Category: Fibromyalgia Exercises

Discover effective exercises for Fibromyalgia that can help reduce pain, improve flexibility, and boost energy levels for better symptom management.

  • How Emotional Therapy Can Benefit Fibromyalgia

    I am so excited to share this interview with you. I hope that it helps you as much as it helped me.

    Please introduce yourself and tell us a little bit about your therapy practice.

    I graduated from Central Michigan University with a Bachelor of Science in Psychology in 2009.  I went on to graduate from the University of Michigan in 2013 with a Master of Social Work degree. I  became a School Social Worker for 3 years working mainly with students with emotional and behavioral disabilities.  Throughout this process, I became diagnosed with several autoimmune diseases. This not only changed my life, but it also changed my perspective.  I learned firsthand that there are few supports to help emotionally cope with this major life change. After 3 years of struggling I took my wellness into my own hands through research and finding ways to not only manage my disease outside of the doctor’s office, but to ultimately create a life for myself I could still be happy and fulfilled by. Having been successful in doing this and reflecting on my purpose, I made it my mission to help others experiencing the same difficulties.

    In my practice, I provide a validating space for people with chronic illness to make sense of their experiences. I help them work toward effective disease management, process the difficult emotions that come up, and learn skills and tools to help them be successful living life with chronic illness.

    How long have you been treating patients with chronic illness and/or fibromyalgia? Also, How did you get started?

    I started my practice in 2017 – The idea came from my own personal struggle finding a therapist’s support when I was trying to navigate my first job after my diagnosis. I couldn’t find a therapist who I felt really understood what I was going through or that could offer me tangible skills or tools for managing my illness and figuring out how to integrate it into my life.

    What kind of therapy do you provide for chronic illness?

    I work with a variety of modalities depending on what I feel would be most helpful for the client.  I strongly believe in Cognitive Behavior Therapy, as it is heavily supported by research to be helpful for managing chronic illness and chronic pain. I also incorporate Mindfulness, Ecotherapy, encourage creative expression, Exposure Therapy where necessary (a type of CBT), Solutions Focused Therapy, and Narrative Therapy techniques. 

    We essentially create a plan of action to address the concerns that the client views as most distressing and work from there. Some major areas of interest are typically stress management, grief/loss specific to chronic pain/ illness, communication, problem-solving, relationships, and symptom management, or overall disease management.

    In what way(s) can therapy help a person fighting fibromyalgia?

    Therapy can help through creating a plan unique to the person’s concerns (because these look different for everyone) as well as just having a supportive space to talk about and process everything that has happened, is happening, and will happen. They can build skills for symptom management, get resources and problem solve with a professional as things come up for them in real-time. Therapists can also help with pain management, relationship difficulties that arise inevitably from the added stress, and lifestyle changes required after diagnosis and put together a stress management plan to help reduce added distress. Seeing a therapist does NOT mean or support the belief that fibromyalgia is ‘all in your head’, in fact, it can be empowering and help you regain control over something that feels so uncontrollable at times.

    In my area finding a therapist that takes new patients and my insurance is nearly impossible. In addition, finding one that also has experience helping people with a chronic illness like fibromyalgia is even more of a challenge. Therefore, can you recommend techniques that a person can use on their own?

    This is a challenge regardless of specialty, mainly because therapy is undervalued and therapists are underpaid by insurance companies. This is a whole other issue, but it trickles down to the client. There ARE more and more therapists specializing in this area though, and I think they need is becoming more and more visible.  Most therapists I know who specializes in this area, do so because they have a chronic illness themselves.  We are very good at referring to each other around the country where we can because we understand the need for clients to feel supported by someone who understands this unique struggle.

    I recommend searching Psychology Today in your area and looking under the therapist’s specialty areas to make sure they specialize in chronic illness. In regards to insurance, there is a great resource called Open Path Collective which is a national lifetime sliding scale program where you can find a therapist for the rate of 30-60$.  You pay a one-time fee and belong to it for LIFE so if you ever move and have to switch therapists, you can jump right back on there and find someone who will honor the same fee.

    For those looking to find a therapist, what questions do you recommend asking to find the “right fit”?

    First, ask yourself, ‘What do I want the focus of therapy to be for me?’ Usually, therapists offer a free 15-minute consultation via phone or video, which is a great way to get to know if they are a good fit.  During the consultation, they may ask you what your top 3 concerns are, and these can become your goals to work on in therapy.

    You can also ask if they have previous experience supporting clients living with a chronic illness, and what their approach for this population of clients typically is (if that is what you want the focus of your therapeutic work to be on).

    Also be aware that for us, it is unethical to ask for or elicit testimonials or reviews from past clients, so if a therapist doesn’t have a lot of ‘reviews’ online, this is why.  It is not necessarily a reflection of their ability or work.

    Many people are fighting a physical chronic illness and a mental illness. First, do you find that to be true among your clients? Finally, do you think there is a connection between the two?

    Absolutely. One of the things I educate my clients about is the fact that Depression is the number 1 co-diagnosed condition with ANY chronic illness.  I also let them know that both anxiety and depression can be a part of their symptom cycle and a result of the circumstance of living with a chronic illness.  I also see a LOT of trauma related to medical experiences and stigma, which can result in PTSD or anxiety relating to medical situations or events and navigating society with a visible or invisible disability. This area doesn’t get a lot of mainstream attention, but it’s more common than you’d think in the chronic illness community.

    Please feel free to add anything else here that wasn’t asked. We would love to hear more about your practice and the services you offer.

    I speak at local support groups for all sorts of chronic illness populations and am always happy to speak or present if I’m available. I’m located in the state of Florida and offer telehealth or virtual sessions, which is a great convenient for people whose conditions fluctuate unexpectedly.  I also have an in-person office in St. Petersburg, FL, and am currently working on an online school filled with courses and tools for people with chronic illness to access anywhere, anytime. I take Medicare and private pay and offer superbills for people who have access to out-of-network reimbursement with their insurance. I also am an Open Path provider and offer a sliding scale to a limited number of clients as available.

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • What is the percentage of people who recover from Fibromyalgia?

    What is the percentage of people who recover from Fibromyalgia?

    I’ve had FMS symptoms for almost 43 years.

    No one recovers from FMS. There is no cure. If someone tells you that they “used to have” FMS, they are mistaken. Their diagnosis was wrong.

