Chronic pain changes our immune systems

https://goo.gl/LMhArw

Chronic pain may reprogram the way genes work in the immune system, according to a new study by McGill University researchers published in the journal Scientific Reports.  

“We found that chronic pain changes the way DNA is marked not only in the brain but also in T cells, a type of white blood cell essential for immunity”, says Moshe Szyf, a professor in the Faculty of Medicine at McGill. “Our findings highlight the devastating impact of chronic pain on other important parts of the body such as the immune system.”

Chronic pain – pain that lasts six months or more -- is one of the most common causes of disability worldwide. Despite enormous efforts to find new therapeutic strategies, however, effective treatments for chronic pain remain elusive.


6 Books That Help Chronic Pain Sufferers

http://goo.gl/hjPhJm

When you suffer from chronic pain, your everyday activities almost come to a standstill. If this sounds like you, and the typical treatment modalities have not provided much relief, there are some interesting books you should probably take a look at.  The alternative methods and strategies outlined in these six can potentially relieve, or at least alleviate, your chronic pain, no matter which area of your body is affected by pain.


Patients who are not prescribed opioids find more improvements in physical function, study

http://goo.gl/NgNh3j

Opioids such as morphine, codeine and Tylenol 3 can be effective for treating pain, however, a new University of Alberta study finds that patients with neuropathic pain taking opioids report no improvements in physical functioning compared to those who were not prescribed opioids.

"We studied patients with neuropathic pain from nerve injuries such as diabetic neuropathy and pinched nerves, and the ones who weren't prescribed any opioids had statistically lower disability and higher physical functioning scores," says Geoff Bostick, associate professor of physical therapy at the Faculty of Rehabilitation Medicine and lead author of the study published in Pain Medicine.

The study looked at 789 patients across Canada who provided baseline measures of self-reported function, and again at six and 12 months after treatment. Adjusting for severity of the symptoms, the research showed physical functioning and disability did not improve in patients with neuropathic pain who were prescribed opioids compared with those who were not prescribed.

"Even though opioid medications can be a powerful pain killer, it does not necessarily mean improved function will follow--pain is not the only factor in determining function," explains Bostick.

"It can be difficult helping people move when they have pain, but as a physiotherapist I know the importance of physical function and we have to help find a way to promote movement, even if it is painful."

As a pain expert, Bostick understands the important role opioids play in the treatment of pain.

"Pain is very complex, and people experience pain at very different levels. Opioids can help people with severe pain be more comfortable, but if they are not also facilitating improved function, the impact of these medications on quality of life should be questioned."


African American Pain Treatment Disparities

https://goo.gl/RwJbwb

Healthcare disparities are inequalities that exist when members of certain populations do not benefit from the same health status as other groups. Historically, cradle-to-grave disparities have been an ongoing tragedy for African Americans. This includes not only the high percentages in disease rankings such as heart disease, cancer, stroke, and diabetes, but also procedures such as pain treatment.

One example is the hospital emergency room waiting time to see a physician for African Americans compared to whites with pain symptoms that suggest acute coronary syndrome. An analysis of the National Hospital and Ambulatory Care Survey data was conducted on adults with visits related to acute coronary syndrome. Adjusted average differences in waiting times (time to see a physician) for African Americans and whites were compared.

A total of 15,438 visits related to acute coronary syndrome symptoms were made during the 7-year study period. Among patients going to the emergency room with symptoms suggesting acute coronary syndrome, African Americans waited 30% longer to receive care compared to whites. In addition, this difference in waiting time persisted during the study period, even after the implementation of the Healthy People initiative to eliminate disparities such as this.


Hospitals Put Pharmacists In The ER To Cut Medication Errors

http://goo.gl/TPSdLf

Medication errors can be caused by something as simple as bad handwriting, confusion between drugs with similar names, poor packaging design or confusion between metric or other dosing units, according to the Food and Drug Administration. But they're often due to a combination of factors, which makes them harder to prevent.

At Children's in Dallas, there are 10 full-time emergency pharmacists, more than anywhere else in the country, and they are on call 24 hours a day. The pharmacists provide a vital safety net, according to Dr. Rustin Morse, chief quality officer and a pediatric ER physician.

"Every single order I put in," Morse says, "is reviewed in real time by a pharmacist in the emergency department prior to dispensing and administering the medication."


