Donald Corenman MD DC | Spine Surgeon Colorado

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dustingfab
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May 14, 2012 at 6:26 am

Post count: 27

in reply to: TLIF? #6196

Thanks for the clear explanation Dr. Corenman. So a fusion regardless of location of the spine replaces pain for stiffness. And with stiffness, a person would need to change their lifestyle and level activity.

dustingfab
Member

April 24, 2012 at 6:35 am

Post count: 27

in reply to: Vertebral Artery Stenosis secondary to cervical bone spurs (DDD) #6103

I agree completely. That makes a lot of sense.

So according the my doc, I do not have myelopathy. Yippee! Yet I’m a candidate for an ACDF procedure? The pain is there, that is one thing I know for sure. I still plan to set up second opinion visits with other surgeons.

dustingfab
Member

April 23, 2012 at 2:58 am

Post count: 27

in reply to: Vertebral Artery Stenosis secondary to cervical bone spurs (DDD) #6078

Thank you Dr. Corenman. Although, I think I exhibit myelopathy symptoms I need to make sure I hear it from my doc’s mouth. I need to ask him to define and to let me know if I have myelopathy.

What he has been saying is “at some point we need to decompress the cord/nerves” But not necessarily specific on staying whether I have myelopathy or the signs you mentioned previously.

dustingfab
Member

April 20, 2012 at 12:54 am

Post count: 27

in reply to: Vertebral Artery Stenosis secondary to cervical bone spurs (DDD) #6039

Yes, I think I exhibit some signs of myelopathy:

Lhermitte’s sign – mild to moderate

Hyperreflexia – my muscles/extremities twitch all day long. The pins and needles sensations that was felt from head to toe pretty and much calmed down since September. Now parasthesias is limited to feet and hands.

Imbalance & incoordination – where symptoms were more acute summer 2011; but no more

No clonus or hoffman’s sign

dustingfab
Member

April 19, 2012 at 4:20 pm

Post count: 27

in reply to: Vertebral Artery Stenosis secondary to cervical bone spurs (DDD) #6036

The exact impression of the recent C-spine MRI stated stable alignment, multilevel degenerative spondylosis. There is increase in size of left midline disc extrusion at C5-C6 resulting in left ventral cord impingement.

The initial MRI about 10 months ago stated: C3-C4, C5-C6, C6-C7 disc herniations. C5-C6 mild to moderate stenosis. Mild stenosis at C6-C7.

A few weeks ago my neck was severely inflamed and swollen. I experienced pain, stiffness, shoulder and arm pain and numbness. And I was significantly weak.

I noticed the swelling about the end of Feb, but I figured it was a symptom of my right shoulder surgery (Jan 2012). And I would say most of March is when my neck stiffness and discomfort went from mild to moderate to moderate to severe.

My symptoms calmed down by the time March ended and I was back to experiencing mild neck stiffness and pain. Then the TIAs happened within the first two weeks in April only a few days apart.

I’m so confused. And the only other symptoms that have been pretty consistent is the numbness and tingling in both hands and feet.

Maybe I am getting better and I’m not realizing it. When my symptoms presented over 10 months ago, they were acute. Now my symptoms are chronic and I’ve been on relafen 1000mg QD. Fortunately, I can function and I’m dealing with my chronic symptoms. But is it safe to wait. Perhaps my symptoms will remain chronic and not necessarily get worse.

More importantly, if an ACDF cannot prevent future TIAs. Then I feel like I am back to square one. Whats the point of going through a major surgery that will put me somewhat out of commission for about 3 months and in therapy possibly longer. Thank you Dr. Corenman for this forum.

dustingfab
Member

April 19, 2012 at 10:39 am

Post count: 27

in reply to: Vertebral Artery Stenosis secondary to cervical bone spurs (DDD) #6034

Thank you Dr. Corenman. I have to complete the blood work before I follow up. The results were already forwarded to my neurologist. So I assume this isn’t serious as I haven’t received a phone call to return to her office sooner than later.

The spine specialist stated he didn’t see any significantly large bone spurs that would potentially impinge the vertebral artery. But I should make sure to follow up with a neurologist.

Due to the recent C-spine, he is insisting on an ACDF. Which freaks me out. But I can only agree to this if it will decrease my risk of further TIAs/strokes.

Thank you again for reading and providing your feedback.
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Donald Corenman, MD, DC

Average rating:

81 reviews

Eric S

Sep 26, 2021

by Eric S on Donald Corenman, MD, DC

Successful pars repair at 46 years old

Back in November of 2018 (at 46 years old) I came from Vancouver BC to have a pars repair done with Dr. Donald Corenman at the Steadman Clinic in Vail Colorado. I'm finally posting this review nearly three years later in late 2021. The reason I waited so long was I wanted to know the final result before I posted my review. Unfortunately in that time Dr. Corenman has retired. Nevertheless, I want to post this review of Dr. Corenman and his staff at the Steadman Clinic in their excellent treatment of my L5 pars interarticularis.

