Tag: fibromyalgia pain

A comprehensive look at Fibromyalgia pain, its symptoms, triggers, and effective strategies to manage and alleviate discomfort.

  • 20 Signs of Chronic Fatigue Syndrome Isn’t Going Away

    20 Signs of Chronic Fatigue Syndrome Isn’t Going Away

    Is Chronic Fatigue Syndrome Real?

    Chronic fatigue syndrome is a debilitating illness that takes many forms, has numerous symptoms, and no known cure is available from the standard medical community.

    You might have some skeptical friends who doubt you are actually ill, perhaps they think you are simply malingering. However, chronic fatigue syndrome is a very real disorder affecting millions of people worldwide. Yet often patients can be told ‘it’s all in your head’, or suffer comments from family and friends like ‘oh yes I get really tired too’, both of which show a complete lack of understanding that the illness is in fact very real.

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    Unfortunately, its common name, chronic fatigue syndrome doesn’t help people’s perception that it’s not a real illness and it’s simply tiredness. The illness has two other names, Myalgic Encephalitis (ME) and Systemic Exertion Intolerance Disease (SEID). Perhaps SEID helps describe the illness best as it does state a key feature of the illness i.e., the inability to tolerate exertion either mental or physical.

    Whatever you decide to call the illness, it is DEFINITELY real.

    Fatigue is not the only symptom, although it is the one that most often typifies the disorder. And, this fatigue isn’t simply a feeling of being a bit tired or sluggish. A good night’s sleep doesn’t help the fatigue which gets worse after mental exhaustion or physical activity and can take several days of bed rest to recover from.

    Several other symptoms accompany the overwhelming and unrelenting fatigue including:

    Is There A Chronic Fatigue Syndrome Test?

    There is no available test or biomarker for the illness. And, what makes this disorder baffling is the severity, type, and a number of symptoms individuals suffer from.

    No single cause of chronic fatigue syndrome is known, and in fact, it can be caused by multiple things, but it is likely that trauma or several traumas of some description triggered it.

    For example, trauma can come from one or more of the following:

    • Hormone imbalance, such as adrenal fatigue.
    • Bacterial infections, such as pneumonia.
    • Immune system problems.
    • Mental health issues, such as stress and emotional trauma.
    • Gene mutations.
    • Viral infections, such as glandular fever.
    • Trauma from physical accidents.

    How Long Does Chronic Fatigue Syndrome Last?

    Because there is no test available, a diagnosis from your doctor is generally only arrived at by ruling out other illnesses such as hypothyroid, sleep disorders, kidney problems, etc. Additionally, a diagnosis can only be given after you have had the symptoms for at least 6 months.

    Unfortunately from a naturopathic point of view, this is 6 months during which time you could have already started testing to find out what lies at the root cause(s) of your chronic fatigue syndrome. It’s also 6 months during which time your symptoms and illness may be getting worse.

    Some people mistakenly believe that they cannot recover from chronic fatigue syndrome because standard allopathic medicine has no ‘cure’, there’s no ‘pill’ they can be given to make chronic fatigue syndrome go away.

    At the other end of the spectrum, others think if they just wait it out, chronic fatigue syndrome will disappear of its own accord. While this might happen, if you are lucky, it’s pretty unlikely. Without getting proper treatment, which gets to the root cause(s) of your particular form of chronic fatigue syndrome it can not only last for many years but during that time, gradually get worse.

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    Time can pass without your symptoms worsening, or new symptoms making an appearance. There can even be periods of time when you start to feel a little better. But there will be times too when you relapse and get worse. This is the point when your health declines even further.

    You may be the type of person who is willing to wait it out to see if you can recover by yourself. However, I know from my experience that had I found the right naturopathic help and treatment sooner, my health would not have declined to the extent it did.

    Chronic fatigue syndrome rarely develops overnight, but there is usually an event or series of events that lead up to it. The tricky thing is that it’s often not until you start getting treatment do you realize what those triggering events were.

    During your journey with the illness, you’ll get many signs chronic fatigue syndrome isn’t going away. Most of the signs sneak up on you slowly. You adapt your life around your illness which can mask the reality of your worsening health condition.

    The signs show themselves in various forms, some are physical, some mental, some behavioral, and some environmental. Many you may think do not relate to your illness at all. However, even the signs that show up in your home and work environment are rooted in your illness.

    Additionally, there are a multitude of signs you should take careful note of to gauge if your chronic fatigue syndrome is not only hanging around but actually becoming worse.

    It is foolish to ignore any of these signs as they are signals your illness is progressing and you need to seek out the right form of treatment if you want to have any chance of recovery.

    Each individual has their own unique journey with chronic fatigue syndrome. Some have a particularly debilitating form of the illness leaving them completely bedridden. Others have a less severe form that gradually deteriorates as the illness progresses. Whatever form your chronic fatigue syndrome takes, there will be signs that it’s not going away…

    Do You Recognize Any Of These Signs?

    1. You Don’t Feel Like Socializing – You may have been a bit of a social butterfly in the past. Always one of the first to eagerly accept invitations to enjoy lunches, family BBQs, nights out with the girls, gallery openings, shopping trips, dinner out with some fine dining, invitations to parties, etc. But now you realize you haven’t had an outing in months, you just declined an invitation to a close friend’s wedding too.

    In fact when was the last time you enjoyed a social occasion. Come to think of it, the last time you went out you left early and couldn’t wait to get home, crawl under the covers, and sleep. And now, it just all seems like way too much effort to take part in any socializing at all.

    It’s going to take too much energy to work out what to wear for starters. Then you need to get in the car and drive half an hour to get there. Don’t even mention how exhausting it is to have to make polite chitchat to people who, if you’re honest, just drain your energy. Nope…..all too hard, you just stay home.

    2. You Can’t Cope With Even The Slightest StressKnown for your calm demeanor and your ability to just get on with things now you find you’re flying off the handle with the least provocation.

    You arrive at work feeling pretty exhausted, get settled at your desk with the first coffee of the day, and proceed to open your email. Scrolling through your emails, you ask yourself when did you start getting so many emails, how are you expected to reply to all these emails in a day?

    Your stress level is already rising when your colleague walks up to you and asks a simple question about a project you are both working on and you not only don’t have the answer but you want to scream at him/her to just go away.

    It’s only 9 am and already you feel completely overwhelmed and terrified that you’re going to drop the ball. Your workload hasn’t increased, in fact, it’s currently the quietest time of the year in the business but it’s all too much to deal with, you just don’t have the mental energy to deal with a normal workday in your normal efficient way.