Migraines worsen as women approach menopause

http://goo.gl/xLmVAw

Migraine headaches heat up as women approach menopause, according to a new study from researchers at the University of Cincinnati (UC), Montefiore Headache Center, Albert Einstein College of Medicine and Vedanta Research.

"Women have been telling doctors that their migraine headaches worsen around menopause and now we have proof they were right," says Vincent Martin, MD, professor of internal medicine in UC's Division of General Internal Medicine and co-director of the Headache and Facial Pain Program at the UC Neuroscience Institute.

The risk for high frequency headache, or more than 10 days with headache per month, increased by 60 percent in middle-aged women with migraine during the perimenopause--the transitional period into menopause marked by irregular menstrual cycles--as compared to normally cycling women, says Martin, the study's lead author.


Implementing the Affordable Care Act (ACA): A Roadmap for People with Disabilities

For policy wonks....

http://goo.gl/5UzHvK

The Patient Protection and Affordable Care Act (ACA) is one of the most significant and widely debated pieces of healthcare legislation in generations, and it has altered the way that people with disabilities will receive health care and ancillary services for generations to come. Implementing the Affordable Care Act (ACA): A Roadmap for People with Disabilities is the first in a series of three reports regarding the implementation, impact, and enforcement of ACA.

This first report in the series provides a roadmap for monitoring the implementation of ACA and for making sure that this important federal law supports the outcomes the disability community has prioritized.

People with dementia gain from learning self-management skills

http://goo.gl/amWfC1

Research involving Bangor University and published in the journal International Psychogeriatrics, found that attending weekly 'self-management' group sessions which encouraged socialisation, discussion, problem solving and goal setting fostered independence and promoted social support amongst people with dementia.

The groups, led by trained facilitators, were focused on providing people with a better understanding of their dementia and ways to cope with it. Participants were supported in their ability to manage their own symptoms, treatment and lifestyle changes with information and expert help. They were then encouraged to share ideas and strategies for dealing with their condition and were encouraged to record notes and reminders in a handbook.

"Developing dementia can be a scary and isolating experience. We developed a group programme to help people with dementia manage their condition and find ways of dealing with the changes in their lifestyle. We found early evidence that empowering people to manage their own symptoms and bringing them together helped them feel more confident about managing everyday life with dementia," said lead researcher Dr Catherine Quinn, Senior Research Fellow in The Centre for Research in Ageing and Cognitive Health (REACH).

"All this has helped to enhance their quality of life. The group members became friends and supported each other, and we found that they benefited from being able to learn from each other."


Psoriasis patients have reduced access to efficient treatment method with age

Gee, I wonder why....
http://goo.gl/nrPObE

Researchers who have examined if patients of varying ages have the same access to the most efficient psoriasis treatment, found that an age increase of 30 years resulted in an average 65 per cent reduction in likelihood of obtaining treatment with biologics. The study is described in an article published in the British Journal of Dermatology.

A group of researchers led by Marcus Schmitt-Egenolf at Umeå University has, in a cohort study, investigated the effects of ageing in terms of access to modern pharmaceuticals in psoriasis healthcare. The study, which is the first of its kind, found that elderly patients have reduced access to the relatively new treatment of psoriasis using biologics. Biologics are medications that either target T-cells or block immune system protein and is more efficient but also more expensive than the corresponding, conventional and systematic treatment. The study shows that the patient's access to this treatment method was reduced with every year of ageing.


“Big Pharma” & Privilege: Or Why I Wish Allies Would Stop Using This Phrase

http://goo.gl/fdrIUR 

This is an actual response to my friend’s post about chronic pain. I’m being kind and not putting names up. Some of you out there might be nodding your head to what is being quoted here right now. I am not exaggerating when I say that this was the second time in the same day I’d seen these sentiments said by 2 different people, and I’d not spent much time on social media yesterday. Being active in the chronic illness and disability communities, I see these statements on a daily basis.  I see the effects on those who it’s said to that don’t live their lives out in the public.

I expressed in a frustrated moment on Facebook that when I hear the words “Big Pharma” I stop listening, because I assume it’s going to be filled with a bunch of unscientific nonsense. And that got challenged, because obviously I’m making assumptions that aren’t nice. Yet I encounter the same situation day in and day out, and I have many friends with chronic illness and invisible disabilities who also express this same sort of experience happening to them regularly.

So let me take a big deep breath here as I calmly say this: I am sick of being nice about this shit, and I’m horrified that those fighting in the social justice realm are constantly ignoring what disabled people are telling them about their experiences.