    You learn to cope with FMS. You learn what your limits are and how to protect your energy. You may have many comorbid conditions such as clinical depression, chronic headaches, irritable bowel syndrome, sleep disturbance, chronic fatigue syndrome, etc. You learn how to deal with each of these conditions. You learn what modalities help you feel better. You learn what drugs help you.

    You exercise to the best of your ability without exhausting yourself or your energy. Walking and water exercises are the gentlest. You have a sleep study to determine if you have apnea or if you need sleep aids. You may need narcolepsy drugs to keep you alert at work.

    You continue working if at all possible. Studies have been done that show that those who continue working do the best in the long run. Effort on through and keep being active.

    FMS does go into remission from time to time. Enjoy it while it lasts. Stress or injury can trigger flares. Retirement helped me a lot! Less stress and time to rest led to a reduction in pain and fatigue. I’m no longer plagued by chronic fatigue.

    Constantly read about FMS and about strides being made in diagnosis and treatment. Stay up to date on the current FMS news. Also, read Lyme Disease materials. The symptoms are very similar.

    Persevere! For another perspective on what we face, read about the “spoon theory”. The author of this piece has MS, not FMS, but her coping method works for us also.

    Above is one theory for which people said fibromyalgia in not recoverable, Read the 2nd theory below for more information.

    Defining Recovery in Fibromyalgia

    Before addressing statistics, it is essential to define what recovery means in this context. Unlike acute illnesses that can completely resolve, fibromyalgia often follows a long-term course. For some, recovery may mean complete remission of symptoms. For others, it may refer to significant symptom reduction to the point where daily life is no longer disrupted.

    Recovery can be classified into several categories: complete recovery, partial remission, and functional improvement. Complete recovery implies a return to pre-symptom health with no ongoing medication or therapies. Partial remission involves reduced symptom severity and improved quality of life, though some level of discomfort may remain. Functional improvement means individuals are able to resume work, maintain relationships, and engage in daily activities, even if some symptoms persist.

    What the Statistics Show

    Research suggests that complete recovery from fibromyalgia is relatively uncommon. Most studies estimate that between 5 to 10 percent of individuals may experience complete remission over time. This number varies based on the population studied, the definition of recovery used, and the type of treatment applied.

    A larger portion of individuals—approximately 30 to 50 percent—experience substantial improvement in symptoms with consistent treatment and lifestyle adjustments. These individuals may not be fully cured but reach a point where fibromyalgia no longer dominates their lives.

    Children and adolescents diagnosed with fibromyalgia tend to have higher recovery rates compared to adults. In some pediatric cases, up to 40 to 60 percent of individuals may experience complete or near-complete recovery. The reasons are believed to involve differences in neuroplasticity, stress resilience, and early intervention.

    Factors That Influence Recovery Outcomes

    Several variables affect the likelihood of recovery from fibromyalgia. Early diagnosis and prompt intervention play a significant role. Patients who receive a diagnosis early in their symptom progression and begin treatment quickly tend to have better long-term outcomes.

    Psychological resilience and mental health also heavily influence recovery. Those who address co-existing issues such as anxiety, depression, and trauma through therapy often report more improvement in physical symptoms. Mental and emotional wellness creates a foundation for sustainable progress.

    A multidisciplinary treatment approach, combining medication, physical therapy, cognitive behavioral therapy, and lifestyle changes, has been found to increase the chances of functional improvement. Physical activity, particularly low-impact aerobic exercise and stretching routines, has shown consistent benefits in symptom management.

    Another critical factor is patient engagement. Individuals who actively participate in their treatment plan, maintain consistency, and make informed lifestyle changes are more likely to report improved health and reduced reliance on medication.

    Socioeconomic status, access to healthcare, and support systems also influence recovery. Those with consistent access to medical care, strong family or community support, and stable life conditions often have better outcomes.

    Why Complete Recovery Remains Rare

    Fibromyalgia is still not fully understood. The condition involves central nervous system sensitization, abnormal pain processing, and sometimes co-existing conditions like irritable bowel syndrome, chronic fatigue syndrome, and autoimmune disorders. These interconnected issues make it difficult to achieve total resolution of symptoms.

    Furthermore, because fibromyalgia does not present with visible physical changes or markers in diagnostic tests, it can be misunderstood or dismissed, leading to delayed treatment. This delay significantly reduces the chance of full recovery.

    Another reason recovery percentages remain low is due to the chronic nature of pain processing disorders. Even when external stressors are removed and symptoms improve, the nervous system may retain a memory of pain that continues to produce discomfort without a physical cause.

    Living Well Without Full Recovery

    While the percentage of people who recover completely from fibromyalgia is limited, many individuals can live fulfilling lives through effective management. Acceptance of the condition, realistic expectations, and long-term coping strategies can empower individuals to reclaim control and improve their quality of life.

    Modern treatment focuses less on a cure and more on self-efficacy, lifestyle modifications, and symptom management. Programs that teach pacing, stress reduction, nutrition, sleep hygiene, and physical activity have transformed how fibromyalgia is treated.

    Many patients report that while their symptoms remain, they become manageable. They learn to identify triggers, adapt their routines, and develop a sense of agency over their health. This transformation is not measured solely by medical standards but by the ability to live a purposeful, joyful life despite the condition.

    Conclusion

    The percentage of people who recover from fibromyalgia completely remains low, with estimates ranging from 5 to 10 percent. However, a much larger group achieves significant improvement and functional wellness through dedicated treatment and lifestyle changes. Fibromyalgia may not always be curable, but it is often livable.

    Understanding recovery in fibromyalgia requires a shift in perspective—from expecting a complete resolution to aiming for meaningful progress. With the right tools, mindset, and support, many people do more than just cope; they thrive.

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • I’m 22 and considering getting a cane for days when my Fibromyalgia Flares up

    I’m 22 and considering getting a cane for days when my Fibromyalgia Flares up

    How do I be confident using the cane in public when I look like an otherwise healthy, able-bodied person?

    I can’t give you a direct definite answer to your question. But I will share a couple of things with you. When my oldest daughter was 13 she had surgery for scoliosis. She walked back to the surgery suite turning back, smiling and waving.

    Totally secure in what she was doing. 13 1/2 hours later they came out and told me that she was paralyzed and would never walk again. Fortunately, God’s bigger than that. Three months later she was wheeled to the hospital doors and with the aid of some braces, she walked out to the car.

