment

    However healthy habits like getting enough sleep, eating healthy foods, and regular exercise will help you find relief from tiredness and nausea. Because it can also help to reduce fatigue and vomiting by avoiding bad habits such as cigarettes, consuming excess alcohol and etc.

    Therefore in order to treat an underlying condition, your doctor may prescribe medication.

    Understanding Home Caring

    However staying hydrated can help relieve fatigue and nausea by drinking clear liquids. Because maintaining a healthy level of activity that does not involve exercising too much can also help to prevent or reduce these symptoms.

    Understanding Fatigue and Nausea Preventions

    Tiredness can affect the overall well-being of you. So take the following steps to prevent tiredness and nausea from beginning:

    • So get plenty of sleep every night (usually 7 to 8 hours).
    • Therefore manage your schedule in order not to make your job too stressful.
    • However refrain from excessive drinking.
    • So non-smoking and medicine abuse.
    • Because Eat food and drink plenty of water.
    • Therefore periodic exercise.

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  • New Research Brings New Hope to Diagnostic Testing of Chronic Fatigue Syndrome

    New Research Brings New Hope to Diagnostic Testing of Chronic Fatigue Syndrome

    Chronic syndrome of fatigue can be a disconcerting disease.

    It presents a constellation of vague symptoms to people with the condition, but there is no easy or fast way to diagnose it.

    For decades, the condition has been mystifying medical experts.

    But new research gives them hope that they will finally understand the mechanisms behind this disease and will soon be able to develop a new way to quickly diagnose it.

    It is estimated that there are between 800,000 and 2,5 million Americans with chronic fatigue syndrome (CFS) or myalgia encephalomyelitis (ME).

    However, according to the Centers for Disease Control and Prevention (CDC)Trusted Source, only about 20 percent of those people were diagnosed.

    Understanding New Clues Looking

    In the hope of finding a way to quickly identify the disease, Stanford University researchers tested a variety of blood markers from 192 CFS patients called cytokines and compared them to 392 healthy patients taking cytokines.

    Last week, they published their findings in the National Academy of Sciences ‘ Proceedings.

    Cytokines are proteins that can affect the immune system and inflammation in the blood.

    The researchers tested 51 cytokines and concluded that 17 were associated with ME / CFS and its severity level with “a statistically significant.”

    The more severe the symptoms of the disease, the higher the number of cytokines.

    According to the authors of the study, 13 of the cytokines associated with the disease were pro-inflammatory.

    “There has been a lot of controversy and confusion around ME / CFS even if it’s a real disease,” said Mark Davis, PhD, professor of immunology and microbiology, and director of Stanford’s Institute for Immunity, Transplantation and Infection. “Our findings clearly demonstrate that it is an inflammatory disease and provide a solid basis for a blood test for diagnosis.”

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    The disease can affect anyone, but people between the ages of 40 and 60 are more common. Women are more likely to develop the disease than men, and according to the CDC Trusted Source, it is more likely to occur in the Caucasian people.

    ME / CFS symptoms include a lower level of activity, sleep problems, and a “post-exertional discomfort” where a person may “crash” after mental or physical exertion. People with ME / CFS may also have memory or thinking problems and symptoms worsen when they are standing or sitting up.

    “I’ve seen the symptoms of this disease compounded by hundreds of patients,” said Dr. Jose Montoya, Stanford University’s Professor of Infectious Diseases and lead author of the study. “For 35 years now, it has been observed and discussed, sometimes with the burden of being described as a psychological condition. But the syndrome of chronic fatigue is not at all a figment of the imagination. This is real.

    “According to the CDC, the disease also economically hits people, rising from $17 billion to $24 billion annually in medical bills and lost income.

    Understanding Helping Tests

    Dr. Sybil Marsh, a family medicine physician at the University Hospitals Cleveland Medical Center, said that if patients develop symptoms of the disease first, the possibility of a diagnostic test could result in huge changes.

    “It’s not something you can go in and think you’ve got it right away,” Marsh said to Healthline.

    She clarified that, before they can be treated, patients must have symptoms for at least six months.

    “All the underlying signs and illnesses are also caused by something else,” she said.

    Marsh said if patients could be treated earlier— within days or weeks of having symptoms— they wouldn’t face months of medical uncertainty.

    Marsh also pointed out that knowing the mechanism behind the disease could mean finding a cure for the illness one day.

    “We won’t know how to treat it until we know what the process is,” she said.

