Donald Corenman MD DC | Spine Surgeon Colorado

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connect2maryk
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October 9, 2014 at 10:28 am

Post count: 8

in reply to: How To Get A Diagnosis #11506

Dear Dr. Corenman,

My question this evening is concerning the multiple lucencies in vertebra C2 and T2. I had completed all labs for multimyeloma and they were negative. My daughter’s boss’s husband is an oncologist. After reviewing the scan he too, believes as well they are benign. The neurosurgeon I see on campus has suggested an MRI to be repeated in 6 months to be safe. He said that a bone biopsy was, “No walk in the park.” I have also seen a “movement” neurologist (Upper right quadrant pain and neuropathy). He ordered a brachial plexus MRI w/wo contrast for the neuropathy and pain in my right upper quadrant. The results were no lesions, no compression, musculature was normal, right lung apex was unremarkable. No lymphadenopathy was seen. The report again noted multiple hemangioms/lipomas redemonstrated with C2-T2.
Is it possible the multiple hemagiomas are causing weakness and pain in my neck, right arm, right shoulder and shoulder blade? The diagnosis that was given before the MRI (brachial plexus) was brachial plexus neuritis. This was after an examination. My husband said that every time I was tested for sensations on my right side with the pin tip I felt it was the dull end. I know the lower portion could be from my spondylothesis or previous schwannoma surgery, but this upper body pain has me unable to drive a car, blow dry my hair, etc…
The neurosurgeon said he can fix the neuropathy for my legs and feet with invasive bone fusion, but I am still trying to fine answers for this debilitating pain in the upper quadrant. He himself was at a loss. Many, Many thanks in advance, Mary

connect2maryk
Participant

July 26, 2014 at 5:08 am

Post count: 8

in reply to: How To Get A Diagnosis #11218

Dear Dr. Corenman,

Thank you for all your suggestions and directions it has been very helpful. I am still bouncing back and forth in the system. I am due to have a CAT Scan of the L5-S1 next week to view fractures.
I had a cervical CAT Scan on the 15th, the neurosurgeon asked if my doctor had informed me of the lucenies. I had not been notified. I requested my report from member services today and it read, “Numerous small lucencies are noted throughout the vertebral bodies and posterior elements. Findings raise the possibility of a marrow replacing process such as metastatic disease or multiple myeloma. No evidence of a pathologic fracture.
I emailed my doctor to tell her the surgeon informed me and I requested my report. She responded with ordering bloodwork for multiple myeloma. Two years and counting with no one believing me.. if I didn’t insist on a recheck for my Schwannoma I wouldn’t be as far as I am today. Does every lucency suggest cancer? Thank you- Mary

connect2maryk
Participant

July 18, 2014 at 1:38 am

Post count: 8

in reply to: How To Get A Diagnosis #11188

Dr. Corenman,
Thank you so much for your response!!! My schwannoma was on the right side. I had a laminectomy of L1, L2 and portions of L3. They started gradually after the schwannoma. The debilitating pain was gone. I did have issues with my back, but the paled in comparison. I was surprised that the sensation that lingered was my left second toe (glass sensation). I was surprised because it was my right side that was affected.
Last week I was sent to a new neurosurgeon and he confirmed your thoughts of L5 nerve injury, but he told me that the feeling of “walking on glass” is not related to that specific area. I should be having the sensation on the top of my feet?
You are an absolute blessing with this board. I have had so many responses from physicians where I believe they feel it is psychological… but the pain is so very real.
Thank you so much,
Mary
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Viewing 3 posts - 1 through 3 (of 3 total)

Donald Corenman, MD, DC

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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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connect2maryk

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