Category: Lupus

Understand Lupus, its symptoms, causes, and available treatment options to manage this chronic autoimmune disease and improve your quality of life.

  • Why Do I Need A Referral To See A Pain Specialist?

    Living with chronic pain is not easy, and when it’s time to seek out a pain specialist who understands the intricacies of chronic pain and the options for treatment, your family physician is your first resource. Most pain clinics require a referral from that family physician in order for the pain clinic to accept you as a patient. Chronicillness.co Site of the United States is no exception. In order to receive award-winning medical treatment from our pain specialists, a referral from your family physician is needed.

    Why do I need a Referral?

    One of the most common questions that we get is “why do I need a referral?” The most common answer is that it’s really up to your insurance company, and to alleviate any insurance discrepancies we ask that patient’s come by referral. Without getting too complicated, referrals depend on whether you have a PPO or an HMO, whether you are using a provider within your network or not, and whether it’s an emergency situation. In any situation where you’d need to see one of our pain specialists, it’s your best bet to get a referral.

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    How do I know if I need a Referral?

    Can’t my family physician just treat the pain? The short answer is yes and no. Your family physician can prescribe over-the-counter medications to help alleviate the pain, but simply alleviating the pain is not diagnosing the problem or treating its source. If you’ve tried pain medication from your physician, and you’ve tried options such as massage and exercise (things that are probably not covered by insurance), and you’re still in pain, it’s time to get that referral to see a pain specialist.

    How do I ask for a Referral?

    Many family physicians have become much like family friends, treating you and your family for generations. So when it comes to asking to seek out a professional that isn’t your physician, sometimes it can be difficult to ask for that referral. And, in some cases, physicians don’t want to give you that referral. Either way, if you have been on pain medication and it’s not working, you must ask for a referral to see a pain specialist. Here are some tips for asking:

    • Discuss with your family physician the amount of pain you’re still in. Let him know that the medication is not working well enough, and you’d like to get to the source of the problem to solve it, not just cover it up with painkillers.
    • Discuss the various treatment options that you’ve already tried with your physician, and ask if he can suggest any others. If he has run out of options, it’s time to see a specialist.
    • Asking for a referral is like ripping off a band-aid. You know it has to be done, but you don’t want to make anyone feel bad.
    • As you ask for your referral, it is also a great time to ask your physician to send a letter to Chronicillness.co Site of United States explaining your medical situation.
    • Finally, check with your insurance to make sure that Chronicillness.co Site is within your network.

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  • How Accurate is the 1 to 10 Pain Scale?

    Do you have a high pain tolerance? How do you know it’s higher than another patient? One of the most difficult aspects of pain management that our doctors deal with is an individual’s pain tolerance. The infamous one-to-ten pain scale is unscientific, and inaccurate when dealing with individuals who feel pain differently. What might be a two-to-one person might be an eight. Even when the patient explains to the pain doctor the amount of pain they’re in, we’re still stuck as to how much pain they are truly feeling. But all of that might be changing.

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    The Pain Scale

    Pain is subjective and unquantifiable. When you visit the physician for chronic pain symptoms, or perhaps when you’re in labor, your doctor will have you rate your pain on a scale of 1 to 10. When my wife was having our first little one, the nurse said “rate your pain on a scale of 1 to 10, 10 being the kind of pain you’d feel if you were hit by a truck and then run over twice.” It’s an interesting way to describe pain, but effective.

    The pain scale, though not entirely effective, does make pain measurable for doctors. On your first visit, your pain might be an 8, but on your third visit, your pain might be down to a 3. This tells the pain doctor that they are doing the right things to get you back into life and relieve your pain.

    Pain Scale MRIs

    Recently, scientists at Brigham and Women’s Hospital in Boston were able to “observe changes in blood flow to specific regions of the brain as chronic back pain patients held uncomfortable positions inside the scanner,” according to ABCNews.com. “As the patients’ brains were registering the distressing sensation, the investigators watched blood flow activate or ‘light up’ different regions. They could then measure that blood flow during those painful episodes.” This, many believe, is a huge step to categorically defining the amount of physical pain that a patient is feeling.

    According to Dr. Ajay D. Wasan, an assistant professor of anesthesiology and psychiatry involved in the research study, the “network involved in processing pain” is well understood. The fact that a person’s attention to their pain is a key element in their pain tolerance leads Dr. Wasan to believe that “drugs that might change a person’s ability to pay attention to their pain or be distracted from their pain” might become exceedingly important aspects of pain management down the road.

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  • Tips for Tent Camping with Chronic Pain

    Many of our United States pain patients love the outdoors, and the United States is a wonderful place to be over Memorial Day Weekend. Everyone in the valley heads north to escape the start of summer and relax with friends and family. However, if you can’t afford an RV, tent camping can be a seriously daunting aspect of the weekend.