    “The treatment is really about managing symptoms right now and coping with this disorder,” explained Marsh.

    Individuals with ME / CFS are usually generally treated for symptoms such as fatigue, pain, and issues with concentration, but there is no medication treating the condition itself.

    “Often people get depressed because of all the things they’ve got to lose and cut out of their lives while they’re waiting to get better,” said Marsh.

    For now, the Stanford researchers hope their work will propel the medical field to solve this disease’s mystery. We also said further studies need to be done to confirm their results for larger study populations studied over longer periods of time.

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  • Strong Evidence Found that the Syndrome of Chronic Fatigue is a Physical Condition

    Strong Evidence Found that the Syndrome of Chronic Fatigue is a Physical Condition

    Understanding CFS Physical Condition

    New research suggests that in people with chronic fatigue syndrome, because a specific biomarker of inflammation is present for years.

    So people with chronic fatigue syndrome frequently find it difficult to understand how they feel exhausted and painful.

    Because most people suffering from the disorder have had their symptoms dismissed as being “all in their minds,” so much like a mental illness. Therefore that’s not necessarily true.

    New research shows the first “strong” proof that chronic fatigue syndrome (CFS) clinically referred to as myalgic encephalomyelitis (ME) is a physical disorder that can be caused by an infection.

    Therefore “We now have evidence confirming what millions of people already know about this disease, that ME / CFS is not psychological,” said Dr. Mady Hornig, Director of Translational Research at the Center for Infection and Immunity and Associate Professor of Epidemiology at the Mailman School in Columbia in a press release.

    Because Columbia researchers published a study that described changes in an individual’s immune system that contribute to the condition.

    “This study provides what has eluded us for so long: unequivocal proof of ME / CFS immunological failure and clinical biomarkers of illness,” said Dr. W. Ian Lipkin, Director of the Center for Infection and Immunity and Professor of Neurology and Pathology at the Mailman School in Columbia.

    The Columbia team says their work supports the hypothesis that after a serious infection, such as infectious mononucleosis, CFS may be caused in a “hit-and-run” fashion.

    The cross-sectional study, published in the Science Advances journal, included examining 298 CFS patients and 348 individuals without the condition blood plasma samples.

    Because in those with the disease, the researchers found different bio-markers produced by the immune system. So in those who have had the disease for less than three years and those who have had it for more than three years, they also found differences.

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    Those who had the disease for a shorter period of time had higher amounts of different cytokine types, or molecules that regulate the defensive response of your body to inflammation and infection.

    In general, the Columbia team reports early-stage CFS patients have elevated interleukin-17A levels, a recognized biomarker of a compromised immune system.

    However the researchers added that the elevated levels of biomarkers seem to subside after three years because after an infection, the immune system became drained after failing to calm down. So they compared it for an extended period of time to an engine running at high gear.

    So “Our findings will speed up the diagnosis process after first fall ill individuals as well as discover new therapeutic approaches based on these early blood markers,” said Hornig, the study’s lead author.

    Historically, the proper diagnosis of CFS has been concerning. The Institute of Medicine (IOM) states that no diagnosis has yet been made for up to 91 percent of the 2,5 million individuals who have chronic fatigue.

    So a panel of experts at the IOM recommended earlier this month that chronic fatigue be identified as a systemic aversion exertion disease (SEID) and diagnostic criteria that better reflect scientific research be developed.

    Because a prominent culprit in Interleukin-17A Autoimmune Disorders affects not only people with CFS.

    Numerous chronic inflammatory conditions such as multiple sclerosis, psoriasis, and rheumatoid arthritis are associated with high levels of this specific cytokine Trusted Source.

    However interleukin-17A is a potential target for Trusted Source biological therapies intended to dampen the immune system of the body in order to alleviate symptoms of these conditions.

    Therefore in the United States January Cosentyx (secukinumab), a psoriasis drug that targets interleukin-17A to relax the body’s immune response, was approved by the Food and Drug administration.

    Because an infection may also trigger psoriasis, an autoimmune disorder. So CFS is a common complaint in people with psoriatic arthritis, an inflammatory joint disease that may cause late-stage psoriasis in people.

    However before researchers would test existing or experimental drugs on patients with CFS to target interleukin-17A, they say they need to replicate their results in a study that follows patients to observe how their levels of cytokine differ over time.

    So there must be a better understanding of CFS before effective CFS treatments can occur so that it can be diagnosed earlier.

