Living with Neuropathy - Welcome to the group

After living with my husband's pain for the last fifteen years, I learned NEVER to say the words, "I understand." How on earth could I understand the torment that man lived with? I'd watch him get up and literally crawl across the floor into the bathroom because it was too painful to walk. He'd take his shower and I'd hear him throwing up as he got dressed and then he'd emerge from the bathroom, kiss me on my cheek, ruffle my hair as if nothing was wrong and disappear into the work day.
I STILL hear him throwing up in the morning from his pain, but now I hear his sobs from my recliner in the den because I can't lie flat beside him due to my own pain shimmering down my legs 24/7. Now, he doesn't leave for work and neither do I. Two careers gone because lives of pain took their place. Lives of intimacy gone only to be replaced by mornings of agony.
How do you share such things with people who only learn about blood pressure, heartrates, and scales as measurement of pain? You don't. You simply say my pain is 9 because if it was a 10, I'd be in the hospital.

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After living with my husband's pain for the last fifteen years, I learned NEVER to say the words, "I understand." How on earth could I understand the torment that man lived with? I'd watch him get up and literally crawl across the floor into the bathroom because it was too painful to walk. He'd take his shower and I'd hear him throwing up as he got dressed and then he'd emerge from the bathroom, kiss me on my cheek, ruffle my hair as if nothing was wrong and disappear into the work day.
I STILL hear him throwing up in the morning from his pain, but now I hear his sobs from my recliner in the den because I can't lie flat beside him due to my own pain shimmering down my legs 24/7. Now, he doesn't leave for work and neither do I. Two careers gone because lives of pain took their place. Lives of intimacy gone only to be replaced by mornings of agony.
How do you share such things with people who only learn about blood pressure, heartrates, and scales as measurement of pain? You don't. You simply say my pain is 9 because if it was a 10, I'd be in the hospital.

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@sunnyflower. and others

I'm having to beg my doctor to increase the dose of my morphine prescription back to what it was before the scs implant, because the scs isn't working. He grudgingly agreed to increase it by 15mg. I moved down from 30mg tid to 15mg tid, which I realize now was a big mistake. In a message on the portal he said he would fill the prescription for 30mg bid, but wants to discuss it with me at my next appointment. My therapist is almost as angry as I am that I'm having such a battle with the doctors, trying to get a therapeutic dose of medication.

@faithwalker007 has been referring to the CDC guidelines, and I'm reading the recommendations. What has stood out is the recurring phrase, "There is insufficient evidence to prove that long term opioid use for chronic pain (naming neuropathy among other things) is ineffective." Another common theme is that "the clinician must prescribe medication sufficient to allow some quality of life, and must explain to the patient the balance between the benefits and the risks."

Doctors like to quote the CDC guidelines as proof that opioids don't treat either long term pain or neuropathy pain. That's a false interpretation of the recommendations. Between now and my next appointment, whenever that is, I'll be compiling a list of things I read to convince him that my experience has been that when I cut back on my dose, the pain increases. And to convince him that I'm not at risk of selling it for a profit, or that I will take more than is prescribed - I'm more likely to take less in case the system works so slowly that I would run out.

When every other medication has failed to work, I'm less concerned about the mechanism as I am about pain control. Telling me over and over that it's not a pain killer, but a pain signal interruption, falls on increasingly frustrated ears. I'm not stupid. I know the allegations that prescribers make, assuming that I'll just lie down and do what I'm told. I'm beyond tired of fighting to maintain my right to have access to the only medication that's helped long term reducing my pain.

Time to take my allocated bedtime pain pill, so end of rant.

Jim

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I am so sorry @jimhd

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@faithwalker007 my thoughts and prayers are with you and your husband. I don’t have near the pain you do but feel many times each day that I am going to lose my mind. Pain is such an insidious thing that takes your whole essence away from you most of the time.

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After living with my husband's pain for the last fifteen years, I learned NEVER to say the words, "I understand." How on earth could I understand the torment that man lived with? I'd watch him get up and literally crawl across the floor into the bathroom because it was too painful to walk. He'd take his shower and I'd hear him throwing up as he got dressed and then he'd emerge from the bathroom, kiss me on my cheek, ruffle my hair as if nothing was wrong and disappear into the work day.
I STILL hear him throwing up in the morning from his pain, but now I hear his sobs from my recliner in the den because I can't lie flat beside him due to my own pain shimmering down my legs 24/7. Now, he doesn't leave for work and neither do I. Two careers gone because lives of pain took their place. Lives of intimacy gone only to be replaced by mornings of agony.
How do you share such things with people who only learn about blood pressure, heartrates, and scales as measurement of pain? You don't. You simply say my pain is 9 because if it was a 10, I'd be in the hospital.

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@faithwalker Renee, your writing cuts me like a knife. You write too well. I can't bare how you describe your life, as it is mine, and all of us here. I have this deep forgiveness inside of me, as people that don't live this, cannot understand it. If they are inappropriate and their responses to me don't quite "cut it," I am happy for them. It means they are well, and for that, I am greatful. No one should understand this, ever. LoriRenee1

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@contentandwell @lioness. I have hip bursitis and S I joint disfunction for a couple of months now, my orthopedic doctor gave me a cortisone shot, then recommended PT. I don't think the shot did much. PT was helpful but it's still there. He doesn't want to give me any more shot. Now I'm feeling discomfort in the other hip. I'm just about giving up. I've not been walking much but today I ventured to Starbucks which took me 40 minutes! Almost twice the time it normally takes. My physical therapists use laser to bring down the inflammation and gave me lots of exercise to do at home. They don't accept my Medicare HMO, but they do give me a cash discount which still costs an arm and a leg. Fortunately my daughter had arranged with them to bill her from now on. I hope I'll get better soon, my next trip to my orthopedic doctor will be for my spinal stenosis which too had gotten worse with all that sitting in the last 9 months. I have never been sedentary in my life until this year. Enough venting, sorry. Just found out my hip doctor is the team doctor for the football team the Chargers!

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@contentandwell . I don't blame you I hurt since shot so don't know either it didn't help with entraped nerve pain . I was talking to a lady that has alot also and I did know about turmeric but she said she takes it twice a day and feels good it cuts down on the inflammation . So am going to start that I love it in my Golden milk going to have to get skim milk all that milk fat won't be good for my waistline lol

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