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    • Have the mindset that tent camping will be a breeze because mindset truly plays a large role in how you will feel this weekend.
    • Don’t take on too much. We can’t stress this enough. When it comes to tent camping, setting up the tent and getting it organized should not be one of your priorities. Do not overstress your body. Allow friends and family to do the work as you take on less strenuous tasks.
    • Have a big enough tent to give you room to stand up. Make it as convenient as possible for when you must climb into the tent, change in the tent, or anything else.
    • Place the tent in a shaded area. As we all know, this United States sun can sneak up on you and just a few moments of direct sunlight can truly heat up that tent and make it very uncomfortable.
    • Spend the money on a nice air mattress. United States pain specialists can’t stress this enough. Sleep is paramount, and being able to sleep comfortably while camping can make or break your Memorial Day Weekend. Have enough blankets to keep warm and a comfortable pillow.
    • Maintain a healthy diet and exercise routine. I know, it’s vacation, but that doesn’t mean you should skimp on your healthy lifestyle. One of the biggest downfalls of every patient’s camping trip is their lack of healthy alternatives to camping food. Changing your diet can dramatically affect your chronic pain.
    • Have a comfortable chair available. Whether you enjoy the hammock or a simple fold-up chair, make sure it’s comfortable for long periods of time. You want this weekend to be relaxing and calming, and a comfortable chair will help.
    • Choose a campsite near a bathroom. Once again, we can’t stress this enough. If you began to have a rough episode, walking to a bathroom that’s even 20 feet away can seem like miles.

    Getting outdoors and back into life is paramount for patients living with chronic pain. Breathing in that fresh air, relaxing under those towering pine trees, and listening to the breeze without a care in the world can bring about much-needed calm and peace. The kind of calm and peace that has been known to ease chronic pain. While getting up north for a camping trip might not be your favorite thing to do, consider the benefits of spending time away from the stress of life. Those positives might outweigh the negatives when it comes to camping, whether you have an RV or tent.

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    Official Fibromyalgia Blogs

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    Fibromyalgia Stores

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  • Breathing Exercises to Calm Pain

    Here at The Chronicilness.co of the United States, we know that living with chronic pain can be stressful. But one of the best ways patients can help reduce the stress in their lives is by learning how to relax through breathing exercises.

    Deep breathing helps lower stress in the body because breathing deeply sends a message to the brain to calm down and relax. The brain then sends this message to the body. Deep breathing also causes certain things that happen when stress occurs, such as increased heart rate, fast breathing, and high blood pressure, to decrease.

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    Another good thing about breathing exercises is that they are easy to learn. Patients can do them whenever they want, and they don’t need any special tools or equipment. Patients can also try out different exercises to see which works best.

    The following methods focus only on breathing exercises, but there are other ways, such as combining breathing with things like yoga, imagery, and meditation.

    The first exercise presented is called belly breathing and is simple to learn and easy to do. It’s best to start there, especially for patients who have never done breathing exercises before. The other exercises are more advanced, but all of these exercises can help patients relax and relieve stress.

    Belly breathing is easy to do and very relaxing. Patients can try this basic exercise anytime they need to relax or relieve stress.

    Sit in a comfortable position.

    Put one hand on your belly just below your ribs and the other hand on your chest.

    Take a deep breath in through your nose, and let your belly push your hand out. Your chest should not move.

    Breathe out through pursed lips as if you were whistling. Feel the hand on your belly go in, and use it to push all the air out.

    Do this breathing 3 to 10 times. Take your time with each breath.

    After mastering belly breathing, patients may want to try one of the following more advanced breathing exercises.

    4-7-8 breathing This exercise also uses belly breathing and can be done either sitting or lying down.

    To start, put one hand on your belly and the other on your chest as in the belly breathing exercise.

    Take a deep, slow breath from your belly, and silently count to 4 as you breathe in.

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    Hold your breath, and silently count from 1 to 7.

    Breathe out completely as you silently count from 1 to 8. Try to get all the air out of your lungs by the time you count to 8.

    Repeat 3 to 7 times or until you feel calm.

    Roll breathing The object of roll breathing is to develop full use of the lungs and to focus on the rhythm of breathing. It can be done in any position, but while learning, it is best to lie on the back with knees bent.

    Put your left hand on your belly and your right hand on your chest. Notice how your hands move as you breathe in and out.

    Practice filling your lower lungs by breathing so that your “belly” (left) hand goes up when you inhale and your “chest” (right) hand remains still. Always breathe in through your nose and breathe out through your mouth. Do this 8 to 10 times.

    When you have filled and emptied your lower lungs 8 to 10 times, add the second step to your breathing: Inhale first into your lower lungs as before, and then continue inhaling into your upper chest. As you do so, your right hand will rise and your left hand will fall a little as your belly falls.

    As you exhale slowly through your mouth, make a quiet, whooshing sound as first your left hand and then your right-hand fall. As you exhale, feel the tension leaving your body as you become more and more relaxed.

    Practice breathing in and out in this way for 3 to 5 minutes. Notice that the movement of your belly and chest rises and falls like the motion of rolling waves.

    Practice roll breathing daily for several weeks until you can do it almost anywhere. You can use it as an instant relaxation tool anytime you need it.

    Caution: Some people get dizzy the first few times they try roll breathing. If this happens, slow breathing down and get up slowly.