    3. You Can’t Stand Noise And Bright Lights – Summoning all of your energy, you pull an outfit together from the back of the wardrobe, slap on some makeup, and get in the car determined to enjoy a night out. The friends you are meeting up with are fun, you enjoy their company and you’re looking forward to a few laughs.

    It’ll be great to enjoy a couple of hours of lighthearted chat and catch up with everyone. Something to take your mind off how lacking in energy you are is just what you need.

    As you walk into the venue you’re hit with a wall of flashing lights above the band in the corner who is playing way too loudly. OMG, you didn’t realize there would be music and definitely didn’t expect the flashing lights. Your friends are there already, getting stuck into a few drinks, yelling to each other to be heard above the music.

    They wave to you and you realize this was a BIG mistake, you just can’t do this. The music is pounding in your head and the bright lights flashing on and off are make you feel like you’re about to throw up.

    Waving to your friends and shaking your head, you start backing towards the door. All you can see is the startled looks on their faces as they see you turn on your heel and get out of there as fast as you possibly can. And now you have another problem, how on earth are you going to explain you’re weird behavior to your friends who you just ran out on?

    4. You Don’t Sleep Well At Night – You used to be such a great sleeper. Getting between 8 or 9 hours of sleep was easy for you. Now, however, getting a solid 8-hour sleep seems to be a thing of the past. In fact, you can’t remember when you slept soundly through one entire night.

    Not only that but something seems to have happened to your body clock because you can’t fall asleep easily either. Sometimes you fall asleep, only to wake up again an hour later and you’re wide awake with no hope of dropping off to sleep again.

    Lately, you’ve also developed a pattern of waking up at around 3.15 each morning and at that time you’re wide awake and there is absolutely no hope of getting back to sleep before the alarm goes off. And when you do wake up, you feel just as exhausted as you did before you finally got to sleep.

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    5. You Develop Feelings Of Isolation – You seem to have lost touch with family and friends. And, it seems as if nobody understands what you are going through with this illness.

    It doesn’t help that you’ve been on the receiving end of comments that suggest ‘you’re just being lazy or that ‘everyone gets tired from time to time, after all, we all have such busy lives. Nobody seems to understand what you’re going through.

    Your doctor can’t help you and you don’t know where to turn for help. It feels as if you are truly alone and nobody understands that you are actually ill.

    6. You Are No Longer Able To Work Full Time – It hurts, you were at the top of your game, climbing the corporate ladder, doing great and the future was looking very bright indeed. Thinking you could recover you kept on pushing through, ignoring the signs your body was giving that it was all too much for you.

    Now you’ve arrived at the heartbreaking realization that you no longer have the capability to continue on your present career path because you simply cannot work a full day. You are seriously considering giving up your full-time position and looking for a job that is less taxing. It seems that working a few hours a week is all you can manage with your current state of fatigue.

    7. You Dread Being Asked To A Function – Once the life and soul of the party, you now cringe if someone asks you to a function as you simply don’t have enough energy to work AND socialize. Your well-meaning friend doesn’t understand you are ill, after all, you look OK on the outside, you definitely don’t look sick and you work full time in your career. So what could possibly be wrong with you?

    Not only that, but you declined the last couple of invitations they gave you. It’s beginning to look as though you just don’t want to spend time with them and you know that pretty soon the invitations will stop arriving if you don’t attend something soon.

    8. You Develop Intolerance For An Increasing Number Of Food Types – Lately, you’ve noticed everything you eat seems to set off a reaction and you start sneezing, your eyes water, and your nose runs uncontrollably. Only by taking an antihistamine can you get it to let up. And what’s with that strange blotchy rash on your chest?

    But yesterday the glass of wine, latte, and cheese sandwich you had were all OK, today….. not so much. Now you need to work out which one of those items is causing you to react, or is it all of them, yikes? Eliminating several foods from your diet has already been carried out, but it seems the list of your food sensitivities just keeps getting longer. Soon it will be very difficult to choose food that you won’t react to.

    9. You Feel Depressed – You feel utterly helpless, and don’t know where to turn for help with your illness. Everyone around you seems to be enjoying a happy and healthy fun-filled life.

    But you are trapped and unable to move. Lately, you’ve started feeling angry that people seem oblivious to your condition. All you want to do is stay curled up in bed all day while your thoughts just keep dragging you down further and further. You are considering a visit to the doctor for some medication. Perhaps he can give you something to lift your mood, some ‘happy pills’. But you are not sure if you want to start medicating your feelings away, doesn’t seem right somehow.

    10. You Suffer An Increasing Number Of Crashes – Lately it seems like the amount of activity you are able to carry out is becoming less and less before you crash. You used to be able to work part-time, carry out normal domestic chores and shop each day.

    However, lately, you can’t do all the cleaning and shopping you used to do before you have to take to your bed to recover. Experiencing a crash used to happen maybe once a month when you overdid it with the cleaning and you’d spend the next two days in bed. Lately, you seem to spend more time in bed during the week and less time on chores and activities.

    11. You Take Longer To Recover From A Crash – During the last month, you’ve spent more days in bed than out of bed. Recovering from a crash normally takes a couple of days, then you can get up and resume your semi-normal life.

    Lately, though it seems each crash takes four or more days in bed before you recover sufficient energy to just get up and sit on the sofa. You feel scared that soon you will become completely bedridden if things keep on going this way. Your life is becoming increasingly abnormal with more of it spent in bed as you have no energy to do anything else.

    12. Your Home Environment Is A Cluttered Mess – As you look around your home you realize it looks like a horrible mess. It hasn’t been cleaned properly for ages but, more than that there is clutter everywhere. The kitchen is full of dirty dishes and half-empty food containers and there’s a coating of dust over all the furniture. Dirty laundry has piled up, you’re running out of clean clothes to wear and the laundry basket is overflowing.

    There are old newspapers, magazines, and garbage everywhere, and every surface is cluttered with ‘stuff’ everywhere. Your home used to be so orderly, you took pride in your organizational and housekeeping skills.

    But now that you take a good look around, your home is in disorganized chaos reflecting the chores you haven’t managed to do due to your lack of mental and physical energy. Gazing around, you realize it’s pretty disgusting. You knew you were letting things slip as your energy disappeared. But how did it get this bad?

