Good morning all. I have DDD in my neck and low back. I have had back pain, and subluxation requiring chiropractic care since I was 14. So my spine has been deteriorating at that location since that age at L4-L5. I have always had adjustments at my cervical and thorasic areas all that time also, but never the dibilitating pain that occurred in my low back. Anyway, my point is that anyone that says DDD is a normal part of the aging process, and also considers it a process that everyone shares is a fruit. I want one person to tell me they have DDD and any of its common associated conditions and that it just came out of the blue from getting older. That they had no symptoms, and are not in pain of some form. I am not talking about a corpse that while they are checking it for science and they say DDD is there with no history. That person can't talk. Had to vent, had a pain management doctor insinuate this belief and also HE proceeded to tell me the pain level of giving birth as an 8. I said "and that is based on what?" I wanted to say personnal experience to his arrogant ass, but held back. He recommended "injections" all over of course. Didn't discuss any pain medication, other than to note I was on oxycodone/ APAP at 5/325 1 to 2 tablets/day. Prescribed by my PCP who I know doesn't want to deal with this medication or the xanax I take and have taken for over 10 years on and off. I had Panic disorder and was put on Paxil 10 years ago. I was also told I have IBS many years ago. It seems I have had nervous system disorders of some type since an early age. My system has always been hyped up for some reason. My stomach and system in general has always been sensitive to abuse that deals with lack of sleep, caffeine, and other meds that cause hyping. This could go on even longer, sorry. So my own PCP read in the pain docs notes that fibromyalgia should be considered. I never really investigated fibro but I did catch something on the internet that said there is a high rate of IBS in Fibro patients. Over the summer my brother passed at 48 from brain cancer. At that time started having these bizarre attacks of diarrhea with unreal spasms and cramping that went on for hours. It happened like 4 or 5 times and one incident caused me to go to the ER via ambulance. All testing was negative. My usual bowel activity is constipation, so for me diarrhea is a rare thing unless something is wrong. When I read about the IBS and fibro I was like holy crap. I made an appointment with my PCP the same day. That is when she presented what the PM doc had stated. She put me on Lyrica the same day.
So here is the basis of my post, if you have read this far, sorry. Long story. I started the Lyrica and noticed a difference within the 1st 24 hours. There are many side effects and odd symptoms with taking this med. I have not really had any of them, other than off balance. Which I have at times anyway. Some tiredness after being on it for a number of weeks. I think I need to up my dose to 450mg a day rather than 300mg. I see a rhuemo today which I hope deals with this medication and will adjust it. Since starting this medicine aching, sometime burning, and spasm type pain I was having in my upper back, hips, and groin to my knees has abated. If I over do physically I am still feeling it, and areas affected by direct nerve/ pain stimulus is there. It seems pain that had no exact cause has been improved greatly. The mechanism involves the nerve/ stimulation barrier. Lyrica does something with calcium and it causes some kind of interference with the impulses caused by over stimulated sensory nerves. These effect the muscles causing a number of unpleasant symptoms. It is worth a shot if you have a lot of muscle pain, I was told that I had mysofascial pain syndrome, which mimics fibro. I felt it is hard to distinguish between the two, especially after this. I would like to know if lyrica works for those who have been diagnosed with MFS. Worth a look, must read full pharmacology report on Lyrica, before considering. You don't want to miss anything, as wonderful as this medication seems there have been people that said the side effects were too much. Take care. I will post after seeing rheumo about anything new. Chris A. =D>