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  • New Studies Showed Mixed-But-Promising Results for New Lupus Drug Anifrolumab

    New Studies Showed Mixed-But-Promising Results for New Lupus Drug Anifrolumab

    Lupus patients have been waiting a while for some good news. Only one drug, belimumab (Benlysta), has been FDA-approved for lupus in more than 50 years — and that happened back in 2011. Since then, scientists have been trying to develop additional therapeutic agents (and failing for various reasons). But research presented at the 2019 American College of Rheumatology/Association of Rheumatology Professionals (ACR/ARP) Annual Meeting in Atlanta suggests that a new lupus medication, anifrolumab, might have the potential to get approved and make its way to market.

    The manufacturer, AstraZeneca, is expected to file for FDA approval in 2020. It’s hardly a slam dunk: The company conducted two phase 3 trials on anifrolumab, and one of them did not hit its primary endpoint, though secondary endpoints suggested that the drug had benefits. The second phase 3 study, which was presented for the first time at the recent ACR/ARP meeting, yielded more consistently positive results.

    “I’m optimistic and hopeful that this drug will be approved,” says Chronicwoman medical advisor Vinicius Domingues, MD. “We have one [phase 3] study that was technically negative but with a lot of positives because of the secondary endpoints, plus a second [phase 3] study that was all positive. Patients should know that this is promising.”

    What the Studies Found

    The first phase 3 trial was called TULIP 1 (Treatment of Uncontrolled Lupus via the Interferon Pathway). Last August, AstraZeneca reported that anifrolumab failed to meet its primary target in TULIP 1, which was a “statistically-significant reduction in disease activity… as measured by the SLE Responder Index 4 (SRI4) at 12 months.”

    SRI4 is a composite score that is often used to measure disease activity in patients with systemic lupus during clinical trials. According to SRI4, anifrolumab was as flop: Patients who added the drug to their treatment regimen did not, on average, fare better than those who added a placebo.

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    However, secondary endpoints in TULIP 1 found that anifrolumab beat the placebo. Those secondary endpoints included a different composite score of disease activity, called BICLA (British Isles Lupus Assessment Group-Based Composite Lupus Assessment), as well as reduced reliance on corticosteroid drugs.

    The results of TULIP 1 appear in the journal Lancet Rheumatology and were discussed at the 2019 ACR/ARP meeting.

    TULIP 2, the second phase III study of anifrolumab, used BICLA as its primary endpoint — and met it. TULIP 2, which was also presented at the 2019 ACR/ARP meeting, found that the drug beat the placebo as far as BICLA was concerned. It also determined that patients using it had greater improvements in skin disease and decreased use of corticosteroids.

    While it’s true that researchers deliberately switched to a primary endpoint that they were likely to meet when moving from TULIP 1 to TULIP 2, there’s no clear consensus among rheumatologists that SRI4 is “better” than BICLA. In fact, a 2014 study compared these two outcome measures and determined that either one could “likely be an optimal primary endpoint” in a given clinical trial.

    According to Northwestern University rheumatologist Michael Putman, MD, reporting on the trials for RheumNow, the SRI4 requires 100 percent improvement in some domains, “whereas with the BICLA you can get a little better across the board.” That might be part of why one endpoint seemed to work and the other didn’t, he said.

    How Anifrolumab Works

    Anifrolumab is a monoclonal antibody that inhibits type 1 interferons, proteins that are involved in inflammation. Some lupus patients (but not all) have a “high interferon gene signature.” Scientists are simultaneously developing a test that can be used to identify those individuals. “It can be used to help predict who may or may not respond to this drug,” says Dr. Domingues. “This is an example of precision medicine, and it’s how cancer is being treated nowadays.”

    “There has been a case building for many years about the importance of interferons in the pathogenesis of lupus,” Timothy Niewold, MD, Judith and Stewart Colton Professor of Medicine and Pathology and Director of the Colton Center for Autoimmunity at the New York University School of Medicine, told the ACR Daily News. “One of the most exciting recent developments is that drug companies have created agents to target the interferon pathway. It’s been a rocky road, but there have been some positive results.”

    If anifrolumab gets the green light from the FDA, patients who haven’t responded well to other lupus treatments — especially those who have a high interferon gene signature — might benefit by including it in their current drug regimen, says Dr. Domingues. (The drug would be an add-on, not a replacement.)

    If the drug eventually gets approved, label specifics such as recommended dosing and warnings about side effects would be revealed at that time. In the TULIP 2 study, participants in the treatment group used 300 mg of anifrolumab via infusion every four weeks. Serious adverse events were rare and occurred more frequently among those in the placebo group. The most common side effect experienced by those using anifrolumab was shingles, which occurred in 7 percent of anifrolumab users.

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  • Taking Hydroxychloroquine for RA or Lupus Can Reduce Heart Risk by 17%

    Taking Hydroxychloroquine for RA or Lupus Can Reduce Heart Risk by 17%

    The anti-malarial drug lowers cholesterol and blood sugar makes blood less sticky, which is good for reducing blood clots and heart attack risk.