    Therefore “Early diagnosis can provide different care options that are likely to vary from those that would be available in later stages of the disease,” Hornig said.

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  • My 11 Lessons Living with Chronic Fatigue Syndrome from My Aunt

    My 11 Lessons Living with Chronic Fatigue Syndrome from My Aunt

    Just imagine that. You’re happy about life. You’re sharing your life with your dream man. You have a couple of kids, a job that most of the time you enjoy, and hobbies and friends to keep you busy. Instead, the mother-in-law is moving in one day.

    You don’t know why. You haven’t invited her, and you’re pretty sure, either, that your husband didn’t. You keep thinking she’s going to leave, but you note that her bags have been completely unpacked, and she changes the subject every time you bring up her imminent departure.

    Okay, that’s not unlike how I had chronic syndrome of exhaustion. As with most people with CFS, you see, for me, chronic fatigue syndrome came in the form of what I thought was a simple stomach flu. I mentally prepared for a few days of suffering and uncomfortable interruptions, as you would for a short-stay visit with your mother-in-law and believed life would return to normal in a few days. That wasn’t the case. The symptoms took up residence in my body, especially a crushing fatigue, and it would seem five years later that my metaphorical mother-in-law has moved in for good.

    It’s not the ideal situation, and it’s one that keeps worrying me, but it’s not all bad news. Some things have been taught to me by the years of living with “her.” I think everybody should know that now that they have this wealth of information.

    1st is It’s not all bad to live with CFS.

    Like any respectable relationship between MIL and DIL, there are ups and downs in life with chronic fatigue. Sometimes for fear of her wrath, you can’t lift your head off the pillow. But other times, if you walk smoothly, you may go weeks, even months, without a major confrontation.

    2nd is It comes with some benefits to live with your Aunt.

    The other day I was asked by a friend if I wanted to join her in selling chocolate almonds to the neighborhood. The response was a simple one, “No. Tonight I’m going to entertain my mother-in-law. “Living with this less-than-wanted house guest doesn’t come with many upsides, and now and then I think it’s fair to use it as a (valid) excuse.

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    3rd is The Aunt can’t beat.

    You can’t beat CFS physically or metaphorically, even though you’d like to, as some might “beat” or cure another illness. Some attempts at battling, defying, or otherwise beating it will only make life worse with it. That’s said.

    4th is a little kindness is going a long way.

    I found it best to show compassion in all respects when coping with this unwelcome resident of my life. A nurturing, peaceful, and patient approach will often yield periods of what is known as “remission” in CFS lingo a period in which symptoms alleviate and one may increase their activity levels.

    5th is Do Not involve your Aunt in extreme sports in any circumstances.

    CFS ‘ real kicker is a nasty little thing called the post-exertional malaise. Simply put, after taking part in rigorous physical activity, this is the all-kinds-of-terrible you feel 24 to 48 hours. So, while your mother-in-law may seem to enjoy her time on the BMX course, she’ll make you pay later. There’s no going to be any telling what injuries she can get and how long you’ll have to hear about them.

    6th is Everything you do: choose your fights.

    The condition of chronic fatigue rarely loses a chance to be heard when, say, you’re having a late night with friends or you’re trying to do some hard gardening. Understanding that, when it’s worth it, I’m just going to fight this infection. To me, it means saying no to issues like the community office or the PTA’s voluntary work. But a concert by Garth Brooks? YEAH HELL!

    7th is You’re not going to win every fight.

    My mother-in-law is a wonderful character. There will certainly be bad times that we call “relapse” in CFS-speaking. I can’t stress enough the ability to accept defeat as the first step towards healing when this happens. I use these moments to drink lots of tea with the MIL for my own sake, reassure her that everything is going to be OK, and convince her to watch Downton Abbey with me until she’s able to bury the hatchet.

    8th is Now and then throw her a bone.

    It might sometimes feel like your MIL is in need. She needs to relax, today she doesn’t want to dig the weeds, life is too hard for her, she wants to be in bed at 8 p.m. at the earliest. The list continues and continues. Throw her bone now and then, for goodness ‘ sake! Yes. That’s scratching. Give her all her bones, and then some. I promise that you will be worth the pay-off in terms of your safety.

    9th is If Aunt comes along, the best of friends won’t mind.

    I have always had great friends, but in the last five years I have never appreciated them more. They’re nice and obedient and don’t mind when my mother-in-law wants to slow us down on a vacation — or even if she suggests that we’re staying home instead!

