FMS | The Moments You Love to Hate: How to Deal with Flare-ups Before & After They Happen

This picture is a summary of my present state.

(Forgive any typographical errors below. I am tired.)

There is a reason fibromyalgia is considered an invisible illness.  If you were to meet me in my everyday life, more than likely it would not be evident to you that I have an illness. Actually, usually when I feel my worst, I tend to dress my best–lots of colourful pretty dresses–and so it has been for the past two days.

I am in the midst of a flare-up.  I cannot say that it was sudden or unexpected or something like that.  I’ve been running myself a bit ragged, and having started classes again means that I am outside every single day…which is never a good thing for me given my immune system.

Still, I am far from saddened by this development, because I was already expecting it to happen, which is winning half of the battle.  The other half is taking precautions. Sure, you may not be able to stop a flare-up, but you can make an effort to diminish its impact on your life.

Image found: http://nickdeck.com

So, what do I do when I recognize I am going to have  a flare-up?

  • Pare back on everything that is unessential – If I don’t have to do it, then it remains on the back-burner until I can.
  • Start consuming even more fresh fruits/veggies and water – I try rid myself of anything that may be adding to internal discomfort.
  • Put myself on a schedule – Given that fibro fog can be a way of my life, I already know that I am going to be more forgetful and less able to concentrate. So, writing everything down that needs to be done for the day is one way to help me keep on track.
  • Disregard my sleeping schedule/ Sleep when possible & necessary – Wait…what?  How does that make sense?  Well, because I already know that I am heading into a moment of high insomnia, it makes little sense for me to stress about whether or not I am sleeping when I am suppose to be sleeping.  To me, there is a lot more stress to be had from worrying about sleeping than simply accepting the fact that I may not sleep.  I cut stress wherever I can: internally and externally.
  • Walk & stretch/ Generally increase activity level – It may seem counterintuitive. However, walking and stretching (increased activity) helps me to diminish the pain experienced daily.
  • Practice Opposite Action As a dialectical behavior therapy advocate, I use the skills of this approach in my daily life.  Opposite Action or Opposite to Emotion Action is exactly what it sounds like…doing the opposite of what you feelFor example, if I were feeling angry, then I would engage in actions that were opposite/opposing anger, such as smiling or watching a comedy.  With fibromyalgia, it means that I make an attempt to do exactly what I think/feel I cannot. Writing this post is an example of Opposite Action.

 

Truly, however, there is no right path to take in dealing with your FMS flare-up.  

You have do what works for you and what feels best to you.

Check out this article by FM Net News: “Hurdling the Impact of Painful Flares”

Until Next Time,

D.

Update:

ATR Challenge Day 11 – Doing what I can (is what’s right in my life). 🙂

Many, Many Thanks to My New Followers!

It’s one of those hazy Roman September mornings: the kind that isn’t so hot that you feel like your only option is to remain indoors, fixed permanently in your bed or under your shower.  Still, it is the kind that makes you a bit lazy about getting up or even bothering with finding mental clarity.

Rome, on these kinds of days, becomes a centrifugal blend of noises: the distinct songs of cicadas, the cobblestone scraping of straw brooms, the random knock of a hammer, the friendly greetings of neighbours, the midday ring of the church bells and the frustrated blares of traffic.  It’s that kind of morning.

Leaves stand still, birds have gone incognito, laundry dries on clotheslines, and there isn’t a soul in sight–even if voices can be heard in between the sadness of moving sirens.

I’ve woken–sort of–to this kind of day: depleted of energy and bogged down in thoughts.

Go through the routine: meditate, stretch (on bed, too tired to stand), effectively putz around room and find: necessary papers, missing perfume bottle, a collection of hairpins, and worn out fortunes from the local Japanese/Chinese restaurant that has yet to reopen since the start of summer and is “Chiuso per Ferie,” feel pleased that the room has been swept, books have been stacked, and mind has woken just a bit more.

I take a look at my computer: glance at Facebook, post something personal and then professional; think about email and decide to avoid it for now; visit school/work blog and then personal, and find myself at this moment of…

Gratitude.

Thank you to my new followers for taking a chance on supporting my blog.  Thank you to my old followers for your continued support.  Thank you to my visitors for acknowledging my presence.

All of you have made this hazy day much less hazy–

You let me know that I continue to take the right steps on my path.

Until Next Time,

D.

P.S.

Interested in the Gratitude Journal in the image above?