    If you take the anti-malarial drug hydroxychloroquine (Plaquenil) as part of your treatment for lupus or rheumatoid arthritis (RA), you may be getting cardiovascular protection as an added bonus.

    That’s welcome news because it’s estimated that about half of lupus patients experience heart complications, and heart attacks occur at younger ages in lupus patients than in the general population. Even as young adults, black and Hispanic women with lupus often have plaque build-up in their arteries that hikes their risk of heart attack. And experts have long known that people with RA are more likely to develop heart disease, even if they don’t show signs of clogged arteries: inflammation from arthritis disease activity is thought to be the link.

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    Because hydroxychloroquine (HCQ) has been associated with lower levels of cholesterol, blood sugar, and the tendency of blood to clot — all cardiovascular risk factors — researchers looked at the association between HCQ use and the occurrence of heart attacks, strokes, and blood clots (in lungs or deep veins). The results were presented at the 2019 American College of Rheumatology/Association of Rheumatology Professionals annual meeting in Atlanta.

    Using a health database that covers the entire population of British Columbia in Canada, researchers compared lupus and rheumatoid arthritis patients who had experienced a cardiovascular event with up to three matched patients who did not have a cardiovascular incident. Most of the patients were female (64 percent) and their average age was 74. In total, researchers studied 532 lupus cardiovascular cases and 1,249 controls, as well as 9,736 RA cardiovascular cases and 28,720 controls.

    HCQ use was categorized by the most recent date covered by a prescription and divided into those currently using the medication (within last month), those who recently stopped using it (used within 30 to 365 days), those who stopped using HCQ more than a year previously, and those who had never taken it.

    After controlling for such other factors as kidney disease and the use of glucocorticoids, disease-modifying anti-rheumatic drugs, and heart disease medication, lupus and RA patients currently using HCQ were 17 percent less likely to have a heart, stroke, or blood clot.

    In contrast, those who had discontinued HCQ within the last year were 8 percent more likely to have one of the cardiovascular events.

    When people stopped using HCQ more than a year ago, the risk of cardiovascular events was no different than those who had never been prescribed HCQ.

    In another hydroxychloroquine study presented at the meeting, Johns Hopkins researchers looked at blood levels of HCQ in lupus patients who developed a blood clot (including heart attacks and clot-caused strokes). They found that patients with the highest levels of HCQ in their bloodstreams were the least likely to have developed a clot.

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    The researchers cautioned that following the suggestion of the American Academy of Ophthalmologists to reduce HCQ doses in an effort to prevent damage to the retina (which occurs in about one out of 5,000 patients taking HCQ for more than five years, according to Johns Hopkins), may also reduce or eliminate the benefit of HCQ in preventing blood clots.

    If you’re taking hydroxychloroquine and are concerned about your dosage and how it may affect your heart disease risk or the odds of vision problems, talk to your rheumatologist and ophthalmologist to understand your risk factors and make the right decision for you.

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  • Could the Weather Affect Lupus Symptoms? New Study Suggests Warm, Humid Weather Does

    Could the Weather Affect Lupus Symptoms? New Study Suggests Warm, Humid Weather Does

    As the temperature increased, so did the risk of rash, joint inflammation, kidney problems, and other lupus symptoms.

    Shifts in weather patterns have long been associated with a variety of health ailments, from seasonal allergies to migraine and joint pain. Now a new study suggests that changes in the outdoor environment may make people who have lupus more susceptible to flare-ups of specific symptoms.

    The study, presented at the 2019 American College of Rheumatology/Association of Rheumatology Professionals Annual Meeting in Atlanta, analyzed data on 1,628 patients with lupus who had checkups between 1999 and 2017 as well as environmental and atmospheric data from the U.S. Environmental Protection Agency. The goal: to determine whether the environmental weather conditions 10 days before a checkup would correlate to changes in patient symptoms.

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    According to the authors, “there is a strong association between changes in atmospheric and environmental variables 10 days prior to patient visit and organ-specific lupus activity at the visit.”

    Although they did not find a connection to systemic flares that impact all organs, they determined that certain environmental factors were strongly linked to flares of specific symptoms: As the temperature increased, so did the risk of rash, joint inflammation, kidney problems, serositis (inflammation of smooth tissue membranes), and hematologic problems such as anemia and low white blood cell count.

    Windy conditions were also apt to lead to a spike in hematologic problems, plus an increase in neurological and pulmonary symptoms. Reports of joint inflammation and serositis increased in more humid weather, and an increase in air pollution (fine particulate matter) correlated to an uptick in rash, joint, serositis, and hematologic flares.

    Although more research is needed to confirm the results, “these findings are the first step to vindicating the great majority of lupus patients who are convinced that their disease is influenced by weather changes and who inspired this research,” lead study author George Stojan, MD, assistant professor of medicine at Johns Hopkins Lupus Center, said in a press release.

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    Official Fibromyalgia Blogs

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    Fibromyalgia Stores

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  • Fibromyalgia vs. Lupus: What’s the Difference?

    Fibromyalgia vs. Lupus: What’s the Difference?

