Back pain.. kinda long post...

New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

Regular Member

Date Joined Oct 2007
Total Posts : 92
   Posted 10/29/2007 8:27 AM (GMT -6)   
Hello everyone.. I’m new here and just wanted to say hi. I’m 29 and have been having back issues for the past few years. The problems originally started 3 years ago, at which point it just felt like a pulled muscle in between my shoulder blades. My doctor sent me to PT for 4 weeks, which didn’t really help much until they used ultrasound and estim. After a week or 2 of PT with the ultrasound my back actually felt better. I went back to my normal life and thought all was well. Fast forward 2 years which places me about 8 months ago. I start having the same problems, I think it was angered by my job which had me using a machine that was to short so I was leaning over 1,000-2,000 time a day 6 days a week. My doctor again sent me to PT for 6 weeks, but this time it didn’t help so much. I started getting some shooting pains in my arm, and sometimes my feet would feel like bricks. My physical Therapist had my Dr. prescribe me a tens unit, which gave me some relief, but it seems to stop working (pain relief wise) if I use it too often, so I limit my use of it. I wasn’t sleeping well, so my Dr. prescribed me 20mg Oxycontin for bedtime. This seemed to get me about 6-7 hours of sleep a night, which was greatly welcomed. At first I would only use it a few times a week, and I was fine with that. After the 6 weeks of PT I didn’t really notice it getting any better, so my doctor ordered X-rays and an MRI and referred me to a different Dr. (a neurologists). The MRI shows arthritis in my spine a bulging disk and the beginning of DDD. At this point my doc prescribes me 5mg Percocet (2 at a time every 6hrs prn). At first I didn’t use the Percocet very often, 240 of them lasted me 3 months. The neuro. Was very uncaring and said “it doesn’t look that bad” and just acted like it shouldn’t hurt me at all. He sent me to a pain doc to get cortisone shots in my neck. The pain doc wasn’t to convinced that it would help, but we proceeded with them anyways. Now I’ve been sick before, but these shots made me SO sick!! I couldn’t go out in the sun, or get too warm or else I almost passed out. I walked around for about a week and a half either beat red or Casper white! I was always on the brink of passing out, and continuously nauseous. On top of that I guess I constricted my neck muscles a lot when they did the injections and it made me stiff as heck for about a week. He said see if the shot helps and if not he can try it a little differently. Well it didn’t help, so I had to go back and get a second set done. This time he gave me 15mg of diazepam to make sure me and my muscles we relaxed. The second shot didn’t make me as stiff, but it did make me just as sick and did nothing for the pain. So the pain management doc and I decided I was done with the shots. This pretty much brings us to current time. In the passing of that time the pain has increased, so I have been taking my Oxycontin nightly and the Percocet daily 2-3 times a day. I am now dependant on the oxycodone, and I can’t go without taking it or I end up in pain and feeling icky (I know these are WD symptoms). I went back to the neuro guy last week hoping he would have some other ideas. All he told me was I’m to young for surgery and he doesn’t want me taking the pain meds anymore. I asked, “so what are my options” all he did was ignore the question and wrote a script for Celebrex. So I called my regular Dr and got the name of a different neuro for a second opinion. I feel like the guy didn’t even care I was in pain, and kinda got the feeling that he thinks I’m just looking for drugs. As of now I take oxycodone (I didn’t like taking so much apap) 20-40 mg a day(240 will still last longer than a month), 20mg oxycontin at bedtime, Norflex 1 or 2 times a day and naproxen at bed time. My insurance company won’t fill the Celebrex until I try 2 other NSAID (hence the naproxen)… Cheap *&*(*&*s! I know for sure I do not want to be on the oxy for much longer, I hate being tied to these pills. I’m not really looking for an answer from anyone here, I just wanted to let this out of me! The whole thing is very angering and depressing. I’m only 29, and it really sucks how I feel. I recently lost my job due to taking to much time off, so now I have that to deal with on top of it all : ( … Well Thank you for listening!! And sorry this was so long.

