My Personal Opioid Crisis

My Personal Opioid Crisis
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Christine Tender Points

As our nation faces the difficult reality of drug abuse, I struggle with my very own opioid crisis. I’m sorry for the families who have lost loved ones due to addiction and overdose. However, I’m just as concerned about those of us who suffer from acute pain and are not abusers in any way. How will the proposed restrictions on pain medication affect those of us who suffer from acute pain and are in no way abusers?

For more than 40 years, I’ve experienced excruciatingly painful myofascial muscle spasms. When they occur, the pain is so strong and so severe that it moves my body involuntarily and completely eliminates my ability to function. (Thank you, fibromyalgia.) Unfortunately, because of the location of my particular pain, I am not eligible for trigger-point injections, which are commonly prescribed to prevent and relieve this condition. Initially, these episodes occurred only once or twice a year. If I were lucky (that’s a relative term here), the spasm would last only a few hours, and it would subside on its own. Other times, I wasn’t so “lucky.” Those times, the pain was stronger than I was, and the emergency room was my only option. Over time, the length, severity, and frequency of these episodes increased.

I was then referred to Kaiser’s pain management program (which I highly recommend). In addition to learning many pain-relieving techniques that I now employ regularly, I was prescribed a variety of narcotic pain relievers until finding one that did not produce the intolerable side effects I’d previously experienced. Now, instead of an hours-long wait in agony at an emergency room, I can take a pill and experience relief within minutes. I’ve regained a sense of control over the pain that I came to fear worse than death itself, and my quality of life has substantially improved.

But I’m concerned about the future. I’m concerned that the discussed prescribing limits will hinder my doctor’s ability to decide how much pain relief I require. I’m concerned about the effects such limits will have on physicians. Will they refuse to adequately medicate pain patients, worried about compromising their medical licenses if they do? I’m concerned that plans to protect the general public from drug abuse will result in a lack of pain control for those who really need it.

It’s not that I want to take these therapies. I’m fully aware of the negative effects they are having on my internal organs. However, it’s the only solution available for acute pain right now. More funding and research on new and different ways to alleviate pain are desperately needed. I’m hopeful that in the face of our current crisis, we will apply more collaboration and creative thinking. I look forward to being pain-free in the future without the use of dangerous treatments.

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Note: Fibromyalgia News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Fibromyalgia News Today, or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to fibromyalgia.

Diagnosed in 1990, Christine has experienced fibromyalgia (FM) symptoms since childhood. After a career in aerospace finance she was trained as an FM support group leader by the Arthritis Foundation and participated in groups on both the east and west coasts. Designated a Leader Against Pain by the National Fibromyalgia Association (NFA) she advocated for increased funding and awareness for FM. She is the author of “More Than Tender Points: A Fibromyalgia Memoir,” available on Amazon. An Upstate New York transplant now living in Southern California, she credits the sunshine for improving her symptoms.
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Diagnosed in 1990, Christine has experienced fibromyalgia (FM) symptoms since childhood. After a career in aerospace finance she was trained as an FM support group leader by the Arthritis Foundation and participated in groups on both the east and west coasts. Designated a Leader Against Pain by the National Fibromyalgia Association (NFA) she advocated for increased funding and awareness for FM. She is the author of “More Than Tender Points: A Fibromyalgia Memoir,” available on Amazon. An Upstate New York transplant now living in Southern California, she credits the sunshine for improving her symptoms.
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