Visit Rosetta Thurman’s Happy Black Woman for more details.

P.P.S.

ATR Challenge Day 10: Getting up & Getting Grateful! Thanks! 😀

 

ATR Challenge: Day 7 & Rilke’s “Live the Questions”

Where Has The Time Gone

My face today. 🙂

Just a brief note to check-in about the Challenge. All is well.  The things for which I am grateful and consider right are the new relationships that I am developing and the new habits that I am forming.

For the most part, what is right is my simple state of being: in myself, in the moment, in connection with others.

Some Words of Encouragement

“Be patient toward all that is unsolved in your heart and try to love the questions themselves, like locked rooms and like books that are now written in a very foreign tongue. Do not now seek the answers, which cannot be given you because you would not be able to live them. And the point is, to live everything. Live the questions now. Perhaps you will then gradually, without noticing it, live along some distant day into the answer.” – Rainer Maria Rilke

Until Next Time,

D.

FMS | Was it Chickenpox? ( Article: Is Herpes Virus Connected to Fibromyalgia?)

Image found: http://krnb.com/

Seriously, now.

Another balmy Saturday. Me? Glued to computer screen with fingers on auto-type while my mind wonders about what fruit will be available in the rapidly depleting fruit section of my local supermarket.

In between finger taps, the consistent yappage of my neighbour’s invisible dog, and my acknowledgements that the world isn’t so bad after all, a random thought comes to mind. Well, not really a thought, but a memory; one that I thought was pretty useless…until now [cue dramatic suspense music here].

Picture it, me at 16 and in my last semester of high school…confined to my bed because of the chickenpox.

Yes, I know.  Chickenpox is something you get as a kid, not as a teenager when everything is all about image–actually, I didn’t really care, but still–and the sight of a pimple can send even the most popular of cheerleaders into a moment of panic.

But that was soooo long ago.

It’s one of many memories I shoved far into the black hole of my mind, so much so that even when I see the resulting scars on my face, I don’t register them as having anything to do with chickenpox.  It’s my defense mechanism checkmate, especially because I am into denial and apparently amazingly good at suppression.

Let’s get back to this moment though, where I am sitting on my bed and typing this post that I’d like to be less than 300 words.

For whatever reason, the words chickenpox and fibromyalgia flashed across my mind and thus my auto-typing fingers tapped them right into Google search and hit the Enter button.

The result?

Well, it seems that a lot of people have been wondering about the relationship between chickenpox and fibromyalgia, although there doesn’t seem to be a great deal of research about it.

Still, it might help to check out the links below to understand why some are wondering:

Is Herpes Virus Connected to Fibromyalgia?

Virus Related to Fibromyalgia?

FMS | ATR Challenge: Day 5 (Back to School/Back to Illness)

I was expecting it.  After all, it was bound to happen.  Three days into the first week of classes, it hits me hard: a cold.

Okay, for the average person, a cold is not such a big deal. If you live with fibromyalgia, however, a cold can turn your world upside down…at least, it can mine.

Already you have to deal with the usual symptoms (pain/nausea/fibro-fog/fatigue/etc.), now imagine adding on the stress of having a cold, which only exacerbates the symptoms you normally have while adding a couple more???! Seriously, it’s no fun.

The point is that yesterday I found myself feverish, anxious because I was feverish, nauseous because I am often nauseous but also because of being ill, alert because I was anxious because I was feverish and nauseous.  It’s brutal.

So, what did I do to counter this situation?

I headed over to the Mayo Clinic’s website to look up information on the common cold and how to treat it.  Of course, most of what was there was common sense:

  • Pain Relievers (have it, but don’t want to use it–I try to keep it natural)
  • Decongestant Nasal Sprays (have it, but don’t want to use it–I try to keep it natural)
  • Cough Syrups (don’t have it and probably wouldn’t use it–I try to keep it natural)
  • Drink lots of fluids (I drink about 2 litres of water every day)
  • Try chicken soup (I am vegetarian/vegan almost)
  • Get some rest (I suffer from insomnia a lot, so who knows)
  • Adjust your room’s temperature and humidity (Rome in September–I turned off the fan)
  • Soothe your throat (I’ve got water and salt for gargling)
  • Use saline nasal drops (don’t have it and probably wouldn’t use it–I try to keep it natural)

So, this what I did: made some lemon/honey tea, drank water, had something hot to eat (rice with vegetables), ate some fruit, tried to rest, turned off my fan and gargled with salt water.

