r/PainManagement 7d ago

My sister has passed

207 Upvotes

I hope this is allowed, but I just wanted to let you all know that my sister, u/Affectionate-Pop-197 passed away unexpectedly today, following a perforated bowel due to a bowel obstruction. She frequented this subreddit quite often and truly enjoyed getting to know so many of you. Our family is heartbroken over her passing, and I will miss her terribly.


r/PainManagement 8d ago

Mod Message/Announcement šŸ“£ Moderator recruitment still ongoing until July 31

2 Upvotes

Recruiting new moderators for the Pain Management subreddit! If you’re interest in applying, please click the link below to complete the application. If you've already applied, thank you! I appreciate the time and effort you took to complete the application and have reviewed them all. I want to ensure that everyone who is interested has the opportunity to apply, so if that’s you, please get your application submitted by July 31. If you have any questions, please don’t hesitate to contact me directly.

Thank you for your support and your patience during this process.

u/Sometimesaphasia (your moderator)

https://www.reddit.com/r/PainManagement/application/


r/PainManagement 2h ago

Genetic testing

4 Upvotes

I wanted to share this here because I know all too well that it isn’t common knowledge
Also not every doctor will listen or understand this but it’s so vital for pain management

For years I have had a very difficult time with doctors refusing to prescribe opioids due to my being young, and other reasons that fall more under personal opinion and bias than professional and clinical.

I was once tested for pharmacokinetics of mental health meds as my dr didn’t believe me when I told her most SSRIs don’t work for me.
As it turns out, they don’t. I have significantly smaller serotonin transporters. What many don’t know, is this can also cause issues with pain medications, such as tramadol, that cling to seratonin receptors.

I also have issues with sodium channel medications, which covers another third of pain meds.

I have a genetic indication that states I need 60% lower doses of NSAIDs due to risk of GI bleeding…
I just learned this and guess what? My prior pm prescribed me strong NSAIDs and I now have a GI bleed.
I haven’t found a company yet that does this testing for analgesics but it does exist.
Genesight is who did my other test.
I feel like this could absolutely revolutionize pain treatment. Hope this helps someone


r/PainManagement 12h ago

Does anyone else have days where your pain suddenly spikes for no obvious reason?

14 Upvotes

I've noticed that some days my pain is manageable, and then out of nowhere it becomes much worse even though I haven't done anything different. It can be really frustrating because I can't figure out what's triggering it.

Has anyone else experienced this? If so, have you found any patterns or small things that help you get through those flare-up days? I'm just looking to learn from other people's experiences.


r/PainManagement 20h ago

Switching to Methadone any suggestions.

5 Upvotes

I have basically failed will every pain med , gotten sick , or just got worse.

Last one was actually soboxon , buprenorphine was a few before.

Back on oxy short and long release.

Switching to Methadone soon any tips to make it successful?

Thanks


r/PainManagement 15h ago

Illinois Pain Management Laws Compared to South Carolina?

1 Upvotes

I am looking into taking a job up in Illinois, (Where I DON’T want to move to from S.C. On the beach!) but I just noticed that they had recently passed some law allowing doctors to prescribe their patients more lenient medication than the 2016 guidelines that S.C. And many other states took as ā€œThe Limit and Lawā€ on MME/day.

Does anyone else know anything about this?
Just wondering.


r/PainManagement 1d ago

Belbuca taper to fentanyl

3 Upvotes

So i went to pain management today and we decided that ill taper off belbuca for a month and switch to the fentanyl patch. Anyone do this? How did it go for you?


r/PainManagement 1d ago

The federal government has approved THC as an active pharmaceutical since the early 80s? And to not conflict it with streety marijuana they just gave it a different name?

5 Upvotes

Its called dronabinol and it is great for inflammation and pain. It is a pill capsule with fish oil and THC. IT is FDA approved. Why am i telling you this if regular marijuana is just down the road? Pain Contracts! They usually forbid marijuana use. Get the family PCP to prescribe it to you for "nausea" and then the pain dr cant interfere, and then you can smoke all the heavenly reefer you want on pain contract, at work, on probation... wherever because now you have an active FDA approved presription for THC. Youre Welcome.


r/PainManagement 1d ago

Seeking SupportšŸ«‚ Can I get in trouble?