    10th is Consider the things that you can’t change.

    I didn’t agree with all of this living arrangement. I begged and pleaded with my MIL to reside elsewhere. I even left her stuff on the doorstep, hoping she’d get the hint, but there was no point in it. It seems to stay here, and it’s better to.

    11th is You can change some things.

    No doubt, it can leave you feeling furious, defeated, and weak when a disease barges into your life unannounced and takes up residence. Nonetheless, for me, there came a point where those emotions had to take a back seat and reflect more constructively on the issues that I could improve. I might be a mother, for example. I would take tai chi, and in reading I could go on a new career. These are activities that I find enjoyable, rewarding, and my “mother-in-law” always finds them quite good!

    If one thing with this disease has become apparent during my experience, it is that we are all called to make the best of our living situations. Who knows that? One day I will wake up and may have found other rooms for my metaphorical roommate. But I’m not holding my breath, safe to say. I’m glad to do the best of it for today and take the lessons as they come. How do you cope with the condition of chronic fatigue? Inform me about your observations!

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  • 7 Coping Strategies That Helped Me in My Chronic Fatigue Syndrome

    7 Coping Strategies That Helped Me in My Chronic Fatigue Syndrome

    My husband and I call “The Dark Years” from 2002 to 2008. I went from a high-energy go-getter virtually overnight to being mostly bedridden, with debilitating aches, increasing tiredness, vertigo, and recurrent bronchitis.

    Doctors gave me different diagnoses, but the most reliable seemed to be chronic fatigue syndrome (CFS) or “an unexplained autoimmune disorder.”

    The worst part of having a condition like CFS apart from the horrible symptoms, the loss of health, and the indignity of people who believed that I was really sick was the mad, full-time job that was looking for ways to get better. I developed the following seven habits through some painful on – the-job training, which eventually enabled me to manage my symptoms and get back on the path to full health.

    Before I start, it is important to acknowledge that CFS is a specific disease and that it will achieve varying degrees of health for those who have it. I was fortunate enough to regain my healthfully, and I saw several others do the same. Everyone has their own path to health and I hope these suggestions can help you find yours whatever your potential is.

    1st Coping Strategy is Taking Charge

    Make sure that you know that you are responsible for your own recovery and that you are your professional advisors.

    I realized that I needed to change my approach after years of hoping to find the doctor with the cure. I came with a friend to advocate for me at every appointment, along with a list of questions, a chart of my symptoms and therapy research. I had third opinions and refused any treatment if the provider could not produce two patients for whom it had worked, and one year later they were still healthy.

    2nd Coping Strategy is Persistently Experiment

    Be open to major changes and ask your hypotheses.

    I had a lot of experiences with my diet during the early years of my disease. I left out rice, sugar, dairy and meat. I tried cleaning anti-Candida, being vegan, cleaning Ayurvedic for six weeks, and more. When none of those worked, I decided that food couldn’t cure me though eating healthy helped a bit. I was mistaken. When I questioned that conclusion, I was only able to recover my health.

    I took on a strict, raw vegan diet after five years of illness that I had ruled out four years ago as too extreme. I felt better within 12 months.

    3rd Coping Strategy is Heart Nurture

    Establish a daily practice that can help you manage hard emotions, such as journaling, peer counseling, or meditation, that could sabotage your healing efforts.

    I was part of a peer counseling community and had sessions with other counselors on a daily basis, two-way listening and sharing. They lasted from five to 50 minutes anywhere.

    These sessions enabled me to stay on top of the grief, fear, and anger that might otherwise have led me to give up or feel unable to make the big changes I needed to make in diet and lifestyle.

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    4th Coping Strategy is Believing

    Adopt a fiercely self-confident attitude and ability to be healthy.

    I decided to become more optimistic when the person leading a mind-body class I was in scolded me that my cynical attitude was “not serving” me. I started looking for therapies that weren’t useful data, not indicators I’d never recover. Exercises such as writing a letter of dismissal in my head to the nervous critic helped me build my muscles of hope.

    5th Coping Strategy is Healing Need

    To set up your home in a way that supports your healing, use organizing principles.

    Practicing qi gong on a daily basis was an important part of my recovery, but I was a chronic qi gong procrastinator before I cleaned out half of our family room to create a beautiful practice space with all the equipment, I wanted a timer, CD, and CD player in a closet.

    6th Coping Strategy is Medical Information

    It will make you a more effective advocate to have a handle on your medical information.

