Ask your doctor or pain clinic

Posted by wishingtobepain @wishingtobepain, Nov 19 1:04pm

Just recently moved back to Missouri from Washington state when I found out my pain clinic here was not prescribing narcotics any more.
I asked them for listing of doctors or clinics in area that still do, they had no issue with printing out for me. I found a wonderful doctor, that I'm very comfortable with that prescribes narcotics.
I was taking 15mg of extended release morphine up to 3 times a day. Now I am taking 2 50mg tramadol up to 3 times a day. I honestly think it works better than morphine.
Just a thought since most of us our dealing with not getting meds we've been on. I was on morphine for over 12 years, the pain clinic just says no and doesn't offer anything for pain or offering to help with withdraws. I really didn't have much withdraw symptoms, but went 3 weeks without pain meds, and it was not fun!!

@wishingtobepainfree If you ever need a great doctor who does prescribe pain meds, see Dr. Joseph Regimbal in Lakewood/Tacoma area. He was great to me when we lived there.

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I had great DR at UW that prescribed all my meds. I think WA state was not quite as strict as Missouri and Kansas are. Makes me sick that people with true pain issues cannot get pain meds because of the crazies that abuse, especially when you have been taking with no abuse or selling of drugs.
That's why I thought I would share my experience.
Hope you are doing well.
Happy Holidays

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I wish I had options besides opioids. I can't take NSAIDs. I can't take tramadol or toradol oral. I can't take lyrica, cymbalta, or neurontin. I already have a Spinal Cord Stimulator and have had numerous physical therapy sessions and PT actually makes my pain worse. So… what options do I have besides opioids? I'm game for any other options! Let me know if anyone has ideas to send past by specialist besides "the DEA wants us to decrease your opioids."

Liked by Hank

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@faithwalker007…. How many opiods do you take? or were you taking? The doctor lets my husband take 2 of the 10's a day.. I can get by somewhat with
1 and a half of the 535's a day..of course 3 are better…. They should surely give you enough to keep the pay at bay. I can't take any of those that you also cannot take. We have almost no options… We who can't tolerate the other things! Last time they tried me on one Lyrica pill. I went into atrial fib and had to stay in the hospital for three days. It is no joke for us sensitive girls! Opioids are it I'm afraid. Maybe change pain doctors? Are you near Lakewood or Tacoma? Try to see Dr. Regimbal. He gave me all meds I needed when we lived there.

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You poor thing on not being able to take these meds. Have you tried medical Marijuana or CBD products, or just pot in general?
That's about all that comes to mind. Maybe others have better ideas.

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@maryflorida

@faithwalker007…. How many opiods do you take? or were you taking? The doctor lets my husband take 2 of the 10's a day.. I can get by somewhat with
1 and a half of the 535's a day..of course 3 are better…. They should surely give you enough to keep the pay at bay. I can't take any of those that you also cannot take. We have almost no options… We who can't tolerate the other things! Last time they tried me on one Lyrica pill. I went into atrial fib and had to stay in the hospital for three days. It is no joke for us sensitive girls! Opioids are it I'm afraid. Maybe change pain doctors? Are you near Lakewood or Tacoma? Try to see Dr. Regimbal. He gave me all meds I needed when we lived there.

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I'm living just north of Kansas City, Missouri. This is home for me.
Was taking 15mg extended release morphine, allowed 3 per day. Now I'm taking 100mg of tramadol 3xday.
I'm also on Lyrica, Cymbalta, meloxicam, muscle relaxers, sleeping pills, etc. I deal with degenerative disc disease, 3 herniated discs, fibromyalgia, but the worst is nerve damage in my lower right abdomen and pelvis. Not sure if you have heard of AIP, that's another issue I have, the good thing is haven't suffered from in several years. When that hits I barely move and can't even carry on conversation the pain is so severe even taking morphine. The nice thing switching from morphine to tramadol is the tramadol is not extended release. I was so lucky finding the dr here that I'm seeing, he also switched my muscle relaxers to something stronger. My abdomen spasms almost 24/7..
Sure hope you find a dr in your area that will help you.