    Fibromyalgia and lupus are both chronic diseases with no cure, can both cause some similar symptoms, and can both take a long time to get the right diagnosis. But fibromyalgia — often called fibro — and lupus are two very distinct health conditions with very different causes and treatments, despite having some features in common.

    Lupus is an autoimmune disorder that involves widespread inflammation and impacts many organs throughout the body. Fibromyalgia a disorder that causes widespread chronic pain and tenderness. Unlike lupus, fibromyalgia is not an inflammatory or autoimmune disease.

    Still, many signs and symptoms of fibromyalgia and lupus overlap and it’s not uncommon for fibromyalgia to be misdiagnosed as lupus, says rheumatologist George Stojan, MD, an assistant professor of medicine at Johns Hopkins University School of Medicine and co-director of the Johns Hopkins Lupus Center in Baltimore, Maryland. Both fibromyalgia and lupus can cause muscle/joint pain, brain fog, and fatigue. Both are also more likely to occur in younger and middle-aged women.

    Interestingly, another factor that makes fibromyalgia and lupus difficult to differentiate from each other is that some people have both at the same time. “Having both lupus and fibromyalgia is extremely common,” says Dr. Stojan. “In our cohort here at Hopkins about 30 percent of lupus patients have fibromyalgia too.”

    People with other rheumatic diseases such as rheumatoid arthritis, osteoarthritis, and axial spondyloarthritis are also at an increased risk of also having fibromyalgia.

    Read more to learn about the different symptoms of fibromyalgia vs. lupus, how fibromyalgia and lupus are each diagnosed, and how treatments for fibromyalgia and lupus differ.

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    The Basics of Fibromyalgia

    The U.S. Centers for Disease Control and Prevention (CDC) estimates that about 4 million American adults have fibromyalgia. While doctors don’t know what causes fibromyalgia, it is a disorder in which people often experience widespread chronic pain and sensitivity to touch, in addition to many other symptoms (more on this below).

    Unlike lupus, fibromyalgia is not an autoimmune disease, which occurs when then body’s immune system mistakenly attacks your own cells and tissues. Fibromyalgia is not related to inflammation, nor is it a joint or muscle disorder caused by physical injury.

    People at higher risk of fibromyalgia include women, the middle-aged, and those with certain diseases, including different types of arthritis, or a family history of fibro. While fibro can impair your quality of life, it doesn’t damage your tissues and organs, or cause medical problems like heart disease. It is not life-threatening.

    Common Symptoms of Fibromyalgia

    Widespread musculoskeletal pain all over the body

    Fibro’s hallmark symptom is persistent pain in soft tissues and muscles all over the body. It may involve tender points, or areas of tenderness in specific parts of body. Frequently described as a deep ache, fibro pain may move around, persist for long periods, and disappear.

    Fatigue

    More than nine in 10 fibromyalgia patients experience exhaustion. Fatigue can be especially noticeable when you first wake up in the morning, even when you’ve gotten plenty of sleep; light activity can make pain and fatigue worse.

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    Cognitive issues

    People with fibro can have difficulty concentrating or switching between tasks, frequently referred to as “fibro fog.”

    Tension or migraine headache

    More than half of patients with fibromyalgia have frequent headaches.

    Weird body sensations

    Some people with fibro report tingling, burning, numbness, or creepy-crawly sensations in both arms or legs.

    Other symptoms

    Fibromyalgia patients often also have irritable bowel symptoms, pelvic pain, and jaw/facial pain.

    Read more here about fibromyalgia symptoms.

    The Basics of Lupus

    The Lupus Foundation estimates that 1.5 million people in America have a form of lupus. Lupus is an autoimmune disease that occurs when your immune system cells — which are supposed to protect the body from different germs — start treating normal, healthy cells like invaders, attacking them and causing flare-ups that can affect the joints, skin, heart, lungs, kidneys, and almost any other system in the body.

    Women of childbearing age (between 15 and 44) are at the highest risk of developing lupus, according to the CDC; some 90 percent of people with lupus are women. People of color — particularly African Americans — are at a higher risk of lupus than white people are, and the disease tends to affect populations differently. Native American and black patients tend to have higher mortality rates than white patients, while Hispanic and Asian patients have a lower risk of lupus.

    There are several types of lupus, but most people refer to the most common form: systemic lupus erythematosus, also known as SLE. About 70 percent of people with lupus have SLE, according to the Lupus Foundation of America. Lupus can cause a range of complications; some, such as heart disease and kidney disease, can be severe and even life-threatening without early and proper medical treatment. Regular medical care that utilizes an integrated team of specialists is important to help lupus patients avoid life-potentially serious complications.

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    Common Symptoms of Lupus

    Painful, swollen joints

    These are usually far from the center of your body, such as joints in the fingers, toes, ankles, wrists, knees, and elbows.

    Swelling around the eyes and extremities

    Kidney inflammation can cause fluid retention that can make ankles, feet, legs, hands, and sometimes eyelids feel puffy and swollen.

