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People Prescribed Opioids for Pain Aren't Automatically Junkies
in Health &middot February 10, 2016

People Prescribed Opioids Are Not Automatically “Junkies”

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in Health &middot February 10, 2016

People Prescribed Opioids Are Not Automatically “Junkies”

To say that I am upset about the response to one of the 2016 Superbowl ads is an understatement. You probably saw it and side eyed it because we can all agree that no one wants to see Superbowl advertisements for medications used for stomach and digestive problems. I’m with you on that one. I’m talking about the black-and-white ad for people with OIC, opioid-induced constipation. The problem was how people responded to that ad. For example:

Was that really an ad for junkies who can’t shit? America, I luv ya but I just can’t keep up

— Bill Maher (@billmaher) February 8, 2016

I get that this was supposed to be funny. And I’ll agree that it is definitely ironic that politicians keep talking about the opioid epidemic while the FDC approves a drug for OIC. But here’s the thing – there is a difference between people who are prescribed opioids and people who are “junkies.: There is a difference between people who are on opioids for chronic pain and addicts, although we also as a nation need to look at how we treat addicts because that, too, is an illness.

So today I’m taking this anger and frustration and putting them to good use. It’s time to talk about how people prescribed opioids for chronic pain are not automatically addicts.

People Prescribed Opioids for Pain Aren't Automatically Junkies

The only thing I’m addicted to is coffee. Let’s start with that. I am not addicted to my pain medication. When I am in less pain overall – as in my when main arthritis treatment has kicked in – I don’t take as much. The only thing I need from my opiate is pain relief, and if I can get that from other things, I don’t take it. What things? In addition to my pain medication, I use a heating pad, NSAID, yoga, chiropractor, higher steroid dose, etc. I do everything I possibly can to reduce my pain, and just because that can involve an opiate does not mean that I am an addict.

And another thing – I don’t want to take my pain medication, but it is without a doubt the only reason why I haven’t been to the ER since May 2014. Also, I really don’t enjoy spending my time rolling on the floor sobbing from pain. And I have a rather high pain tolerance; I keep burning my fingers in my toaster due to short bread problems and that’s a 3/10 for me. My pain tolerance is high and I’m still in excruciating pain on a regular basis because, you know, I live with a highly active autoimmune disease attacking my body. I don’t want to take my pain medication, but it’s so much better than the alternative.

My opiates are not my main pain-management treatment. Not by a long shot. I’m switching to Stelara injections from Rituxan infusions, and I also take the maximum amount of NSAID (anti-inflammatory) you can in a day. Actually, I take 3 medications daily for my arthritis pain, 3 daily for my fibromyalgia pain, plus 1 weekly for my arthritis. On top of that, I do yoga and walk every day, I use a heating pad for my fibromyalgia as needed, I see a chiropractor every week, and I do physical therapy exercises from my knee surgery every day. Oh, and I’ve also changed my diet. So my pain medication is NOT my primary source of pain relief, but it is the one thing I can take that immediately makes a large difference in my pain. And you want to shame me for that, for something I can’t control when I’m trying my best to feel better?

[bctt tweet=”If you think all people prescribed opiates are junkies, you need to reevaluate what you think you know because most are #PatientsNotAddicts”]

Statistics about Chronic Pain and Opioids

Let’s look at some statistics in case my personal experience is not enough for you. A study in the American Journal of Psychiatry found that 78% of people addicted to opiates were not prescribed the drug for any medical reason. A study by the Partnership for Drug-Free Kids found that 9 in 10 chronic pain patients tried a non-opiate based treatment before relying on opiates. Oh, and my favorite statistic? 96% of chronic pain patients on opioids do not become addicted. That’s right. Ninety-six percent.

[bctt tweet=”78% of people addicted to opioids were never prescribed them. 96.7% of people prescribed opiates for chronic pain aren’t addicted. Learn more about how they’re #PatientsNotAddicts.”]

