Wednesday, September 30, 2009

Small Business Tip: Firms Working to Take Some Pain Out of the Workday

This is the last day of the month and a close to Pain Awareness Month. Not a big small business event? You’d be surprised. Thousands of small business owners are taking steps and making accommodations to help employees living with chronic pain stay productive.

Fibromyalgia affects more than five million Americans and is one of the most common, chronic widespread pain conditions, yet it is often called an invisible illness. The disorder is one of the most common chronic widespread pain conditions in the United States.

This short streaming video reveals some of the ways small business owners and entrepreneurs are making changes to help the millions of Americans living with chronic pain.

Please follow me on Twitter to learn more about small business trends and events to give you a competitive edge in business at http://twitter.com/danitablackwood

Monday, September 28, 2009

Fibromyalgia: an overview

I didn’t intend to get into a theme this week, but this paper arrived in my inbox this morning, and given both the prevalence of fibromyalgia, and the often ‘fuzzy’ management that can be provided, I thought it might be worthwhile taking a look at it.  The paper itself is a pre-print, but has been revised earlier this year and is probably the final version.

The outline of the paper covers diagnostic criteria, and briefly discusses the place of neuroimaging (if only we could get that done readily here!), but notes that many other conditions overlap or mimic FM such as hypothyroidism, tendonitis, ankylosing spondylitis, as well as chronic fatigue, suggesting some sort of common pathway in either the peripheral or central nervous system, raising the possibility of some common treatment approach.  So far though, it’s not clear – and it’s important to rule out these other conditions that all have their own management approach before deciding that FM is what the problem is.

The next section of the paper reviews the current state of knowledge around pathophysiology as a basis for treatment and rehabilitation.  Both peripheral and central sensitisation seem implicated in FM, leading to amplification of sensory impulses that alter pain perception.  Increased excitation of various peripheral structures can in turn lead to neuroplastic changes in the central nervous system – winding up the whole experience for the person in the middle of it!

Imamura, Cassius & Freni, the authors of this paper, briefly review some of the factors thought to play a role in the reduced threshold for neuronal firing, including elevated levels of substance P, calcitonin gene-related peptide, bradykinin, and so on.  Included in their review are CNS factors such as the altered non-REM sleep of people with FM – and that this is associated with the severity of symptoms; the association between depression and FM; and neuroimaging studies showing a change in regional cerebral blood flow to pain-related structures in people with FM.

If these aspects of FM can be explained to people with the pain problem it could make a significant difference to their own attitude toward their pain.  For many people, it can take several years before a diagnosis of FM is made: during this time the beliefs and approaches of many practitioners can influence their understanding of their pain – and sadly, some practitioners are not empathic and can take a somewhat pejorative approach to people with the disorder.  Knowledge can lead to understanding – and understanding can lead to a sense of empowerment.

Moving through the paper, the authors indicate that treatment needs to be based on the proposed model of fibromyalgia.  That is, it needs to address central mechanisms rather than peripheral ones (so, no more NSAIDs, opioids or corticosteroids!), and the overall approach needs to be ‘rehabilitative’ – I’d suggest biopsychosocial as the model!  The shift is from curing the problem to improving health status and health -related quality of life.

There are two arms of management for fibromyalgia:

(1)  pain relief through medication and ‘physical’ strategies to reduce peripheral and central sensitisation

(2)  cognitive behavioural approaches to manage sleep, fatigue, mood, cognitive problems, headache, migraine and other problems associated with FM.

Although the authors suggest ‘education’ as a cornerstone – I’d rather suggest helping the person to reconceptualise their problem as one of pain processing.  Education can be seen as simply providing information – reconceptualising is about helping the person see themselves and their pain problem as something they can manage, something only they can do – and something they can do.

The remainder of the paper looks at pharmacological approaches and the rationale for using tricyclic antidepressants and/or serotonin/norepinephrine-reuptake inhibitors, and tramadol because of their effect on reducing afferent transmission at the dorsal horn or increasing the activity of the descending inhibitory pain systems.

It should be noted that even these drugs don’t always reduce the pain and all have their own array of side-effects – so they need to combined with self management.

Nonpharmacological approaches are then reviewed.  This is where the interdisciplinary team can take the lead because these approaches are both effective – and once learned, don’t consume health resources in quite the same way as medications can.

Exercise gets the nod – remembering that exercise can include enjoyable daily activities such as walking, gardening, dancing and playing with the dog, not just going to a gym!