    Unintentional weight loss (or sometimes gain due to swelling)

    Unexplained weight loss — not due to dieting, other illness, or medication side effects — can be a sign of lupus. On the other hand, weight gain caused by fluid retention can also be a sign of the disease.

    Rashes and skin lesions

    The characteristic rash across the cheeks and nose (called a malar rash) is one of the most recognized symptoms of lupus, although a similar-looking rash can also occur in other skin issues. Another type of lupus skin issue is a discoid rash that causes raised, red, and scaly patches.

    Sensitivity to sunlight and cold temperatures

    Sun exposure can cause a lupus rash to develop or flare. People with lupus are also at risk of developing Raynaud’s, a condition in which the small blood vessels in the hands and feet suddenly constrict when exposed to cold or stress.

    Other lupus symptoms include fever; neuropsychiatric issues such as depression, anxiety, seizures, or psychosis; brain fog; fatigue; headaches (including migraine-like attacks); mouth ulcers; kidney problems; and chest pain.

    Read more here about lupus symptoms.

    Symptoms that Lupus and Fibromyalgia Have in Common

    • Pain
    • Cognitive issues
    • Fatigue
    • Headaches

    Key Ways Fibromyalgia and Lupus Are Different

    Despite the similarities in some of the symptoms, there are a few clear differences doctors and patients should be on the lookout for, says Dr. Stojan.

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    1. The nature of fatigue: Fatigue is common during a lupus flare, but it will subside once the attack is over, says Dr. Stojan. In fibromyalgia, however, exhaustion is more chronic — it’s less likely to come and go.

    2. The nature of pain: Although both fibromyalgia and lupus can cause muscle and joint pain, lupus pain persists until it’s treated, says Dr. Stojan. The pain of fibromyalgia comes and goes. “The transient quality of the symptoms is a reliable sign that pain is not related to lupus,” he says.

    3. Whether skin is involved: Fibromyalgia doesn’t cause nose and/or mouth ulcers or rashes like lupus does, such as the typical “butterfly” rash on the cheeks and bridge of the nose that can pop up during a lupus flare.

    4. Whether there is inflammation: In lupus, a patient’s immune system starts to attack organs and other body tissues, leading to widespread inflammation that will likely show up in lab tests or imaging, says Dr. Stojan. Fibromyalgia, on the other hand, does not cause inflammation.

    Getting the Right Diagnosis

    There are no definitive tests for either fibromyalgia or lupus, so differentiating between the two relies mostly on a thorough history of your symptoms, a physical exam, and sometimes blood tests or imaging to rule out other conditions. Read more here about how fibromyalgia is diagnosed.

    Your doctor will ask you to describe your pain — and if they suspect fibromyalgia, may perform a “tenderness” test, pressing on several parts of your body to gauge where the tenderness is, and how severe it is.

    Your doctor will likely also ask whether you experience fatigue, wake up tired every morning, or have trouble concentrating or experience brain fog — and for how long you’ve had these symptoms.

    Your doctor may order some blood tests in order to rule out diseases that can cause fatigue, such as hypothyroidism type 2 diabetes. They may order blood tests to check for levels of inflammation in the body or for antibodies that could signal an autoimmune disease. One test ordered to help confirm or rule out lupus is the blood test for antinuclear antibodies (ANA). A positive test can be one sign of lupus, but it doesn’t necessarily mean you have it. “ANA is a very common marker people have in the blood. Almost one-third of people in the U.S. will test positive — and that alone doesn’t mean you have lupus,” Dr. Stojan says. However, most people who have lupus will have a positive test.

    If you have a positive ANA test and other signs that point to lupus, your doctor may do additional antibody tests that help confirm or rule out the illness.

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    Your doctor may also order imaging tests like X-rays or MRIs to narrow down the cause of your symptoms. Neither fibromyalgia or lupus cause erosion in the joints (the way rheumatoid arthritis does) or visible inflammation of the lower back (the way axial spondyloarthritis does).

    Treatment for Fibromyalgia vs. Lupus

    Neither disease has a cure, but medication can treat symptoms and help prevent serious lupus complications. The medications used to treat lupus are very different from those used to treat fibromyalgia.

    For fibro patients: Some drugs commonly used to treat depression, called antidepressants, may ease pain and fatigue; these include duloxetine (Cymbalta) and milnacipran (Savella). Anti-seizure medications, frequently prescribed to people with epilepsy, can also help manage pain in fibromyalgia. Among these, the FDA has specifically approved pregabalin (Lyrica) for the treatment of fibro.