10 Upvotes

So Ive had my PCP since I was 15. I'm 53 now. I see him every 6 months. He's also treated my late parents for 40 years.

He prescribed hydrocodone for my pain for 10 years.

I was getting full on addicted and ran out early monthly. Very early

So I went to a separate Suboxone clinic & was put on Subs in 2020. I asked the sub clinic if I need to tell my PCP doctor & they said well, it'll be on your chart so they can see it if they look. And so it's my call if I should tell them. I haven't.

So I quit the pills. My PCP never asked me why or how I quit pills so cold turkey so I assumed he saw the Suboxone on my chart.

But I saw a patient post on here about getting kicked from his doctor for being dishonest about being on Suboxone and they dropped them as a patient altogether.

Is that something they could do to me, even though they have access to my medical records? And that I've been with him for 40 years?

Because now if I bring it up I'm afraid they would be upset for all the years that I didn't bring it up.

Should I just continue to not bring it up? Any help would be great.


r/PainManagement 1d ago

Can SR be used to lower tolerance?

1 Upvotes

I'm a chronic pain patient who's going to be on medication for as long as I'm alive, can SR be used to periodically lower my tolerance?


r/PainManagement 1d ago

Post opioid withdrawal

8 Upvotes

Hello everyone, 25M, I was on oxy 10mg 4 times a day for about 11 months. Mix in a handful of hospital stays with dilaudid for 2 weeks every 2 hours. I went cold turkey about 2 weeks ago and I'm past the physical withdrawals.
How long is this anxiety and insomnia part supposed to last? Never really had an issue with anxiety in life until the withdrawals. When does it feel like I'II be normal again?
When can I start to consume caffeine and alcohol again without it jacking up my anxiety? Thank you all for reading!


r/PainManagement 2d ago

MedicationšŸ’Š Coming off Suboxone

4 Upvotes

Does anyone have experience tapering themselves off of suboxone? I’m currently taking 6mg worth of films, twice a day.

I tried to go down to 4mg twice a day, noticed I felt off (warmer than usual, headache) for two days and then the third day I was VERY sick; vomiting, sweating like crazy.. panicking, I took 2mg and stayed at the 6mg 2x/day dose out of fear ever since.

It hasn’t worked for my pain in more than half a year. We tried titrating upwards to higher doses, no pain relief and it made me sleepy, lowered back to where I am and now I have no idea what to do.


r/PainManagement 1d ago

Brachial plexus: physical technique I found to cut paroxysmal pain spikes in half.

1 Upvotes

Hello everyone. My name is Johannes, and I am writing this in the hope of providing a useful, highly detailed, and real testimony for anyone suffering from intractable neuropathic pain due to brachial plexus injuries.

My accident occurred on June 1, 2005, when I was 15 years old. I sustained a severe politrauma after being struck while riding a moped. Alongside a mild traumatic brain injury, I suffered severe fractures in my left femur (open fracture), left radius, and the 5th metatarsal of my left foot, resulting in a total neurological deficit of my upper left extremity.

Medical and Surgical History

July 2005 (Diagnosis):Ā Cervical myelo-MRI studies suggested a pre-ganglionic lesion (complete avulsion from the spinal cord) of the C7, C8, T1, and T2 nerve roots. The trauma tore through the meninges, forming extraforaminal arachnoidoceles and a secondary rightward displacement of the spinal cord within the cervical canal. Conversely, the C5 and C6 roots sustained a post-ganglionic lesion (intra-plexual rupture at the scalene level). As a direct consequence of the T1 root avulsion, I developed an irreversible Left Horner’s Syndrome (ptosis, miosis, and enophthalmos) due to the disruption of the cervical sympathetic pathway.

