Tag Archives: pain pills

COPD – the beginning. Pain – the end

COPD (Chronic Obstructive Pulmonary Disease) is not painful.  We simply cannot breathe easily.  Some of us are on supplement oxygen – others chug along noisily, some less noisy.

“Question: Is having pain in the lung typical of COPD?

Answer: Chronic lung pain is not commonly associated with COPD. However, pain can come from the wall of the chest and not directly from the lungs – this in fact can be seen in COPD. Pain in the chest can come from coughing very hard and straining the muscles of the chest. Pain in the chest can be due to a rib fracture from coughing hard. Pain in the back of the chest can come from osteoporosis, or thinning of the bones. Check with your healthcare provider to find out the cause of your pain. If you have new chest pain, or have pain that frightens you, call 911 to go to the emergency room at the nearest hospital.”

 http://www.nationaljewish.org/healthinfo/conditions/copd-chronic-obstructive-pulmonary-disease/faq/

The problem for some of us is that COPD leads to other stuff – some of it painful – none of it desirable.  That is where I am – I have gathered a bunch of other stuff since my 1997 stay in Harrison Medical Center.

Do to inattention at putting on my stockings when I needed to – timing is crucial – the Cellulitis/Lymphedema is back and trying to heal.  It should have healed by now.  A brief stay in Harrison gave a great jump-start of healing my left leg but the healing has been set back and that means the pain is unrelenting.

A problem seems to be that the long homemade brush had an end tied cord that caught in the bristles of the soft baby brush and ripped the half healed sores open when I was in the shower to gently cleanse the wounds before my husband wrapped them again.

I did not know why it was so painful until I lifted the brush to rinse it and saw the cord end stuck in the soft bristles. I have recut the length of the cord so it cannot happen again.

Pain overtakes a life – it has taken over mine…and no blame except to me.   It has been over a year since my legs got bad and lymph fluid wept and the ‘blame’ is my own doorstep.  I let other stuff get in the way of getting my stockings on. I dropped the ball – as it’s turned out – on my own left foot.

I have never liked taking pain pills for any reason but for a lung patient – it is harmful.  Trouble is, right now – I do not care.  What good is saving your lungs when pain keeps you awake and in agony?  Crying in pain chokes off my airway and I still my mind to focus on deep breathing.  I take a pain pill to sleep and I take a pain pill to endure being awake waiting for my leg to heal.

Should I be afraid of becoming a drug addict?  At this point, I’m more afraid of not wanting to wake up to another day of the same pain.

Funny how drug abuse by drug addicts shut down pain relief for people who medically need it.  Doctors become afraid to prescribe pain pills for fear their patients will become addicted….and patients become afraid to take it.

Read the latest policy by the state – to track:

““Having a patient’s prescription history gives prescribers a more complete view of patient care when they prescribe or dispense controlled substances,” Washington State Secretary of Health Mary Selecky said in a press release. “This new service is another tool for patient care and safety.””

Read more: http://pugetsoundblogs.com/kitsap-crime/2011/10/14/state-to-begin-monitoring-prescriptions-for-pain-medication-in-2012/#ixzz1cT5a9dJ1

Josh Farley’s “State to begin monitoring prescriptions for pain medication in 2012” article is timely.

The only people tracked here are medical patients and their doctors.  The druggies and drug dealers remain in a dark, untracked place of anonymity.

If doctors are leery of writing scripts for pain medications for their patients – what will happen to those patients forced to endure unrelenting pain?

Yes, Josh – I think this is an invasion of people’s privacy.

Thanks for reading…. Sharon O’Hara

Pain Matters – Anger, Sad Study Results

Pain matters – not only to the person feeling it – to the whole family. The idea that our own feelings of anger and sadness might increase our pain level mean we could learn to control the anger and sadness, lessening pain and – if it works on the respiratory system – we can lessen and control the breathing rough times.

Could the same Utrecht University study results apply to lung patients?  It seems a strong possibility based on my own recent experience.

For lung patients it’s important to remember that pain pills negatively affect the respiratory system – we can’t just take them as others might, for pain.  Ask your doctor or Pain Center.

The importance of the study may be seen in the next two paragraphs:

“The treatment effects were significant, showing notable positive differences in physical (pain, fatigue, and functional disability) and psychological (negative mood and anxiety) functioning, and impact of FM for the TC in comparison with the WLC. Clinically relevant improvement was found among patients in the TC group.

“Our results demonstrate that offering high-risk FM patients a treatment tailored to their cognitive behavioral patterns at an early stage after the diagnosis is effective in improving both short-and long-term physical and psychological outcomes,” says junior investigator Saskia van Koulil. “Supporting evidence of the effectiveness of our tailored treatment was found with regard to the follow-up assessments and the low dropout rates. The effects were overall maintained at 6 months, suggesting that patients continued to benefit from the treatment.””

I asked if they had done a separate study for men and discovered that few men get fibromyalgia and was not included in the study.

