← Return to Decision re: artificial disc replacements in cervical spine

Discussion
Comment receiving replies
@dlydailyhope

@nadiachar
I had ACDF surgery on my c5-c6 due to cervical myelopathy. I was 52 at the time. I was misdiagnosed for over 5 years and now have some permanent spinal cord injury. My cord showed flattening/effacement and I had bone spurs/osteophytes and disc bulge causing stenosis. My symptoms were daily headaches, neck/shoulder pain and knots, tinnitus in ears, arm/hand weakness/numbness (regularly dropped things/handwriting worsened), bladder control issues, heaviness in legs/slowness in walking when I used to walk very fast (even when my brain wanted my body to move faster, it wouldn’t), etc. Cervical myelopathy is slow spinal cord injury over time. It is really only stopped from progressing through surgery. They used my own bone from my bone spurs to use in the fusion “cement” at c5-c6. After surgery, most of my symptoms improved except for residual arm/hand weakness.

Now, I have a new broad disc herniation at c6-c7 which is pressing on my spinal cord and nerve roots causing new myelopathy and bilateral radiculopathy symptoms. I recently had right hand carpal tunnel surgery and also have ACDF surgery planned for c6-c7 surgery in 2 weeks (3rd week in May). My myelopathy symptoms have returned and this time are major balance issues, arm/hand weakness, some neck pain, bladder control issues/frequency and slower walking. I am 55 and a single parent of a teen and want to stop the spinal cord injury from progressing further. After surgery, I will then have c5-c7 fused and will have some limited range of motion turning my head/neck but it is worth it not having many symptoms below the level of my spinal cord compression which could become permanent.

Have you been to a neurologist for EMG/nerve conduction studies of upper and lower limbs? Did your orthopedic spine specialist check your reflexes and watch you walk/your gait for signs of myelopathy?

Jump to this post


Replies to "@nadiachar I had ACDF surgery on my c5-c6 due to cervical myelopathy. I was 52 at..."

Thank you very much for sharing. It helps a lot to hear of the experiences of others.
I have seen an orthopaedic surgeon in Canada and had consultations with two neurosurgeons from Germany both of whom I trust. I do not think I have overt signs of myelopathy at this time but wish to decompress my spinal cord and improve the biomechanics while still a candidate for disc replacement to avoid it. Auto-fusion is occurring so the window will close. I wish you the very best in your upcoming surgery. It must be really difficult to be single-parenting while going through this. I hope you get the support you need to heal and recover well.

I think I accidentally responded to you in the wrong place, sorry! I hope you will see it below under another response posted for me.
Thank you both for sharing. I am trying to learn as much as possible as I make my decisions.

@dlydailyhope It sounds like you are going in the right direction. You already know what's involved since you've had one procedure already. I think your head turning will be the same as it is now after this surgery. Most of that is done by C1 & C2 with some help from C3 and C4. It will make your spine stiffer and take away some forward bending or arching backward. I'm glad you are sharing your journey so others may learn from you. Good luck with your surgery.