Did it work?  

Well, I am feeling a heck of a lot better this morning, except for the migraine concentrating itself over my right eye.

Either way, I feel good enough to head out to my class in the afternoon–and that’s the most important thing for today.

So, what was right yesterday?

Many things: 🙂

  • I woke up and did my daily meditation/stretches
  • I worked, read, wrote, and knitted som
  • I went to class and participated fully
  • I recognised and fully acknowledged that I was getting a cold
  • I did my best to prevent the cold from persisting
  • I took it easy and reminded myself that I was trying my best.

Remember: Do You!

A while back, I posted about the following article on going to school and managing fibromyalgia symptoms as well as asking for accommodation by Kristen Stewart on EverydayHealth.com: Succeeding at School with Fibromyalgia.  It’s worth taking a look at again, if you have already, and if you haven’t, then take a look now.

——-

Each day I try to remind myself that my path is unique and cannot be walked by anyone else and cannot be compared to anyone else’s.  

Walking it may not always be easy, but it is always worthwhile.

 Until Next Time,

D.

FMS | ATR Challenge: Day 4

Is it Day 4 already???!! 

Four days may not seem like much to celebrate, but given my goal of sticktoitiveness, I am super glad that I have stuck to it, i.e. both the meditation/prayer challenge (Day 26) and the Acknowledge the Right Challenge (Day 4).

The happiness is also because, as a person with fibromyalgia, I find myself often in a position where I have to give up the things that I want to do or am doing.  So, any progress made, however small, in showing myself that I can do/have it must be acknowledged.

As to what was right yesterday? Well, many things:

  • I got up (despite the weather, aches and pains, and general lack of sleep)
  • I did my daily meditation/prayer and stretches
  • I went to class and met new people, and feel very upbeat about the courses I am taking
  • I met a new friend and spent a good deal of time talking.
  • I got some reading/writing/work done
  • I spoke with my mother, which is always a good thing.

For today, I thought I would leave you with a link to a great Yoga International article on the benefits of yoga for people with fibromyalgia: “The Art of Surrender: Yoga & Fibromyalgia.”

Happy Wednesday!!

&

Remember that making progress on any path

means putting one foot in front of the other!

Until Next Time,

D.

 

 

ATR Challenge: Day 3

So, I’ve made it to Day 3. 😉

Let’s begin with what was right about yesterday:

  • I did my daily meditation/prayer
  • I went school
  • I wrote some and read some
  • I spoke with my mother
  • The weather was far better than expected
  • I went to bed at a reasonable hour
  • I received some good news
  • I enjoyed being outside in nature

What about you?  What was right in your life yesterday?

In case you’re wondering about the video above, it is what I’ve been listening to in the mornings for my daily meditation and stretches–perhaps you might enjoy it, too.

 

FMS | Please, Tell Me What I Can Eat….

Seriously. 😉

If you are like me and have been diagnosed with fibromyalgia as well as other comorbid illnesses, such as polycystic ovarian syndrome (PCOS), irritable bowel syndrome (IBS), Reynaud’s syndrome, then your relationship with food might be a complex one–and that probably is an understatement.

Eating the wrong foods or food combinations can mean more inflammation, pain, digestive issues, insomnia, fatigue, hair loss and gain (facial), decreased libido, mood swings, etc. And who wants more of that?

Especially, if you have comorbid diagnoses, you may find that the food recommended for one illness, may be discouraged for another illness. Sometimes it feels like a lose-lose battle.

Still, we must not despair. There is always a path to healthier and active living, if we choose to seek it.

For me, I live be a golden rule when it comes to living in my body.  I think of my body like any vehicle that I would drive. It is my personal vehicle, and so this rule applies:

Food is the Fuel

Exercise is the Engine

As long as the combination of those two factors is balanced, then I feel at peace with my choices. Whereas exercise may be limited to what my body can do at any given time and may not be a daily experience (although I try to make it so), food is something that I ought to consume daily for basic functioning and overall well-being.

However, food, the fuel that our bodies need to sustain us, is one aspect of self-care that can create havoc, for people with fibromyalgia, in our otherwise solid treatment plans.

Over the last six years, I have undertaken the task of discovering what foods my body can tolerate.  Perhaps this task is a leftover from my days as a personal trainer/fitness instructor or maybe it’s just that I want to feel the best I can every day. Whatever the case, I have been experimenting with foods in order to find a FMS+ plan that is nutritionally sound and interesting.