Liked by Hank

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@maryflorida

@faithwalker007…. How many opiods do you take? or were you taking? The doctor lets my husband take 2 of the 10's a day.. I can get by somewhat with
1 and a half of the 535's a day..of course 3 are better…. They should surely give you enough to keep the pay at bay. I can't take any of those that you also cannot take. We have almost no options… We who can't tolerate the other things! Last time they tried me on one Lyrica pill. I went into atrial fib and had to stay in the hospital for three days. It is no joke for us sensitive girls! Opioids are it I'm afraid. Maybe change pain doctors? Are you near Lakewood or Tacoma? Try to see Dr. Regimbal. He gave me all meds I needed when we lived there.

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I never did answer you and I apologize. I’m in 30mg OxyContin bid and Percocet 10mg qid for breakthrough pain. I have the following disease states:
Migraines headaches
Epilepsy
Irritable Bowel Disease
Small Intestinal Resection
Traumatic Osteoarthritis in my left knee
Complete and total right knee replacement of my right knee
Lumbosacral plexopathy
Torn rotator cuff in left shoulder
Torn rotator cuff in right shoulder
Ruptured and separated labrum surrounding right shoulder
Right wrist carpal tunnel
High Risk for Infectious C. difficile Colitis (hx of infections so far)
Complex Regional Pain Syndrome Type 2 (Causalgia)
Symptoms include severe neurological, nerve, and physical pain including muscle cramps, joint pain, migraines, stomach cramps, hand and foot pain, hip and back pain, mobility limitations, and sensitivity to touch. Heat and cold changes to the body- areas affected by pain can change by more than 1-2 degrees.
I also have a DRG Spinal Cord Stimulator from Abbott/St. Jude which handles approximately 20-25% of my Pain load on Good days, 10-15% on average days, less on bad.
My total pain management covers about 40% of the pain load.

Liked by lorirenee1

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@faithwalker007

I never did answer you and I apologize. I’m in 30mg OxyContin bid and Percocet 10mg qid for breakthrough pain. I have the following disease states:
Migraines headaches
Epilepsy
Irritable Bowel Disease
Small Intestinal Resection
Traumatic Osteoarthritis in my left knee
Complete and total right knee replacement of my right knee
Lumbosacral plexopathy
Torn rotator cuff in left shoulder
Torn rotator cuff in right shoulder
Ruptured and separated labrum surrounding right shoulder
Right wrist carpal tunnel
High Risk for Infectious C. difficile Colitis (hx of infections so far)
Complex Regional Pain Syndrome Type 2 (Causalgia)
Symptoms include severe neurological, nerve, and physical pain including muscle cramps, joint pain, migraines, stomach cramps, hand and foot pain, hip and back pain, mobility limitations, and sensitivity to touch. Heat and cold changes to the body- areas affected by pain can change by more than 1-2 degrees.
I also have a DRG Spinal Cord Stimulator from Abbott/St. Jude which handles approximately 20-25% of my Pain load on Good days, 10-15% on average days, less on bad.
My total pain management covers about 40% of the pain load.

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@faithwalker007
Renee, with a 40% pain reduction, what would you say your overall pain level is on a 1-10 scale? Just trying to quantify how much residual pain your meds, stimulator, etc. leave you with. Another question, more rhetorical, do you think one person can handle pain better than another person? Is there anything to what I used to hear about how some people are more "stoic" than others, meaning they do not feel the pain as much as another person might? Interested in your opinion. Best, Hank

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@jesfactsmon

@faithwalker007
Renee, with a 40% pain reduction, what would you say your overall pain level is on a 1-10 scale? Just trying to quantify how much residual pain your meds, stimulator, etc. leave you with. Another question, more rhetorical, do you think one person can handle pain better than another person? Is there anything to what I used to hear about how some people are more "stoic" than others, meaning they do not feel the pain as much as another person might? Interested in your opinion. Best, Hank

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@jesfactsmon @faithwalker007 Hank. Interesting questions. I am particularly interested in the latter as I have been prescribed some painkillers that according to the MME dosage scale I feel should leave me in no pain but it still is unbearable for many hours a day,
Especially the bottom of my feet. It is not even half of the MME scale but if I ask for more it would put me there. Renee, is this me being unable to handle pain appropriately? If I still feel pain is it appropriate to ask for me if it puts me at the halfway mark? I feel so very selfish and hope the myofascial release therapy will eventually cure it but even if it does it could take up to a year. Is 3-4 hours out of bed a day acceptance? I still feel my quality of life is so poor I cannot do more than wash dishes or make the bed on good days. Thanks so much for both of your wise opinions.