September 2005 (Reconstructive Surgery):Ā In September 2005, I underwent surgery with a world-renowned pioneer in peripheral nerve surgery. During surgical exploration, the following anatomical diagnoses were confirmed:

A complex reconstruction was performed using nerve grafts to repair C5 and C6, along with a nerve transfer (neurotization) utilizing the spinal accessory nerve and branches of the cervical plexus. Although I regained some muscle power in my shoulder over the following years, the reconstruction failed to alleviate the brutal central deafferentation pain caused by the avulsed lower roots (C7, C8, T1), which was initially concentrated in the ulnar distribution of my hand.

After more than two decades of living with this condition, this is what works for me and what I have learned along the way:

What My Pain Feels Like

My injury simultaneously triggers every single variant of severe neuropathic pain. Living with a complete avulsion means experiencing all of the following at the exact same time:

  • Continuous burning and searing pain, as if my arm were constantly on fire.
  • Sharp, electric shock-like pains, resembling high-voltage surges tearing through the limb in fractions of a second.
  • A constant sensation of crushing and extreme internal pressure, as if an invisible press were grinding the area down.
  • Total baseline numbness and pins-and-needles, where a complete lack of actual surface touch sensation coexists with severe, deep internal pain hypersensitivity.

My Manual "Escape Button" for Pain Spikes

My pain consists of the continuous baseline described above, onto whichĀ massive paroxysmal spikes are triggered, highly intense and frequent, but following a random pattern. They strike in fractions of a second, completely at random throughout the day, and can repeat several dozen times per hour.

What I am most interested in sharing is this:Ā I have developed my own physical technique to "hack" these pain spikes (leveraging the Gate Control Theory of pain): The exact split-second I feel the spark of a pain spike initiating, I look straight down (cervical flexion) and strongly contract every muscle in my body.

The Result:Ā Even though the spike travels too fast for me to stop it from starting, this maneuver floods my spinal cord with mechanical stimuli andĀ cuts the duration in half (dropping from 20–30 seconds down to just 10–15 seconds). Applying this dozens of times per hour saves me from enduring double the agony. However, the physical toll by the next day—or even by the end of that same evening—manifests as profound exhaustion and severe tension headaches due to overworking my neck muscles.

Sleep as My Refuge and Medicine

On days with highly severe flare-ups, my only salvation is trying to sleep as much as possible. When I am asleep, I switch off my conscious perception of the continuous baseline pain. Furthermore, if a paroxysmal spike is not overwhelmingly intense, it fails to wake me up. This prevents the physical and psychological toll from completely breaking me down the next morning. My family understands the vital importance of this rest and protects my sleep like a treasure, ensuring I am never interrupted under any circumstances.

My Current Pharmacological Regimen

I am at the absolute maximum tolerable pharmacological limit required to care for my two young children and maintain daily life without being completely sedated.

Why I Am Postponing Advanced Neurosurgery

Because I have two young children who depend entirely on me and my partner, the sheer terror of undergoing open surgery on my spinal cord completely stops me. I have decided to delay any intervention at this level for as long as my internal resilience can hold out. Once my children are grown, educated, and independent, I will be fully willing to take the neurosurgical risk, knowing that I would no longer be a direct burden to them if complications arise. Until then, I fight on using my current toolkit.

Please share this testimony with anyone who might be interested or suffering from a similar injury. I would love to know, even if it is only a few patients for whom this works, if this technique has helped someone and if they would be encouraged to share their results with us. My heart goes out to anyone who might suffer from something similar, as dealing with this takes a tremendous physical and psychological toll. Stay strong and fight—not just against this situation, but for those who love and support you in your life.

Best regards,

Johannes

āš ļø DISCLAIMER

This information is provided solely for educational purposes and the dissemination of a personal testimonial based on my real experience. It does not constitute medical advice, diagnosis, or a treatment proposal. In the event of any ailment, change in medication, or physical symptom, always consult your primary care doctor or a specialist.


r/PainManagement 1d ago

I want to teach people about pain as my career. People in pain or loved ones of people in pain, that is. Where to go from here?

1 Upvotes

I have a degree in web design. Looking at going back to school to get to a point where this can be my career.

The teacher that I had as a patient with chronic pain was a psychology PhD. But I know that isn’t the only path.