    It took about two years of PT but she got to the point that she was able to put the wheelchair away and use two canes. Then later she went to one cane. She’s had 2 more major surgeries to stabilize her back and she now walks with a walker to help take some of the pressure torque off her spine. So never give up! Keep fighting!

    Click here to Get this or Visit Fibromyalgia Store

    The second thing that I want to share with you is my disability. I have a lung disease that requires me to be on high flow oxygen. For several years after being put on oxygen random strangers would walk up to me in Walmart and ask me why was I on oxygen?

    I didn’t look sick! I spent a lot of time trying to explain things to people but it was really almost offensive. I don’t offend easily. But it bothered me enough that I got to the point where I started looking at people and asking Really!?! And what exactly does sick look like! There are many times that I’ve caught myself watching someone park in a handicapped space and get out of the car looking perfectly able.

    I often wondered why they seemed to need a handicap spot. At some point, I made the connection and reminded myself that I had NO IDEA what their health issues were, and frankly, it was none of my business and not mine to judge. I take care of my own issues and usually find that I’m left with little time to squander on placing judgment on other people. It’s not my place to judge.

    So my point is this. Do what you need to do to take the best care of yourself that you can. Don’t even worry about what other people are going to think! You won’t be able to do anything to change it anyway. People that are that worried about your health, they’re going to find something to be critical of no matter what you do.

    Don’t waste your energy on them. You do the best that you can do to take as good of care of yourself as you can. It will help you in the long run and will remove some of your burden in the short run. Take care!

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • What are aggravating factors for Fibromyalgia Syndrome?

    What are aggravating factors for Fibromyalgia Syndrome?

    This can be a difficult question to answer because fibromyalgia affects everyone in differing ways; however, there is one overarching thing that makes it worse, not moving. Although it can feel horrific to move at times, not being active will only make things worse.

    On really bad days all I can muster is walking my dog 10–20 minutes 3–4 times in the day. It’s not a lot but it helps. I’ll also do light stretching on really bad days. Just making sure to not spend the whole day on the couch or bed and getting up every so often and moving around will help.

    Click here to Get this or Visit Fibromyalgia Store

    On days when I still hurt a lot but I’m not absolutely fatigued I’ll call a friend to meet me at the dog park. This helps because it distracts me from the pain while getting me moving for an hour or two (sometimes taking breaks to sit on a bench).

    Having my dog has helped me tremendously with my fibromyalgia for the sheer fact of forcing me to move every day, no matter what. Plus it’s nice to have companionship when you do feel terrible.

    Another thing that can really aggravate is a bad diet. Sugar especially is bad because it causes inflammation, poor digestion and can cause bad crashes when I’m already fatigued. Same with fatty foods.

    The first thing I suggest to anyone dealing with fibromyalgia is to talk to their doctor about medication. Even though I’m a believer in making good life choices and having your body heal itself, if the pain is so bad that you cannot even begin to think about exercise or am exhausted at the thought of trying to buy healthy food and preparing it, medication can help get the ball moving.

    I take Cymbalta for my pain and it’s helped enough where I could start doing yoga again, which in turn gave me the motivation to eat better.

    Make sure to eat well and eat protein (protein powder in a shake with lots of veggies, fruit, and yogurt are great) because I find it hard to keep muscle since I cannot exercise hard enough/regularly enough to sustain it. I also stretch thoroughly before bed and when I wake up in the morning because sleeping for 8 hours makes me quite stiff in the morning.

    And finally, smoking, too much stress, or not getting enough sleep can all aggravate fibromyalgia. Meditation is a great way to help with stress levels and being able to endure the pain. There are great apps and websites that have free or cheap meditation. They have helped me tremendously by not letting me fall into a depressive episode during a flare-up.

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Please avoid these things if you have fibromyalgia?

    Please avoid these things if you have fibromyalgia?

    I’m not telling you what not to do, but a way to get to the point where you can do things. Avoiding things with fibromyalgia is a slippery slope. It reinforces how disabled you are. You need to be active, but very slowly increasing what you’re doing

    Go to a physiotherapist and tell them you want to start SLOWLY you are able to move your knee fives. Do it. Tomorrow do six times, and soon. Each day add one muscle group with the same gradual increase. Start doing very short walks just half a block a day for a week, then ¾ block a day for a week. People will say that’s not going to help. Of course, initially, you won’t notice a difference, but after a few weeks, you’ll find you can do a surprising amount.

    Tai chi is a very gentle exercise and if you go for only 10 minutes initially and gradually increase You will feel better mentally too. Get input from a physio as to the best muscle groups and how to exercise them.

    One of the things that fibromyalgia patients often do his nap during the day. However hard it is, don’t nap. Go to bed at the same time every day and get up at the same time (set an alarm if necessary) Saturday and Sunday too. Getting back into a regular sleep pattern.- patients always said it was impossible.

    I’d say if you went to Japan, within a week your sleep pattern would change. So you can do it! It takes determination, but it does help. Sleep disturbance is a major problem with fibromyalgia and it’s not helped by napping. If you wake up in the middle of the night get up for a few minutes have a drink of warm milk or a small snack and go back to bed. If you’re in pain use a hot pack or whatever works for you while you’re having your drink.

    Click here to Get this or Visit Fibromyalgia Store

    Eat meals at regular times. Remember how miserable young children get when they don’t get food on time. Get massages, go swimming in a warm pool ( most Ys have an evening when a small pool is warmed for very young children. Try an aquatic exercise class and remember to start slowly (5–10 ) minutes to start increasing by 10 minutes a week.

    One of the big keys to improving fibromyalgia is to consciously get your body back into a routine. Another thing I saw over and over was someone in the early strange of working this program was they’d go out and mow the lawn or spend two hours at the grocery store and lifting heavy bags. Tell everyone when you start what you are doing and that you are working very slowly.

    Initially, you need to get lots of help, but after a month you will find you can do a little more. Buy prepared meals or get delivery. Get family members to load the dishwasher, do the laundry for the first few weeks. That’s all exercise. Do not lie around in bed. Read, play music, etc get friends over for tea or coffee go to the movies. 