Forum Moderator

Date Joined Jan 2005
Total Posts : 9146
   Posted 10/29/2007 8:54 AM (GMT -6)   
Hi Mach,

And welcome to our CP family. I hate that you have to be here but since that's what your body needs right've come to the right place. People here truly understand and care. I'm heard stories similar to yours. "You're young, don't want to do surgery nor have you take pain med. No solution offered." That makes me furious!! Age doesn't matter. Pain is pain! and you should be treated with respect. You are NOT a drug seeker and they should be able to recognize that. I can and I'm no doctor.

about all I can tell you is don't take 'no' for an answer. Get a neuro who will respect your issues and deal with them. I also have arthritis in my spine and it's miserable. I'm probably considerably older than you and I get great pain care from my primary. He's not afraid of the 'pill police'.

Please keep posting and let us know how your days are going. It's very comforting just to know someone is out there who cares. Feel free to email me also. Just click the little envelope under my name.

Co-Mod Fibromyalgia & Chronic Pain Forums
Fibromyalgia, Ulcerative Colitis, Insulin dependent diabetic, collapsed disk, dermatitis herpetiformus, osteo arthritis in spine and other locations.

The only difference between genius and stupidity is that genius has it's limits. Albert Einstein: (1879-1955)

Forum Moderator

Date Joined Feb 2003
Total Posts : 16570
   Posted 10/29/2007 9:07 PM (GMT -6)   

Hi Mach,

Welcome to HW although we love newcomers, we hate to see someone else afflicted by chronic pain. That neuro was a complete idiot, cause guess what, pain does not have an age limit. You don't have to be 90 years old and be allowed to hurt. My chronic pain started many, many years ago. I was 19yrs old 1st time I ever had to see a dr for my back. He said he had never seen anyone as young as me to have the intense muscles spasms that I was having. He did not doubt my word that I was in pain either.

Get yourself another opinion and it may take more than 2. We have all at some point had to find another dr. I have arthritis too, the weather changes we have been having has at times just about reduced me to tears.

Hang in there and I hope you will come and hang out with us. Susie

Regular Member

Date Joined Oct 2007
Total Posts : 92
   Posted 10/30/2007 3:11 PM (GMT -6)   
Hello again,
Just thought I'd pop back in, to ask a question. how many people out there who have chronic pain are able to manage it without the use of opiates? I really want to get off the oxy, but I fear the pain that comes when I don't take it. thanks for the kind words! I am lucky to have a good primary care doc. He has no problem refilling my scripts, and I only have to see him every 3 months. He believes me about the pain, I think. I'm assuming he must believe me, or else he wouldn't have written such strong meds... Right? I just need to find a better neurologist? Or should I seek a different kind of doctor?


New Member

Date Joined Oct 2007
Total Posts : 6
   Posted 10/30/2007 11:55 PM (GMT -6)   
I have a very bad back sice I was 19 I amnow 44 and I never took anything for the past 15 years until I finally ruptured a disk a few months ago. The only thing that kept the pain level down was really trying to find all the little movements that would make my back worse. I got up rolling off the bed...made sure that last step on a flight of stairs or walking off a curb I made sure I took it slow. After a long long time I knew every movement that would throw my back out and got to know all the feelings in my back so days before I knew I would throw my back out I took a step back and I would relax so I could get over the hump and get back to normal without having my back go out on me. I play a lot of sports and finally this year I made one very large mistake playing basketball and made a spin move (Which I knew was a no no) and it went out on me.

But generally you got to learn what you can do and set limits that way you can at least get off the meds a few months at a time and take them when you really need them and in the end you'll get some kind of normal life.
New Topic Post Reply Printable Version
Forum Information
Currently it is Wednesday, August 15, 2018 6:09 PM (GMT -6)
There are a total of 2,993,059 posts in 328,014 threads.
View Active Threads

Who's Online
This forum has 161212 registered members. Please welcome our newest member, LymePie.
317 Guest(s), 13 Registered Member(s) are currently online.  Details
Kent M., CashCat, physedgirl09, compiler, cashlessclay, Serenity Now, Redwing57, Tudpock18, Hawaii3654, songlady, RobLee, helpwithlyme, Steve Smith