Issues after cervical fusion. Normal?
Had cervical fusion C3 to T1. Felt good after till recently. 2/6/25. Have pain occasionally in my neck. A little bit burn wondering if this is normal.
Interested in more discussions like this? Go to the Spine Health Support Group.
Connect

@lisalucier wow, hugsss. I'm so sorry to hear of all of these things. These are major hurdles.
My experience after my C6-C7 C7-T1 fusion left me with tons of pain just like before surgery, but some is a different feeling of pain. Like it's hard to describe.
I have opiods given and they have no effect on the pain it's extremely frustrating. I'm a single parent my youngest is 12 and is going through toughtimes, also a major argumentative, defiant and major source of stress (which makes healing difficult).
I had to check myself back into the hospital about a week after the surgery due to feeling as my throat was closing and extreme pain.
After a picc line IV antibiotics for weeks due to a possible infection/ fluid collection in my neck.
My neurosurgeon said give it a few months to see if my pain remains sooo high then we think about fusing 2 more levels (for a four level fusion) 😭😭
If my throat still feels like I'm being choked and like I have a baseball in it, would it make sense to think my throat would be even worse after going back in to fuse 2 more levels?
I'd have nothing to lose I guess at that point.
I have zero energy the same as you (more than normal). Takes me the whole day to get minimal things done.
I've been trying to drink protein drinks because my appetite isn't great and I'm cooking less than before which isn't alot.
I have a speech therapist apt again to try to help my voice, when I speak or try to sing my voice is shaky at points. I'm hoping that inflammation will reduce more as time goes on but it'll be 2 months post op on the 13th.
My pain level baseline is 8 to 8 1/2 out of 10. Often gets to9 to 9 1/2.
It's a struggle.
I hope physio will help with ROM.
I feel for you. We're in this mess together. 🖤 I have no advice that could be positive unfortunately.
Ice, heating pads, pain cream, baths.
Same as before the surgery.
Take things on slow mode. More mindfulness and self care is necessary.
-
Like -
Helpful -
Hug
2 Reactions@mariacabral the anterior & posterior cervical surgery I had was something about my spinal cord that the doctor noticed. He said it had to be fixed or there would be problems in the future.
I had not been experienced any pain.
The surgery went well.
I'm sorry you are having to deal with so much from yours. What does the physical therapist say about it? Has the doctor ordered an X-ray of it to check everything?
-
Like -
Helpful -
Hug
1 ReactionHello! Thank you for sharing and for your help @yesibeleive.
My doctor ordered an X-ray; the disc is misaligned, but as it’s the second one, he says it’s normal and that my problem is muscular, so he prescribed muscle relaxants. I’m tired of taking muscle relaxants, anti-inflammatories and so many medicines with side effects; they’re affecting my life, my work... The physiatrist recommended a chronic pain specialist, who suggested a cervical epidural block with X-ray guidance as the first option, or as a second option, corticosteroid injections with ultrasound guidance and possibly radiofrequency ablation. I’m still thinking about and looking into these options. I really appreciate your feedback and sharing. Thank you!
View Translation
@gothghoul many thanks for sharing! I'm really sorry to hear that it's been difficult for you too 🙁
My doctor makes me feel as though everything is out of the ordinary, and as though I have extremely rare symptoms, and says the problem is probably down to my incorrect posture. I’ve come to the conclusion that he’s no longer the right person to help me, so I’m trying other specialists... and different solutions. Stay strong and keep hope alive, and thank you so much for sharing! Huggs
View Translation
-
Like -
Helpful -
Hug
3 Reactions@mariacabral
Thanks so so much!!!♡
It's extremely frustrating and invalidating when they day dumb things like that.
They give me an incredible hard time getting any pain relief meds. They don't have to navigate life like we all dool 24/7 365, and are expected to act pleasant and try to manage as a non challenged person in alot of instances.
I wish you the bestest of luck!!! I think you've made a very wise decision to look towards other Dr's/ specialists. We just have to keep reaching out for physical and or mental health support.
If we're not heard then keep pushing on until we are taken care of in a proper way.
Sending you tons of hugs and lots of patience in your journey.
✨️🌷
Thank you for your message
-
Like -
Helpful -
Hug
1 Reaction@mariacabral
I can relate to your story, in 2001 I had posterior cervical surgery C2 - C6, it was prompted by only able to raise my arms 4 or 5 inches. The pain was unbearable like 2 jackhammers full blast 24 hours a day. My neurosurgeon cut a window in my spine to take the pressure off my spinal cord. It was an improvement to my condition, but 2 years later I started with pain again, this time in a anterior approach all the discs were removed and replaced by cages, screws and a titanium rod. I was out of work again for 3 months as I was with the first surgery. The college I worked at had a horrible plan for disability; only $100 dollars a week. At the same time my mother was with me she had colon cancer and heart failure. You mention massage, I cannot have a massage due to pain, Lerhmette's disease. Feels like I'm being electrocuted, every disc in my spine is injured in some way because of DDD, spondylolisthesis, stenosis and spurs etc. I didn't have PT for these two surgeries. I experience problems swallowing and recently had my esophagus stretched, it helped. In addition, I had 5 other joint replacements both hips, both knees, and left shoulder replacement. For these I did water therapy which is much better for me. During the first surgery left hip my foot dropped.
I've had it all and when I became inoperable I was offered a morphine pump. last week I received my third pump (they need to be replaced every 7 years). I thought the arthritis would take me out from my job, but in 2010, I contracted sepsis that attacked my epiglottis, only 4 in a million adults get this, after discharge I discovered I had brain damage and couldn't go back to work. I couldn't read, all the letters melted on the page. In a year my ability to read came back, but not to the level I had before. I had to surrender and go on disability. I do meditation and prayer. On You Tube there are meditation tapes some to help you sleep, others to relax. Try them. The only choice is to go where the disease takes me, I don't have to like it, but gaining acceptance helps. Keep trying, you'll become aware of what helps. Good luck.
-
Like -
Helpful -
Hug
2 Reactions