    I am a man who is congenitally disorganized. So, after years of papers flying all over the place, a friend helped me create a physical notebook with tabs for Articles, Notes from Health Appointments, Medical History, Current Medicines and Lab Results.

    I had all my laboratory results sent to me, so I alphabetized them with tabs such as Lupus, Lyme, Parvovirus and Parasites.

    7th Coping Strategy is Be Open

    Talk openly with your friends and family and invite them on your healing journey to help you.

    I finally got over my delusion after five years of suffering that I didn’t need help. When people started coming to appointments with me, spending time exploring solutions with me, and visiting me, I had the confidence to take on the strict diet of healing that had previously felt too hard.

    Breslov’s Nachman, a Ukrainian Hassidic rabbi of the 18th century, famously said that “a little bit is also good.” Wherever you are in your recovery, taking steps to affirm only one part of your path could make a real difference in bringing you to a healthier future.

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  • For Chronic Fatigue Reduction Use These Hack 10 Diet Tips

    For Chronic Fatigue Reduction Use These Hack 10 Diet Tips

    Chronic tiredness is far from the tiredness of “I need another cup of coffee.” It’s a deteriorating disease that can affect your whole life.

    No big research on the impact of diet on chronic fatigue syndrome (CFS) have been performed to date. Nonetheless, Jose Montoya, MD, a medicine professor and Stanford’s Chronic Fatigue clinic expert, reported that diet tends to have an effect on chronic fatigue.

    “The diet may affect CFS, but we know very little about what specifically could work for everyone,” Montoya said. “We know that some food items make their symptoms worse or better for some, and people should pay attention to them.”

    While more work still needs to be done, there are many things you can do to help boost strength and ensure a healthy, well-balanced diet is being consumed.

    1st is Inflammatory Ditch Foods

    Since inflammation seems to play a role in chronic tiredness, Montoya suggests following an anti-inflammatory diet and adding anti-inflammatory foods such as fish and olive oil. Inflammatory foods such as sugar, fried foods, and processed meat should be limited.

    2nd is Stay Hydrated

    While it is not a cure for chronic fatigue to drink more water, it is still necessary. Dehydration is considered to intensify fatigue. It is important to stay hydrated in order to improve or maintain health.

    3rd is Make Food Journal

    A food newspaper is a great way to discover foods that make your symptoms better or worse. Having a record of how you feel every day to share with your doctor is also beneficial. Track how you feel and what you eat to find patterns every day. Because 35 to 90 percent of people with chronic fatigue have symptoms associated with irritable bowel syndrome, any stomach upset or discomfort should be given special consideration.

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    4th is Talk to Doctor

    It is tempting to cut everything you can in the face of a nebulous, debilitating illness like chronic fatigue, but there is no proof that the effects are helped by a highly restrictive diet. Talk to your doctor before removing any foods from your diet to prevent your body being overtaxed and important nutrients being cut off. Just follow a diet for elimination if you think your doctor or dietitian are right for you.

    5th is Diet Experiment

    You can feel better or worse with certain foods. For example, some patients in Montoya noticed improvements after removing gluten or high-carbohydrate foods from their diets while others had no effects. Since there is no standard diet for CFS, finding what makes you feel the best might be worth experimenting with your diet.

    Consulting with your dietitian or doctor is best to tailor a schedule of food to your specific needs. Through paying attention to how particular foods make you feel, you could start on your own.

    6th is Reduce Caffeine

    Caffeine appears to be a great way to enhance your power, but it has consequences. According to Montoya, caffeine could give you a false sense of energy and cause you to overdo it. For some people, a bit of caffeine may be good. Just be careful not to over-exert yourself and ensure that your diet does not impact your sleep.

    7th is Meals Plan

    Most people with chronic fatigue sometimes feel too tired or hungry to feed. When you lose weight and struggle throughout the day to eat enough, Experts advise more often trying smaller meals and adding small snacks between each meal. Eating more often can help keep up your energy. It may also be easier to tolerate smaller portions.

    8th is Vegetable Diet

    Fill up on vegetables that are not starchy. To get their special nutrients and advantages, seek to include vegetables of all colors throughout the day. Red vegetables, for example, are full of antioxidant phytonutrients that help to reduce inflammation. Yellow vegetables, including vitamins A, C and B6, contain essential vitamins and minerals.