    Gradually increase the amount you do as your physical fitness improves. And it will. Can you wiggle your foot five times? Of course, you can. You won’t feel bad tomorrow when you wiggle it 6 times. You can increase daily or alternate days. If you work and sit all day, get up stretch and go for a short walk down a corridor or to the washroom. Sitting in one place really stiffens you

    Depression makes management of pain more difficult, so if you are depressed go and see your doctor and get help. Pain clinics and acupuncture can sometimes help. Meditation, relaxation creative imagery with a therapist can help

    I have helped many people with fibromyalgia and they usually do very well. The key is to go slowly. If you overdo it you’ll get discouraged. One of my family does sweet nothing for days and then vacuums the house from top to bottom. He then lies in bed for a few days moaning and groaning and feeling martyred. He sabotages any recovery.

    Doing things slowly may be frustrating. The house may be in a mess, you may be living on take-out, frozen pizza, etc. But it’s not forever and your family and friends should understand if you explain.

    If prescribed take antidepressants, and pain medication. I advise fibromyalgia patients not to get on tranquilizers like Valium Type drugs. They really don’t help fibromyalgia and it’s easy to become dependent. Also, they mess up sleep patterns. A nonaddictive medication for sleep that works quite well with no hangover is Melatonin with L theanine. Just check with your pharmacist that it won’t interfere with any of your other medications

    Ask your pharmacist. I know Costco has it So do many stores selling healthy foods, vitamins, etc.

    Good luck. If you really commit to this I guarantee you will improve your quality of life. This is not about what to avoid? It’s about getting going and taking control of your illness.

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • What do the stories of Survivors tell us about Fibromyalgia and Chronic Fatigue Syndrome?

    What do the stories of Survivors tell us about Fibromyalgia and Chronic Fatigue Syndrome?

    A wonderful database of patients who have accomplished a remission from Fibromyalgia and Chronic Fatigue Syndrome has been created by Chronic-illness Community has video-interviewed several survivors and he has made these available for review.

    The stories he presents and the stories I have heard from patients contain similar reports of survivorship, and it is exactly the healing journeys of these survivors that point to the causes and the diagnosis of Fibromyalgia and Chronic Fatigue Syndrome. Those methods that heal Fibromyalgia and Chronic Fatigue Syndrome, in that they are beneficial, intimate the causes.

    Almost universally, survivors report reaching a state of mind and certitude that change must be made in their minds and bodies, and they evolve passionate and willful determination to increase physical activity and optimize nutrition (see discussions below).

    Exercise

    Aerobic exercises are painful and exhausting for Fibromyalgia and Chronic Fatigue Syndrome patients, who usually have deconditioned and weak bodies. Gentle efforts like Aqua therapy and walking were often common first efforts made by survivors. Gentle Yoga and Tai Chi are also mentioned.

    Aqua therapy is useful because the buoyancy of water relatively negates gravity; relieving stress on strained ligaments as deconditioned and weaken muscles are being exercised and toned. Keeping the body upright is a big effort for people with Fibromyalgia and Chronic Fatigue Syndrome.

    Prolonged bed rest takes a toll on invalids and gravity-deprived astronauts alike. Perhaps a successful escalated exercise program could be ruck sacking, whereby about 10% of the person’s body weight is put into a backpack.

    Click here to Get this or Visit Fibromyalgia Store

    Strengthening the back

    To build a strong back, which is the underpinning of strength for the upright human tower, survivors should model themselves after military personnel, and one of their best training exercises for back strengthening is called “rucking“. The idea is to walk around for at least 30 minutes, or whatever can be tolerated in the beginning, and for three times a week with a knapsack (also called a rucksack) on the back.

    The contained weight of the rucksack should equal about 10% of body weight, or less for openers, and go up to 15% over time. An hour of this kind of activity burns over 300 calories. The posture engendered by the weighted backpack exercises back muscle groups that strengthen the back, and which counter the common human habit of bending forward for much of the workday.

    This exercise is reputed to be one of the reasons that U.S. military troops are such fierce competitors on the battlefield – strong backs. Of course, as you might guess, when military fighting experts pursue this activity with abandon they advance to 60+ pounds and hours of trekking. But for us common folk, who just want to survive the ravages of everyday life, the above-detailed weights are adequate.

    The healing journey

    The diagnosis of Fibromyalgia and Chronic Fatigue Syndrome is correlated with the recognition that the only person who knows what is wrong with you is yourself. Your sense of frustration, hopelessness, fatigue and constant pain often accompany a final realization that no one knows what is wrong with you.

    This self-realization more or less suggests the diagnosis of Fibromyalgia and Chronic Fatigue Syndrome. There is a high degree of correlation between these symptoms of human suffering and the common inability of medical professionals to discern that Fibromyalgia and Chronic Fatigue Syndrome are explanatory.

    Doctor diagnostician impairment

    Many doctors openly deride the diagnosis of Fibromyalgia and Chronic Fatigue Syndrome. Many other doctors are too conservative to go out on a limb to proclaim something for which they have no objective evidence. Doctors are a conservative lot. Many doctors fear what their community of peers might think of them if they begin making the diagnosis.

    Are they thought of as money-seeking opportunists? And with about 4% of the population to be diagnosed, it becomes like potato chips. Once you start making the diagnosis where do you stop when your popularity escalates and more people make appointments. Can your conservative doctor image withstand scrutiny from your peers, especially since you cannot show them objective proof and clinical evidence for your decision-making?

    Let me assure you that most doctors have little taste for becoming the Fibromyalgia and Chronic Fatigue Syndrome King or Queen within their communities, and where doctor survivorship depends upon patient referrals from their peers. The dynamics of covering overhead expenses take into consideration that many who suffer from Fibromyalgia and Chronic Fatigue Syndrome are indigent. Medicaid remuneration to doctors barely covers overhead expenses, if even that.

    Click here to Get this or Visit Fibromyalgia Store

    Initial survivor insights

    What the survivors often did next, after self-realization that they were on their own, was to begin to introduce fundamental changes into their lives. Some began with nutrition. Some began with exercise. The order of introduction of these new habits did not seem to make a difference.

    A key characteristic of the survivors is that they had certitude about their quest, and kept at it for weeks and months; over which time they noted small incremental improvements. These small benefits provided feedback, reward, and instilled enthusiasm to continue the efforts. Eventually, after months of effort, fatigue and pain faded into remission. But healing does not end here.