Here’s the issue at the heart of the misunderstanding: 100 million Americans are affected by chronic pain, more than those with heart disease, cancer, and diabetes combined. We are the ones suffering the most from people making light of our struggles. We are the ones being treated like addicts while our bodies attack us. We are the ones suffering. Would you say that someone living with cancer was drug seeking and looking for opiates to get high, not for pain relief? Why would that be okay to someone living with chronic pain?

For more information, check out Maia Szalavitz’s article “How the War on Drugs Is Hurting Chronic Pain Patients” and Pat Anson’s article “Survey: Most Pain Patients Don’t Abuse Painkillers.”

Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

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Comments

  1. Chelsea Jacobs says

    February 10, 2016 at 9:59 am

    ABSOLUTELY RIDICULOUS. So freaking insensitive. People are dumb.

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    • Kate Mitchell says

      February 10, 2016 at 3:00 pm

      Yup! I just don’t understand how these people don’t critically think about these things before posting. Especially since these are people in a position of influence!

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  2. Theresa Hammons says

    February 10, 2016 at 11:45 am

    Great blog Kate! If only those who judge had to live 1 day in the life of a chronic pain sufferer…all of this “shame” would go away. The real shame is that people who truly need relief are ridiculed and made to suffer more because of the addicts and the “junkies”. Lack of education is truly the real root of this issue! Thank you for taking your time to help educate all and for your support of those who suffer with chronic pain!

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    • Kate Mitchell says

      February 10, 2016 at 3:00 pm

      Thank you! You’re absolutely right – lack of education is the root of the problem.

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  3. Emily of Em Busy Living says

    February 10, 2016 at 12:48 pm

    My mom takes different pain medications daily from a botched back surgery that left her with terrible nerve damage and constant back/leg pain. I hate knowing that people (like the ones you described) would think of my mom as a junkie or make it more difficult for her to find the relief she needs to live a semi-normal life.

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    • Kate Mitchell says

      February 10, 2016 at 3:01 pm

      That’s what it really comes down to; these people don’t think about how we’re just trying to live a semi-normal life. It’s really unfortunate.

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  4. Andrea Darst says

    February 16, 2016 at 2:32 pm

    Thank you for discussing this! It is so frustrating for people who are on opiate medications for legitimate reasons! I, unfortunately, have a bad back, and have been on pain medication for almost 4 years. I tried everything: physical therapy, yoga, injections, had a disc decompression, and on and on. Nothing worked! For those who deal with back pain, you know that if your back is spasming and/or throbbing, it affects your movement in the rest of your body. My only option right now is a disc fusion surgery, which at the age of 34, is not something I want to do! The surgery has only about a 50% success rate, and fusing discs puts pressure on the rest of your discs, which then means more surgeries. So here I sit, in limbo, with only my pain medications to help relieve the pain. Sadly, my body is addicted to these, but I have been on the same dose for more than 2 years, and I take them as prescribed. I pass every drug test that is required by my pain management doctor, and still the pharmacists every month look at me like I’m a junky! Then, there’s the FDA “cracking” down on opiates, which they should look at people who are prescribed them for no reason, but I wish they’d do it on a case-by-case basis and not take away the medication from those who really need it. Such a frustrating situation!

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    • Kate Mitchell says

      February 23, 2016 at 1:21 pm

      Oh my goodness! I’m so sorry that you’ve had to deal with all of this, too. You bring up so many good points here. Best of luck!

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    • JAM661 says

      May 10, 2016 at 12:59 am

      Andrea, you are not addicted to your pain medication but dependant on them. Basically many things can cause changes to your body when you suddenly stop taking them. For example you stop taking your blood pressure medication for your high blood pressure. Depending on how long you have been on the medication and what it is stopping it suddenly could cause your blood pressure to sky rocket to a much higher reading then you had before you even took the meds. Another example coffee. If you just stop drinking it you could find yourself a few hours after you would normally drink it having a major headache, tired , having a hard time concentrating and so on. Are you addicted to your blood pressure medication. NO! Are you dependant? Yes. Every addict who addicted to there opiate meds is dependant on it. However, not everyone who is dependent on there opiate medications is an addict. There is a big difference.

