Opana (Oxymorphone)

Discuss different Pain Management Options; Medication options including side effects and Worldwide variances in names etc.
Lernica
Posts: 960
Joined: Fri Jan 14, 2011 10:31 pm

Re: Opana (Oxymorphone)

Post by Lernica »

Hi Betty,

Welcome to HOPE. You are among friends. I'm sorry for all the troubles you've had and for your epic journey to obtain a diagnosis and a cure. I am sure that with time and rest you will heal. Please keep in touch and ask us as many questions as you like about coping with and managing your pain. We've all been there.

All the best with your continued recovery.

Lernica
Athlete until pain started in 2001. Diagnosed with PN in Nov. 2010. Probable cause: 3 difficult labors, 5 pelvic surgeries for endometriosis, and undiagnosed hip injuries. 60% better after 3 rounds of shockwave therapy in Cornwall, Ontario (Dec - Feb/12). 99% better after bilateral hip scopes for FAI and labral tears (April and July/12). Pelvic pain life coach Lorraine Faendrich helped me overcome the mind/body connection to chronic pain: http://www.radiantlifedesign.com
donstore
Posts: 463
Joined: Mon Nov 08, 2010 6:13 am
Location: San Francisco

Re: Opana (Oxymorphone)

Post by donstore »

Betty,
I like the Airgo Active Seat Cushion from Amazon. Hang in there. You are still early in recovery.

Best Wishes.

Don
Mild to moderate PN for 5 plus years, pain controlled by lyrica and opiates.
Nerve block (unguided) 9/10 Dr. Jerome Weiss - sciatica for 5 months but got numb in painful perineal/scrotal area - he diagnosed entrapment - but no more cortisone for me
Potter MRI 5/11 - rt STL entrapment of PN at Alcocks
Consult with Dr. Hibner Feb. 2012
Bilateral inguinal hernias diagnosed by dynamic ultrasound - surgery on 6/20/13
Feeling a little better, a few more months will tell
Betty
Posts: 4
Joined: Wed Apr 20, 2011 4:43 pm

Re: Opana (Oxymorphone)

Post by Betty »

I asked Dr Renney if he was pion free and he said only about 75%. I would be happy with 75% relief. I know it has only been 4 months but it feels like years. I have tried cymbalta, fentynol, lyrica and I have bad side effects from these..nausea and headaches. What else has anyone found that helps the burning pain? I love to walk but I find that that is causing me more pain. Is anyone else doing any type of exercise?
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Celeste
Posts: 574
Joined: Sat Sep 18, 2010 2:24 am
Location: central Ohio

Re: Opana (Oxymorphone)

Post by Celeste »

Betty, I know Dr. Renney didn't get total relief, but you're right, it's important to be able to accept whatever you can get. He told me that he takes Klonopin if he gets a flare sometimes. It's like Valium, and lots of patients use one or the other. Have you tried either of them? You can take them with other things if there's something that you find that does help.
PNE as a result of childbirth, 2002. Treatment by the Houston team, with neurosurgery by Dr. Ansell in 2004. My left side ST and SS ligaments were found to be grown together, encasing the pudendal nerve.

I am cured. I hope you will be, too.

There are no medical answers on the forum. Your only hope is to go to a doctor. I was very happy with the Houston team, which has treated the most PNE patients (well over 400), more than any other US provider.

http://www.tipna.org
calluna
Posts: 1058
Joined: Mon Sep 27, 2010 11:57 pm

Re: Opana (Oxymorphone)

Post by calluna »

I have the same cushion that donstore recommended - Togu Airgo Active Cushion - and it has made a big difference for me. it is particularly helpful when I have to sit on a firm surface, such as a car seat. It is expensive but very well made, and you can inflate it more or less as you choose, it comes with a little pump.

With regard to medication: there is amitriptyline, nortriptyline, and gabapentin. All have varying amounts of side effects, but there are many people on here who are taking various combinations of these to good effect. Also there is tramadol - I have found the slow release version to be better at damping down pain spikes, and it is also easier to stop taking than the ordinary sort.

But the single biggest help for me has been from the psychology services at my GP - CBT for help with pain management.
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ezer
Posts: 689
Joined: Sun Sep 19, 2010 6:53 am

Re: Opana (Oxymorphone)

Post by ezer »

Betty wrote:I asked Dr Renney if he was pion free and he said only about 75%. I would be happy with 75% relief. I know it has only been 4 months but it feels like years. I have tried cymbalta, fentynol, lyrica and I have bad side effects from these..nausea and headaches. What else has anyone found that helps the burning pain? I love to walk but I find that that is causing me more pain. Is anyone else doing any type of exercise?
Betty,
It is imperative to increase the dosage very slowly. In fact much more slowly than what the manufacturers recommend. It is the only way to avoid as much as possible the side effects that come with that type of medication.
2002 PN pain started following a fall on a wet marble floor
2004 Headache in the pelvis clinic. Diagnosed with PNE by Drs. Jerome Weiss, Stephen Mann, and Rodney Anderson
2004-2007 PT, Botox, diagnosed with PNE by Dr. Sheldon Jordan
2010 MRN and 3T MRI showing PNE. Diagnosed with PNE by Dr. Aaron Filler. 2 failed PNE surgeries.
2011-2012 Horrific PN pain.
2013 Experimented with various Mind-body modalities
3/2014 Significantly better
11/2014 Cured. No pain whatsoever since
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