    Remissions and recurrences

    Another common experience of survivors seems to be a tendency to have recurrences of symptoms of fatigue and pain. Each recurrence was once again beaten into remission via reinstitution of the same efforts that gained initial benefits.

    Hormones and endorphins

    I believe that hormones are intimately involved in the healing process that Fibromyalgia and Chronic Fatigue Syndrome survivors report. The biggest endocrine gland in the human body, the brain, is directly connected to the biggest concentration of nerves in the body and the spinal cord, and these neural and endocrine tissues are intimate and maintain inter-communication throughout our lives.

    The brain secretes hormones and senses hormones. The master gland in the human body, the pituitary, lies at the base of the brain and is part of the brain. The pituitary gland secretes hormones into the blood to regulate most of the other glands in the body. Brain tissues command the pituitary, and thoughts command the brain. “I think and therefore I am” is not an abstract philosophical idea, as Voltaire seemed to indicate when he stated this as part of his philosophical discussions of reality.

    Thinking and healing

    Thinking literally causes what you become. These concepts have been an integral part of the biological sciences since the 1960s. Initially, these physiological insights were studied and recorded within a field called “Psychosomatic Medicine”. Later, in the 1980s these ideas became more broadly incorporated into the field of “Psychoneuroimmunology“.

    A more appropriate name is “Psychoneuroendocrinimmunology“. Anyone interested in the scientific underpinnings of these physiological concepts should study the writings of Dr. Candace Pert.

    Click here to Get this or Visit Fibromyalgia Store

    Thinking wellness

    What the survivors self-discovered is that they could think and act their way to wellness. Each time they instituted an effort that had restorative potency, their brain-generated thoughts evoked positive neural signals that incited positive hormonal ebbs and flows, which in turn stimulated cytokine and endorphin ebb and flows causal of feelings of well being and actual tissue healing.

    The runner’s high is not a myth. Endorphins released by exercise are the body’s internal opiate system. Endo-cannabinoids are another internal feel-good and healing system.

    The extensive body of clinical endo-cannabinoid science explains why Cannabis has been so helpful to those with Fibromyalgia and Chronic Fatigue Syndrome, and to those who have been daring enough to attempt the use of Cannabis in face of the massive federal propaganda campaign that has been waged against this miracle herb for the last 75 years.

    Conclusion

    Qualities that seem to define the thoughts and behaviors of survivors:

    • Recognition that no one understands their illness
    • Belief in self
    • Passionate planning
    • Willful pursuit
    • Determination to heal
    • Dedicated exercise
    • Natural nutrition quest
    • Peer pressure rejection

    The healing pathway:

    1. Resignation to pain and hopelessness
    2. Turned to anger
    3. Turned to stubborn refusal to accept fate
    4. Turned to passionate planning
    5. Turned to dedicated effort
    6. Turned to sense of improved wellbeing
    7. Turned to sense of conquest
    8. Turned to wellness

    Fibromyalgia and Chronic Fatigue Syndrome Diagnosis

    Once a person has realized this transcendence of life experiences, and has sensed true benefits, these very experiences provide self-evidentiary proof that what they have been suffering has been Fibromyalgia and Chronic Fatigue Syndrome.

    The survivors will have made their own self-diagnosis, and they will realize that their own self-taken actions are the optimal route to recovery.

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • My Fight with Fibromyalgia (My Best Way to Tackle this Illness)

    My Fight with Fibromyalgia (My Best Way to Tackle this Illness)

    I don’t know if my way is best, but I’m nearly symptom-free. I take medication and I slowly increased my exercise and activity.

    The worst:

    In the spring of 2008, my fibromyalgia (technically fibromyalgia syndrome or FMS) was destroying my life. I couldn’t move without crippling pain. I would move in small increments like going to the bathroom or switching from the bed to the couch. I needed help getting to appointments. If my ride’s car didn’t have soft seats, I was in agony.

    Medicine:

    Sometime that summer, I was prescribed Lyrica. It wasn’t the first thing I tried, but it was the first thing that helped. It made a big difference. I did a little bit of housework, a little bit of caring for my kids, and I could get myself to appointments.

    I lived like that for years. I got Social Security Disability Insurance (SSDI) after a long appeals process. A couple of times, I tried to be productive and return to school or get a job. Both attempts failed.

    Exercise:

    In 2012 or 2013, I began physical therapy for the FMS. Fortunately, they started me in a therapy swimming pool. That way, the exercises weren’t “weight-bearing.” It did add a little bit of resistance, but really it was less than holding a 1 pound weight. I started with 5 minutes of exercise – plus after I got out of the pool, they would stretch my legs gently.

    I don’t remember how many months I continued with them. I think it was close to a year and a half. They added two minutes a week at first. Later, they added five minutes a week. With the added minutes, they added exercises. I was much stronger when they finally started having me work on the land. Eventually, I could exercise for 30 minutes weight-bearing. At that point, they discharged me.

    Click here to Get this or Visit Fibromyalgia Store

    With all this exercise, something very nice happened. The constant widespread pain declined. It was still pretty bad when I was discharged, but not agonizing. I also disagreed with the discharge because I still couldn’t do a lot of basic household tasks. The fact was, I still wasn’t as strong as the average couch potato.

    At home, I kept doing the exercises. I really liked the reduction in pain. Then, I got a virus and I was sick for a week. The FMS symptoms worsened to the point that I couldn’t do the exercise routine anymore.

    It wasn’t at its worst. I decided on a plan. I chose a YouTube exercise video for beginners. I picked one that used the whole body and seemed to be a true beginner level – for average people. In order to make it possible for me, I started with the first 5 minutes of the video.

    I did it every morning. After a week, I added a minute. I kept adding minutes in small numbers week after week. When I was finally doing the whole video, I felt better all the time again.

    Activity:

    In 2015, I decided that I could manage a part-time job. I did a job search, which is a story in itself. August of 2015, I began working 15 hours a week. The job involved some walking and some stairs, which worried me at first.

    The walking and stairs turned out to be a good thing. Don’t get me wrong; it hurt to walk and climb stairs. But they were absolutely necessary to my job. And since I care about work ethic, I did both with a positive attitude. My symptoms improved further.