    For lupus patients: Many different types of medications can be used to treat lupus, including:

    • Non-steroidal anti-inflammatory drugs (NSAIDs) to relieve pain and inflammation
    • Hydroxychloroquine or chloroquine, a malaria drug that is also useful at treating lupus flares, joint pain, and skin rashes
    • Glucocorticoids, or steroids, to relieve inflammation and treat flares
    • Immunosuppressive medications, such as azathioprine, cyclophosphamide, methotrexate, mycophenalate mofetil
    • Targeted biologics, such as rituximab (Rituxan) and belimumab (Benlysta), which reduce the activity of the immune system by targeting specific immune cells
    • Other medications to help manage complications of lupus, including those for cholesterol, blood pressure, osteoporosis, and others

    Patients with lupus and fibro can also benefit from healthy lifestyle practices, too, including:

    • Exercise: Regular physical activity can help manage symptoms of fibro or lupus, and may improve mood, fitness and function. Swimming, walking, tai chi, and yoga are smart options. Exercise can be very important in helping people with lupus reduce their risk of cardiovascular disease complications. Consult a health care provider or physical therapist about a new exercise regimen, so it can be adapted to individual needs.
    • Diet: Though there is no specific diet recommended for lupus or fibro, a healthy eating plan may boost your immune system, help manage co-existing conditions, and promote overall good health. Read more about a following a healthy diet for lupus and a healthy diet for fibromyalgia.
    • Sleep: Getting adequate rest is vital for both conditions. It’s recommended that adults between ages 18 and 64 should aim for seven to nine hours nightly.
    • Complementary practices: Some patients report that activities like meditation, acupuncture, deep breathing, and massage help them relax and ease symptoms.

    While lupus and fibro may have some symptoms in common, they are ultimately distinct conditions with very different causes and treatments. Visiting a health care provider can help you get to the bottom of your symptoms quickly and begin the correct therapies. The faster you start, the faster you can start feeling better.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

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    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

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  • Most Dangerous If You Are Facing Both Multiple Sclerosis or Lupus

    Most Dangerous If You Are Facing Both Multiple Sclerosis or Lupus

    Understanding MS and Lupus

    Multiple sclerosis (MS) and systemic lupus erythematosus (lupus) are both serious diseases resulting from a failure to function properly in the body’s immune system.

    In MS, myelin, the protective layer around your nerves is damaged by the body’s immune system. It interferes with your brain’s contact with the rest of your body. The effect is a variety of symptoms, for example:

    • dizziness
    • bowel and bladder problems
    • weakness in the limbs
    • numbness in the limbs
    • vision problems
    • fatigue

    Physicians are debating whether MS should be considered an autoimmune disorder. The MS material that would activate the immune response of the body (the antigen) has not yet been identified by scientists.

    Rather than an “autoimmune disease,” MS is sometimes referred to as an “immunemediated” condition.

    Lupus is an autoimmune disease that responds to healthy antigens by the immune system. These are proteins that activate the immune response of the body.

    It’s as if the immune system can’t tell the difference that the immune system is supposed to attack between antigens that are supposed to be in the body and pathogens or other foreign “invaders.”

    The immune system attacks different parts of your body with lupus, such as:

    • joints
    • skin
    • internal organs

    Understanding the Link Between Lupus and MS

    Usually, doctors determine you have MS by eliminating other conditions, such as lupus. It can be difficult to diagnose both MS and lupus. Diseases such as lupus and another autoimmune disease, such as rheumatoid arthritis, may also overlap.

    These diseases also tend to “cluster” in families, which means you may have one autoimmune disease while a sibling or parent has another type of disease.

    While MS and lupus are unlikely to occur, it is common for someone with MS to be misdiagnosed with lupus because of common symptoms of these diseases.

    MS has several other “mimic” conditions, apart from lupus, including Lyme disease. Part of the confusion is that MS does not have a single diagnostic test.

    Understanding MS and Lupus Management

    It is not possible to cure either lupus or MS. A variety of drugs can help control symptoms. If you have both conditions, some treatments and changes in lifestyle can help both of you:

    • Have a lot of rest. Rest often helps to shorten a flare and can help you cope with symptoms of weakness and fatigue.
    • Commit to regular physical exercise. This can sometimes help you get faster through a lupus flare, and if you deal with MS symptoms, it can help improve your strength and coordination.
    • Eat a good diet. For everyone, a healthy diet is recommended. But there may be some dietary restrictions for people with lupus. People with MS may also be advised in their diet to get more vitamin D.
    • Practice relief from stress. Taking a meditation class or learning breathing techniques for relaxation can help you cope with a chronic illness. For people with lupus, learning to de-stress may be even more important, as stress can trigger flares.

    How the development of lupus and MS in an adult is hard to predict. You may have moderate lupus all your life, or to be very severe, it may improve. MS symptoms may also become severe over time, but your life expectancy is usually not affected by the disease itself.

    Giving’s

    If you have any of the above-mentioned symptoms, or you feel something “just isn’t right,” don’t hesitate to talk to your doctor.

    To decide what’s wrong, it may take some time and a number of tests. But the faster you can start treating it, the sooner you know what you’re dealing with.

    Diagnosis and treatment affect both MS and lupus. If you experience symptoms, being proactive about your health and engaging with your doctor can help you meet this challenge.

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    Official Fibromyalgia Blogs

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  • 10 Most Early Signs of Lupus

    10 Most Early Signs of Lupus

    Understanding Lupus

    Lupus is an autoimmune disease that causes swelling and various symptoms. Lupus has a different impact on everyone. Many people only have a few mild symptoms, while others have a lot more severe.

