Overcoming Fibromyalgia

 

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Found via Google image search.

Over the years, I have found that physical illness involves three aspects of self: body, mind, and emotion.  It is not  just about the body healing itself.  It is also about the health of the ongoing dialogue that occurs between the body  and the mind, and the resulting emotions.  Of course, the body heals in its own time, but our thoughts can also assist in how healthy we perceive ourselves to be and ultimately are.  This is what might considered as “thinking our way to good health.” Visualizing a healthier version of ourselves can do wonders to begin or continue the process of actual healing.  However, the reverse is also quite true.  Beyond whatever factual illness we may have, our minds can contribute a hefty dose of additional symptoms, with which we must also contend.  Some might refer to such occurrences as psychosomatic symptoms.  For example, depression is not just something that impacts the mind.  It impacts the body’s ability to function effectively as well.  Depression is associated with physical symptoms, such as chest pains, fatigue, muscle and joint aches, digestive issues, headaches, weight loss and gain, and even back pain.  Add to that sleep disturbances and sexual problems, it might seem as though I have been describing fibromyalgia because the symptoms are quite similar.  These physical symptoms of depression are temporary, however, while fibromyalgia symptoms are chronic.

For a long time, the general consensus among doctors was that fibromyalgia was all in the mind, that it was merely psychosomatic, that it was not real.  Although there are still some who maintain disbelief, research has shown that fibromyalgia, the second most common rheumatoid disorder, is “now considered to be a lifelong central nervous system disorder, which is responsible for amplified pain that shoots through the body of those who suffer from it.”  Fibromyalgia is not something that you can just think away. No amount of visualization will permanently remove the impact that fibromyalgia can have on its sufferers.  That is the reality.

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The Broken Column, 1944 by Frida Kahlo. Image from noijam.com, found via GIS.

As the illness progresses, daily life can feel quite surreal. Perhaps you felt great yesterday, but today you feel as though you are broken in many places.  It may feel that there is no way to hold yourself together.  It is not just the pain that hurts.  It is ever-increasing isolation, diminishing self-sufficiency, and the loss of words that comes with the fog that overtakes the mind.  It is also the ongoing disappointment as you begin saying “no” to work, loved ones, and even yourself.  Having fibromyalgia means being broken, being scattered into tiny fragments of self that you try each to recover and bind together

S0, how does one overcome this?

Until there is a definitive cure found by medical experiences, there is no way to overcome fibromyalgia.  At least, not in the sense of the illness ending.

Instead, see overcoming fibromyalgia as a daily process.  For example, on days when you wake up to a flare, challenge yourself to do more than you think you can–perhaps that might be sitting up in bed, or talking to a friend on the phone.  On days when you feel great, challenge yourself to do less than you think you should–perhaps that might be leaving work on time or a little early (if you are still working), instead of staying late because you are trying to make up for lost time.  This is basically opposite to emotion action, a DBT skill that asks practitioners to 1) acknowledge and allow for their emotional state, and 2) act in the opposite manner than their emotional urge would prefer. For example, if you are angry and your emotional urge is to hit someone, opposite to emotion action would have you choose an action that is opposite to your emotional urge, so perhaps hug someone.


When we allow ourselves (mind, body, emotions) to give into illness, we allow for that illness to have enormous control over how we experience life.  Yes, you may feel ill today, but instead of focusing on feeling physically ill, try focusing your mind on what can you can do (in spite of your illness).  Contrarily, you may feel physically great today, but instead of focusing on feeling great, try focusing your mind on what you can do to ensure that you feel better tomorrow (this may mean holding yourself back a bit).

 

If we acknowledge our limitations and challenge our thinking, then this may be helpful in avoiding compounding our physical illness with our emotions.  Depression can be resulting factor of chronic illness.  For those of us living with fibromyalgia, learning how to cope with feelings of depression is vital to our survival.  Thus, finding ways to celebrate ourselves and the steps we take to feel better is key. Every day try doing to following (in no particular order):

  • Create an action plan (a.k.a. To Do List) based on your current physical state
  • Journal about your physical symptoms and your emotional state
  • Exercise in whatever way possible, whether that is doing a light stretch or going for a walk.
  • Eat well. Avoid foods that exacerbate symptoms.
  • Talk to someone, whether in-person, on the phone, or online.
  • Smile for no reason. Trust me, it helps.
  • Be mindful in each moment. Be aware of your thoughts and how your thoughts are influencing your emotions and actions.
  • Pay attention to the calendar. Know the month and day you are in.  It is very easy to lose track of time.
  • Set long-term achievable goals (but challenge yourself).  What is it that you believe you can no longer do/achieve because of fibromyaglia? Try to find ways to modify what you wanted to do so that it accommodates your illness.
  • Feed your spirit.  This does not mean join a religion. Do something to help others.

