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Angelika Byczkowski

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Angelika Byczkowski

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Angelika Byczkowski is a patient with Ehlers-Danlos syndrome who blogs at EDS Info.

Blame the pain, not the opioids

Angelika Byczkowski
Patient
March 29, 2019

I’ve noticed a frightening trend in the latest research on patients taking prescribed opioids: whatever the negative outcomes, researchers attribute them to the opioid medications instead of the underlying pain.

The many detrimental outcomes these studies find are exactly what you’d expect from a person suffering long-term chronic pain. They don’t recognize or calculate into their studies that opioids were prescribed to ease intractable pain.

It’s like stating that …

Read more…

Blame the pain, not the opioids

A patient’s opposition to the anti-opioid movement

Angelika Byczkowski
Medications
March 21, 2019

I recently read an article — “California Doctors Alarmed As State Links Their Opioid Prescriptions to Deaths” — that infuriates and frightens me I’m furious that doctors are being persecuted for opioid prescriptions written years ago, and frightened that my doctor here in California may be pressured to stop prescribing them for my painful genetic disorder (Ehlers-Danlos).

Twenty-six states have already implemented arbitrary restrictions on our …

Read more…

A patient’s opposition to the anti-opioid movement

How the war on opioids has harmed some patients

Angelika Byczkowski
Patient
January 30, 2019

In a recent article for Pain Medicine News, “4 Steps Every Provider Must Take Before Prescribing an Opioid,” two lawyers detail the voluminous documentation doctors must collect and maintain to protect themselves against all these new anti-opioid rules.

When even so many doctors don’t understand chronic pain, it’s no surprise that lawyers don’t either. They are trying to fit the practice of pain management into a legal framework to defend themselves …

Read more…

How the war on opioids has harmed some patients

Stop the war against patients with intractable pain

Angelika Byczkowski
Patient
July 10, 2017

An open letter to doctors still prescribing opioid medication when necessary:

Thank you so much for standing up for us pain patients. My chronic pain comes from a genetic connective tissue disorder (Ehlers-Danlos Syndrome), so there is no treatment or cure for my slow, but relentless, physical deterioration as the collagen holding my body together falls apart.

I, like so many other pain patients, spent years (1982-1995) trying other therapies (yoga, acupuncture, …

Read more…

Stop the war against patients with intractable pain

When impossible pain is, in fact, possible

Angelika Byczkowski
Patient
June 28, 2017

I had my first outpatient surgical procedure when I was still in high school and needed a plantar wart removed from the sole of my foot. As the doctor injected the area with a local anesthetic, he explained he did these procedures all the time, and I wouldn’t feel a thing. After a short wait, he began to dig out the deeply embedded wart with a hooked scalpel.

With the first …

Read more…

When impossible pain is, in fact, possible

The subtle arrogance of good health

Angelika Byczkowski
Patient
September 4, 2016

Until my physical ailments began worsening rapidly in my late 40s, I was a high achiever, proud of my “kick ass” attitude, thinking I was so competent I could surmount any challenge life threw at me. Life appeared to be straightforward, and I didn’t understand why this didn’t seem to be the case for so many other less fortunate folks.

Though I worked hard for my accomplishments and sometimes struggled, there …

Read more…

The subtle arrogance of good health

In today’s society, chronic illness is viewed as a personal failing

Angelika Byczkowski
Patient
May 16, 2013

When I recently read the phrase, “I’m embarrassed to be sick,” it made my stomach clench and my breath catch.  That’s exactly what I’ve been feeling: this vague sense of social unease even with close friends, a reluctance to be seen or even talk to people–especially those that knew me before I became chronically ill.

At the age of 55, after a lifetime of seemingly …

Read more…

In today’s society, chronic illness is viewed as a personal failing

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  • Most Popular

  • Past Week

    • Retirement isn’t the end of medicine, it’s a second act [PODCAST]

      The Podcast by KevinMD | Podcast
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      Mustafa Kemal Çalık, MD | Physician
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    • Paid for twice

      Physicians paid for G2211 twice. Most never bill it.

      Michael Duben, MD | Physician Finance
    • Hospital IT approval has no path for clinician-built tools

      Sanjay Khicha, MD and Gautam Nayak, MD | Health Technology
    • Physician well-being is not an individual problem

      Heather Buckley | Conditions and Diseases
  • Past 6 Months

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      Richard A. Lawhern, PhD | Conditions and Diseases
    • Retirement isn’t the end of medicine, it’s a second act [PODCAST]

      The Podcast by KevinMD | Podcast
    • Sensory processing in autism and the brain’s volume control

      Josette Pelatan, PhD | Conditions and Diseases
    • What maternity care deserts cost a town

      Manisha Kaliaperumal | Health Policy
    • Why medicine needs a national physician license now

      Vaishali Popat, MD, MPH | Physician
    • A cold cost $945. The cost of primary care is broken.

      Susan Newman, MD | Physician
  • Recent Posts

    • Paid for twice

      Physicians paid for G2211 twice. Most never bill it.

      Michael Duben, MD | Physician Finance
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