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Anonymous
Fibro and PLIF

I have Fibro and have for years. Luckily mine is not debilitating. I am curious as to how Fibro patients heal after PLIF surgery. Anyone have any experience with this? I know everyone heals at a different rate, but I wonder if actually getting up and around will be more difficult due to the Fibro pain in addition to the back pain.

I have Grade II spondololisthesis, severe DDD, spondylosis and stenosis at L5-S1...

I am looking at a two level fusion L4-S1 on March 10th.

User offline. Last seen 5 weeks 7 hours ago. Offline
Joined: 07/03/2008
Posts: 287
Points: 578
Hi - I think it's increased my flares

I'm not officially diagnosed with fibro, but during my recovery, I can tell that I've had a few days feeling like I've got the "flu" and then it lifts. During the 9 weeks I was off work, I probably had 4 times of 2 days like this. Since returning part time, I've had a flare last Friday. I've also noticed the fog is worse.

Right off though, immediately after surgery, not sure if it was due to the IV antibiotics and the muscle relaxers, I haven't had the allover aches as much as now that I'm not taking all the meds and returning to work.

I know everyone is different. I hope you have the best of luck with your surgery and recovery.

Melisa

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ALIF L4/5 07/08, PLIF L3-5 12/08, ACDF C5/6 06/09, ACDF C4-6 08/09, PCDF C4-6 03/10, ACDF C6/7 03/11, Hardware removal posterior C4-6 11/11. Several MRIs, 3 myelograms, discogram, several lumbar ESIs. OA, DDD, DDJD. Just plain tired of hurting.

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