    9th is Skip Processed Foods

    Typically, heavily processed foods have fewer nutrients than their entire counterparts. Loading up on plants, such as legumes, fruits, vegetables, and whole grains, is important to support the needs of your body.

    Don’t know what you should eat? Researches recommend sticking to foods that are “as close as possible to how Mother Nature made it.” For example, choose popped maize instead of corn flakes or brown rice instead of pasta.

    10th is Healthy Fats

    A sprinkle of walnuts, a few slices of avocado, a few ounces of trout: good fats such as omega-3 fatty acids can be easily added all day long. Healthy fats are important for the health of the brain and heart and can help to reduce inflammation as well.

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  • CFS (Chronic Fatigue Syndrome) is Never Let You Be Happy

    CFS (Chronic Fatigue Syndrome) is Never Let You Be Happy

    Understanding Chronic Fatigue Syndrome

    Chronic fatigue syndrome (CFS) is a disorder characterized by extreme fatigue and exhaustion that cannot be explained by an underlying medical condition.

    CFS also be called myalgic encephalomyelitis (ME) or systemic intolerance exertion disease (SEID).

    CFS causes have not yet been fully understood. Viral infection, psychological stress, or a combination of factors are some theories.

    Since no single cause has been identified and many other conditions give rise to similar symptoms, CFS can be difficult to diagnose.

    CFS tests are not available. Before making a diagnosis, the doctor will have to rule out other sources of your exhaustion.

    While CFS was previously a controversial diagnosis, as a medical condition it is now widely accepted.

    Therefore while it is most common among women in their 40s and 50s, CFS can impact anyone. So there is no remedy at the moment, but symptoms can be relieved by medication.

    Here’s what you need to know about CFS, including symptoms, options for treatment, and outlook.

    Understanding CFS Causes

    It is unknown the cause of CFS. Investigators suspect that factors that may lead may include:

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    Understanding CFS Risk Factors

    In their 40s and 50s, CFS is most commonly seen among people.

    Sex also plays an important role in CFS as women are more likely to be diagnosed with CFS than men, two to four times Trusted Source.

    Other factors that could increase your CFS risk include:

    Understanding CFS Symptoms

    CFS symptoms vary depending on the individual and condition severity.

    However fatigue is the most common symptom. which is serious enough to interfere with your daily activities.

    The ability to perform the usual daily tasks with fatigue will last for at least six months in order to be diagnosed with CFS. Despite bed rest, it must not be healable.

    After physical or mental activity, you may also experience extreme fatigue. This may last after the operation for more than 24 hours. Includes

    Understanding CFS Diagnosed

    As of 2015, CFS exists in about 836,000 to 2.5 million Americans, according to the Institute of Medicine. Nevertheless, it is estimated that 84 to 91% have yet to be identified.

    Because there is no screening for medical tests for CFS. Similar to many other conditions, its symptoms. So most people with CFS do not “look sick,” and doctors may not know that they necessarily have a lack of health.

    However tour doctor will rule out other potential causes and check your medical history with you to receive a CFS diagnosis.

    Understanding CFS Treatment

    However there is no clear treatment for CFS at the moment.

    Therefore that person has different symptoms, so different types of treatment may be needed.

    So work to create the best treatment plan for you with your health care provider team. Therefore we can go over the therapy’s potential benefits and side effects with you.

    Understanding Home Remedies

    Changes in lifestyle can help to reduce the symptoms.

    Therefore limiting or reducing your intake of caffeine can help you to sleep better and ease your insomnia. Nicotine and alcohol should also be limited or avoided.

    If it affects your ability to sleep at night, try to avoid napping during the day.

    Develop a routine for sleeping. Go to bed every night at the same time and try to wake up every day around the same time.

    Understanding Medications

    Normally, the symptoms cannot be treated by any drug. With time, the symptoms may also alter, and your drugs may also need to.

    CFS can cause or be a symptom of depression in many cases. Low-dose antidepressant therapy or referral to a provider of mental health may be required.

    If you don’t get a restful night’s sleep if changes in lifestyle, your doctor may suggest a sleep aid. Medication that reduces pain can also help you cope with CFS-related aches and joint pain.

    It will need to be personalized to your needs if drug therapy is necessary. Work closely with your doctor. There is no single-size-fits-all CFS diagnosis.

    Understanding Therapies

    Therefore acupuncture, tai chi, yoga, and massage can help relieve CFSrelated pain. Please talk to your doctor before you begin any alternative or complementary therapy.

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