Electrical stimulation – this is suggested, although as far as I know, it’s not readily available – Imamura et al. indicate transcranial direct current stimulation as an effective approach, but I haven’t heard much of this as a strategy available in New Zealand.  (If anyone has, let me know).  I’m also not entirely comfortable with this as a self management strategy – it sounds pretty invasive and requires health care input, at least initially.

Acupuncture – this is less well-documented, and results are, as these authors say, ‘controversial’.  They suggest that ‘clinical benefits seem to be of small magnitude and of short duration’ – my main concern would be that unless the person can ‘do it themselves’, it will involve more appointments, so I’d not be comfortable with it as a self management approach.  I hold a similar view of injections – Imamura et al suggest that ‘concomitant myofascial pain, along with instruction in relaxation techniques, may benefit some patients with an associated mysfascial pain component.’ 

The final area reviews, very, very briefly, cognitive behavioural therapy.  The authors indicate its use for ‘associated psychological and psychiatric comorbidity’, but I’d be inclined to challenge this.  The perception of pain involves thoughts and beliefs about the meaning of pain – and the effect of reconceptualising fibromyalgia as not being a ‘life sentence’ or a ‘constant struggle’, and understanding what some of the mechanism are, will bring about changed perception.  Distress reduction, increased sense of self efficacy and more effective approaches to activity, relaxation, cognitions, as well as effective communication skills and working on relationships - these are all integral to living a good life despite pain.

Overall – this is a nice, brief review especially of some of the pathophysiology of fibromyalgia and the rationale for the treatment approaches suggested.  There are plenty of good references, and while it’s not an ‘easy’ read, it’s quite brief and contains the essentials.

 

From Imamura, M., Cassius, D., & Fregni, F. (2009). Fibromyalgia: From treatment to rehabilitation European Journal of Pain Supplements DOI: 10.1016/j.eujps.2009.08.011

Sunday, September 27, 2009

The 3 R's? A Fourth Is Crucial Too : Recess

Egoscue Portland comments on an article in the New York Times.

The best way to improve children’s performance in the classroom may be to take them out of it.

New research suggests that play and down time may be as important to a child’s academic experience as reading, science and math, and that regular recess, fitness or nature time can influence behavior, concentration and even grades.

A study published this month in the journal Pediatrics studied the links between recess and classroom behavior among about 11,000 children age 8 and 9. Those who had more than 15 minutes of recess a day showed better behavior in class than those who had little or none.

Read The Rest of the Blog

Friday, September 25, 2009

SLEEP, SLEEP AND SLEEP A LITTLE MORE!

DAY 30:  I choose  to appreciate my naps since much healing occurs while I sleep.

I really resent having to sleep much of my afternoon away.  A real indicator of health for me will be increased endurance and restfulness so that I will not have to stop and sleep.  I  hate this gradual loss of stamina during the morning so that by Noon I am struggling and finally after lunch I surrender and go for a nap.  On some  stronger days I resist the fatigue and attempt to miss the nap.  Unfortunately, by supper I am ready to collapse.  Therefore, I almost resist the growing body of evidence that suggests that everyone should have a nap in the afternoon!

Dr. Gregg D. Jacobs writes in an article called the ”Benefits of Naps” that  “because the urge for a nap is appreciably weaker than the need to sleep at night, it can be suppressed (or masked by caffeine) but at the cost of increased sleepiness and reduced mood and performance.” He also states that “sleep itself may not be the crucial factor in the positive effects of afternoon naps on improving mood; what may be important is an afternoon period of relaxation common to both resting and napping.” (http://www.talkaboutsleep.com/sleep)  Others who promote naps actually suggest that a power nap will give us more patience, less stress, better reaction time, increased learning, more efficiency and better health.  These sleep advocates even suggest how long a nap to take in order to enjoy specific benefits.  For example, a 20 minute nap increases alertness and motor skills; a 40 minute nap increases memory; and a 90 minute nap increases creativity!  Apparently, it is unnecessary to have a nap longer than 90 minutes since it merely means that the cycle of sleep begins again.  However, I haven’t found any research to determine whether some of those numbers may change for someone who is ill.

What this information does suggest is that if naps are that beneficial to healthy people how much more to those who are ill. The necessity of sleep was reinforced when I read A Stroke Of Insight by the brain scientist Jill Bolte Taylor, who had a stroke at 39 years of age.  She writes, “When it comes to the physical healing of cells, I cannot stress enough the value of getting plenty of sleep.  I truly believe that the brain is the ultimate authority on what it needs to heal itself .  . . I remain a very loud advocate for the benefits of sleep, sleep, sleep and more sleep interspersed with periods of learning and cognitive challenges.”

