As some of ya’ll know & some don’t, I’ve been visiting the ER more than usual. In a period of about 6 weeks, I was in the ER *Five Times* due to pain flares of my fibromyalgia. Each visit they gave me demerol, but occasionally torodol.
I have since gotten an emergency appointment with my fibro/pain management doctor. He told that torodol is an anti-inflammatory & wouldn’t work on fibro cuz it is not an inflammatory condition; I knew that, but it will help cfs inflammation. He also told me that demerol is an anesthetic, not a pain reliever that can treat the pain. This I did not know. He also told me that demerol could also be detrimental to my health and that if I do find myself in the ER, I should get morphine. Finally, he said that regular use of Tylenol 3′s is also detrimental to my health. He stated that ER docs should know all that.
He did quite a few things for me. He administered local anesthesia to my lower back to help temporarily block the nerve receptors from registering pain for a few hours until I was able to obtain the rest of the medication. He gave me a prescription for the Fentanyl patch 25mcg/h. One patch lasts about 72 hours. This medication works with the pain centre in the brain. He also gave me percocet, but no more that 3/day. This is for breakthrough pain from the fentanyl patch. A change was also made from lyrica to gabapentin. They are apparently sibling medications, but the gabapentin is covered by my plan, lyrica isn’t.
OMG! A pain doctor who actually gets it and treats it!
Why is it that when one person has a health issue, it seems like a dozen other people is your circle also have health issues? We’re been up to our necks in it lately.. It started with me on Christmas morning and my fibromyalgia pain getting the best of me (see here: http://bit.ly/AsUG8Q).. Then 2-3…
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If we’re talking weather, I am not a big fan of extreme hot (>40) or extreme cold (
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The Worst Place for Christmas… is the Emergency Room.. Second major flare for December got so bad, yes I actually went to the ER in the wee hours of Christmas Morning.. The only people who are there on Christmas morning are the ones who don’t have a choice, that it is a complete Emergency.. There…
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We got to the Emergency Room near 6pm this evening. It wasn’t busy, yet; it’s Saturday night so ya it will get busy. After registration, I was sent straight out to the ambulatory waiting area in the back of the ER. I was back there for about 10-15 minutes before I was brought back to…
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My biggest issue with my medical issues is me. I have so much trouble accepting my limitations. I am still trying to figure out how much I can and can not do. It’s more the can not that is my issue. I used to be way more than I am now. I used to be…
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My Significant Other is always concerned about the potentially addictive medications I am on. I try and assure him that, while dependant, I am not addicted. He doesn’t see the difference between the two. Unfortunately, when I am tired or just generically fibro-foggy I find it hard to explain. Medical dependance is a body’s need,…
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As many Fibromites have dealt with abuse in their youth, I figured this tidbit of info might be of interest… According to CP24, a local news channel, a recent study shows that women Who have experienced abuse, physical, psychological and/or sexual abuse, have an increased risk to die from heart disease.. I do plan on…
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Here is what has helped me. Before anything, I sit outside for a few minutes each day. Unless it’s the dead of winter (here we can get double digits below zero) I sit outside for a few minutes and get some fresh air and sunlight. And when it is the dead of winter, I use…
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October is Breast Cancer Awareness Month, and February is Heart & Stroke Month. I understand why these medical conditions have a full month of awareness because they are the top two killers of women. But why do conditions like Fibromyalgia and Chronic Fatigue Syndrome not only have one day of awareness, but have to share…
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