so I had back surgery on February 10th they did a XL if procedure, so I had a spinal fusion at L 1 - L2.please pardon me if my grammar looks strange. I do not have a keyboard for my tablet so I am using the touch and talk method. So again I'm a little over 2 weeks out from surgery. My surgeon with a sports and orthopedic surgeon who I was referred to. I was using a 20 milligram Butrans patch and 4 percocets a day. I was in the hospital for 3 days they had a very hard time controlling my pain. They sent me home on oxycotton 20 milligrams 2 times a day and a 15 milligram oxycodone every 4 hours. And I have to say, people I hurt,. They also gave me 5 milligram valium every 4 hours, and 400 milligrams of gabapentin 3 times a day. I have been begging my surgeon to let me take motrin and he just approved it two days ago. The motrin helped considerably, however, When physical therapist, comes over and we do simple stretches and muscle strengthening. I am moaning and groaning uncontrollably in bed afterwards. Please understand does the medication I was on before surgery barely put a dent in my pain. I don't know if I have a high tolerance or what's going on but he feels it appropriate for me to be on what I am. Can anyone let me know if they were on stronger doses after spinal fusion? When I wake up in the morning, I can't hardly move until 30 minutes after taking my medicine. And even then is touch and go. I guess I'll just wait for reply s. I would love to tell you my story and all that is wrong with my back. If I just had a dang keyboard. What I've written has taken about 30 minutes. By the way, I'm a 37 year old female, medically retired from the Air Force after the removal of my large intestines.after they removed my intestines I started getting sick a lot, little things such as sinus infections every month. I used to get nerve blocks for my pain, and they helped. The last two times I had nerve blocks I got viral meningitis. So now the infections disease doctor the leaves that the removal of my intestines crawls in issue with myimmune system. Also, and this is just my opinion, it seems that on really bad days of diarrhea that my pills don't work nearly as long as they should. So there you have it, I'm like the super freak in the medical world I have chronic meningitis, I've had a total colectomy, I have which is rare in itself - but having it in the discs that I have it in is almost unheard of. Literally.
So I have the medication question, also is there anyone else who had surgery around February 10th, 2015. I'd love to know how they were doing, I were that spondylioliothesiss is similar yet opposite to what I've had. Has anyone had it in the l1 area.
Thank you for taking the time to listen, Dixie