Liked by Hank

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Hank,
Women have twice if not more the pain receptors than men biologically. It’s not fair or right to ANYONE to compare themselves to how another handles a pain load. That will drive them into depression faster than a speeding bullet. DO NOT DO THAT TO YOURSELF AND YOUR LOVED ONES.
As for me? I spend most of my day in my recliner, the equivalent to my bed. I spend 40% of my day (on a good day) doing things around the house that will help my husband and me be productive. I organize my craft room, paint, wipe down the kitchen and clean the kitchen IF it’s not overwhelming. I even groom my service dog! Not all of these and definitely not at once.
I spend time with my hubby and play with our dog who is painfully neglected by me on my down days.
This is my life and I have compensated not BECAUSE of the pain but in spite of it.
Pain does not control me. I live my life anyway and I’m happy. I breathe through it and have learned that it is another feature of me that people will either accept or not.
My quality of life is the defining factor and management of that factor affects it, yes.
Just like my seizures, migraines, and other diseases which I have affect it.
But they don’t DEFINE OR CONTROL who I am. I am Renee, child of God, wife of James, mother of Sean, and warrior.
That is who I have always been and will continue to be.
Please, people, don’t let an indicator, something your body is using to try to help you, overwhelm you into taking your purpose for life away.

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@bustrbrwn22

@jesfactsmon @faithwalker007 Hank. Interesting questions. I am particularly interested in the latter as I have been prescribed some painkillers that according to the MME dosage scale I feel should leave me in no pain but it still is unbearable for many hours a day,
Especially the bottom of my feet. It is not even half of the MME scale but if I ask for more it would put me there. Renee, is this me being unable to handle pain appropriately? If I still feel pain is it appropriate to ask for me if it puts me at the halfway mark? I feel so very selfish and hope the myofascial release therapy will eventually cure it but even if it does it could take up to a year. Is 3-4 hours out of bed a day acceptance? I still feel my quality of life is so poor I cannot do more than wash dishes or make the bed on good days. Thanks so much for both of your wise opinions.

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As I have told Hank, management of your pain to a goal of acceptable quality of life for YOU is what is important. You need to decide what is realistic and acceptable.
Pain is a feature of your life now but it need not control you. If it is, stop letting it. I know that’s easier said than done. I walk that path everyday.
Talk to your pain specialist about a realistic goal regarding your pain management and then task yourself and them to REACH IT.
You and your team may never actually reach that goal but it will be a journey and an enlightenment of your life to merely to begin it.

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@jesfactsmon

@faithwalker007
Renee, with a 40% pain reduction, what would you say your overall pain level is on a 1-10 scale? Just trying to quantify how much residual pain your meds, stimulator, etc. leave you with. Another question, more rhetorical, do you think one person can handle pain better than another person? Is there anything to what I used to hear about how some people are more "stoic" than others, meaning they do not feel the pain as much as another person might? Interested in your opinion. Best, Hank

Jump to this post

Hank, my overall pain on a 1-10 scale depends on the day but for two hours of the day it rests at 6. As I told my pain specialist, it then climbs to a 7/8, I take my meds, it dives back to 6, four hours later it climbs to a 7/8 and stays there even with pain meds. By night fall I’m around a 8/9. I take my next long term pain med so I can try to sleep but by then I’m in so much pain, sleep is impossible. I take my next pain meds and I finally doze about 3am only to wake around 6 or 8am and start the day again!

