The Two Faces of Conventional Care – National Report on Pain



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This year, while I write almost exclusively on integrative care – which includes conventional, complementary, and self-care – I tend to skip the conventional model because I've moved away from medicine Western a decade or so ago. welfare. In fact, when I switched to integrative care, I quickly reached my second partial remission of complex regional pain syndrome, nine years and older.

I would not like to touch conventional medicine. Despite being a major skeptic of the many surgeries, procedures and medications that our doctors prescribe for us suffering women who are, in my opinion, primarily a profit regime for the medical facility, the model Western is beneficial for my well-being. More specifically, I use drugs that, without a doubt, give me a better quality of life.

That being said, if I had followed all the advice of my western doctors, I would have probably kicked in for months because of an avalanche. over-care that included their recommendations for an intra-thecal pump implant, two spinal cord stimulators, multiple surgeries, countless medications (including infusion medications) and hundreds of tests and procedures that I categorically refused. I call this type of medicine a "clinically induced trauma".

Cynthia Toussaint

On the rise, I take three daily medications for my pain – and they continue to serve me admirably. I often take these treatments for granted because I have been using them successfully for so long. In fact, this article is a good exercise to help me remember that the conventional part of integrative care occupies an important place in my arsenal of wellbeing.

Thirty-two years ago I had to leave my dancing career and return to my suburban childhood home. My world has quickly imploded and I have no hope for the future. I slipped into a suicidal depression – and my level of anxiety became so tortuous that almost everything I saw and heard became distorted and scary.

In the worst case, I could only look at a wall and be incommunicable. A psychiatrist put me on the benzodiazepine, Klonopin (clonazepam), for my anxiety and my pain – and the result seemed to me magical. Almost immediately my anxiety disappeared and I entered my first CRPS remission (at the time, RSD). To this day, I do not know how I would have survived without this medal.

About five years later, after my undiagnosed CRPS ravaged my vocal cords and I could not speak, my internist was able to survive. put on Axid (nitazidine), a gastric acid reducer, that in one way or another, one way or another m & # 39; did talk again without pain. I am a talkative – and when I can not verbally express myself, I become very desperate. This drug continues to be a gift of God to me.

When I was finally diagnosed nearly 14 years in CRPS, the best thing my doctor did, beside believing me, was to prescribe Neurontin (Gabapentin). insisting that I could not get pain relief before a minimum of 900 mg., I started walking short distances after being bedridden for ten years mainly at 600 mg. It remains a miracle drug for me.

Thirty-five years into high impact chronic pain, it can be a shock to hear that I rarely take opioids. But there are times when my breakthrough pain is so unbearable, the only thing that gives me a smidgen of relief is a 5 mg. Vicodin (hydrocodone.) And when restorative zzz become elusive due to fibromyalgia, I sometimes take a milligram or two of Flexeril that makes a world of difference because I wake up refreshed!

These are my successes, but my battlefield has also been littered with drugs that have done a lot of harm. My horror stories include once using a fentynal patch as prescribed by my doctor, which, I'm sure, almost killed me. I woke up with major hallucinations and I was unable to reason. Fortunately, I managed to get on the phone my panicked doctor who ordered me to rip the stamp just in time.

I was vaccinated against the infusion, Benlysta, for a disease that I had not, I was sick for years with symptoms resembling mono-symptoms. In fact, this doctor refused to allow my third infusion because she thought it could kill me. Once for a bursitis flare, I received a cortisone injection that not only gave me insomnia and anxiety (working in Europe, no less!) She caused a diabetic episode that decreased by chance. I know that in some cases this is not the case. Scary, scary.

Two years ago, when I was floored by mold poisoning, I listened to my well-meaning mother and made a mistake while visiting my internist . She even injected me with a series of antibiotics, prednisone and an inhaler that did nothing for my illness but which actually removed my lower body remission. The following year was a nightmare as I pioneered myself to my level of pain. There is a lot more, but you get drift.

I boast and believe deeply in the caring angels of integrative care. Complementary and autonomous care consists mainly of non-invasive therapies without side effects. And that 's the good place I like to be when it comes to pain management.

There can be no denying, however, that conventional medicine is a potential actor in our well-being. But since this modality involves so many artificial and artificial things that involve invading our bodies, we must be extremely tired of the possible harmful side effects, including disability and death.

Just Sayin & # 39; …

Cynthia Toussaint founded For Grace in 2002. It's a non-profit organization dedicated to raising awareness about gender disparity in the pain treatment. She also frequently contributes to the National Pain Report

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