    13. Your Brain Fog Is Getting Worse – This morning you can’t find your purse. Rushing to get breakfast ready, your mind is racing. How can you have lost your purse? Trying to frantically retrace yesterday’s steps you think about where you could have left it. Maybe it’s still in the car? You turn to get the milk from the fridge, open the door, and Bingo! There’s your purse, on the top shelf of the fridge. It’s been there all night so at least you didn’t lose it.

    The only harm done seems to be that your lipstick is now a bit frozen and too solid to put on. But why on earth would you have put your purse in the fridge?

    Oh well, all’s well that ends well, you go upstairs to get some documents you need for work and at the top of the stairs can’t remember what you came up for. Down you go again, then you remember…… the documents!

    People at work are starting to notice you seem to be a bit forgetful and a couple of comments have been made about your lateness getting reports in on time. Actually, it’s starting to become a bit embarrassing, you used to be the one everyone could rely on.

    14. You Are Unable To Exercise – Your weekly routine for years was always to exercise about 3 or 4 times each week. You didn’t go mad, just some cardio or weights and the odd class to break up the monotony, it’s always been a great way to keep your weight under control.

    You’ve kept your exercise routine pretty steady for years and enjoy a good fitness level. So you know that motivation isn’t a problem for you.

    But last time you did 20 minutes on the treadmill you spent 4 days in bed recovering. Always a regular exerciser, now it seems that even a gentle 10-minute walk in the park is too much for you. But you know if you push it beyond 10 minutes, you’ll end up in bed for days recovering.

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    15. You Seem To Be Suffering From Anxiety – Never normally an anxious type of person, you’ve noticed strange feelings surface that you realize could be symptoms of anxiety. That weird churning feeling in your stomach that you know is not indigestion.

    Often you feel dizzy and light-headed, but sort of restless at the same time. The other day you couldn’t find a space to park the car and your heart started beating out of control and you felt as if you were going to pass out or vomit, or all three at the same time.

    In situations, you can normally handle you now feel completely out of control. The slightest upset seems to trigger many of these weird symptoms and feelings.

    16. Your Eating Habits Are Out Of Control – Having always been conscious of maintaining a healthy diet, why on earth are you craving french fries and sweets every single day? Come mid-afternoon the lure of all that fat and sugary wrapped goodness luring you from the vending machine becomes too hard to ignore.

    Watching TV in the evening you’ve just eaten an entire container of ice cream on your own. Healthy salads, fresh lightly steamed vegetables, salmon, and free-range chicken have lost their appeal. All you want now is fatty oily pastries, deep-fried food, and chocolate.

    17. Your Hair Starts Falling Out – People have always commented on your crowning glory, you’re gloriously shiny healthy looking lustrous hair. During your shower this morning the water stops draining away and on closer inspection, you find the reason.

    No need to call the plumber, it’s just your fallen hair clogging the drain. As you start to dry your hair you notice lots of hair in the brush. Your once thick hair is thinning and the texture is wiry and it’s kind of frizzy too. Unfortunately, it can no longer be described as a crowning glory so thin and straggly has it become.

    18. You Develop An Irritated Bladder – It seems you can no longer get a full night’s sleep as you are constantly awake with the need to pee. Not only that but when you pee it burns badly.

    After checking with the doctor you find there is no infection, however, it seems you have developed an irritated bladder. Your stomach feels a little tender and you have the annoying need to go to the toilet several times a day. It’s not only annoying but makes many activities impossible. For example, going to see a movie is now completely out of the question as you’ll miss half the movie while you spend so much time in the toilet.

    19. You Experience Balance Issues And Muscle Weakness – Realizing your normal exercise routine is out of the question you try some simple yoga. However, it seems that even the relatively simple tree pose is too much for you.

    Normally your balance is pretty good, but doing tree pose you find it impossible to balance on one leg. When you try cobra pose you find your arm strength has deserted you too. You simply cannot push yourself up on your arms, they are too weak. All of the simple poses you normally do are also out of the question. Looks like you’ll need to start practicing restorative yoga instead.

    20. You Try To Sit Down As Much As Possible – The thought of standing in the shower for even five minutes is too much for you. You’ve started taking a bath each morning instead.

    You use a rolling stool to sit on while doing chores as much as possible. Cooking, ironing, and laundry tasks are all carried out whilst sitting. Shopping expeditions are now a thing of the past, it’s too difficult to stand in queues and walk around stores. Instead, you’ve started ordering your groceries online so that you no longer have to make a trip to the mall.

    Putting It All Together

    By taking note of new or worsening symptoms, and changes in your work and living environment you can recognize the signs your illness is giving you that it’s here to stay. It’s not going to disappear of its own accord. Now is the time to find a naturopath/ functional medicine practitioner experienced in treating chronic fatigue syndrome who can help you recover.

    Please feel free to leave a comment below.

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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

  • Nurse Receives Complex Regional Pain Syndrome Compensation

    After slipping on a wet floor and injuring herself, a nurse developed severe Complex Regional Pain Syndrome (CRPS), a condition that is known for causing a plethora of extremely painful symptoms. Due to the condition having such a negative impact on her life in every capacity, Ronty Rhodes Solicitors helped her to secure £50,000 in complex regional pain syndrome compensation.

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     How the accident caused CRPS to develop

    Kathleen Ann McLeish, a 60-year-old nurse from Edinburgh, slipped on a wet floor, fell, and broke her wrist in 2011 while working as an emergency nurse practitioner. She was working in the Emergency Department of the Edinburgh Royal Infirmary at the time of the accident, and there were no signs to indicate that the floor was wet. 

    After the initial accident took place, Kathleen momentarily fainted in the resuscitation room and was immediately sent to the A&E department where, after receiving X-rays, a black slab was added to her fractured wrist. She was sent home with painkillers, and two weeks later, she was admitted to the hospital and underwent surgery to have an external fixation placed on her wrist and lower arm. She was expected to make a full recovery, but soon after the surgery, her fingers became swollen and extremely painful. Although no infection was discovered by professionals, Kathleen was prescribed antibiotics.

    Symptoms of CRPS

    Six weeks later, the fixation was removed from Kathleen’s wrist and lower arm, and she began to attend physiotherapy on a weekly basis. Although a reasonable degree of movement returned to her wrist and fingers, she still felt stiffness, restricted movement, and swelling in her hand and wrist. By September the same year, three months after the initial fall took place, Kathleen was continuing to experience a feeling of tightness around her wrist, as well as considerable swelling in the fingers on her left hand, intermittent color changes, and occasional shooting pains.

