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Thread: prescription pain meds

  1. #11
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    anything with Tylenol bad for the kidneys anti-inflammatories are also bad for the kidneys that is why my pain management doctor gave me oxy I tried to take it only when I really need it like to sleep

  2. #12
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    Hi Jaha!

    What is Costchondritis? I'm asking because I see you have a few of the same diagnoses (COPD, Neuropathy) as me. Also, it's in your ribs so I was wondering if you have any T disk problems?

    Thanks!

    Quote Originally Posted by Jaha View Post
    WG Mom,
    I am currently taking pain meds Oxycontin and oxycodone, it is prescribed to me by my PCP. In addition to Wegs, I have Fibromyalgia, in Costchondritis my ribs, COPD, neuropathy in hands and feet. Then there is the nerve damage from the shingles in my breast and back that lasted for over 10months. I'm on 15mg of Preds, always trying to taper, when I get to 10 I have a flare and have to up it which is destroying my shoulder joints and my knees. I have been on all the immune suppressant so far and am currently on 2000mg per day of Cellcept, Bactrium and Rtx infusions every six month. I think it is safe to say that if your daughter is in pain her PCP should be able to give her something and it may be just temporary that she would have to take them. Best wishes to your daughter to live a better pain free life.

  3. #13
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    Costochondritis is inflammation of the tissue and nerves, in my case between the ribs. It is also called Tieze syndrome and I think I might have spelled both of them incorrect. I was told that it sometimes takes along time to calm down and can flare from time to time. I do have degeneration in my thoracic disks going on. I had an open lung biopsy almost 5 years ago and have had shingles on that side from front back. So who really knows where the pain is coming from, I'm going to see a neurologist later this month maybe they will tell me something totally different.
    Jana


    Do not fear anything, just do it afraid!
    It does not matter how slowly you go, as long as you do not stop!


  4. #14
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    I also had costocondritis about 12 years before I was dx'd with Wegener's. So weird to think I may have had symptoms for years. I'm so sorry to hear you have that, it really hurt.

  5. #15
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    Wow! I haven't been here since February!
    Quote Originally Posted by Jaha View Post
    Costochondritis is inflammation of the tissue and nerves, in my case between the ribs. It is also called Tieze syndrome and I think I might have spelled both of them incorrect. I was told that it sometimes takes along time to calm down and can flare from time to time. I do have degeneration in my thoracic disks going on. I had an open lung biopsy almost 5 years ago and have had shingles on that side from front back. So who really knows where the pain is coming from, I'm going to see a neurologist later this month maybe they will tell me something totally different.

  6. #16
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    If wegeners is involved then a long term pain management strategy ought to be created with a good medical team. What works this year may not be appropriate in 5 or 10 years. My general practitioner, although she means well, could easily prescribe counter-productive meds. It takes a team that you feel is competent.
    Charting daily weg symptoms, pain level 1-10, and dates gives a lot of info for the team to go on.

    At 25 if bedridden and in excruciating pain I would take oxycodone minimally even though it makes me nauseated. Percocet and vicadin have things in them that make me worse. Dilaudid was the only thing that worked when severe spine and nerve damage occured, but only two doses one night in er then the pred took over and a little oxycodone got me through a few days. I have a whole bunch of it if I need it but almost never take it unless it's excruciating and can't sleep. Level 8-10 pain should probably be treated. Seems cruel for a doc to withhold help at that stage.

    Addictive personality or not, if taking narcotics pain meds preventively for more than a few weeks then the body will develop tolerance and undergo withdrawal if discontinued abruptly. Call it "dependent" if not addiction. But it takes a slow taper to stop those stronger meds. Caution.

    Anxiety is often related to severe pain. So sometimes adding a safer anxiolytic can reduce the amount of pain medication needed to control pain.

    I write down every single pill I take and the time and always ask myself "Do I really need this?"

    Sent from my SM-G925V using Tapatalk
    Best wishes,
    Tom
    ----------------------------------
    2 years untreated. Dx w/ biopsy - 2000
    Tx Plan:

    NUTRITION
    RESTORATIVE SLEEP
    RAISE ANABOLISM
    REDUCE ALL INT / EXT STRESSORS

  7. #17
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    I am a pain management patient that is 100% supportive of people taking pain medications when they have legitimate medical reasons to take them. I have degenerative disk disease in my low back and neck, with my back being the absolute worst. I have needed spinal fusion surgery for a couple of years now, and when I finally decided to take the plunge and get it done (because the pain is so horrid), they find Wegeners and none of my specialists will medically clear me for the surgery until I am done with the treatment for Wegs in a year or two. So, my only comfort is my pain meds. I have been taking some form of pain med for the past 10 years now, so I've gone through a lot of different kinds. Right now I take MS Contin ER 45mg twice a day (morphine extended release), Dilaudid 2 mg every 4 hours, and Zanaflex muscle relaxer 4 mg every 6 hours. I have tried fentanyl patches in the past, but the "night" sweats I get from Cytoxan and prednisone caused me to sweat those patches right off. I've had hydrocodone (no longer works), oxycontin (really doesn't work, either), and I guess my next steps are an increase in morphine, a pain pump, or pain shots.

    I think people that have abused prescription pain meds have honestly ruined it for the rest of us that are using the meds as directed and as intended. No, pain meds do not control 100% of my pain and I've never expected them to. I have accepted that most days, my pain level from 1-10 will be around a 4 and that is something I live with. I also understand that I am watched like a hawk by my pain management physician, they count my pills every month to make sure I'm taking them, they check my pee, heck, even the Drug Enforcement Administration watches every prescription I fill and sends my primary care doctor a letter several times a year so he knows I'm getting pain meds. I think it is a JOKE the way the government watches me as if I've broken some major drug laws - and I'm the one that has never been arrested in my life! But if this is what I have to go through to get a little bit of pain relief each day, then so be it.

    Teri
    Teri from Texas
    Diagnosed w/WG March 2015
    "Lord my God, I called to you for help, and you healed me." - Psalm 30:2

  8. #18
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    Quote Originally Posted by txrepub4God View Post
    I have tried fentanyl patches in the past, but the "night" sweats I get from Cytoxan and prednisone caused me to sweat those patches right off.
    I wrapped the patches with that sticky elastic gauze tape to hold em on.

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