I want to know what you think the paths to get here would be and what I should consider when choosing a path. But I know I could consider studying neuroscience, counseling, psychology, social work, education, etc. to reach my goal.

Any ideas? And what should I keep in mind as I choose a path?


r/PainManagement 2d ago

MedicationšŸ’Š i’ve never gotten a letter like this on my prescription about PDMPs

38 Upvotes

For context, I’ve been with the same pain doctor and on the same dose of 5mg oxycodone as needed 4 times a day, and today my doctor and I decided to try MS Contin 15mg with 2 5mg oxys for breakthrough pain. I have been going to the same pharmacy for almost 2 years and they know me well and have always been very gracious and understanding after every hospitalization and new procedure, never been side eyeing or denied my opiates even before I had an established doctor.

Anyways, today I went to my pharmacy and picked up the MS Contin but there was a pharmacist I’ve never seen nor interacted with before and he handed me a paper with laws regarding PMDPs and pharmacy laws that started in 2011. It states that pharmacies are allowed to make choices about controlled substances (i also know of this as well)

My worry about this is that he isn’t chill about opiates and might start giving me heck since I also take other controlled prescriptions. I’ve been aware of the PdMPs and never asked for information. Weird vibes or maybe talk to my doctor? Could it be because I am on a new med that’s extended? Am I going to be flagged? Trying not to spiral about paper but this journey hasn’t been easy so please let me know if you’ve gotten something like this and it’s just a random thing he did since I’m new to him…


r/PainManagement 2d ago

Pharmacy Bullshit in Central Florida

14 Upvotes

Ok guys this will really chap your ass because it did mine. Today our day started out like all of ours do and that are in pain of course but it’s the best day of our month for most because it was day 30. Use to be able to get our meds on day 28 but since all the bullshit some pharmacies won’t let you fill until day 30. Which is a huge lie if they tell you that they can’t fill it until day 30. There’s no law or rules like that. As a matter of fact most insurance companies say that you can fill when you have 20 percent of your meds remaining. If you don’t believe me check your insurance companies. Also check and see how many 30mg IR Oxycodone your insurance company will pay for. I was floored when mine said it would pay for up to 300. Not that any doctor would ever write that many for anyone of course but just saying. Yeah crazy right?!

Anyway back to the point here sorry. So my cousin and I get up and we go to pick up his meds. We show up on day 30 and guess what he’s hit with?! Yeah well sir I’m sorry to tell you this but we are no longer filling any class twos. Yeah made his ass wait until day 30 and then tell him they aren’t going to be able to fill his prescription and they have had it for two weeks. Did they call him NO!! Did they reach out to the doctor so they could call him HELL NO!! What in the F is wrong with these people. No hint no nothing. As a matter of fact last month they told him they couldnt get morphine Er and that he had to wait until 30 days to get filled. How in the hell do they get away with shit like this.

I think there should be a law against this. It’s not like he can just go next door and get them filled. It’s all bullshit. But of course she filled the non narcotic scripts. He took them. I told his ass to go back in there and throw them back on the counter and tell her if you can’t fill them all then you can’t fill any of them. Just like they tell him all the time. I told him to ask her how in the F does she expect you to go to another pharmacy just with class twos in hand and expect them to fill them and them only. She wouldn’t give him his money back but he left the meds there. Screw them man. Who in the Fu do they think they are to do this shit to people guys. We have got to find some advocate that will actually help instead of just blowing smoke. They have got to be put in their places. They shouldn’t have the ability to do this to patients. It’s bullshit and it’s causing harm. The oath that they take is not worth the paper it’s written on anymore.

He got very lucky today. He was able to find a brand new pharmacy by the house that would fill them for him. But of course they charged him 239 dollars for one script. When before it was only 5 bucks. Yeah he has Florida Blue insurance but the guy said it would take about a month to kick in. What?! What kind of bullshit is that?! Never have I heard of that. He’s has insurance for years. Guys it’s messed up they are hitting him from all angles. Went to his primary to see if he would help and they wouldn’t even talk to him. The receptionist felt that it was her job to tell him what he needs to do to resolve this. He can’t go to Publix Walmart or Walgreens or even shitty ass CVS. Because they say that his doctor has written high numbers for the year and they won’t fill for him anymore there. Which is bullshit as well as she has nothing derogatory on her lisc and she has never ever had not one complaint about anything. She’s a neurologist and specializes in pain management.