Here is what I’ve discovered about my body:

Foods it Likes

(Tolerates…because I can’t really say that I, personally, enjoy all of these foods):

  • Leafy Greens – Bring on the lettuce, cabbage, endive, etc.  I cannot express to you how much I detest endive…but I live in Italy and am a bit lazy with food preparation, so endive is bound to be present in the bagged salads that I buy.  Oh well.
  • Water – Natural. Okay, this may seem a bit strange, but it is my reality.  My body loves water in its most natural state, not effervescent (fizzy). There is little else beyond water that my body can handle as a liquid. It’s simply not on.
  • Fruits – The crunchy kinds.  Any kind of fruit that has a crunch to it, my body seems to appreciate more than fruits that could be considered juicy (or very ripened).  So, that leaves me with pears, nectarines, apples, etc. HOWEVER, I have learned that I can only eat these in moderation or, at least, rotate them out. I can also eat bananas, mangoes, susine gialle (I don’t know the English name), and grapefruits, but even more infrequently.
  • Nuts & Dried Fruits – Don’t get too excited.  I can eat two things from this category fairly often, but still I understand that I need to keep them in moderate amounts: peanuts & dried cranberries. That’s it. Sometimes, I can have almonds, but not as often.
  • Eggs –  Although I am not a fan, I can eat them and do.  I, however, rotate them in my diet, because I am not partial to the taste.
  • Seafood – Yes, I can eat seafood BUT not all. My body, for whatever reason, cannot handle frequent consumption of  certain fish, such as salmon and tuna.  Shellfish, however, gets a green light.
  • Yoghurt – Notice, I didn’t write milk.  I can eat all yoghurt (as far as I know).  I feel best, however, when I eat Greek yoghurt, which I eat frequently and often in combination with my nuts and dried fruits–it’s my little treat.
  • Gelato – Not often, but I can eat gelato.  I don’t know about ice-cream. Also, I have to stick with plain flavours. Ideally, the gelato should be gluten-free (gluten is sometimes used as a thickener).  So, nothing with cereals or candies, etc.
  • Chocolate (dark or white) – Again, not often, but I can eat chocolate every now and again.  Like gelato, should be ideally gluten-free and it cannot contain any kind of cereals and is best without dried fruits (which is often raisins, which I cannot eat).
  • Diet Soda Ideally, caffeine-free. Looking to spice things up liquid-wise?  Well, I can have diet soda fairly regularly, BUT because of my IBS, I understand that I need to limit my consumption.
  • Other vegetables – Mushrooms, olives, cucumbers, zucchini, garlic, onion, leeks, chives, scallions.  All of those get the green light.
  • Oils & other fats – I cook with olive oil. Period.  I do have butter in my refrigerator, but use it infrequently.
  • Seasonings – Well, most, as far as I know.  I tend not to season my foods, except with curry, black pepper, powdered/liquid garlic, rosemary, thyme or pimento.  And even these are used sparingly.
  • Gluten-free Products – WAIT…Please, don’t get excited, I can eat gluten-free cookies/biscuits…but not all, and it’s sort of a game of roulette.  I never know how my body will react to things.  Also, even though I have been able to eat these things, doesn’t mean that I think that it is good for me.  So, only when I am having a particular craving will I make the effort to purchase these.  They can also be great for making the crust of a low-carb/gluten-free cheesecake.
  • Cheeses – Apparently, I can whatever cheeses are available, but in severe moderation. 🙂 I am partial to softer cheeses, such as brie or cream cheese (which I use to make my low-carb/gluten-free cheesecake).
  • Fake Sugars – Yes, I can use them and do to add flavour to my cooking or sometimes to my water.  Fake sugars, however, are tricky and it is important to understand which ones work for you and which don’t.  My body, for example, cannot tolerate sugar alcohols in any form, whether as a sweetener or in the presence of a food (including gum and mint).

Okay, so those are the major (if not complete list of) items that I can eat.

—–

What I Choose Not To Eat…

The list of items that I ought not to eat is very long.  Notice that I write ought not to eat.