    Making a diagnosis of CRPS

    Due to her persistent symptoms, she consulted her doctor who then diagnosed her with complex regional pain syndrome in her left hand, which was directly caused by the fracture she obtained from the initial fall. CRPS is a poorly understood condition that affects approximately 1 in 3,800 UK people each year and is usually caused by an accident or trauma. It typically affects the limbs and is known as one of the most painful of all medical problems, often causing extreme sensitivity, prolonged pain, stiffness, and cognitive impairment.

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    The impact of CRPS on Kathleen’s life

    As a sufferer, Kathleen’s life has changed in a negative way. The symptoms she experiences prevent her from completing many day-to-day tasks, often leaving her reliant on assistance from others. 

    She has had to make many lifestyle changes in order to maintain her independence. She has had to adjust the clothes she wears, and only wears clothing with zips as opposed to buttons as she struggles to dress independently. In addition to this, Kathleen has had to employ a gardener due to the severe pain she experiences. She has also had to give up swimming and playing the piano, both of which are hobbies she enjoyed taking part in. 

    Her confidence at work has been affected and, due to the fact she feels socially isolated from her friends and family, she has become depressed, has put on weight, and has had to be signed off work in order to recover.

    Making a successful compensation claim

    Due to the way Kathleen’s life has been affected, and the fact that no verbal, signed, or visible warning was given to her to confirm that the floor was wet, the Court ruled the NHS responsible. Kathleen was issued a sum of £50,000 in complex regional pain syndrome compensation – a sum which should help to improve her quality of life and ease some of the burdens she feels as someone who suffers from CRPS.

    Contact us

    If you suffer from CRPS as a result of an accident or injury that wasn’t your fault, you could be entitled to compensation, just like Kathleen. If you suspect this may be the case, read up on how the CRPS law process works, get in touch with our expert team of lawyers by calling 0808 123 0003 or filling in our online contact form, and discuss your case in more detail.

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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

  • Dry Body Brushing and Fibromyalgia

    The Benefits of Dry Body Brushing

    Fibromyalgia and Chronic Fatigue are often associated with toxic overload and therefore, finding ways to reduce the toxins in our bodies are crucial to good health. Dry Body Brushing is a great addition to your daily routine.

    Many of us opt for a massage as this helps with our aches and pains. However, what the massage is actually doing is moving and draining lymphatic fluid, getting it to freely circulate around the body. Exercise also has the same effect. However, unless we are very lucky, daily massages are just not an option for most people and we may not be up for exercise every day. Dry Body Brushing is free, quick, and easy, taking just a few minutes every day.

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    Just 5 minutes of brushing brings great health benefits.

    Not only is the skin the largest organ of the body but it is really important for elimination and detoxification. The lymph is responsible for helping to remove toxins from the body and the skin accounts for the removal of about one-third of your body’s toxins.

    Often when our body is toxic, this in most cases is reflected on our skin in varying degrees ranging from dry and lackluster to oily and acne. Whilst nutrients are delivered to other areas of the body first before the skin, it is the skin that is the first organ to show signs of dis-ease. Toxic overload can also leave us lacking in energy and suffering from digestive issues.

    The benefits of Dry Body Brushing include:

    • Increasing circulation which in some cases has improved cellulite.
    • Sheds dry skin cells which encourage new cell renewal which ultimately results in brighter skin.
    • Releases toxins through the improvement of lymphatic drainage.
    • Stimulates the nerve endings which just feels great.
    • Helps to eliminate clogged pores and therefore assists absorption of nutrients.
    • Helps digestion.
    • Tone the muscles.

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    Directions:

    • For best results, use a natural bristle brush.
    • Always brush on dry skin before a shower.
    • Work in circular, brisk, upward motions always towards the heart and in the direction of the lymphatic flow.
    • Start at the ankles and work up.
    • On the back work from the neck, down towards the lower back.
    • Use circular counter clock-wise strokes on the stomach
    • Lightly brush over the breasts
    • Ensure that you never brush over inflamed, sunburnt skin or skin cancer.
    • Always shower after body brushing to wash away the sloughed-off skin cells. Follow up with a moisturizer.

    Annet King, Director of Global Education for  The International Dermal Institute says that “body brushing helps to remove stagnant toxins that break down connective tissue leading to the cellulite, however, ultimately there is no conclusive evidence but as a quick fix to plumping the skin, this may be one of the short-lived results of body brushing”.

    As with adopting any new regime, it will take time to see results and it is recommended daily brushing for a minimum of 30 days to experience some changes. For a more thorough lymphatic cleansing, you should brush daily for 3 months to see the benefits.

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    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

  • Bringing A CRPS Insurance Claim Or Claiming For CRPS Under A Critical Illness Insurance Policy

    Cases involving CRPS can be tricky, however, as experts, we can help you overcome difficulties you may face when claiming. Find out more here.

    Complex regional pain syndrome (CRPS) is an extremely painful condition that’s poorly understood by many. There are two types of CRPS, known as CRPS Type 1 and CRPS Type 2, both of which are notoriously difficult to diagnose due to the similarity in symptoms, which include sweating, discoloration to the skin, burning pain, and sensitivity to touch, pressure, and movement. If you are a CRPS sufferer who has developed the condition as a result of an accident, injury, or trauma that wasn’t your fault, you may be able to claim damages. When making a claim, however, you may face a number of difficulties; CRPS is extremely debilitating and can cause mobility and concentration difficulties, fatigue, and pain, which may make it arduous for sufferers to engage in the litigation process and partake in appointments they may need to attend. To find out more about the problems you could face and how we could help, continue reading.

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    A Misunderstanding

    Every complex regional pain syndrome sufferer knows all too well how poorly understood the condition is, which is why it’s so important to ensure your solicitor has a good understanding of CRPS and knows the ins and outs of the symptoms and consequences associated. Having a good knowledge of the condition won’t only enable your solicitor to produce a detailed and accurate report, but it will also allow them to understand when you’re having a bad day, whether it be due to pain, fatigue, or something else associated with the illness.

    At Ronty Rhodes Solicitors, we specialize in CRPS compensation claims and have worked alongside many sufferers in the past, which has provided us with the knowledge we need to understand what our patients experience on a daily basis. With this knowledge and expertise combined, we are able to provide flexibility for our clients and can accommodate their individual needs to make them feel as comfortable as possible; for example, if a client feels more comfortable speaking over the phone, our specialist lawyers are always happy to pick up the phone. In addition to this, our clients can always feel safe in the knowledge that we have the ability to report accurately and correctly, which in turn will have a significant impact on the overall value of the claim.