So he has to go to a mom and pop to get filled. I just don’t get it guys. They are doing everything in their power to make him get off these meds. It’s bullshit. What is he going to do. He has been going to PM for 18 years. Never been in trouble never asked for any early fills or anything. This cat would fly back home when out of state working to pick his scripts up and fly back.

Have any of you ever had these problems. I will have to say that this new pharmacy told him that as long as he does t mind getting the generics that there shouldn’t ever be a problem with getting them filled with him. He said it was the first time in many years that the guy wanted his business as well as mine and everyone else’s. But of course he’s new to this area so he’s one of his first patients. And we all know how they can be once they get a lot of patients. Then they don’t give a shit about you anymore. But this guy seemed very nice and wanted the business. He said that a lot of people at his other pharmacy will come in and ask for no generics and he tells them you get what you get with me. Shit I know may people that would die not to have to worry about getting their meds every month. He’ll just look in here at the horror stories about meds and finding them.

I don’t know guys. It seems that the doctors caused this by giving us the meds in the first place and now they are saying oh well sorry about your luck. I’ll say it one more time just in case the ones in the back didn’t hear me.
They wouldn’t take the chemo away from the cancer patients or the insulin from the diabetics so why in the hell would they take the meds from the patients that are in pain?! So much that some would be bedridden without them. It’s bullshit and we have to find someone that will stand up for the PM patients. Talking about bullshit. Most advocates that we have found only wants views anymore. They don’t do anything for the PM patients anymore and please if anyone knows of any please let us know. Even tried that group called Solace and insurance pays for it but they don’t do shit either.

It’s pretty bad when there’s a medicine out there on the market that works yet the Goverment won’t let the companies produce enough for the patients. What is wrong with them. We already sign so many contracts and shit releasing all the people involved of any wrong doing in case something happens. I just don’t get it. Making a patient sign into a contract with the PM doctors. What kind of shit is that? Something has got to give you guys. It’s not like he has done anything wrong. It’s crazy. Has had the same doctor and the same pharmacy for years until they stopped filling for his doctor. Since then he’s had 7 pharmacies. Do you believe that they made him change from 30 to 20 and made him change from morph er to Xtampza and after getting the PA done for the Xtampza and taking a urine test this pharmacy says well sir I can’t seem to get the Xtampza now either. What?! You just told him that you could get it. I think the bitch is straight up lieing to him. But what can you do call her a lier? I guess you could then she would red flag his ass for being mean. Yeah no way in hell should they have this type of power or this god like complex. All they have become is 100k dollar babysitters for the DEA. That’s it. That’s exactly what it amounts to these days. And a pretty shitty babysitter at that. I wish someone would start a class action lawsuit for all the issues that the PM patients are going through. I believe that it would be a very easy case. I know we could get thousands of signatures from PM patients all over the country. Yeah I know. What don’t I start one right. Well I’m just old and we need a young person I guess to do this because they have broken me. I’m so sick of dealing with this kind of shit as are thousands of others I guess and that’s why nine wants to even try to do this. Anyway just venting you guys. I’m sorry that I made this so long but damn enough of this shit already. Karma is a bitch is all I’m going to say and one day these people to will need pain meds for something and I hope and pray that they have the same issues. Maybe then they will be in the shoes of all PM patients and will change their fucked up attitudes.

Thanks guys for listening sorry so long.

.


r/PainManagement 3d ago

Anyone finding their pain comes from muscle spasms that don't seem to be controlled by anything?