There is no guarantee that the above will work for you.  These are just the steps that I have found helpful along the way.  Yes, every day, I find that fibromyalgia diminishes some aspect of me.  Sometimes it is very difficult to see the positives in each moment. Still, if I do not try to make my reality better for me, then who will?

I hope these words offer comfort to anyone who is having a hard time today.

Until Next Time,

D.

 

 

Fibromyalgia & Maintaining Hope

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Maintaining hope is a matter of discipline.  Hope isn’t not magically bestowed upon you. It’s not something packaged in the form of the latest prescription your doctor wants you to try.  You can’t purchase it from your neighbourhood 24-7 pharmacy. You learned it from someone somewhere at some point in your life, oftentimes in childhood.  Hope is a skill.  As such, the old adage of  use it or lose it applies to it as well.  This is especially true if you have a chronic illness.

Having a chronic illness isn’t the end of the world, although it may feel like it.  To be blunt, it sucks to have a chronic illness.  However, in the difficulties that having any illness can bring, there is wisdom and compassion to be gained.  Still, being constantly ill or never knowing when next illness will strike can create feelings of hopelessness and helplessness, which can lead to or may signal depression.    In fact, despite being a mental health counselor and expressive therapist, I have felt hopeless and helpless at various points in my illness–a good portion of it being related to having to redefine my self-concept, rather than the illness itself.

I found that the more I refused to let go of what/who I was, the more frustrated and sad I became.  However, each time I conceded to a limitation and took steps to adjust to it, I felt freer and more hopeful.  As I have written many times, chronic illnesses take away many things from you, but they also give something to you.  Whether or not you choose to understand that there is a gift (or gifts) is up to you.

Chronic illnesses, as much as they can create havoc in your life, they also can make things really simple, especially decisions. Still, you have to see through the chaos of your symptoms (physical and mental) to the clarity of your will.  To help myself see beyond the difficulty of the any moment related to my fibromyalgia, I ask myself the following question:

Will I allow my illness to devour me?  

The answer is always no. I refuse to be held hostage to my illness.  Like all other things about myself that I cannot change, I have accepted that my illness is a part of me.  I don’t need to focus on changing it.  I need to focus on living with it, learning from it, and moving beyond it.  This is how I maintain a hopeful attitude about my life and my illness.

I no longer see my illness as something I need to or can fix.  If the experts come up with something definitive in the future that will alleviate me of my illness, then great.  Otherwise, I choose to focus on making peace with having fibromyalgia, rather than fighting it.  In those moments when I am feeling my worst, I choose to focus on how my illness is helping me, rather than how it may be hindering me. 

My hope is grounded in the belief that I can live successfully with fibromyalgia, regardless of what it takes away…because I believe it always gives me something in return.  Because of this belief, I also know that I can and will always find a way to help myself, even if the way is not immediately shown to me. I suppose what I’ve learned is that

Hope is about riding the waves of uncertainty…with a keen sense of direction. 😉

  D.

Check out this post by a fellow  Wordpress blogger: When Chronic Illness Causes Depression

5 Positive Negatives of Fibromyalgia…

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Yeah, I said it. There are some good things about having fibromyalgia…It’s just took me a while to figure out what they were.

  1. I can now predict bad weather.  That’s right. You no longer need to watch the news or visit weather.com, just call me (maybe I’ll answer) and I’ll tell you, because from the moment there is a shift in the weather my body knows it.
  2. I can relate to older people. You’ve got a pain in your back, side, arm, elbow, neck? Feeling weak and creaky? Can’t remember where you left…wait, what was it again? Wonder why everybody is moving so fast?…Well, I do, too. Let’s commiserate and wonder how we got here.
  3. I’ve hit a personal low. So, I can only keep going up from here on out.  There’s nothing quite like losing utter sense of self, having your livelihood stripped from you, and becoming reclusive. It put so many things in perspective, which leads me to…
  4. I’ve learnt to keep things real simple. Drama? No, thank you. I’m interested in the direct line from point A to B. Fix the problem or remove it.
  5. I’m mentally stronger.  Oh, I used to get bogged down in so many emotional situations that I really had no business being in…just because I thought these four little words: I can handle this.  I applied those four words to all sorts of situations: work, relationships, life changes, etc. What I’ve come to learn is that even if I am capable of “handling” a situation, it doesn’t mean I should.  In the end, the stress of unwarranted drama (i.e. drama for the sake of drama) only leaves me feeling emotionally and physically ill.  And no, I do not think you are mentally strong if you subject yourself to situations that will only increase your stress levels. Mental strength, to me, means being able to make the tough decision of not getting involved when there isn’t a need.