Obviously, I need to positively approach my naps so that negative emotions don’t hinder the benefits of this afternoon rest!  I need to imagine how my cells are healing and how my immune system is getting stronger while I sleep.  I need to trust my body’s wisdom and know that when I no longer need long naps I will no longer sleep as long as I do!  And apparently, I am in good company as I nap since the following were self-proclaimed nappers:  Albert Einstein, Leonardo Da Vinci, Thomas Edison, Winston Churchill, Johannes Brahms, and   Eleanor Roosevelt.  If naps were good enough for them, I guess they are good enough for me too!

Wednesday, September 23, 2009

Ambassadors For Christ

We are therefore Christ’s ambassadors, as though God were making his appeal through us   (II Corinthians 5:20-21 NIV).

Our pastor recently preached on this passage. I usually associate this verse with foreign missions, but as I listened, I was impressed with a new thought.

He mentioned that the word “ambassador” means having a mission or assignment to carry out. This verse does not say that Christ’s ambassadors are only the healthy, the strong, the mobile, or the mentally alert. It says that we – all believers – are on this mission for God.

Many days I may feel I don’t have any “assignment”– I may not be able to physically “do” anything from my perspective. I then thought about ambassadors to other countries. I’m sure there are times when every day is not packed with activity, yet they still remain as a constant presence, ready and prepared to represent their country.

I can do the same. There may be long periods where I feel there is no “mission” I am capable of carrying out for God, yet His Word says otherwise. We are God’s only vessels on this earth. He has chosen us as well as the healthy and strong to represent him. If nothing else, our continued perseverance and faith is an assignment which may have significant effects in someone else’s life.

Our pastor also reminded us that an ambassador’s home is not where he is serving. He is living their temporarily until his mission is accomplished. I am actually doing that now on earth, and some days I am ready for my assignment to be ended because I just want to go home. But the Lord knows what only I can do for him, and until that is finished, He will keep me here. One glorious day, I will be able to say, “mission accomplished”. May I also hear the Lord say, “well done thou good and faithful servant”.

Prayer: Heavenly Father, thank you that you choose not only the whole and healthy but the weak and infirm as your vessels, for when we are weak, then you are strong. May we look on every day as an opportunity to represent you and do it well. Amen.

ABOUT THE AUTHOR
Bronlynn Spindler is a wife and mother of three grown daughters and lives in Fredericksburg, VA. God’s grace and strength give her the ability to deal with chronic back pain, depression, headaches, and fibromyalgia. You may contact her at spindler@cox.net.

