Ankylosing Spondylitis Support Group
Ankylosing Spondylitis (AS) is a chronic form of arthritis--it is an inflammatory disease that causes joints, cartilage or other fibrous tissue (such as ligaments and tendons) to turn into bone. Ankylosing spondylitis is part of the group of rheumatic diseases. The disease is characterized by progressive stiffness, tenderness, and pain in joints. Pain can be episodic and...
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I have been taking oxycontin, perc's and peroxicam for my mucle aches as well, pain all over my body joints, with inflamation flare ups, cant make a fist, and drop things when i think i have a good grip, popping noises in my half mobile hips, hurtin all the time, cant sleep well at night, hurts to straighten my leg's from fetal position, like stretching a rubberband, going into some sort of spasm that goes to my ab muscle's. What is that? I was diagnosed with AS 6 month's ago and got on enbrel 2 months ago. What can really help me so i can get off these meds?
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Being on medication for the rest of my life is still something that I am coming to gribs with myself. I find that is most helpful to keep a close eye on what I'm taking and discuss all medications with my doctor. If you are taking a prescribed pain killer than OTC medications can be highly dangerous. Not to mention the more likely you are to getting ulcers from having AS.
I have ulcers and the years that I took OTC's made them near deadly. All pain solutions should go through your doctor but I recommed this line of treatment.
There's something else that works wonders for spondylitis: Vitamin D and L-Arginine. They help control pain and inflammation and of course, you can't forget about exercise. It's the best thing you can do to slow the progression of the disease: walking. stretching, yoga, massage therapy....
But let me be perfectly honest. You can never expect to be 100% pain free with spondylitis. No matter what we do or what we take we will always have some pain and stiffness. It's just something we have to learn to live with, as depressing as it is.
I start on the fifth. I've been in and out of PT since 2005, after a car accident.
In late 2005, I went to a physical medicine doctor to finally get some answers about my true injuries.
He sent me for a different kind of PT (one which focused on pain relief, stretching and gentle strengthening) and to an osteopath (who ended up discovering that my autoimmune markers were elevated).
I am happy to say that 95% of the time, I no longer suffer from the pain that made me seek treatment last year. However, I also deal with the pain of my autoimmune condition.
Aside: Long term use of potent opioids can cause pain to feel worse than it is. I forget the pharmacokinetics of it, but it does not have anything to do with dependence or tolerance. It effects the way your brain processes pain. Are you on anything besides the biologic and peroxicam to deal with the inflammation? A DMARD perhaps, or even a low dose of prednisone?
This is not true in my case. In fact, it seems to be the only thing that can help me break the crippling fatigue associated with my AS. When I have a flare up, I seem to need the big guns as being misdiagnosed and having AS treated as a disk herniation, led to gratuitous use of narcotic analgesics on the part of my doctor, and myself. Things have changed a bit, I'm not slaved out to pills but i have just about 0 quality of life without them. this is my current dilemma, in fact. Please advise before it's too late because I fear going back to narcotics but they seem to be the only thing that allows me to live a somewhat functional life.
I KNOW you don't want to hear this but, exercise REALLY helps with the pain! Also if the embrel isn't working, try something else! Oxy is VERY addictive. I talk Sulfasalzine, Vimovo (naproxen w/stomach med), Robaxin (muscle relaxer)Tramadol during the day and Hydrocodone at night. I KNOW the pain is terrrible, but moving really helps. Try swimming or water aerobics, very low impact, but helps w/the pain!
I get Epidurals every 3-4 months. Those trigger point injection & epidurals have done wonders to block the pain. I no longer use a cane too.The pain meds are from my PM doctors. Plus they also find it important to get sleep.As he told me sleep is a strong part of the healing process.during a Flare-up.
PLEASE BE VERY CAREFUL USING OXYCONTIN! I was on it for years then ended up in the ER with a intestines blockage and needed to have surgery to remove 6ins. I was told it from the Oxycontin..