Chronic Pain Support Group
Physicians and professionalsdefine pain as chronic if it lasts longer than three to six months and is persistent. It's distinct from acute pain that is a direct result of injury or trauma. This support group is dedicated to those suffering from chronic pain. Discuss treatments that have worked for you, find advice for your specific experience, and find support. You're not...

David.
I had almost the same symptoms, by the time I saw My surgeon I couldn't walk or sit. he took one look at my MRI and scheduled emergency surgery, 4 days later. when I woke from surgery he told me that my disk was shattered. and it was a good thing I hadn't waited any longer. Only mild low back pain now, when I do too much. Good luck at the Drs. and feel better.
Sharon
I am sorry that you are in so much pain, I hope that you can get to the pain management Doctor soon, and that he can take care of you. Hun, it sounds like you also have nerve pain, and if you do, you might want to ask your Doctor to give you a referral for a Doctor that works with spinal cord stimulator's (SCS). An SCS is a device that gets implanted inside of your body and controls your nerve pain, and it will not make you woozy.
If your pain is created by nerve pain the SCS trial will help you. Try to find a Doctor that works with the device, get into the trial and see if it helps. Hopefully it will! Take care and see you soon!
Anyway I hope most of the people in your life understand what you are going through as best they can. Maybe on a good day try to talk to them about it. There is a Letter to Normals on here that I found out about that is really good and helps put words to what we are feeling. Try to find it. It is really helpful. Also everyone on here is so nice and understanding. That has helped me so much. Good luck!
I try to stay positive. I am an active member of my local church, and I love all of them. There are so many great support systems available.
Hang in there and get connected with the good people here.
David.
I am so sorry that you are having such terrible pain...that sciatica is a beast!
I encourage you to see someone else regarding your back pain. I also might see about a herniated disc surgery, I am not an advocate of surgery and I have not had one on my back...so...I should shut up--however--it could be a fixable thing.
I have had several personal friends who have had a herniated disc that was causing them agony...they waited like their MD's told them too -conservative care first- and the disc did not go back into place. They had the surgery and, except for one friend...completely asymptomatic. It sounds like with your numb foot, the disc may be pressing on your spinal cord or nerve root.
Anyway...whatever happens, I hope you are able to get the relief you need and feel more quality of life and work. NO ONE should "just get used to it".
HUGS
i'm so glad you came over to our board. i think you're going to like it here - pain can be SO tough to live with, and when it gets to the point where you have it coming from more than one place/diagnosis, it can
be downright overwhelming. try as they may, it's hard for people who aren't living it to understand. but you know all of this, and i'm clearly
rambling. my point is that it's great to be able to talk to a LOT of people who *do* understand! sometimes i feel like i'm literally at
the end of my rope, and no one in my life gets it ... but here they do.
hopefully your life will be a little less stressful with us to talk to!
now that i've finished my after-school special monologue (lol), i have to say that i've personally never had any experience with sciatica, although my uncle - he's just a few years older than you - has recently been having some issues with it, and MAN is he in pain.
i can't believe how much pain, and we're talking about one tough guy!
no WAY would a tylenol 3 cover that; i don't think it would even touch it. not for me, anyway. i'm not sure how much the lyrica is helping, but it certainly doesn't sound like much.
it certainly sounds like the best thing for you will be a pain management doctor, and you're already on top of that, which is great. the dr you have right now sounds like an absolute sadist. don't you just love it when someone who has *no* clue as to how much pain you're in tells you what you should be feeling, how much medicine should be handling your pain, etc.? and i'm pretty much willing to bet my bank account that this woman has never had sciatica in my life ... am i right? i'm sure i am, or she would be helping you out every way she could.
one piece of advice, though: at least until you get into your PMD (pain management dr), please speak up! don't be afraid to tell her that what she's giving you isn't working, or to ask for something stronger. what is she going to do? at worst, tell you no. at which point you're no worse off than you already were. if you don't speak up, however, not only will she think that she was right in your case and that you *don't* need anything more, but think about the next person who's in major pain and relying on her for help: she'll be even more stubborn and set in her ways with them, too. obviously you're biggest concern right now is you, but there's a second benefit to speaking up, which is also nice. :D
many of us here have been judged by doctors, nurses, family members, friends ... i know it can be intimidating when you think that the person you're dealing with doesn't believe you, or all of what you're saying, is judging you, etc.- but you have to stand up for yourself, because *you* know what is true. it's NOT your fault that these things happened to you, and NO ONE has the right to judge you because they did - the should just be grateful that they aren't in a similar place. i don't know what your support system is like, but it's so important to be your own advocate. sometimes you can only rely on yourself.
i hope i don't sound as though i'm talkking down to you or telling you things that you already know ... i've just been there before, and i hate it when people are living in pain because the 'healers' think they know best. i really hope that things start to get better for you; please keep us updated!
xoxo, misa
ps) when can you get into your PMD? i would call and see if they have any cancellations if i were you - and keep calling. many times people with pain can't make their appts, you know? also, are you staying on with your current dr? aren't i nosy?