    Diagnosis Delay

    Cases that involve CRPS are notoriously complex; the condition is extremely difficult to diagnose as there is no single test that can be carried out to give you a definitive yes or no answer. In order to receive a diagnosis and determine what has actually caused the CRPS, a variety of tests can be carried out, which can take some time. Before bringing a compensation claim for CRPS, a full diagnosis must be obtained. There must also be a causal link between the trauma you have sustained which was not your fault and the CRPS. At Brian Barr, we work on a day-to-day basis with a number of expert medical consultants, who not only prepare medical reports but treat patients with CRPS.

    An Unfair Stigma

    Although work has been carried out to improve the stigma attached to CRPS, a degree of stigma still remains. Unfortunately, this stigma often influences experts to suggest that sufferers are lying about their symptoms or observe a sufferer’s medical history to look at past psychological difficulties which may have made them vulnerable to the condition. At Chronicillness, we understand how frustrating this can be for patients and will act on a sufferer’s behalf to earn as much compensation as possible to improve the quality of life for those who have suffered the consequences of CRPS. When using our services, no patient will be dismissed, ignored, or doubted; our expertise lies in offering the very best support to every sufferer.

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    Finding Evidence

    In order to give any CRPS sufferer the best chance of succeeding when making a CRPS insurance claim, it’s imperative that evidence is gathered right from the start. In order to gather as much evidence as possible, the following must take place:

    All medical records must be reviewed in detail, so all aspects of the case are fully understood;
    The injured party must visit experts as soon as possible and they must also receive the right treatment/ rehabilitation to give them a good chance of managing their condition moving forwards;
    Any witness evidence should be prepared and detailed to allow others to fully understand the impact the condition has had on the sufferer in terms of day-to-day activities.

    All in all, it’s important to remember that you employ a specialist to handle your personal injury claim; experts will have a clear understanding of your condition and, as a result, will have immediate access to suitable individuals who can offer expertise and assistance to you during your claim. These individuals can range from treatment providers, medical experts, and knowledgeable legal advisors who will make a positive impact on the result of your claim. With a team of law experts and a breadth of experience under our belts, we know which questions need to be asked and which investigations must be carried out in order to obtain the evidence you need to succeed in your claim.

    CRPS Insurance Claims

    It may be the case that you have a critical illness insurance policy that does not list CRPS as a particular illness under which the policy will pay out. However, due to the debilitating nature of the condition, it is sometimes possible to claim under the ‘Total and Permanent Disability’ criteria contained within a critical illness policy. Ronty Rhodes Solicitors can assist with this. If you have such a policy and suffer from CRPS and do believe that you satisfy the criteria under this policy, get in touch with us to discuss the details of your case by calling us for free on 0808 123 0003 or by filling in our online contact form.

    https://teespring.com/stores/fibromyalgia-6
    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 Favorite Celebrity is Going for Fibromyalgia & Raising Awareness – Lady Gaga Fibro Warrior

    Lady Gaga “comes out” as a Fibro Fighter

    Have you noticed the media frenzy this past week? Fibromyalgia is trendy!!

    Lady Gaga declared on her Twitter feed that she too battles with Fibromyalgia.

    As she opened up about her chronic pain, her canceled tour dates, and her stay in hospital; social media went into meltdown.

    Love her or hate her, Lady Gaga’s announcement has definitely divided opinions.

    I have never been a huge visitor to Fibromyalgia support forums. However, it has been “eye-opening to say the least to see how opinions have been divided.

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    In one camp you have those, like me who think that this is great for raising awareness.

    People are finally starting to ask questions about this relatively unknown and misunderstood condition. Facebook went into overdrive. Instagram was buzzing and Twitter, well just tweeted. Daytime TV interviewed doctors who gave the low down on Fibromyalgia. One of our regular presenters got a crash course in pronouncing the word as well as learning what the symptoms are. In some respects, it felt better late than never. All of sudden, we are validated. Just sad that it has taken so long and a celebrity suffering to bring Fibromyalgia out in the open. Good on Gaga!!

    Sadly, on the other side of the fence, there are those sufferers who are playing the “my Fibromyalgia is worse than yours” game. They have declared open season on Lady Gaga.

    They are questioning her motives for going public. Doubting that she could even have the condition given her long and energetic live performances. There have been those that have suggested that she would be better using her wealth by contributing to research. They deem this preferable as opposed to sharing her story. And believe it or not, there are some who are “whining” about her being in hospital. If she can “rest in the hospital, why can’t I?” Really???

     I am sure that she can think of better places to rest and recuperate without being admitted to hospital.

    The reality of this condition is that nobody is immune, the pain has no regard for celebrity status. Because Fibromyalgia is so different and unique to each individual it is difficult to judge one set of symptoms against another. Fibromyalgia can prove to be more debilitating for some than others. We know that it tends to go hand in hand with so many other conditions such as Chronic Fatigue or Irritable Bowel Syndrome.

    For those of us with Fibromyalgia and chronic pain, it is important that we extend compassion not just to fellow sufferers but also towards ourselves.

    It is imperative that we don’t turn our pain into some sort of competition by judging one another as to who can do what. We should be celebrating our successes and commiserating when the going gets tough. Not putting each other down because somebody had a good day!

    I have, in some small part, been on the receiving of those who have doubted the severity of my condition. I have been slated for holding down a full-time job and for not taking medication. All good reasons apparently to question my diagnosis by other Fibromyalgia sufferers.

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    Therefore, I have to say that I do feel for Lady Gaga. Although never a fan, I admire her honesty and her admission that shows she isn’t the superhuman everybody thought she was. By coming out and talking of her struggle with pain, she has made herself vulnerable to the doubters and naysayers. I am hoping that she also becomes an ambassador and a voice for those who genuinely suffer in silence.

    She has the same frailties and struggles as the rest of us who suffer with this condition.

    And, yes truth be told, she has more money than most. Without a doubt, she will have access to some of the best doctors and healthcare. However, at the end of the day, her pain and fatigue will be as soul-destroying and debilitating as it is for the rest of us.

    As we all do, she will have good and bad days. Sadly, she will have flares and periods of stability. She is now after all a Fibromyalgia Warrior battling with the rest of us. Therefore, she is as deserving of our support as any other brave soul battling chronic pain.

    Whatever your thoughts are on the performer, she has brought the word Fibromyalgia into the public domain and that can only be a good thing. I for one, wish her all the love and luck in the world.

    I think the priority now for Fibromyalgia warriors everywhere is to jump on the Gaga bandwagon.