What about you?

What is it about having fibromyalgia that you have come to appreciate?

 

CW | Saying “Whatever” to Fibromyalgia’s Grey Days

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“It must suck to have fibromyalgia,” says [Insert Name Here].

The sky is grey today.  I knew that before I properly woke up.  I could feel the grey grinding my bones, shaping my body into something that it wasn’t just a few hours before. Like the darkening clouds, the grey attempts to conceal my memories, blot out what I meant to today.

The grey binds itself to my feet, my arms, my head, my stomach.  I smell the grey, taste it, and touch it as I rub my limbs, my temples, my chest.  I hear it blend in with persistent beats of the hot water that pours down my back.  I see it etching whatever into the lines on my face, or perhaps that could just be an issue of age.

I cannot help but laugh–It’s a never ending competition between us, grey and me.  Grey tries its best, and so I must try even harder.

I’ll wear black today.

 

 

 

 

 

 

Fibromyalgia | A Hungry Illness

This Cold Hard Floor: II, watercolour and ink painting by Diedré M. Blake, 2006

This Cold Hard Floor: II, watercolour and ink painting by Diedré M. Blake, 2006

It’s sunny with a gentle breeze today in Rome, and the streets are filled with all sorts of people: tourists, vendors, eco-friendly bicycle transporters, fake gladiators, and me, wearing my too-bright 1970’s dress and carrying a somewhat worn red Chinese umbrella.  As I walk through the city, my mind registers that I am alone…no, not just alone.

I look around at the people who are busy making something of their lives or trying to.  I see their desperation, from the vendors hoping to sell their wares to the couples hoping to purchase romance.  Everyone is hungry for something.  What about me?

When I first came to Rome, I felt out of sorts, as though I had no self-concept, no sense of self.  My self was wrapped up in my illness, and bogged down by one word that represented the annihilation of my reality: fibromyalgia.  Fibromyalgia ate whoever I was, and she was no longer me.

Still, clinging to a part of self that no longer exist makes no sense.  So, I let go and became no one.  As no one I had nothing, no place, no connection, just some vague notions of a past and some hope for a future.  The only thing that existed for me was my illness. Fibromyalgia was my reality, although it was not my self.

However, fibromyalgia is a hungry illness.  It takes and takes and takes and takes…and it has taken many things from me.  It has gorged upon my confidence. It has satiated its thirst with my tears. So much so, that there is no a void, waiting to be filled.

Gelato, bottles of iced water, freshly squeezed juice are all sold along Via Fori Imperiali.  Fresh water runs freely from the fontanella in front of the Colosseo metro station.  I am thirsty. I am hungry. I am tired.

I’ve only been out of my house for 5 hours, but I am desperate to go home, hungry for quiet and the peace that comes from being alone with whatever and whoever I am and am not.

Until Wednesday,

D. 

Creative Writing | Survival 1

art,swimming,under water,pool

drink, take, spill, need, pills

wake, sleep, scream, feel, fall, breathe, void

— do you believe me? 

3 Tips to Getting Unstuck from that Rut

 

Image from MadameNoire.com. Click to read their article, "The 'Itis: Foods that are making you sleepy at work"

Image from MadameNoire.com. Click to read their article, “The ‘Itis: Foods that are making you sleepy at work”

All right. I’ll admit it. Somehow I managed to get myself in a rut. It’s not a pretty situation. Seriously, especially as someone with a background in psychology. I should be able therapize myself out of this…right?  Of course, but it’s not easy.

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First thing first: Identify the sticking point. 

What I mean is, examine the period before recognizing that you are stuck. Try to identify any factors that may have contributed to this experience.  In my case, it’s been this trip back to Rome which has caused a massive disruption to my physical functioning.

Image found on Google Images

Second thing second: Write your desired state of being.