“Dr. van Middendorp’s response follows:

There were two reasons why men were not included in this study. First, because of the female preponderance in fibromyalgia. This makes it very difficult to include enough men with fibromyalgia to draw reliable conclusions. Second, because men and women differ in emotions, ways of dealing with their emotions, and in reported and experimental pain levels, they cannot just be regarded as one group. Resultantly, we decided to focus our study on women only. There was not a separate study done in men.”

“Anger amplifies clinical pain in women with and without fibromyalgia –

Sensitizing effect of anger and sadness not limited to fibromyalgia patients”

Researchers from Utrecht University who studied the effect of negative emotions on pain perception in women with and without fibromyalgia found that anger and sadness amplified pain equally in both groups. Full findings are now online and will publish in the October print issue of Arthritis Care & Research, a journal of the American College of Rheumatology.

The Utrecht team theorized that specific negative emotions such as sadness and anger also would increase pain more in women with FM than in healthy women. Their study examined the effects of experimentally-induced anger and sadness on self-reported clinical and experimentally-induced pain in women with and without FM. Participants consisted of 62 women with FM and 59 women without FM. Both groups were asked to recall a neutral situation, followed by recalling both an anger-inducing and a sadness-inducing situation, in counterbalanced order. The effect of these emotions on pain responses (non-induced clinical pain and experimentally-induced sensory threshold, pain threshold, and pain tolerance) was analyzed with a repeated-measures analysis of variance.

Self-reported clinical pain always preceded the experimentally-induced pain assessments and consisted of reporting current pain levels (“now, at this moment”) on a scale ranging from “no pain at all” to “intolerable pain.” Clinical pain reports were analyzed in women with FM only. Electrical pain induction was used to assess experimentally-induced pain. Participants pressed a button when they felt the current (sensory threshold) and when it became painful (pain threshold) and intolerable (pain tolerance). Four pain assessments were conducted per condition, and very high internal consistencies were obtained.

More pain was indicated by both the clinical pain reports in women with FM and pain threshold and tolerance in both groups in response to anger and sadness induction. Sadness reactivity predicted clinical pain responses. Anger reactivity predicted both clinical and electrically-stimulated pain responses.

Both women with and women without FM manifested increased pain in response to the induction of both anger and sadness, and greater emotional reactivity was associated with a greater pain response. “We found no convincing evidence for a larger pain response to anger or sadness in either study group (women with, or without FM), said study leader Henriët van Middendorp, Ph.D. “In women with FM, sensitivity was roughly the same for anger and sadness.”

Dr. van Middendorp concludes, “Emotional sensitization of pain may be especially detrimental in people who already have high pain levels. Research should test techniques to facilitate better emotion regulation, emotional awareness, experiencing, and processing.”

In a related study, a research team from Radboud University Nijmegen Medical Centre found that tailored cognitive-behavioral therapy (CBT) and exercise training tailored to pain-avoidance or pain-persistence patterns at a relatively early stage after diagnosis is likely to promote beneficial treatment outcomes for high-risk patients with FM.

The Nijmegen team evaluated the effects of this approach in a randomized controlled trial. The study compared a waiting list control condition (WLC) with patients in a treatment condition (TC) to demonstrate improvements in physical and psychological functioning and in the overall impact of FM.

High-risk patients were selected and classified into 2 groups (84 patients were assigned to a pain-avoidance group and 74 patients to the pain-persistence group) and subsequently randomized to either the TC or WLC. Treatment consisted of 16 sessions of CBT and exercise training, tailored to the patient’s specific cognitive behavioral pattern, delivered within 10 weeks. Physical and psychological functioning and impact of FM were assessed at baseline, post-treatment, and 6-month follow-up.

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These studies are published in Arthritis Care & Research. Media wishing to receive a PDF of these articles may contact healthnews@wiley.com.

Full Citation: “The Effects of Anger and Sadness on Clinical Pain Reports and Experimentally-Induced Pain Thresholds in Women With and Without Fibromyalgia.” Henriët van Middendorp, Mark A. Lumley, Johannes W.G. Jacobs, Johannes W.J. Bijlsma, Rinie Greenen. Arthritis Care and Research; Published Online: April 21, 2010 (DOI: 10.1002/acr.20230); Print Issue Date: October 2010. http://onlinelibrary.wiley.com/doi/10.1002/acr.20230/abstract

“Tailored Cognitive-Behavioral Therapy and Exercise Training for High-Risk Patients With Fibromyalgia.” Saskia van Koulil, Wim van Lankveld, Floris W. Kraaimaat, Toon van Helmond, Annemieke Vedder, Hanneke van Hoorn, Rogier Donders, Alphons J.L. De Jong, Joost F. Haverman, Kurt-Jan Korff, Piet L.C.M. van Riel, Hans A. Cats, Andrea W.M. Evers. Arthritis Care and Research; Published Online: June 2, 2010 (DOI: 10.1002/acr.20268); Print Issue Date: October 2010. http://onlinelibrary.wiley.com/doi/10.1002/acr.20268/abstract

Arthritis Care & Research is an official journal of the American College of Rheumatology, and the Association of Rheumatology Health Professionals, a division of the College.

Thank you, Dawn Peters, for your assistance!

Part 2 of 2

More later…. Sharon O’Hara