    Symptoms usually start in early adulthood, from puberty to the 1930s. People with lupus usually develop symptoms and then remission periods. That is why it is convenient to ignore early symptoms.

    Since early symptoms are similar to those of other conditions, it does not always mean that you have lupus. Early symptoms may consist of:

    1st Symptom is Fatigue

    Some 90% of lupus suffer from some degree of fatigue. Some people have a nap in the afternoon, but too many sleeps during the day can lead to sleeplessness in the night. It might be hard, but you might be able to maintain your energy level if you can remain active and stick to a daily routine.

    Talk to your doctor if you are experiencing weakening tiredness. There are certain causes of fatigue.

    2nd Symptom is undefine Fever

    Low grade fever for no apparent reason is one of the first signs of lupus. You might not feel you should see a doctor because it may linger between 98.5 liners F (36.9 liners C) and 101 liners F (38.3 linens C). That form of fever can occur to people with lupus on and off.

    Infection, inflammation or imminent outbreaks may result in low levels of fever. Make an appointment to see your Doctor when you have recurrent low-grade fever.

    3rd Symptom is Hair Loss

    Thinning hair is frequently one of the initial lupus symptoms. The loss of hair is caused by skin and scalp inflammation. Many people lose hair by the clump with lupus. The hair dilutes slowly more often. Many people have also beard dilution, eyebrows, eyelids and other body hair.

    Lupus can cause the hair to feel fragile, to break easily, and to appear to be a little ragged, gaining the name “lupus hair.” However, hair loss in those areas may be permanent if you develop lesions on your scalp.

    4th Symptom is Skin Rashes

    A butterfly-shaped rash over the bridge of the nose and on both cheeses is one of the most obvious symptoms of lupus. Approximately 50 percent of lupus suffer from this rash. It can happen suddenly or after daylight. It can appear. Sometimes the rash comes up only prior to an inflammation.

    In other areas of the body, lupus may also contribute to non-itchy lesions. Lupus can rarely lead to hives. Most people with lupus are prone to the sun and artificial light. Some of the fingers and toes are coloring.

    5th Symptom is Pulmonary Issues

    Another potential symptom of lupus is the inflammation of the pulmonary system. The lung becomes inflamed and inflammation could spread to the lungs. The diaphragm can also be affected. All of these conditions can cause chest pain when you are trying to respire. Often referred to as pleuritary thoroughbred pain.

    Lupus breathing problems can decrease the lung size over time. This condition is characterized by continuous chest pain and shortness of breath. Sometimes it is called disappearance (or lung syndrome shrinking). According to the Lupus Foundation of America, the diaphragmatic muscles appear to rise so weakly in CT scan images.

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    6th Symptom is Kidney Inflammation

    Lupus people can experience an inflammation of the kidney known as nephritis. The removal of toxins and waste from the blood makes it difficult for the kidneys to burn. Nephritis usually begins within five years of the start of lupus, according to the Lupus Foundation of America.

    Symptoms include:

    • swelling in the lower legs and feet
    • having to urinate more frequently at night
    • pain in your side
    • high blood pressure
    • blood in your urine
    • darker urine

    7th Symptom is Painful and Swollen Joints

    Inflammation, especially in the morning, can cause pain, rigidity and visible inflammation in your joint. At first, it can be mild and increasingly clearer. Joint problems can come and go, like other lupus symptoms.

    See your doctor if pain medications that are over – the-counter (OTC) don’t help. Better treatment services can be available. However, your doctor should determine whether lupus or any other condition, such as arthritis, causes your joint problems.

    8th Symptom is Gastrointestinal Problems

    In certain people with lupus, heartburn, acid reflux or other gastric disorders are often encountered. OTC anti-acids can treat mild symptoms. Try to decrease the size and avoid caffeine-containing beverages if you get a frequent flow of acid or heartburn. Even, after a meal don’t lie down. See your doctor for additional conditions if the symptoms persist.

    9th Symptom is Thyroid Problems

    Autoimmune thyroid disorder is not uncommon for people with lupus. The thyroid controls the metabolism of your body. A thyroid that is poorly controlled can affect vital bodies like the brain, heart, kidney and liver. It can also lead to a gain or loss of weight. Dry skin, body, and moodiness are other signs.

    When a thyroid is underactive, the condition is known as hypothyroidism. Hyperthyroidism is caused by an overactive thyroid. Treatments to get your metabolism back on track are available.

    10th symptom is Dry mouth and Eyes

    You can feel dry mouth if you have lupus. Your eyes may also feel awful and dry. This is because people with lupus are developing a new autoimmune disorder called Sjogren’s syndrome. Sjogren causes malfunction of the glands that cause tears and saliva, and lymphocytes in the glands may accumulate. In some cases, the vagina and skin of women with lupus and Sjogren can also be dry.

    Other symptoms

    The list of possible lupus symptoms is long. Other symptoms include oral ulcers, lymph nodes that are enlarged, muscle pain, chest pain, osteoporosis, and depression. Anemia, dizziness, and seizures are rare signs.

    Luckily, not everyone gets all the symptoms. While there may be new signs, others often vanish.

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    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store