Take a moment to write how you would like to feel in this moment.  More than likely, you’re not enjoying being in this rut. You want to get out, right?? So, write down how you prefer to feel and what you prefer to do.  Explore all possible helpful factors, looking at what has been helpful in the past and things that you have wanted to try. Perhaps you found that going out for a daily walk always helped you to feel more focused and in touch with your life. Perhaps you’ve wanted to try rock climbing, take a cooking class, go on a meditation retreat, etc. Identify what can shift you out of where you are now.

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Third thing third: Just do it.

Yes, it’s Nike’s slogan, but I think it’s the ultimate weapon in getting out of a rut.  You just have to do it. Identifying where things started to go south, and then exploring ways to shift your emotional states are wonderful in helping you understand that there is a way out.  Still, nothing beats just getting up, getting out and just doing what you have to do.  To materialize what you say you desire, how you say you want to live, and who you say you want to be, you must take positive action.

Found via Google image search.

Found via Google image search.

Positive action is anything that helps rather than hinders, anything that enhances you but does not impinge upon the well-being of others, and anything that moves you closer to your goals.

For me, this is my first positive action: writing this post today.  By writing this post today, I am taking action to make positive change. It’s a small step but an important one because I am keeping a promise to myself and to you, my readers. (By the way, thank you so much for taking the time to read my writing. It means a great to me). 🙂

My second will be to clean my room. It’s my personal belief that your physical state (both self and environment) reflects your internal state. So, if your space is cluttered or disorganized, etc., then so is your mind. So, on that note, it’s time to take stock of my physical state. 😉 It’s amazing what cleaning and clearing your physical state can do to free your mind. Really…try it. 

Now, the above steps are aimed at those who are in the emotional/psychological place to take them.  There are many times that ruts are really depression or beginning of depression. It’s important that you take what you are feeling/experiencing very seriously.  I suggest visiting a counselor/therapist/psychologist to understand whether you are just having a challenging moment or if you have entered into a more severe situation.

Until Next Time,

D.

Fibromyalgia | Jet Lag Anyone? Any Expert Ideas to Share?

View from my Delta fllight back to Orlando.

View from my Delta flight back to Orlando.

Today makes one week since I’ve returned to Rome…and I’m still dealing with jet lag. Yes, indeed. My entire system is off, and I’m finding that I am still going to sleep at my usual hour EST (between 1 am and 3 am).  This means that I’ve been going to sleep between 7 am and 9 am.  The heat, humidity and killer mosquitoes aren’t helping matters.  Thus, I decided to consult those in the know (yes, I should have done this on day 2).  So far I’ve found one like of interest: “Melatonin may help to treat jet lag disorder”.

Well, if you have any other ideas, share in the comments or send me a message! 🙂 Thanks!

Until Wednesday,
D.

Fibromyalgia | Feeling Stuck? Try These 3 DBT Tips

Image from ThisIsYourConscience.com

Image from ThisIsYourConscience.com

It’s no joke when you wake up to feeling that there is nothing you can do to make your life better. This may be especially so when you have a chronic illness like fibromyalgia.  There are just sometimes when your life seems to be going nowhere and the only thing you have to look forward to is another day of symptom management.  Such moods can pass quickly, i.e. given your temperament and support network.

Still, what if it doesn’t?  What if you continue such negative self-talk and feel unable to break the cycle that you’re in? Well, the outcome surely isn’t going to be of benefit to you, your self-esteem, and achieving your goals.

So, before you get to that point, I wanted to share with you 3 tips from DBT (Dialectical Behavior Therapy) that may get you out your rut.

I’ve discussed DBT in various posts, so I won’t go into full details here. Suffice to say that DBT, developed by Marsha Linehan, is a form of therapy that uses the Buddhist practice of mindfulness and incorporates a cognitive behavioral approach to making positive change in your life.

Of course, there is a great deal more that goes into DBT.  The 3 tips below, however, might just be ticket to making this day one that lives you feeling inspired to do more and experience more in your life.

  • Opposite to Emotion Action – Although one of the last suggested techniques to changing your emotional circumstances, Opposite to Emotion is the first technique I turn to when needing to motivate myself.  Opposite to Emotion (from the Emotion Regulation skill set) asks of you to do the contrary action to your present emotion/thoughtsSo, let’s say that your mood is so low and the last thing you want to do is to take care of yourself.  Well, do exactly the opposite, i.e. take care of yourself. In this case, taking a shower, eating well, taking a walk, etc.