    This is a great opportunity now to capitalize on her story and build momentum by telling our stories. If you are feeling brave, why not get in touch with your local press and tell them about your Fibro journey. Post on your Facebook page, start up your own community or share your Fibro days on Instagram. 

    It is certainly a topical subject at the moment and ultimately, this can only be a good thing in educating people about our condition. It is up to us to get our message out there and highlight how many people are actually battling this condition day in day out, out of the headlines, and away from the cameras. 

    Be brave, be bold and tell your story – no meaty outfits required!!

    https://teespring.com/stores/fibromyalgia-6
    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 Does CRPS Affect The Eyes?

    CRPS is a condition known for causing chronic pain and discomfort in the body and, as anecdotal evidence has suggested, the eyes. Find out how CRPS affects the eyes in our blog.

    As a chronic pain condition, complex regional pain syndrome is known for causing a wide range of extremely painful symptoms, such as joint stiffness, swelling, changes in skin texture, and burning, in the affected area. At Brian Barr, we are a leading CRPS lawyer firm that understands how difficult everyday life can be for sufferers of illness. As well as causing pain, CRPS has the ability to spread and cause severe symptoms in other areas of the body, including the eyes. In this blog, we outline how CRPS affects the eyes and what symptoms it can cause. Continue reading to find out more.

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    Although there is no research to prove that there is in fact a link between CRPS and eye problems, there has been strong evidence to suggest so, and many patients in the past have suffered from a wide range of uncomfortable symptoms in their eyes as a result of, what evidence suggests, being a CRPS sufferer. Common symptoms that CRPS patients should look out for are blurred vision, double vision, poor focus, sensitivity to light, and dry eyes, with a less common symptom being droopy eyes. Sufferers have also reported seeing flashes and zig-zags in their vision, with sharp, stabbing, and shooting pains taking place through their eyes.

    Why does CRPS affect the eyes? Unfortunately, there is no definitive answer to this question, much like the question as to why CRPS developed in the first place. As a CRPS law firm, we have worked with many patients in the past and understand how irritating it is to not have the answers to your questions. This being said however, experts do know that the condition can develop in the face and head as a result of a traumatic encounter, such as surgery, a tooth removal, or after having a lesion (wound, bruise, ulcer, abscess, or tumor). It’s a well-known fact that pre-existing CRPS and surgery don’t go hand in hand. Suffering from CRPS in the face or head makes the eyes much more vulnerable to the effects of the disease.

    In order to understand how CRPS will affect an individual patient’s eye, two things must be understood; the initial state of the eye and the type of injury that occurred to the eye. Although there is no cure for CRPS, there are methods of pain relief that can ease any pain and discomfort caused to the eye area as a result of the disease. In a past case, a CRPS patient suffered a trivial swipe injury in his left eye, which caused initial symptoms of redness and lacrimation in the same eye. After two months, he began to experience orbital pain, along with swelling and burning sensations, and was prescribed 100mg of medicine take twice per day for a week. After the next examination, he continued to experience pain and developed moist skin on his eyelid, as well as minimal resolving edema. As a result, his medicine dosage increased to 300mg three times per day for four weeks, which then eased his pain and edema. After three weeks had passed, the man was completely pain-free, proving that, through the right treatments, symptoms can be relieved and sufferers can return to some form of normality. Each patient’s unique circumstance should be considered in order to reach a conclusion.

    All in all, there is some evidence to support the belief that CRPS has the ability to affect the eyes in many ways, however, until sufficient evidence is found, medical professionals are likely to remain highly skeptical. If you suffer from the condition and have experienced problems with your eyes in the past, leave a comment below; as an expert CRPS lawyer firm, we regularly share advice and support to sufferers on our blog and social media pages, so get in touch with us on Facebook and Twitter.

    https://teespring.com/stores/fibromyalgia-6
    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

  • Fighting Battles with Fibromyalgia

    Every day is a battle but who is winning the war?

    Since I began Fibro Warrior, I have often been asked how do I manage to focus on the positives whilst battling Fibromyalgia? The answer to that is what are the alternatives? I guess I have two choices but only one is worth pursuing.

    The truth is that there is certainly nothing positive about having a chronic condition. But given that there is currently no cure for Fibromyalgia, then I feel that I must change and adapt. So read on to see how I do just that….

    When I was diagnosed in 2000, I had already been struggling with Fibromyalgia for 11 years. I didn’t know what was wrong with me and I think in reality those years were the darkest. They were scary in the sense that I feared for my sanity. I knew all was not well but the doctors could find nothing wrong.

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    It was in the early years that this condition robbed me of so much.

    It took my energy, my health, my confidence, and my self-esteem. More tragically, it robbed me of the early years with my baby son, and later in 1997 it put paid to my first marriage. Whatever this was, it was beating me and winning!

    Getting my diagnosis was a massive relief and once I got my head around the fact that it was incurable, I was ready to fight. I made the decision there and then, that I was not going to rely on medication and from then on, things started to change.

    I had two choices, roll over and let Fibromyalgia throw all that it had at me. Become its victim and allow it to keep robbing me until I had nothing left or I couldn’t fight anymore!!

    I chose to start fighting!!

    I didn’t have an army or stash of secret weapons…yet! But, I did have a renewed will to get better. I didn’t know how I was going to do it but I thought I knew what I was up against. It was a start, the battle lines were drawn and I could start and fight back.

    Over the years, I read everything I could get my hands on about the condition. I saw a nutritionist, spent a fortune on alternative therapies and acupuncture. Joined a gym and quit, joined another, and quit again. I took supplements, drank Aloe Vera. I used crystals and aromatherapy oils looking for one that one miracle cure. You have been there, right? You know what I am talking about.

    Well, I am sure you discovered the same as me. There is no miracle cure. One Nil to Fibromyalgia

    As I neared my 50th birthday, there came the realization that with this anniversary there would be another “milestone.” I would have officially battled Fibromyalgia for over half of my life. In all likelihood, I would have to carry on the fight for another 25 years. I knew that there had to be a way of making sure that the Fibro didn’t swallow me up completely. I finally knew that the answer wasn’t going to come in some wonder drug or therapy. It was going to come from within me!!

    Yep, Fibromyalgia, I won this one!! I got the answer you tried to keep from me for 25 years – one all

    It was almost a revelation that my “healing” as much as it could be, was going to start and end with me. No doctors, no therapists, no medication – just me. I truly believed that I had all the weapons I needed right here in my body. It was just a matter of deciding what I had and how I was going to use it.