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  5. kaoruchan180 says

    May 9, 2016 at 7:31 pm

    you know what the worst part is? I have gastroparesis which is made worse by the opiod constipation side effect (it’s in fact specifically the same kind of constipation as the illness causes iirc) and I was on percocet for two years before anyone even MENTIONED it caused constipation at all!

    But every visit with every doctor, even though they weren’t providing the RX themselves, was happy to give me a lecture on addiction. I’ve been on the same dose for 5 years now and no one will refill my prescription because “addiction risk” I was only getting maximum 45 5 mg pills A YEAR. (they expired last month and I haven’t been able to do anything but lie in bed since).

    I’ve been put on so many dangerous medications, some I ended up dependent on, that I was given no warning of side effects. Fuck I have been prescribed shit with known interactions with my other medications and mocked when I complained about it. But no, they want me to be scared of painkillers when the pain has ruined my life and made me hope I hurry up and just die from illness because the pain only gets worse and they cut my treatment instead of giving me help.

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  1. How I Worked To Increase Blog Traffic in February says:
    March 2, 2016 at 8:02 am

    […] People Prescribed Opioids Are Not Automatically ‘Junkies’ […]

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  2. Not All Disabilities Are Visible + $170 to Ulta - Kate the (Almost) Great | Boston Lifestyle Blog says:
    April 27, 2016 at 8:02 am

    […] pain. I’m not going to get into that again, but if you would like to learn more, check out my blog post on it (oh, and Ariana Huffington thought it was a position that should be heard and invited me to […]

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  3. Kate the (Almost) Great | Boston Lifestyle Blog - Opioids for Chronic Pain: How Chronic Pain Patients Use Opioids says:
    December 19, 2016 at 8:00 am

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Dos and don'ts for when someone in your life is di Dos and don'ts for when someone in your life is diagnosed with autoimmune arthritis! What are some that you would add?⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: "So someone you know was diagnosed with Autoimmune Arthritis". Under the Do column (indicated with a green checkmark) is:⁣
"As how they feel about it⁣
Offer specific ways to help⁣
Treat them normally⁣
Ask follow-up questions⁣
Wear a mask around them when sick."⁣
Under the don't don't column (indicated with an x in a red circle) is:⁣
"Say “At least it’s not xyz!”⁣
Say that and not follow through⁣
Assume nothing about their lives has changed⁣
Conflate autoimmune arthritis with osteoarthritis⁣
Pass your cold to an immunosuppressed person".⁣
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Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

1️⃣ Lots of Harley time
2️⃣ Working from home means saving my PTO for fun things!
3️⃣ Lots of duck families (📸 my dad)
4️⃣ What a lot of my days look like - Harley and my current project (needlepoint). And, yes, I’m still in a cast.
5️⃣ Learned how to play Mahjong, which my parents love
6️⃣ Lake views on the 4th

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This is a different part of the foot than I used to deal with, but any problems with my feet and especially my left foot messes with me. While this doctor eventually fixed the problems and even got me diagnosed with RA, every time I go back to his office, I have to fight not to become 17 again. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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Week 25 of #2026Weekly Happy to be in Maine for Week 25 of #2026Weekly 

Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

1️⃣ IVIG 
2️⃣ Lots of beautiful birds have been coming to my mom’s bird feeder!

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What do you have to do every day for your chronic What do you have to do every day for your chronic illnesses? ⁣
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Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

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There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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Weeks 23 and 24 of 2026 Weekly! The last two wee Weeks 23 and 24 of 2026 Weekly! 

The last two weeks were prepping for my infusion, having/recovering from my infusion, and getting caught up after. This meant things were very busy but also I don’t have a lot to show for them. 

1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣

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IDs: 
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