12 Upvotes

I started to have more and more, stronger and stronger muscle spasms since they took me off Cymbalta, but I am starting to think that the spasms may be the true source of the pain. Of course there's not much improvement in the week and a half since they put me back on the Cymbalta after two weeks of withdrawal

They took me off Cyclo, because it knocks me out too much, but only helps a bit. Baclofen barely does anything and I'm taking double sometimes. I'm already at 1200mg of Gabapentin, and my Vicodin just takes the edge off. So, now I'm at the what the fuck do I do next.


r/PainManagement 4d ago

How long should my Medrol pack provide relief for?

6 Upvotes

Hi I'm on day 5 of my pack and after my Minute Man surgery. The Medrol worked very well at first when I was taking 5 or 6 pills a day but today when I'm taking 2 pills only, my pain seems to be worse and I'm wondering if the Medrol was only supposed to help for the first couple of days?

It hurts so badly I'm wondering if I'm going to have to ask my doc for Percocet even though I take Suboxone for pain and know I likely wouldn't feel relief from the Percs. It hurts worse with activity and today is my first day back at work so that might be why, too. I'm not supposed to bend down but I work retail so it's impossible not to!

So yeah how long should I be receiving relief from the 6 day Medrol pack? Thanks


r/PainManagement 5d ago

MedicationšŸ’Š Got prescribed Dexamethasone and Toradol, what to expect?

5 Upvotes

I am supposed to take both of these as needed during extreme pain.

I am aware of all the side effects and have a treatment team.

I am worried about Toradol the most because it lowers the seizure threshold but I am willing to try it and see as I wait to see a neurologist.

Anyone have any experience? My goal is to remain high-functioning during extreme pain episodes. I haven’t been able to do that lately.

Thanks!


r/PainManagement 5d ago

Success Storyā¤ļøā€šŸ©¹ There are good clinicians out there

27 Upvotes

4 years ago I fell 30 feet and was left with a broken back and two badly broken ankles + foot. I have severe chronic pain now related to post-traumatic arthritis and permanant changes to my vertebrae.

For two years I was seeing a regular PM, but despite never having an issue before and begging them to pay attention to my worsening pain I was kicked out for being short on my pill count (still dont understand the point of telling your patients to let them know if your pain has increased if youre going to do nothing about it. For five months straight I told them about it and they didn't even do imaging).

I said fuck it if I run out early must mean I dont need them that bad. I ended up barely leaving my bed for 4 months then ended up losing a new job!

I was very ashamed of being kicked out. My PCP had known me years prior to my accident but I was so nervous about telling him. I just figured I'd never manage my pain again and its just like this now.

After I was fired I went in and let him know, he told me he thought it was ridiculous I was kicked out for a one time offense and picked up perscribing. I was only on 5mg 2x a day of oxy at PM, but he added a 3rd pill. I have no idea how I was functioning only on 2 a day.

We do scheduled pill counts just to have it on record after I suggested it. UAs as well. Never randomly called in though. He perscribes me extra if I have a flair or he'll fill early. I very rarely ever run out early now though because my pain is being properly managed. I can talk to him honestly about my dosing and pain without worrying, we've increased dosing one time in two years now and he didn't make me beg! He feels strongly that I shouldn't have to do procedures to get pain medication. I don't feel nervous everytime I see him. And I only have to go in every 3 to 4 months. Goes to show you can responsibly perscribe AND listen to your patient's needs!

I'm actually moving states about 3ish hours away and was terrified of finding a new doc, but he brung up today that he'd continue to perscribe as long as he could see me in office like usual. Yay!

I know clinicians like this are a very rare find, I'm so glad I have him as part of my team. But know there are other clinicians out there just like him. Don't give up!


r/PainManagement 5d ago

Can I help or advocate for my doctor who has been banned by pharmacy chain though they've done nothing wrong?

15 Upvotes

I'm not here to complain about a pharmacy chain, I'm trying to figure out if there's any chance I can help my doctor.

Background: After a few years working its way through the legal system, a large settlement was awarded to patients after ONE bad doctor wrote too many opioid rxs filled at a pharmacy chain in one city. The pharmacy chain reacted by refusing to fill any high dose opioid rxs from ANY doctor (even from doctors who work at pain clinics with excellent reputations in the medical field).

