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I had the exact same symptoms and the anxiety & depression was overwhelming. I replaced C5 in April 2020. About 6 months ago, I got so frustrated with my nerve pain & opted to go to two different surgeons (1 orthopedic & 1 neurosurgeon). I did the nerve conduction study & it turned out that I was right.. the disc was moving in an incorrect way. Both surgeons advised a fusion on c5. I chose to go with the neurosurgeon for surgery because he knew without the emg what was going on. In my experience, they are much more informative about nerve damage. I had the fusion & so far, so good! I definitely recommend trying it if you’re at your wits end. Take a chance for your freedom!
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Hi. I had a second acdf fusion 3 mos ago. Previous one was in 2005 ay C-5-6 Current one is C3-7. I would like to know if there is anyone that the swallowing problem gets better. It feels like someone is choking me at all times. My dr keeps telling me its going to go away. It's getting worse. Anybody have an answer??
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My surgery has been 5 years. Problems with swallowing has gotten extremely worse. During the past holiday I had a really bad scare. Eating corn I noticed the difficulty in swallowing. I went to the restroom and did my best to regurgitate. Unfortunately I found myself not being able to breathe. I tried to swallow water and it just ran out of my mouth. I could not breathe or talk. Kids became aware and a rush to the hospital started. At the driveway I knew I would not make it to medical assistance. Using the wood porch post I pushed under my rib while I inserted thumb in mouth. I finally chocked up 4 kernels of corn and could breathe Needless to say I have been stressed every since.
I had the Barium Swallow test on Dec 2021 as well as a esophageal test. Nothing wrong according to them.
I have an appointment with surgery doctor the first of August. We shall see.
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Just wondered if you found out what you could do?
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I am 6 weeks out acdf surgery c5-c7. Still have difficulty swallowing and terrible stickiness in throat. Dr said my plate could be more flush which makes me think it could be causing the issues. Have any of you thought about a lawsuit? I would hate foe this to be permanent. Dr says it will improve in a few months.
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I have severe belching also. Mine didn't start till a couple weeks after surgery. I would burp and immediately would feel pressure built back up. It caused me to have anxiety attacks cause the only time I didn't feel pressure is when I was laying down. Drinking anything carbonated made pressure a thousand times worse. But even drinking water caused me to burp and mild discomfort all day
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Yes I had C5/C6 Medtronics Cage infusion I'm having issues swallowing breathing feels like I can't breath at times soar ruff throat try to clear nothing getting concerned spoke to Medtronics Noone seemed concerned!! Any ideas???
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Severe pain in right side neck shoulder area into thoracic numbness in hands legs feet Awful pain after C5/C6 Medtronic cage surgery Dr's now don't seem to wanna get involved ONE said my cage is growing into my vocal cords Hard swallow choking sensation most all time Called Medtronics Noone seemed to care hard swallow rough throat dry voice all time mine was 2007 I've called in 2008 nothing from. Anyone scared I'm going to have to cut hole in my throat at times any ideas
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Health Hero
1626 posts
Hello.

If you are experiencing awful pain after C5/C6 Medtronic cage surgery, it is important to consult with your surgeon. Your surgeon may suggest some treatments such as physical therapy, pain medications, or steroid injections. They may also recommend further imaging tests to identify any underlying issues that may be causing the pain.

Other treatments may include nerve blocks, radiofrequency ablation, and spinal cord stimulation.

It is important to discuss all of your options with your surgeon to determine the best course of action for you. If your surgeons won't talk with you, seek another opinion immediately.
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