I fractured my pars at age 42 back in 2014 when rolling on the gym floor, and was denied treatment by the Canadian healthcare system, probably due to my age. First my GP told me there was no surgical option for a pars defect, which was quite incorrect! I tried to live with it, but the symptoms worsened (periodic random spine slippage and weeks of resultant pain after just bending over to tie my shoe, so I eventually learned to mostly squat and hardly bend). When I finally consulted with Canadian spine surgeons, I was told they believed my pars defect had been congenital (since birth). This was absurd, considering I had done extreme martial arts (including jiu jitsu) for years prior, as well as 5 years of reinforcing steel full time in my 20s, probably the hardest job on the back you can find. No pars defect like mine would possibly have allowed this--ergo it was impossible that I had had the defect since birth. I did however have an asymptomatic congenital spina bifida occulta that made me more susceptible to a pars fracture. In 2014 in one instant, I went from having the strongest back people I knew said they'd ever seen, to being unable to safely bend over and tie my shoe without a non-negligible risk of my spine slipping randomly (which would lead to weeks of pain after each occurrence). This was due to the unilateral L5 pars defect, otherwise known as spondylolysis. It was when lying in pain on the floor 4 years later after maybe the 6th spine slippage event post injury, that I had had enough, and resolved to have surgery. If Canada's "universal health care" said no, I would make lemonade from lemons, and find the very best surgeon in the world at pars repairs. That was Dr. Donald Corenman. Dr. Corenman back in 2018 ran a website https://neckandback.com/ that dedicated many pages to the science of every aspect of pars repairs, from eligibility (good discs on MRI), to best surgical techniques (minimal open compared to minimally invasive), best imaging to use (i.e., O-Arm with Stealth imaging vs. older fluoroscopy), the ideal amount of BMP to use and why not use too much or too little, and much more, all to do with pars repairs, pages upon pages of his site just on the pars, with scientific references and his own extensive expert opinion. As a health research statistician, I was very impressed with this. It was in stark contrast to the websites of other spine surgeons which barely gave the pars a word or two, focusing almost exclusively on fusions. I had found the best surgeon in the world for pars repairs, and so after Dr. Corenman personally screened my MRI to ensure my discs were healthy, I booked the surgery.

Being 46 years old at the time of surgery in 2018, with a 4-year-old pars fracture from 2014 combined with a congenital SBO meant my pars fragment was somewhat atrophied, but it was "very solid", said Dr. Corenman in the operative report. Nevertheless, it was challenging with two things to fix, the pars and SBO, and OR time was around 4 hours. Recovery over the following months was guided by a very clear "Spine binder" from the Steadman Clinic with strict rules of "no BLT" (no bending, lifting or twisting), and illustrated physiotherapy guidelines. They even warned patients to avoid fish oil supplements, which could excessively dampen inflammation and hence slow bone healing. They answered many questions I had during months of recovery, with responses coming from the very supportive Lori Fugate (then director of Dr. Corenman's practice), and Ehrich Bean (then physician's assistant at the practice), as well as a couple calls with Dr. Corenman himself after two of the CT scans. Ehrich Bean offered great advice for taking the spine binder conservatively due to the nature of pars repairs vs. fusions. The final post-op CT scan I had was a couple weeks ago at 34 months post-op, and Dr. Corenman had retired, but I got a very positive and informative call from Eric Strauch (current PA at the Steadman Clinic under Dr. Corenman's replacement there, and who had also worked with Dr. Corenman previously). The staff at the Steadman Clinic were extremely supportive all the way through the process. I should mention, the local Canadian spine surgeon did offer me very good post-operative support including antibiotics as needed to deal with a mild surface incision-site infection early on, booking numerous x-rays when I felt something was amiss, as well as booking all four of my post-op CT scans. I am very grateful for that support also.

My final result shows plenty of solid bone across the pars and a healed SBO, with my vertebral body now a solid bone ring instead of being broken at two places as it was pre-op. Does my spine hold up in the real world? You bet! I have recently dug and moved several yards of dirt and sand and gravel by myself (shovel and wheelbarrow!) to fix our water main, pulled roots from the yard, moved several "portable" (these are HUGE) air conditioners up several flights of stairs my myself, and lifted weights. I now run 2 miles (3.2 KM) several times weekly with a hard 100 meter dash in the middle. I bend deeply before each run I go on, with no spine slippage. My spine feels amazing. I can bend over to do exercise, or real word tasks, with no risk of spine slippage.

My sincere thanks to God, Dr. Donald Corenman, Lori Fugate, Ehrich Bean, Eric Strauch, and the Steadman Clinic, as well as the Canadian spine surgeon who offered me excellent post-operative care back in Canada. You have all given me a new lease on life.

Sincerely,
Eric S

Robert S

May 11, 2021

by Robert S on Donald Corenman, MD, DC

Back Fusion Surgery

I had my entire lumbar spine fused in November of 2018. I had scoliosis , with pinched nerves that were so painful I could hardly walk - and standing for more than a few minutes was impossible. Even sitting was painful.
The fusion surgery produced immediate relief! And the recovery was much easier than I expected.
To this day I can do all the activities I love from hiking, to standing in a stream fly fishing to riding my bike long distances - or just walking down the street with my wife.
Kudos to Dr. Corenman and his staff, (including the two Erics) for taking such good care of me!

Leslie R

Jul 9, 2020

by Leslie R on Donald Corenman, MD, DC

TLIF

I had my TLIF surgery on 6/24/2020 by Dr. Corenman, I can not say enough good things about the Dr or his staff. I was always treated with respect and explained everything throughly, that made it easy for everyone to understand. I highly recommend Dr. Corenman and the Steadman Clinic.

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dustingfab

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