This is because I can eat them, but there will be repercussions.  As long as I am willing to accept the repercussions (major IBS symptoms, random/sudden weight gain, increased pain and fatigue, migraines, increased insomnia), then I’m good to go. 😉

So, what I do I choose not to eat?  Well, I’ll give you general categories:

I discovered how bad it was for me just the other day.  Recently, I bought a bag of gluten-free flour, thinking that I would make myself some awesome Jamaican boiled dumplings. Well…the experience left me in misery.  Sure the dumplings tasted good, but I felt almost as awful as I would have if I were to have used regular flour.  Why?

Well, the foundation of most gluten-free flour is grounded rice, potato starch, sugar, and even some finely grounded nuts, such as almonds.  Remember my list of foods that my body likes?  Well, there you go.  Of course, having spent close to 4 Euros on this bag of flour, I intend to use it all, but sparingly (it’s good until next year).

  • Nightshade vegetables & fruits As much as I love them.  I have said goodbye to tomatoes, bell peppers, potatoes, eggplant (mostly), peppers, and most berries (cranberry exception).  They cause/increase inflammation and possibly insomnia, so it’s just not on.
  • Citrus Fruits – High sugar content, acidic, and too much vitamin C.  Well, all of these things I can do without. I already take a daily supplement of vitamin C, so I can live without them. Of course, as mentioned above, every now and again, I can eat a grapefruit. 🙂
  • Caffeine-heavy products – So, that basically wipes out tea, coffee, sodas, and even chocolate. 🙂  Of course, anything can be consumed in moderate amounts.  Still, I do not drink coffee, and rarely tea or soda. Of course, I mentioned chocolate before.
  • Meats – Like grains. It’s simply not on.
  • Milk – I always find it strange that I can eat yoghurt, but not drink milk. Well, that’s the reality. I can, however, use heavy cream for cooking.
  • Nuts & dried fruits – Too much sugar, too challenging for the body to process. 
  • Alcohol – I’ve never been partial to drinking alcohol. That being stated, alcohol simply presents a challenge for many with FMS. Want to feel more tired? More nauseous? Less restful sleep? Then, drink alcohol. I’m good without it though.

—-

Other things of consumption to think about?

Well, if you smoke, STOP. Smoking increases pain severity.

Chewing gum? Pause. Check the sugar content. Your sugar intake may be having an adverse impact on your health.

Of course, the research on what foods actually help or hinder us is limited.  Each person is different. So, each of us must take responsibility for what we put into our bodies.  Don’t just read this blog or something else and say “Aha! Now I know what to eat!”

Don’t be lazy!

Instead, take this information and use it for your own research. As I mentioned before, it has taken me 6 years to sort this out for myself AND it is still an ongoing process, especially as my body grows older (as a woman, this presents certain nutritional and hormonal issues).

What I’ve come to understand is that, no matter what, I must love my body.

It’s become a mantra…

I must love my body, even when it isn’t doing what I want it to do, even when it isn’t looking the way I want it to look, even when it feels like a stranger to me.  I must love and care for it the best way that I can.

I must shut out the emotional voice of my body that sometimes longs for foods that are unwise for me to eat, and listen carefully to the wise voice of my body that reveals to me the foods that will help me heal and maintain balance.

Food is fuel for our bodies, not a crutch for our self-esteems.

The Take-Away?  Well, I try to follow two basic rules when shopping, especially when I am thinking to buy something new:

  • If the food can live on a shelf longer than one to two weeks, then I don’t buy it.
  • If the food is in a can, bottle, plastic package, then I hestitate to buy it and refer to the first rule.

 

Well, I’m off to the grocery store! Happy Sunday!

P.S. If weight is an issue for you and you are looking for a place to begin, or you are needing inspiration on your journey, then check out fitness motivation speaker and certified women’s fitness, weightloss, and nutrition trainer Erika Nicole Kendall‘s blog:  A Black Girl’s Guide To Weightloss.  Kendall’s blog covers a variety of topics, including fitness, body image, sex, culture, food recipes, and beauty.

FMS | How to (Re)Build a Future…

As a person living with fibromyalgia, I spend a great deal of time thinking.  My thoughts go from the mundane (what can I eat today that won’t cause me to suffer?) to the extraordinary (what would it be like if I could fly alongside the birds outside my window?)…okay, maybe not so extraordinary.

The point is that when my body won’t act according to the demands of my brain, I spend my time reflecting on the present and then on the future. In so doing today, I came to realise that something within me had shifted.

For the firs time in a long while, I was thinking, whole-heartedly and fearlessly, about my future.