    When I was laid off in 2016, I was ready for a job with 30 hours a week and some activity. A year later, I went to 40 hours a week and more activity. Last fall, 2018, I increased my activity again. When I had a smartwatch (I recently lost it), I learned that I’m walking about 9000 steps most days.

    The difference is profound. I still have a ghost of pain all the time, but it’s not a problem. I seldom notice it.

    If I get too much activity, I will feel it. It’s horrible. But since I started working, I’ve gotten more and more careful to monitor my activity. I’ve become aware of the way a muscle feels when it’s starting to reach that point. That means I don’t have problems often.

    Another restriction:

    I have to avoid NSAID class medications except in emergencies. For some people with FMS, they increase symptoms. These include aspirin, ibuprofen, naproxen sodium, and everything related. The safest way to check whether you have this issue is to take a dose of aspirin. It will be out of your system in 2 to 3 days. If it does make you worse, you won’t have to suffer for weeks.

    Of course, in case of a heart attack, I would take aspirin as directed. A couple of days of extra pain doesn’t even matter at that point.

    The over-the-counter pain medicine that doesn’t hurt is acetaminophen (often called Tylenol or Paracetamol).

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • How Fibromyalgia Suffer can start Strength Training?

    How Fibromyalgia Suffer can start Strength Training?

    Exercise helps break the chronic pain cycle associated with fibromyalgia syndrome (FMS) by improving fitness and functional levels, relieving physical and emotional stress, and boosting one’s confidence and self-esteem. While you probably have heard a lot about the benefits of aerobic exercise, you may be wondering about strength training. Women at risk of osteoporosis commonly hear about including strength training activities in an exercise program.

    Should a person with fibromyalgia perform strength training activities? Is it safe? Will this type of exercise hurt you? In the following article, we will answer these commonly asked questions and describe how you can include basic strength training activities in your exercise regimen.

    First Steps

    There are three important steps to take before beginning an exercise program.

    First, let your doctor and other health care providers know about any change in what you are doing to manage your health—including exercise. While exercise has many physical, emotional, and social benefits, there may be health issues you need to address before starting an exercise program, such as unresolved foot pain or back pain. You may be directed to stay away from certain forms of exercise because of other health issues.

    Second, an exercise program is most effective when you do it consistently. Decide on what you are going to do for exercise and where you will do it. If your exercise is not enjoyable or convenient, you probably will not do it regularly. Follow a basic program, like the one at the end of this article, or get the help of a knowledgeable professional—exercise physiologist, physical therapist, doctor, nurse—to formulate your exercise program.

    Does it make sense for you to be outside or inside at this time of year? Do you like to exercise alone or with others? You can exercise at home, in a community center, or in a commercial fitness center. Once you decide what to do and where to do it, make a commitment to yourself to make time in your schedule to exercise. The more hectic your schedule, the more important it is to review your other commitments and plan your weekly exercise schedule. Consider the times of day and days of the week that works best for you.

    Click here to Get this or Visit Fibromyalgia Store

    Finally, anticipate that you may be a bit sore or uncomfortable at first, especially if you have not been physically active in recent months. You should not be in severe pain, however. If you experience severe pain, then you probably have done too much and started too fast. Listen to your body—learn to know the difference between your chronic fibromyalgia pain, the pain of overused muscles, and the acute pain of an injury; they are different.

    One way to help judge your level of pain when exercising is to utilize a 0-10 numerical scale with zero signifying no pain, 5 moderate pain, and 10 the worst possible pain. In general, if your pain is 1-4, exercise as you planned; if the pain rates 5-7, cut back on the amount and intensity of exercise you do that day; if your pain is an 8 or 9, don’t do your regular exercise routine, but you may still be able to perform some gentle stretching and maybe go for a short walk, and if you are experiencing pain that is a 10 it is best if you do not exercise that day.

    While fibromyalgia can be extremely painful, it is important to remember that you are not damaging your muscles and joints when you exercise appropriately. Making good judgments about how much to exercise takes time to learn, but is essential to your successful self-management. With practice, you can become your own exercise expert.

    Adding Strength Training to Your Exercise Program

    Recent research has demonstrated that strength training exercises, when done appropriately, can be safe and beneficial for individuals with FMS. Strength training exercises increase your muscle strength and can make daily activities, such as climbing stairs and carrying laundry, easier. 

    Stronger muscles use less effort to do work than weaker muscles. Some think that by using less effort, your muscles do not get as fatigued. For many years, when FMS was thought to be a disorder of the muscles, people believed that you might damage muscle if you exercised it too hard. Therefore, people with FMS were discouraged from doing strength training type exercises. Today, research demonstrates the safety and benefit of this important type of exercise for the person with FMS.

    Strength training activities can be incorporated into your exercise regimen regardless of your level of experience or fitness. The strength training part of a program ideally should include one exercise for each of the major body areas (legs, chest, shoulders, back, arms, and abdominals). Strength training exercises should be done 2-3 times per week with at least one day of rest between workouts to allow muscles time to rest and recover.

    Exercises can be performed with free weights, machines, stretchy bands, household items (e.g., soup cans), or the resistance of your own body. Exercises can use one or more of the above methods to provide resistance. There is no magic about how you provide resistance. The key is to perform the exercises correctly and regularly, so convenience should be considered when making your decision of what you will use for resistance.

    When beginning a strength-training program for fibromyalgia, you should first learn and master the proper techniques for all exercises. You can learn proper techniques from a book, an introductory session with trained health or fitness professional, or by participating in a class where an instructor will keep a watchful eye on you while you learn with others. More guidance from a knowledgeable professional usually translates into faster learning.

    Click here to Get this or Visit Fibromyalgia Store

    A repetition of “rep” is the performance of an exercise one time, and a “set” is a sequence of repetitions of an exercise performed without prolonged rest. The number of repetitions and sets and the amount of resistance is how strength training exercise is quantified or measured. Begin with a level of resistance that allows you to perform eight repetitions “fairly easily.”

    If you can comfortably lift the weight eight times (8 reps), it is safe to progress to 10 reps the next time you exercise. After you are comfortable with 10 reps, you can try to perform a set of 12 reps. When you can perform 12 reps of an exercise for two sessions in a row, you are ready to increase the weight/resistance slightly. When you increase the resistance, remember to reduce the number of reps to eight and repeat the process of gradually increasing the number of repetitions with the new resistance.