    Firstly, I knew I needed exercise. I had tried all the usual gym stuff, swimming and walking. Invariably, these made me feel worse and induced a flare. I knew that I had to find something fairly gentle on my body but it had to be effective. So began my journey to the Yoga mat. It was and still is amazing.

    Yoga meets you where you are and no two sessions are the same. Positions are adapted to accommodate my Fibro body depending on what I can manage on any given day. I also read up on rebounding (bouncing on a trampoline) and learned that this was beneficial for Fibromyalgia sufferers. So, I bought my rebounder and gradually increased my bounce time from an initial tough 5 minutes to an invigorating and enjoyable half an hour.

    Another win chalked up to me I think Fibro

    I had, over the years dabbled with meditation. This had been born out of my love of all things Tibetan and His Holiness, The Dalai Lama. Therefore it made sense to make a real effort to include meditation in my yoga practice. In addition, I spend the first 10 minutes of every day meditating outside, no matter the weather. (An outdoor gazebo is a triumph).

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    Meditation works!! It takes me to a place where my breath dominates and my thoughts, feelings, and pain are relegated for a short time while I focus on ME. My personal mantra is “It is all about me, it’s all about now”.

    My early morning meditation and yoga sessions set me up for the day. I believe that this sends a message to my Fibromyalgia that I am up, out of bed, and ready to take on my day – strong and determined.

    So, that is my body & mind sorted – what else could I arm myself with?

    I have always been a strong believer that given the right conditions, the body can heal itself. Never one to embrace a medication, I always know that a headache will eventually go away. A cold or flu will run its course and then disappear without a trace. A cut or a bruise will in time, heal as if by magic. So, my next quest was to explore what my body needed to fight Fibromyalgia every damn day.

    I personally believed that the answer would lie in my diet. So, I decided to go right back to the drawing board and carry out a cleanse. I knew that this would give me the opportunity of cutting out large amounts of food, whilst giving my digestion a break. This would then put me in the position of slowly introducing certain foods again and then judging how they impacted my body.

    I opted for a 12-day program that required me to cut out all processed food, meat, caffeine, dairy, and sugar. It was tough for a couple of days but then the magic started. I woke in the mornings with no aches and pains (seriously). My energy increased and the constant fatigue which plagued my days was gone. People started to comment on how well I looked and I was even accused of getting Botox because my skin glowed.

    I felt so good that at the end of the 12 days, I did another 12. I made the decision then to permanently cut out all caffeine and processed foods from my diet. Also, I opted to leave out the meat and just eat fish.

    So, the stage was set for my fight back!

    As time went on, I wanted to learn more about how I could further support my body in its war with Fibromyalgia but I also wanted to pass on what I had learned already. In order to support other sufferers, I decided to sign up to become and Health & Wellness Coach. I then went on to study raw food nutrition. It was learning about what my body needed to function at its optimal. I was giving it a fighting chance against Fibromyalgia.

    Now, I need to be clear here and say that I would not consider myself healed. There are times when the pain is too much to bear, the fatigue overwhelming but compared to how I felt in 1989 there is no comparison. I have learned that with the right foods and being gentle with me when I need it, these flares pass and I live to fight another day!

    Fibromyalgia may win many of the battles but I am determined it will never, ever win the war!!

    https://teespring.com/stores/fibromyalgia-6
    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

  • Explaining Fibromyalgia to Family & Friends

    ….it’s not that easy!

    When it comes to Explaining Fibromyalgia to Family & Friends, it’s a tough one. It isn’t something that comes easily to them or even to you for that matter. No matter how long you have battled with the condition, the reality is that you will always come up against opposition when you are trying to explain how this “invisible illness” affects you every day.

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    I have battled Fibromyalgia since 1989 and I still think that there really isn’t one member of my family that just “gets it.” And to be fair, who can blame them. Most of the time, I look absolutely fine – a little tired maybe. I am not rolling around the bed writhing in pain. I don’t have a raging temperature or covered in some unpleasant rash – I am to all intents and purposes ME.

    It is for this very reason, that those battling Fibromyalgia often feel incredibly isolated and alone.

    Likely, nobody in your immediate circle of family and friends understands what you are having to deal with day in and day out. Sure, you can head off to your local support group or find an online forum. But the reality is, if you are like me you want your family to comprehend your suffering. You want a little compassion and support from your loved ones.

    One of the biggest frustrations of Fibromyalgia is trying to explain what it is. How you got it and how you deal with it. At times it feels like trying to explain the unexplainable. Truth be told, we don’t really understand what we are battling. It just appears from nowhere, takes over your life. You are caught up in the merry-go-round of pain and fatigue.

    So, what are you to do when you find yourself in this situation?

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    How do you explain to your family and friends why you are missing out on the social occasion of the year. Why you can’t do Christmas at yours like you used too?

    Chances are you can’t. And that isn’t because you are not articulate enough or educated enough on the condition – it is because you are too close to the situation. The likely outcome will be that any in-depth conversation will end up in misunderstanding, frustration, and emotions running high on both sides.

    So, what do you do? The answer is you let somebody else do the talking for you. I relied on YouTube to get my message across to my family. It takes away the anxiety and almost makes it less personal when somebody else is recounting their story or sharing the facts. I have a great little video on the site which helps to explain, it is a little robotic but the message is perfect.

    This issue can be a huge source of stress and anxiety to all concerned. So, it is, for this reason, I decided to do something positive to help you and your family.

    I put together a short course which you can share with your loved ones. It contains some strategies for opening the channels of communication along with a couple of videos. There are also two fairly powerful and thought-provoking letters.

    Because I feel so strongly that you should have the support and understanding you so richly deserve, I am gifting this course to you and your family.

    It is my sincere hope that sharing this information with your loved ones, it will give both them and you the knowledge to move forward together united.

    So, head over there now and unwrap your gift with my love and best wishes.

    https://teespring.com/stores/fibromyalgia-6
    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 We’ll Become is Fibro Warrior

    Fate whispers to the warrior, “you cannot withstand the storm.” And the warrior whispers back “I am the storm.” ~ unknown

    I love this “warrior” quote and have referred back to it many times throughout my battles with chronic pain. It is the defiance of answering fate back that most appeals to me. The thought that OK, I have my lot in life but I don’t have to like it or accept it.

    So often now, we see titles such as Chronic Pain warrior, Fibromyalgia warrior, Chronic Illness warrior, Spoonie warrior. They are everywhere, often preceded by the # on social media. But what does it really mean to be tagged, warrior? Do you have what it takes to even be a warrior?