I was imagining myself travelling.  No, not just around my neighbourhood, but to distant places like Japan and South Africa.  I was seeing myself working again with young people, writing, teaching, meditating, advising, and generally being at peace and being happy (which I am now)…

It was amazing.  

And then I realised that this, this freedom to imagine, to dream, was something that I had thought had been taken away from me by illness.  I had preoccupied myself with thinking that I could do no more than I had already done with my life.

After all, I had overcome some major challenges with my illness, had given up my old ways of living, had moved to another country, immersed myself in a new culture and language, and begun studying again.  I’ve even been able to work a bit.

Isn’t that more than enough to hope for?

No, it isn’t.

I still have my dreams and my goals AND I can still realise them.  Even if I don’t exactly know the how of each step that it will take to achieve my dreams, I know that the first step is simply to acknowledge that I CAN achieve them, regardless of illness.

So, live whole-heartedly and fearlessly today, despite the challenges, despite your inner critique, despite the naysayers. Having fibromyalgia doesn’t mean that you have to stop living!

Live for You, live for Now, and live for Tomorrow!

FMS | Article: Aerobic Exercise ‘Most Effective Weapon’ for Fibromyalgia

It’s a bright sunny morning here in Rome and, thankfully, not too terribly hot.  Over the last month, I’ve been engaging in a renewed program of incorporating daily walks as a part of my self-care management.

Now, I don’t mean just taking a walk down the road to the neighbourhood grocery store.  I mean taking a proper walk of between 1-3 hours (dependent upon weather and time).

Back in 2008 when I was finally diagnosed with fibromyalgia, my body was in its most unhealthy state.  I had gained a tremendous amount of weight as I could barely get up due to my fatigue and the pain was unbearable. I simply didn’t see how I could get my body to move and to go about life as usual.  Not only that, the drastic changes in both my weight and overall health had been devastating to my self-concept and self-esteem.

You see, just prior to beginning my journey to becoming a therapist, I worked as a personal trainer and fitness instructor.  I prided myself on my level of strength and stamina.  I prided myself on my little need for sleep (of course, I was in my twenties) and was content with the way my body functioned.

Enter fibromyalgia…and the pictured changed.  I was in misery.  It took me almost a year after my diagnosis (2009) to figure out a strategy to get my body and life back together.

I didn’t want to be a walking pharmacy anymore, dragging around a heavy frame that was only becoming heavier and making my symptoms worse.

I decided that I would walk…even if it was the last thing I wanted to do.  I knew that I would be in misery if I attempted to join an exercise program and I don’t believe in dieting.

Most importantly, I knew that walking was still something I could do. It hadn’t been taken away from me.

I started out with small goals, solicited some friends to join me, and began a 10 minute walk program.  That’s right.  Ten whole minutes.  Early in the morning, a couple of times per week, we would meet up and walk together for 10 whole minutes.  Eventually, we increased the time and frequency, and even (gasp) began a jog/walk program. 😉

Fast-forward five years and here I am, walking for hours.  My body has benefited tremendously from the small decision I made back in 2009.  The simple decision to walk. I take one medication for my illness as opposed to several that I had been taking back in 2008.

You see, we can spend our time trying to find the right medication(s). We can go from doctor to doctor.  We can bemoan our circumstances and ask ‘why me?’ forever or, at least, until our last breath.  None of that really will change anything in the end if we don’t look at how we can take control over our bodies ourselves and lives.

Don’t just leave it up to the latest pill you can pop.  Don’t just give up and say ‘what’s done is done’.  Don’t just decide that you are unlucky or fated to living your life in a way that is displeasing to you.

Decide that you can change it. Decide that you can control it.  It’s your body and your illness.  Decide how you want to live with it…happily.

There is always a path to be found…

Until Next Time,

D. 

Click on the link below for the article!

Aerobic Exercise ‘Most Effective Weapon’ for Fibromyalgia (Excerpt below)

“There is no magic drug against fibromyalgia and, in my opinion, there will never be. Psychotherapists don’t work miracles, but psychotherapy can help and, in a few cases, turn people with fibromyalgia into nonpatients. Drugs may help, but patients don’t like them,” said investigator Winfried Häuser, MD, from Technische Universität München in Germany, who has published widely on fibromyalgia.

“Aerobic exercise is the most effective weapon we have; healthy people profit from continuous physical exercise, and so do patients with fibromyalgia,” he explained.

Dr. Häuser presented an overview of research on fibromyalgia treatment here at the European League Against Rheumatism Congress 2014.