    There are several important keys to remember while performing strength training exercises. Always use proper exercise techniques. Avoid “guarding” sore muscles when you perform an exercise. Contracting muscles around an aching body part leads to more tension and poor posture. Poor posture puts unnecessary stress on other body areas. Exercising with good body posture and technique will work the muscles in a balanced manner and reduce the chance of injury.

    Breathing during the exercise is very important for keeping muscles relaxed, comfortable while exercising, and supplied with oxygen to do the work. To breathe properly during an exercise, inhale and exhale slowly as you perform the part of the movement that requires the greatest effort. As you return to the starting position of the movement, breathe in slowly and smoothly. An easy way to remember this is to “exhale on exertion,” and inhale on the less strenuous part of the movement. Remember, you should never hold your breath while performing an exercise.

    Speed or the pace of a movement is also extremely important to your strength training program. In most strength training exercises there are two parts to each repetition. The first is the concentric or “positive” phase. The concentric phase is when the muscle you are exercising shortens while performing the exercise movement. An example is the biceps muscle, on the front of the upper arm, when you move your hand from your thigh to your shoulder.

    The second part is the eccentric or “negative” phase of the movement where the muscle you are exercising lengthens while you return to the starting position of the exercise. The biceps muscle lengthens when the hand moves from the shoulder to the thigh. Strength training exercises should be performed to a count of two seconds for each of the concentric and eccentric parts of the exercise.

    Our work over the past several years with the SELF-study (Self-management and Exercise for Living with Fibromyalgia) has shown that shortening the eccentric phase can help decrease muscle soreness in people with FMS when beginning a strength training program.

    Strength training exercise has many health benefits for people of all ages. While people with FMS have often been discouraged from performing strength training exercises in the past, evidence today suggests that when performed appropriately, strength training can be an enjoyable and beneficial part of a balanced exercise program. As with any new type of physical activity, it is important to start and progress slowly to allow your body time to learn the exercise and safely adapt to the level of effort.

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Best Books on Fibromyalgia and Other Resources

    Best Books on Fibromyalgia and Other Resources

    Fibromyalgia is complex. If you live with fibro, you know that it’s not as easy as taking a “pill” or any other quick fix and just getting on with your life. Living smarter is about being proactive and taking responsibility for ourselves and our illness, and in that comes empowerment and greater levels of healing.  

    Listed below are the best books and support for fibromyalgia and chronic illness that I have found. The authors are among the very best in their fields. The ‘nutrition’ related books are the very same ones I have used in my business when working with clients and address the very foundation in both diet and endocrine related issues.  

    I have provided and will continue to provide books, resources, and links that will help you to create the best quality of life possible. All of the books, products, and resources have been used or utilized by us for many years. We only promote and stand behind things we have used and believe in as tools, not false cures.

    The books (available for purchase) here below are not listed in any particular order of importance. In fact, for those patients and family members who are new to fibromyalgia, I very highly recommend starting with the book I often refer to as the ‘fibro bible’, 
    Fibromyalgia and Chronic Myofascial Pain, by Devin Starlanyl. 

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    Best Books On Fibromyalgia

    • The Power of Neuroplasticity; Dr. Shad Helmstetter   
    • Molecules Of Emotion”; Candace Pert, PhD
    • Adrenaline Dominance: A Revolutionary Approach to Wellness
      by Michael E. Platt 
    • “Quantum Healing: Exploring The Frontiers Of Mind/Body Medicine“; Deepak  Chopra, MD
    • “Boundless Energy”; Deepak Chopra, M.D.
    • “Superbrain: Unleasing the Power of Your Mind to Maximize Health, Happiness,
      and Spiritual Well-Being; Dr. Deepak Chopra & Dr. Rudy Tanzi
    • “The Mindbody Prescription”;  Dr. John E. Sarno
    • “Freedom From Fibromyalgia“;  Dr. Nancy Selfridge & Franklynn Peterson
    • “Body Ecology Diet Book”;  Donna Gates
    • “Primal Body Primal Mind”; Nora T. Gedgaudas, CNS, CNT  
    • “The Daylight Diet”; Paul Nison
    • Fibromyalgia And Chronic Myofascial Pain”;  Devin Starlanyl & Mary Ellen Copeland
    • “Why People Don’t Heal And How They Can”;  Caroline Myss, PhD
    • “The Maker’s Diet”;  Jordan Rubin
    • “The Power Of Now”;  Eckhart Tolle
    • ” What Your Doctor May Not Tell You About Fibromyalgia“; Dr Paul St Amand
    https://fibromyalgia-6.creator-spring.com/
    https://www.teepublic.com/stores/fibromyalgia-store

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store

  • Chronic Pain Management: Lower Back Pain

    Chronic Pain Management: Lower Back Pain

    Fibromyalgia and lower back pain

    If you have fibromyalgia, then you have likely experienced fibromyalgia related back pain. With many nerves and muscles in the back and around the spine, this is a vulnerable area for anyone but especially those with fibromyalgia and chronic pain issues.

    Chronic pain management techniques are often called for with every kind of back, spine and/or nerve related pain. 

    In fact, because lower back pain is more common today, even in the non-fibro population, it’s no wonder that so many people are challenged with this often debilitating pain. 

    Chronic Fibro Back Pain

    With fibromyalgia, lower back pain is easily exacerbated mostly during activities of daily living. It could be improper sitting, sleeping, or bending the wrong way. 

    This can occur when trigger points are both present and/or active and radiate pain from the lower back into the SI joints, hip flexors, glutes and pelvic area.

    The involvement with SI joints on the upper side on the buttocks also radiates pain to the lower back and even into the pelvic area. Sitting or standing for long periods of time can keep these areas tight and radiating.

    For those with more severe fibro, even shorter periods of sitting can pose the same issue and should be limited, especially with a tendency toward inflammation within the SI joints of the lower back. 

    Elements of Chronic Pain Management

    Although regular chiropractic adjustments can be helpful to keeping the fibro body in better alignment, there are many perpetuating factors that need to be addressed and other chronic pain management tools to be used consistently as well.

    First, the fibromyalgia patient may have a more difficult time allowing the adjustment to ‘hold’ like a non-fibro body …This can stem from the TRP’s that may be active in the body.

    Second, any perpetuating factors such as lack of core strength and/or lack of agility need to be addressed with chronic pain management techniques.