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@faithwalker007

Hank,
Women have twice if not more the pain receptors than men biologically. It’s not fair or right to ANYONE to compare themselves to how another handles a pain load. That will drive them into depression faster than a speeding bullet. DO NOT DO THAT TO YOURSELF AND YOUR LOVED ONES.
As for me? I spend most of my day in my recliner, the equivalent to my bed. I spend 40% of my day (on a good day) doing things around the house that will help my husband and me be productive. I organize my craft room, paint, wipe down the kitchen and clean the kitchen IF it’s not overwhelming. I even groom my service dog! Not all of these and definitely not at once.
I spend time with my hubby and play with our dog who is painfully neglected by me on my down days.
This is my life and I have compensated not BECAUSE of the pain but in spite of it.
Pain does not control me. I live my life anyway and I’m happy. I breathe through it and have learned that it is another feature of me that people will either accept or not.
My quality of life is the defining factor and management of that factor affects it, yes.
Just like my seizures, migraines, and other diseases which I have affect it.
But they don’t DEFINE OR CONTROL who I am. I am Renee, child of God, wife of James, mother of Sean, and warrior.
That is who I have always been and will continue to be.
Please, people, don’t let an indicator, something your body is using to try to help you, overwhelm you into taking your purpose for life away.

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Good for you! I am printing this and will read daily.

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@faithwalker007

Hank, my overall pain on a 1-10 scale depends on the day but for two hours of the day it rests at 6. As I told my pain specialist, it then climbs to a 7/8, I take my meds, it dives back to 6, four hours later it climbs to a 7/8 and stays there even with pain meds. By night fall I’m around a 8/9. I take my next long term pain med so I can try to sleep but by then I’m in so much pain, sleep is impossible. I take my next pain meds and I finally doze about 3am only to wake around 6 or 8am and start the day again!

Jump to this post

I’ve learned to breathe and compartmentalize a lot of the burning and aching. The shooting and lancing pain takes more effort but I can do that too. The cramps hit without warning and James helps with those. We’re getting better as a team in taming those down in quick order but they drive my levels up faster than anything. Standing is something I can’t tolerate but I can’t sit forever. Lol I pay for my wandering.

Liked by Hank

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@faithwalker007

Hank,
Women have twice if not more the pain receptors than men biologically. It’s not fair or right to ANYONE to compare themselves to how another handles a pain load. That will drive them into depression faster than a speeding bullet. DO NOT DO THAT TO YOURSELF AND YOUR LOVED ONES.
As for me? I spend most of my day in my recliner, the equivalent to my bed. I spend 40% of my day (on a good day) doing things around the house that will help my husband and me be productive. I organize my craft room, paint, wipe down the kitchen and clean the kitchen IF it’s not overwhelming. I even groom my service dog! Not all of these and definitely not at once.
I spend time with my hubby and play with our dog who is painfully neglected by me on my down days.
This is my life and I have compensated not BECAUSE of the pain but in spite of it.
Pain does not control me. I live my life anyway and I’m happy. I breathe through it and have learned that it is another feature of me that people will either accept or not.
My quality of life is the defining factor and management of that factor affects it, yes.
Just like my seizures, migraines, and other diseases which I have affect it.
But they don’t DEFINE OR CONTROL who I am. I am Renee, child of God, wife of James, mother of Sean, and warrior.
That is who I have always been and will continue to be.
Please, people, don’t let an indicator, something your body is using to try to help you, overwhelm you into taking your purpose for life away.

Jump to this post

@faithwalker007 Renee I love the words you wrote.

Every time I am asked my pain level I cringe… a chart number just does not put it in perspective. You have the overall pain and then a specific area pain. .. shoulder, back, knee, foot, hand, abdominal, etc. How much do you let that pain take you over. ..

I do not like taking an opiate. I cannot take nsaids nor other meds for pain. I had to up the dosage earlier this year for some thumb surgery. I asked my doctor to lower the number of pills back down and here I am two months later asking him to up the number again. I am having another body issue. I am getting an injection on Monday that will hopefully calm the pain.

Friends tell me I am so strong and so brave. I feel weak and like I am drowning at times. At those times I say some fervent prayers to help me get through them and take one moment at a time. I try to distract myself from pain by occupying my mind with other things. Crochet usually is my go-to, but the surgery earlier this year was for my thumb. My thumb is only up to small amounts of the activity. So puzzles and games on my tablet. I cannot concentrate on novels, so short times reading scriptures, short stories and poems.

My husband starts telling doctors that I can tolerate more pain than he ever could. I tell him to hush up. I see him go through pain daily.. that I could not handle. He is no weaker nor stronger than I when it comes to pain. We all handle pain in our own way. Lately pain has slowed us both. We went for a drive last week. It was painful on our bodies.. but oh the good it did our souls!!

Always put Joy in your life so you will have Happiness in your soul.

ZeeGee

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