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    The definition of a warrior is “one who is engaged in or experienced in battle.” Other meanings include “one who is engaged in conflict or struggle.”

    “A person who has shown great vigour, courage or aggressiveness.”

    For me personally, I often shy away from using the word suffer when referring to my chronic pain journey. I prefer the word battle. My head tells me that this word sends out the message to the universe that I am fighting. Suffering I might be but battling is how I want to be perceived. There are many times when I don’t feel much like a warrior but no matter what life throws at me, I somehow tell myself the fight must go on. The alternatives are too hard to contemplate, so resolutely I “soldier” on determined not to let pain and fatigue get the better of me.

    Now, I absolutely know that I am not unique, nor am I some kind of hero. I am just another warrior who has no alternative than to fight on. I know that for you reading this, you too are a warrior and committed to the battle. How do I know? Because if you were not a warrior, you definitely would not be on a website that looks to support healthy, positive life with chronic pain. You certainly wouldn’t be looking to empower yourself and search for answers if you were not determined and unwavering in your quest for better health.

    We fight for our health everyday in ways that most people don’t understand.

    For those of us battling chronic pain, it’s the little things that most people take for granted that make us strong. The effort to get moving. To get out of bed in the morning, even when it would be easier to stay there. Our determination to keep going when our whole body is crying out enough. The smiles we paint onto our faces mask the tears of pain and frustration.

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    Our abilities to resist the temptation to punch the doctor. You know the one, who tells us that we need to pull ourselves together and snap out of it. It’s the way that we hide our disappointment and sadness when friends and loved ones give us a wide berth for saying “no” one too many times. The relentless march to look normal when we are feeling anything but. It’s the keeping, keeping on when we are so exhausted we just want it all to stop.

    The days when the last thing we want to do is be the victim, but our pain and fatigue overwhelms us anyway.

    For all of these reasons and for many more, we ARE warriors. It is not some tag or label, it is truly our reality. Every day we go to war, engage in battle just to get through the day. We fight with everything we have, just for some normality. We stand strong in our unwavering support and acknowledgment of our fellow warriors. Knowing that nobody understands and lifts them up like another warrior. We are constantly on a quest for the smallest victories – holding down a job, attending a family wedding, a walk in the park, or just getting dressed.

    To every warrior out there battling their chronic pain and fatigue, I salute you. I stand alongside you in your battle for health, wellness, and some sense of normality. Check out how I can support you by clicking this link.

    For my birthday earlier this year, my husband bought me the CD from the Greatest Showman. He wanted me to hear the words from the song “This is me.” Today, I dedicate those words to you.

    I opted to share this emotionally charged clip as opposed to the one from the actual show.  She is scared but she did it anyway!! Enjoy her triumph and if you love the video as much as I do, drop a comment in the box below and let me know.

    “We are Warriors, yeah, that’s what we’ll become.”

    https://teespring.com/stores/fibromyalgia-6
    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

  • This Is Me… This is Fibromyalgia

    Today, I stepped back into a place I haven’t visited in a long time……One year to the day to be exact since I last ventured anywhere close. It wasn’t intentional or deliberate to visit on this day, it just kind of happened. It felt like taking a trip down memory lane. I was curious and I suppose I wanted to see if everything was still the same. Truth be told, it was and it wasn’t.

    The surroundings were familiar enough, nothing much had changed but in a sense, everything had changed. I had changed. That seemed to make all the difference.

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    So where did I go you might ask? Where was this place that had conjured up so many mixed emotions and left me in floods of tears?

    The answer, was right here, the blog!!

    My last post here was on 3rd October 2018. 12 whole months since I had reached out to my fellow warriors with love and support. 365 days, that I haven’t had the confidence to write from the heart and reach out. 52 weeks of being in the wilderness and feeling disconnected from everything and everyone.

    The truth is that I was struggling so bad myself that I felt that I had nothing to give you. How could I make things fantastic for those who came to get support and guidance? I couldn’t even help myself. So, I retreated. I let life happen to me whilst all the time trying desperately to distance myself from the mental and physical pain I was battling against.

    One of my coping strategies, the love of writing fell by the wayside, and once that happened my outlet for expression went too. I bottled everything up inside, giving the appearance all was well in my world, whilst the reality was far from good.

    My self-confidence was at rock bottom and I felt that I had nothing to offer anymore.

    All of my words of wisdom had dried up and I was just another chronic pain warrior, battling through each day with nothing new to share. No advice to give and no words of comfort.

    As I logged on today, I read my last blog post and replayed over and over the video clip that I had attached to the post. It was then and still is today an incredibly powerful version of “This Is Me” from the film The Greatest Showman. As I listened, the words

    “Another round of bullets hits my skin Well, fire away ’cause today, I won’t let the shame sink in.”

    resonated so deep within me that I could have easily sunk to the ground with emotion. I had let shame get the better of me. I was ashamed to really share the struggle…..if I wasn’t Fibro Fantastic then I thought I had nothing anybody would want to hear.

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    But, recently I have been working so hard on authenticity.

    Coming to terms with who I am, who I always was, and who I have become. Acknowledging that if people can’t deal with the real me, then there is no point in having them in my life. I wanted to send the imposter away and take the real Tracey by the hand and bring her out of hiding.

    As I played the video clip Keala Settle’s voice wracked with emotion was like a light going on. It felt as though now, this was my anthem. My mantra. My shout out to the world that I make no apologies. – This is me!!

    I am brave, I am bruised
    I am who I’m meant to be, this is me
    Look out ’cause here I come
    And I’m marching on to the beat I drum
    I’m not scared to be seen
    I make no apologies, this is me

    For now, I am back.

    To share my words and feelings from my heart feels like a huge release. I need an outlet for my journey, the one that has both physical and mental pain as passengers. It has been here all along – my blog, my corner of the virtual world. A place where people stand together, as members of an invisible club, where only we understand the rules.

    Going forward, I don’t know the direction Fibro Fantastic Wellness Coaching will take, but I do know this will be as much about me as it is about you. I can’t help you if I can’t help me. So, for now, I feel that the blog will take on more of a journey feel. Letting you into my new world of struggle, despair, the battles, the highs, and the lows.

    I am still Tracey the Wellness Coach, but I am also Tracey the fighter who is vulnerable and scared of the future, just like the rest of you. But I am home and for now, I will take that!

    https://teespring.com/stores/fibromyalgia-6
    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