    Maintaining strength and agility will always be necessary to avoid injury and stress on the more vulnerable areas of the body.

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    If you have Degenerative Disc Disease and Fibromyalgia, it is important to utilize the most effective but least invasive options to treating lower back pain.

    And like fibro, it can feel progressive, however many experts on treating back pain believe that degenerative disc disease is more of a waxing and waning pain syndrome due to normal wear or aging and not really a “disease”

    With fibromyalgia, we are more “sensitive” to any kind of injections. If you choose treatments including injections such as epidurals, cortisone or even saline/cartilage injections, it is important to know that the fibro body will likely need more recovery time from the injection sites.

    That is normal for a fibro patient. However, doctors treating other conditions in a fibromyalgia patient will not always know this. 

    Don’t neglect the core

    One of the more effective elements to decreasing lower back pain includes core strength exercises, performed slowly and consistently. With chronic pain, it is often overlooked. This can be done in a variety of ways, including in the standing position, with knee lifts and side bends that activate the oblique muscles.

    Hand weights are also optional with oblique work. These type of exercises are great for people who cannot get down on the floor.
    Again, strengthening the core in a safe and effective manner is essential for reducing pain in the lower back and SI joints.
    Lack of strength in the gluteal muscles can also affect pain in the lower back.

    Weakness in the gluteus area can also exacerbate trigger points in the lower body. Core and glute strength support one another while supporting overall conditioning in the lower back region.   

    Another effective exercise is to lie on your back on a mat, and like you are building a bridge with your back, gently lift up from the lower back, put your hands under your back and just lift up and down and hold in the upper position 4-8 times. (See if you can go a little higher with each “bridging” session)

    Decompression Techniques

    Have you ever used de-compression techniques at your chiropractor’s office? This can be a very helpful component of chronic pain management for lower back pain.

    The spine tends to get compressed through activities of daily living and by sitting and/or standing for extended periods of time so decompression is an effective tool.

    We have also found techniques utilizing inexpensive tools that can be used at home. One such tool is a small curved padded device that can aid in de-compression while lying comfortably on the floor or even on a raised table.

    While utilizing any kind of de-compression, it is important to be very relaxed while ‘allowing’ the entire spine to release. It might not feel normal at first. Start with 1-2 minute increments and work up to 5-10 minutes per session. 

    What about the inversion table?

    An inversion table can also be used for spinal de-compression either at home, at the gym or in the doctor’s office.

    Go slow when using inversion, especially with any active trigger points in the neck or back area. It has been found that even going just past 50% on the table can be helpful, so going slow and adjusting to the feeling of being inverted needs to be a consistent process. 

    I use an inversion table at home and my recommendation would be to get a good quality table if buying one for home or office use. I have also used them at the Chiropractors office and we now have one at the gym as well, so they are becoming more widely available. 

    I will provide another caution with inversion, but this won’t be an issue until you are going past about 70% inversion.

    If you have weakness in your ankles, you want to be sure to not only wear shoes while inverting, but also thick socks may be helpful and if you feel too much pressure on the ankles, then come back up as much as needed. 

    A few minutes per day is a good place to start. Again, even at just past 50%, you are taking pressure off the spine. Some people with fibromyalgia and CFS/ME might feel pressure in the head more quickly with inversion.

    For instance, if you ever feel pressure in your head when leaning down, then this is a warning to go slow with increasing levels of inversion

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    The “BeActive” Brace for Low Back Pain

    • The patented pressure pad in the brace applies targeted pressure to the specifc point that provides back pain relief! BeActive is now FDA approved for Class 1 Medical Devices!
    • Helps relieve lower back pain associated with Sciatica!
    • Quick and easy to apply . The Beactive wrap should initially be worn for up to 2 hours at a time. If it remains comfortable, the wrap can be worn for longer periods as needed.
    • Works on either right or left leg! The Beactive wrap fits the calf circumference sizes 12.5 inches to 18 inches measured around the fullest part of the calf. The Beactive wrap is effective when worn on a single leg on the side of the pain.
    • Discreet and easily hidden under clothing.

    Another point of consideration and often a perpetuating factor in those with chronic lower back pain is sitting too long first thing in the morning. Do you wake up and sit in front of your computer or TV first thing in the morning?

    What about Posture?

    How can we become better aware of our posture? Here is a simple move that we can do anytime to remind ourselves of correct posture and improve body memory:

    Draw up from the abdomen into the rib cage and hold.. so instead of merely putting our shoulders back, we first draw up from the abdomen area while increasing the range of motion within the entire back and spine.

    This will also prevent us from putting undue strain on the neck area. You will be surprised at how much pressure you can take off of the lower back when consistently practicing this drawing up from the lower back type of posture. (put a note at your computer/desk or wherever you sit for periods of time)

    Other perpetuating factors for back pain include sleeping positions and mattress quality. Extra pillows around the sides of the body and under the knees can be helpful.

    Even a decrease in upper body strength can increase lower back pain when we attempt to lift something unusually heavy. We cannot afford the extra strain on the lower back due to over-compensation and/or ineffective posture. 

    Yes, overall body strength and agility in the fibro body is an essential part of chronic pain management and will always be important to preventing injury and protecting the more vulnerable areas that are susceptible to pain.

    A New Excellent Tool for Lower Back Pain Management 

    I’ve discovered a new tool for my constant lower back pain which is one of my most troublesome areas of chronic pain; its called the Lo-Bak Trax.

    I’ve been using this for a few weeks and its helped a lot. I love it. Click on the links and wander on over to Amazon and check it out.

    About the product:  Lo-Bak Trax

    1. FDA Cleared to treat: Herniated Discs, Stenosis, Sciatica & Degeneration
    2. Easy, Comfortable and More Effective because you can Target Your Pain
    3. You are in TOTAL CONTROL of the amount and direction of the force applied
    4. Totally Portable, weighs less than 4 lb’s and can fit in a suitcase
    5. Hand welded at 5 different points and comes with a lifetime guarantee against breakage

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

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

    For More Information Related to Fibromyalgia Visit below sites:

    References:

    Fibromyalgia Contact Us Directly

    Click here to Contact us Directly on Inbox

    Official Fibromyalgia Blogs

    Click here to Get the latest Chronic illness Updates

    Fibromyalgia Stores

    Click here to Visit Fibromyalgia Store