 

  • Nonjudgmental Stance – This is one of the last skills that is learned in the first DBT skill set of Mindfulness.  Taking a Nonjudgmental Stance means taking an objective distance from your present circumstances.  It asks of you to 1) observe your experience nonjudgmentally, i.e. without trying to change them, 2) describe your experience nonjudgementally, i.e. without condemnation or praise, 3) participate in your experience nonjudgementally, i.e. allowing yourself to be wholly involved in whatever you are doing.  I use nonjudgmental stance when I find myself in confusion about the actions or inactions I’ve taken in my life.  I aim to get at the heart and mind of my present circumstances, so that I can better understand how to change them.

 

  • Improve the Moment This is one of the four basic skills learned in the Distress Tolerance skill set.  Simply put, do what you can to make the moment better and not worse.  Focus on decreasing levels of stress and, if possible, removing yourself from the environment that may be contributing negatively to your experience.  This is where techniques such as imagery, finding meaning in the moment, utilizing prayer, practicing relaxation skills, taking a one thing at a time approach, taking a literal vacation from the place, seeking or remembering encouragement. 

 

Individually, each one of these 3 tips works wonders.  However, when put all together, I believe that you may experience even a greater shift.  I would add to the tips helping others.  I find that when I take the time to help someone else, it helps me to feel less stuck and more motivated to experience positive change.

 

Until Next Wednesday,

D.

Fibromyalgia| Life in Chaos? 3 Steps to Creating Routine in Your Life

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Know this Feeling? (Image from GIS)

At this point, if you’ve followed my blog, you’ll know that my life is far from what one might call normal.  Still, it is my reality.  A part of that reality is having to deal with the inconsistency of my chronic illness, i.e., fibromyalgia.  There are some days that I feel great, like I could go run a marathon or two, and there are some days when even the thought of opening an eyelid seems like too much of an effort.

With such fluctuations in one’s daily experience, it can feel hard to create a sense of order to your life.  After all, what’s the point of making plans for the next day you’re never sure how you are actually going to be?

Over the years, I’ve engaged in an internal psychological warfare, trying to force myself to feel better when I don’t, blaming myself for real and imagined shortcomings, and even giving up on myself when I fell short of my expectations.

The path to living peaceably with fibromyalgia is far from smooth. However, over the past year, I’ve been working on letting go of my self-frustrations, allowing myself to feel whatever I feel, and strategizing how to take small steps that move me healthily along my path.

Image from GIS

Learn to Enjoy Life. (Image from GIS)

So, here are 3 steps that I’ve found useful to keeping internal order even when everything else feels like it’s in utter chaos:

  • Do 1 Thing the Same Way Every Day: Choose one helpful thing that you will do every day no matter what. Don’t cut corners.  Why? Because it helps to create a 1)sense of routine, 2) shows you that you can do what say you will, and 3) moves you a further step along your path.  So, what are some possibilities?  Depending on where you are in your journey, it could be as simple as taking care of your personal hygiene or working on a personal project (for me, that would be writing).  It’s up to you.  As long as whatever you choose moves you closer to your life goals, then it is A-OK.

 

  • Make Lists: If there is one thing that bothers me most about having fibromyalgia, it is dealing with brain fog and memory issues.  In the past, when I felt like my mind could not focus or I could not remember something important, I would really come down hard on myself. I took a massive blow to self-esteem because I did know how to accept and strategize around my illness.  Now, I make lists, especially if I know there is something important coming up. I would suggest having a bulletin board in a place where you cannot avoid seeing it, and posting your lists there.  If you’re not into the bulletin board idea, then I would suggest posting it on your refrigerator…after all, you have to eat at some point.

 

  • Write Down What You’ve Done Each Day:  At the end of the day, even if you didn’t move from your bed, write it down.  Write down who you spoke to, if you took your medications, if you made it out of bed, what daily goal you accomplished, and any and everything else. Write it down.  I do not mean that you should journal–although journaling is not a bad idea. I mean that you should take notes on what you do or don’t do each day.  It will help you to understand your personal patterns.  If you do this long enough, you can see how your symptoms might be impacting how much of what you can do in a day.  It doesn’t hurt, so try it.

 

I cannot promise you that following these steps will change everything in your life.  I do believe, however, that they are the beginning steps that will take you closer to where you would like to be.  Remember the key thing is consistency.

It doesn’t matter what you decide to do–how big or small it is–just be consistent.  Learn to appreciate the small steps you can take, so that when you are able to take larger steps, you understand the magnitude of your accomplishment!

Happy Fibro Friday! 😉