Has anyone else experienced a non-union of their fusion? (ACDF C6-7) I have ZERO bone growth at 3 months post-op. Still having a lot of pain, but not the same pain as before my surgery. Now it feels more like bone pain. I'm assuming from where the hardware is. I'm in a soft collar to stabilize, but the pain continues. My PCP seems to think I am fabricating the pain for the medication, but that couldn't be farther from the truth. It's really frustrating to be in pain every day and people seem to discredit you. My surgeon understands my pain, but my PCP called his office and told them not to prescribe medications to me that they would be taking care of it. I don't deserve to be treated like this. Any one have any advice? Anyone with the same experience?
Needed to add I am not allowed to take ANY anti-inflammatories at all, because it inhibits bone growth. Since I haven't begun to fuse at all, this is out of the question. No range of motion, manipulations or exercises via PT, so that's out as well. (All per NS) I'm so limited as to what I can do and take for pain control.
I take Celexa 40mg X1 (because my PCP believes my frustration with my pain is depression) Neurontin 100mg x3 a day, Skelaxin 800mg x3 a day, Norco 7.5/325 1x a day which does not decrease the pain (and I have to basically beg for those) ****************************************************************************************************** Welcome to Spine-Health
One of the most important things that members can do is to provide the rest of the community with as much information about themselves as possible. It is so very difficult for anyone to respond when we do not have enough information to go on. This is not meant to indicate that you are doing anything wrong or violated any rule, we are just trying to be pro-active and get the information upfront so that people can start responding and your thread is more effective.
So many times we read about members who have different tests and they all come back negative. The more clues and information you provide, the better chances in finding out what is wrong, The fact that your test results are negative does not mean that you are fine and without any concerns. Many times it takes several diagnostic tests and procedures to isolate a specific condition.
Here are some questions that you should answer:
- - When did this first start? . Year, Your age, etc
- Was it the result of an accident or trauma?
- Are there others in your family with similar medication conditions?
- What doctors have you seen? (Orthopedic, Neurosurgeon, Spine Specialist, etc)
- . Which doctor did you start with? Ie Primary Care Physician . Who are you currently seeing?
- What Conservative treatments have you had? Which ones?
- . Physical Therapy . Ultrasound / Tens unit . Spinal Injections . Acupuncture . Massage Therapy
- What diagnostic tests have you had? And their results (MRI, CTScan, XRay, EMG, etc)
- . Summarize the results, please do not post all details, we cannot analyze them . How many different tests have you had over the years? Similar results?
- What medications are you currently using? (details, dosage, frequency, etc)
- . Name of Medication . How long have you been using this? . Results
- Has surgery been discussed as an option? (If so, what kind)
- Is there any nerve pain/damage associated?
- What is your doctor’s action plan for treating you?
Providing answers to questions like this will give the member community here a better understanding
of your situation and make it easier to respond.
Please take a look at our forum rules: Forum Rules
I also strongly suggest that you take a look at our FAQ (Frequently Asked Questions) which can be found at the top of the forum menu tab or by going to FAQ
There you will find much information that will
- - Help you better utilize the Spine-Health system- Provide pointers on how to make your threads / posts- Tips on how to create your avatar (your picture), posting images, etc- General pieces of valuable information
Please remember that no one at Spine-Health is a formally trained medical professional.
Everything that is posted here is based on personal experiences and perhaps additional research.
As such, no member is permitted to provide
- - Analysis or interpretation of any diagnostic test (ie MRI, CTscan, Xray, etc)- Medical advice of any kind- Recommendations in terms of Medications, Treatments, Exercises, etc
What could be good for someone could spell disaster for another.
You should also consult your doctor to better understand your condition and the do’s and don’t’s.
It is very important that new members (or even seasoned members) provide others with details about their condition(s). It is virtually impossible to help another member when all the details we have areI’ve had this for years, it hurts, I cant move my shoulder – what could this be, what treatment should I get?
Diagnosing spinal problems can be very difficult. In many ways it’s like a game of clue. Especially, when the diagnostic tests come back negative – no trouble found! Then it’s up to the patient and the doctor to start digging deeper. The doctor is like a detective. They need clues to help them move along. So, you as the patient need to provide the doctor with all sorts of clues. That is like it is here. Without having information about a condition, its impossible for anyone here to try to help.Specific comments :Personal Opinion, not medical advice :
--- Ron DiLauro, Spine-Health System Moderator : 08/23/15 22:02 est
•ACDF C6-7 (5/12/15) resulted in a non-union of the 2 vertebrae. I am using a BSG & Forteo injections every night, PT for e-stim, US, MFR, dry needling, acupuncture & another private MT for MFR. My tone is improving, however the bone pain continues.