Complex Regional Pain Syndrome -

Complex Regional Pain Syndrome or CRPS Treatment

originally posted on August 4, 2008;  Re-posted 9-22-09

Complex Regional Pain Syndrome (CRPS), commonly referred to as reflex sympathetic dystrophy or RSD, is a syndrome in which pain, usually burning type, is out of proportion to the injury (either nerve or no nerve involvement). The pain may spread through the entire limb and/or to other parts of the body. Examples of precipitating events that may cause CRPS include the following: fractures, surgery, frostbite, soft tissue trauma, burns, MS, tight cast, strokes, heart attack and amputations. The symptoms are characterized by autonomic dysregulation such as swelling, vasomotor instability (skin becoming pale/cool/cyanotic or red/warm/dry), abnormal sweating, trophic changes (course hair, thick rigid or brittle nails, skin may become coarse or thin, smooth, and tight), hypersensitivity, abnormal motor activity, and decreased bone density.
Medically, CRPS is managed by a variety of medications aimed lowering the rate of nerve firing, reducing inflammation, reducing anxiety, and reducing pain. More invasive measures include sympathetic nerve blocks in the spinal column or ganglion blocks, implanted dorsal column stimulation or decompression, all of which carry the same risks of any invasive procedure.
The main reason for this entry is to share a positive treatment outcome for CRPS using IMT. In general, the physical therapy treatment for CRPS includes reduction of pain to allow the pt. to maintain function. Traditional forms of exercise such as aerobic, pool therapy, ROM, joint mobilization/soft tissue mobilization, exercise emphasizing compression and distraction, functional ex. and exercise that increases blood flow to the extremity or increase proprioception to the spinal cord may be beneficial All exercise must be extremely gentle and nonaggressive especially if not initiated during times of sympathetic blocks.
My past experience with CRPS includes most patients unable to tolerate any manual techniques and very minimal exercise resulting in extremely slow progress. It has been shown in research that early intervention with physical therapy is extremely important to minimize loss of function. The earlier the intervention the more likely to reverse the dysfunction.
Recently I evaluated a pt. with CRPS onset following a bunionectomy. The pt. presented 3 months post op with extremely antalgic gait, inability to bear more than 30% weight on the affected foot, and requiring a walking cast boot to tolerate being on her feet. The patient’s foot was swollen, reddened, and there was no active mov’t in the big toe. Within 5 treatments of IMT including light touch on areas of the body specific to affecting the autonomic nervous system and indirect myofascial release (vs. more aggressive direct techniques) the patient is able to bear 50-50% body weight, ambulate w/o the walking boot with more normality. Gait quality still consisted of slight antalgia, decreased push off and mild trunk shift but the patient is able to walk further and have more energy throughout the day to function. The skin has returned to a more normal color and edema has decreased resulting in less smooth/shiny appearance. The slough and calluses which persisted on her incision long after surgery fell off naturally within 1 week and active ROM has returned in the big toe. Range of motion home exercises are being performed in a warm bath and also passively to isolate different joints of the toe. Ankle ROM exercises are also completed in the bath. In no way is this patient healed or pain free but the quality of the toe/foot appearance, gait quality and tolerance have progressed more rapidly than I have ever seen in the past.
I know I’m more than a little biased towards IMT but I want people out there to know that there is gentle, effective treatment out there that can make life a lot easier and functional if you have CRPS. Please spread the word!! www.missionhillspt.com and http://missionhillspt.com/index.php?page=chronic_pain for success stories of patients who recovered from chronic pain issues.

For more information on the methods used at  Mission Hills Physical Therapy please visit these sites

www.centerIMT.com

www.matrixenergetics.com

www.kimberlyburnhamPhD.com

Sally Skurdahl, MPT

——————————-

Ralph Havens PT, OCS, IMTC

Mission Hills Physical Therapy

928 Ft. Stockton Dr. Ste. 201

San Diego, Ca 92103

619.543.1470

Tuesday, September 22, 2009

"What do I Have?" - Overlapping Symptoms & Coexisting Conditions - Ashley Boynes, Community Development Director, WPA Chapter

One problem that arthritis patients have in getting an affirmative arthritis diagnosis is that many forms of arthritis imitate one another, and even mimic other conditions. This makes it a difficult task for doctors to diagnose certain types of arthritis, and can often lead to frustration in patients, as well.

For one thing, there are over 100 types of arthritis. Additionally, some forms, such as Rheumatoid Arthritis, share many common characteristics with other diseases – specifically chronic and invisible autoimmune illnesses.

With so many symptoms overlapping and so many coexisting conditions, it is no wonder that patients and doctors are sometimes left in a state of confusion over the actual cause of the problem, or problems, at hand.

Conditions such as Rheumatoid Arthritis, Lupus, Fibromyalgia, Sjogren’s Syndrome, and Multiple Sclerosis, for example (just to name a FEW!) have many of the same symptoms: aching joints, muscle tenderness, overall pain and discomfort, stiffness, severe fatigue, headaches, a feeling of weakness, and so on. Many patients with these symptoms have an elevated rheumatoid factor and coexisting symptoms such as vision/eye problems, gastrointestinal issues, etc. Additionally, many of these conditions’ symptoms lull and flare, and are not consistent on a day-to-day or even hour-to-hour basis, which makes it a hit-or-miss situation when visiting a doctor to try to “show” them your symptoms upon physical exam. All of the above conditions are autoimmune in nature, causing a weakened immune system that attacks itself, and that can cause other illness, as well. In fact, many medications and natural courses of treatment overlap for all of the above-named conditions, too. Even more perplexing is that these conditions often coexist in the same patient, at the same time!

With all of this being said, you may wonder why it matters to get an official diagnosis, if many of the symptoms, outcomes, and courses of treatment are the same. Getting an official diagnosis is important because, although many aspects of these illnesses do overlap, each has its own exclusive set of symptoms, as well. For instance – someone with RA may have swelling – but no swelling or inflammation is typically present in fibromyalgia by itself. Depression, while a common factor in any chronic illness, is more closely associated with MS than any of the other aforementioned conditions. Likewise, patients with MS and RA may have vision issues, while someone with Lupus may not. People with Sjogren’s deal with severely dry eyes and mouth, which isn’t always common to the other conditions. Rheumatoid Arthritis is closely associated with certain forms of cancer, heart disease, low-grade fevers, and thyroid problems; and MS is associated sometimes with musculoskeletal issues and food allergies. Lupus patients typically get a red butterfly rash on the face, as well as occasional edema in the lower legs. As you can see, it is important to treat each illness on its own, in order to take care of each individual symptom, despite so many of them overlapping.