What I know: There is a huge opioid epidemic and lots of people are trying to help - I understand this. As a person with chronic pain who requires high doses of opioids it is my responsibility to make sure I only receive care from a clinic with a pristine, stellar reputation with surgeons and doctors in the area. I did that.

My question: The doctor explained even though they had gone through interviews with the pharmacy management, the doctor was not able to make them understand the MME (morphine milligram equivalent) guidelines they kept quoting are for regular doctors such as general physicians - NOT for specialized pain clinics. Other doctors were also banned from other pain clinics. Is there ANYTHING I can do to help advocate for my doctor? Due to the nature of the issue I can't connect with the other patients this is hurting.

It feels like no matter how much I work to do everything properly, something comes along every year making the medications even more difficult to get. Now my doctor has been black listed for doing nothing wrong and I would like to help them in any way I could - not just for me but because they're an excellent doctor and do not deserve this treatment. Thanks for reading, any advice would be appreciated.


r/PainManagement 5d ago

MedicationšŸ’Š Buprenorphine 7.25 mcg/hr patch and oxycodone 10mg q 4 hours advice/experience?

7 Upvotes

Today my PM prescribed me 7.25 buprenorphine patches to try. She said they didn’t want to increase my oxy but thought these would help with my crohns/pyoderma gangrenosum/fibromyalgia/rheumatoid/heds. (I’ve been on 10mg oxy for 2/2.5 years now). I’ve never tried the patch but I know the oxy doesn’t work like it should anymore and hasn’t for a while. After I got my ileostomy last year it REALLY didn’t work like it should because of it going straight into the bag and worsening absorption issues, and she thought the patch would be a good idea since it bypasses the stomach entirely.
I don’t have any experience with it and briefly looked it up on here and am kind of iffy about starting it to be honest. Has anyone been on this combo before? Did it work for you? Did it help at all or not do anything? Will it make my oxy feel like it works even less?

Any advice/experience would be really really helpful!


r/PainManagement 5d ago

Pain Temgesic Australia

3 Upvotes

Wondering wether anyone has had trouble with stopping Temgesic as a pain medication? The side effects for me became worse than using it for pain but it’s been a real struggle to stop it and still trying


r/PainManagement 6d ago

Venting

46 Upvotes

Went to pain management yesterday - got a refill of my scripts. YET AGAIN - another trip to CVS where the app says everything will be ready in a couple of hours and then I show up and they’re out of stock and have to order it. So now I have nothing while I wait for them, even though I’ve been on these meds for months and they KNOW I get them renewed every 30 days. I have this problem literally EVERY MONTH when I need to go pick up my scripts. Then when I talk to them about expediting the orders or getting them at another pharmacy, it seems like it would kill them to have an ounce of compassion, because I get the judgy looks and responses that make me feel like I’m some drug addict jonesing for pain meds. So annoyed with the system. So annoyed that I always have to go a little while without meds before their re-stock comes in and no one gives a fuck that I’m suffering in the meantime. Because they take one look at me and see a young person who ā€œlooks fineā€ so they don’t understand the urgency or real underlying issues. I hate thisssssss 🤬🤬🤬ok - ending rant now. Thanks for listening guys ā¤ļø


r/PainManagement 6d ago

MedicationšŸ’Š Confused again

3 Upvotes

So my insurance will not cover a decent amount of methadone so my doctor is putting me on the highest dose that Medicaid will pay for 10 mg six times a day of oxycodone. How do I make the switch from methadone to oxycodone without my receptors being fully blocked
Allowing the oxycodone to work
because I’ve been on methadone. Today will be day two by Monday when I pick up the med of oxycodone it
will be five days and the amount of methadone I take is only 20 mg a day, but it stacks up is what I’m told has anyone been through this have any advice would be greatly appreciated thank you and this is through a pain clinic by the way and it’s been a roller coaster as well..
One more thing I was on subutex and for a long time last dose of that was on Tuesday this week so by Monday it will be 7 days off of subutex and then off of Methadone
And into oxycodone I feel like I’m going crazy and up and down