All of the similar traits of these types of illnesses can often lead to misdiagnosis, or, a “missed” diagnosis. This is why it is important to share EVERY symptom or change in your health – even if you think it is irrelevant – with your health care professional, so that they can make a reasonable assessment and an accurate diagnosis. The one symptom that you neglect to tell your doctor may be the key in proper diagnosis of your condition.

So how DO they know what you have? In diagnosing forms of arthritis and related conditions, a doctor usually couples a physical examination with bloodwork. Additionally, they also factor in the patients’ personal description of ailments. In many cases, the lab work is used to rule out other conditions, and a diagnosis is often made using a “process of elimination” of sorts. Unfortunately, people who have one form of arthritis (for example, RA) often have another co-existing form (i.e. osteoarthritis or fibromyalgia.) Likewise, patients with one autoimmune condition typically have more than one – often, three, overlapping conditions at once.

Other reasons for coexisting conditions and overlapping symptoms in arthritis patients include medications and lifestyle. Arthritis patients with a more sedentary lifestyle are more prone to obesity which can then lead to diabetes or heart problems. Additionally, many medications can cause nasty side effects ranging from partial blindness to neurological and gastrointestinal problems – and even cancer.

It is important to stay proactive in your health. If you are unsure “what you have” – see a doctor.  A helpful tip is to keep a health journal, and, before your appointment, document every symptom that you have – even if you aren’t sure it is a concern. If you are unsatisfied with a diagnosis, seek a second or even third opinion until your issue is resolved. Do not ever write anything off. If you have these types of conditions, you need to be aware of everything that is going on with your body. Educate yourself on your disease. For instance – if you have arthritis, do you know what type you have? Is it rheumatoid, which is autoimmune in nature? Or, is it osteoarthritis, which is more mechanical; more “wear-and-tear”? Is it another rheumatic condition – bursitis, myositis, gout, Sjorgen’s, Still’s Disease, ankylosing spondylitis? Make sure you understand your illness and the array of symptoms associated with it. If anything new pops up, let your doctor know – it is better to be safe than sorry.

For your information, here are a few quick facts and tips to keep in mind:

  • There are 117 types of arthritis. You can read about them from the Arthritis Foundation here: http://www.arthritis.org/types-arthritis.php
  • There are over 100 known autoimmune diseases – many of which are also considered – you guessed it – forms of arthritis and rheumatic disease.
  • A symptom common to all of these conditions is severe, debilitating fatigue. Another is widespread weakness and pain.
  • Another attribute common to all of these types of illnesses is the fact that they are chronic. A chronic illness is one that is ongoing, long-standing, and typically, permanent. Often, chronic illnesses may be treatable to an extent but have no cure.
  • If you have a chronic illness like arthritis, be certain not to neglect the needs of your spouse/partner, family, and loved ones. It is sometimes all too easy to concentrate on yourself and your symptoms and overlook the needs of others.
  • People with these types of diseases are prone to anxiety and depression. Be on the lookout for any signs of mental or emotional distress.
  • An accurate and official diagnosis is often needed in order for health insurance to cover your condition and provide benefits.
  • The Arthritis Foundation provides brochures and literature on the 117 types of arthritis. Contact us if you need any types of resources or support.
  • Keep in mind that all of these illnesses CAN AFFECT CHILDREN, too! If your child’s pediatrician gives you a diagnosis you disagree with, keep tabs of his/her symptoms and seek out a second opinion.

Please note, too, that we will not be airing a new episode of Arthritis Radio this week, due to the G20 Summit being in town here in Pittsburgh. However, in correlation with this blog, we encourage you to go back and browse our archives – you will learn a lot from episodes 1-8 about rheumatoid arthritis, osteoarthritis, juvenile arthritis, fibromyalgia, and overall wellness.

Check it out here:  http://arthritisradio.podbean.com or search, “Arthritis Radio” on iTunes!

As always, thanks for reading, and be well!

Best,

~ Ashley Boynes

Community Development Director

WPA Chapter