Bilateral feeliing loss in arms

Viewing 3 posts - 1 through 3 (of 3 total)

Author

Posts
anelsen15
Member

May 28, 2013 at 2:25 pm

Post count: 12

#8757

My senior year of college I was wrestling with my godchild and friends in swimming pool, one of them grabbed my neck in from behind and pulled pack twisting and pulling back neck at same time. I continued playing with kids, but back home in evening all of a sudden I lost feeling in both arms and could not seem to move. I had what I would call a panic attack cause of this, the feeling seemed gone but I could still move them and took some aspirin and did not go to ER. THe next day places in upper back felt like a knife stabbing them and I had numbness in both arms. Could anything other than a nerve getting impinged cause this? Doctors have said if was disc would not be bilateral. Ive had alot of wierd symptoms since and does not seem like spine could contribute to all.
MRI shows 2-3 mm protrusions in c5-6 and c6-7, and nerve conduction shows just slight irritation of c5-6

Donald Corenman, MD, DC
Moderator

May 28, 2013 at 9:41 pm

Post count: 8660

#8758

If you did not have immediate loss of motor function in the pool with the pool incident, we can rule out central cord syndrome.

I am unclear what would cause delayed onset of full symmetric loss of motor control with sensory loss that resolved within a short period of time unless something like a stroke or TIA occurred.

Possibly, thoracic outlet syndrome could cause this but this disorder is typically not symmetrical. You can review thoracic outlet syndrome on the website.

Your MRI has ruled out substantial central disc herniations as a cause.

I do not know what could have caused these symptoms. Please keep us informed if you find a specialist who determines the cause of these symptoms.

Dr. Corenman

PLEASE REMEMBER, THIS FORUM IS MEANT TO PROVIDE GENERAL INFORMATION ON SPINE ANATOMY, CONDITIONS AND TREATMENTS. TO GET AN ACCURATE DIAGNOSIS, YOU MUST VISIT A QUALIFIED PROFESSIONAL IN PERSON.

Donald Corenman, MD, DC is a highly-regarded spine surgeon, considered an expert in the area of neck and back pain. Trained as both a Medical Doctor and Doctor of Chiropractic, Dr. Corenman earned academic appointments as Clinical Assistant Professor and Assistant Professor of Orthopaedic Surgery at the University of Colorado Health Sciences Center, and his research on spine surgery and rehabilitation has resulted in the publication of multiple peer-reviewed articles and two books.

anelsen15
Member

May 29, 2013 at 7:34 am

Post count: 12

#8762

Thanks for the reply.
I have a herniated T6-7 disc impinging on spinal cord from injury long ago that does not give me much issues anymore. I have not had that checked after pool injury. I have been tested for MS, MD, RA, and several other things due to the increasing weakness both arms and legs, spacticity in legs, and alot of pain over entire spine. I have severe burning, itching and things crawling feeling in lower neck (especially right side) and the feeling of something catching when get up and down from sitting in low back, both feel very mechanical vs when disc herniation in thoracic did not restrict me in any way just high pain levels. We are repeating MRI of both since been about a year. Doctors are looking into it possibly being fibromyalgia, but some ED and incontinence ive developed has them baffled. Could there be any issue of possibly stretching the nerves of neck when kid had arm around neck and started yanking backwards with foot pushing off in my lower back?
Im very proactive and was doing yoga, exercising , anti inflammatory natural supplements etc and I know I can rehab if I just find out whats going on but no rehab or conservative measures seem to do anything, its much different than my thoracic rehab.
THe only thing that offers any relief is when I go to ER the injection they give offers about a half day of almost no symptoms and when I have had ESI it offers about a day. Inflammatory neurological condition is something I have heard also. 3 different doctors three different opinions on what it is. Frustrating to say the least. The only thing I can say for certain is that everything went south since pool injury.
My next step is a muscle biopsy. Hopefully bring something to light.
Thanks so much for this service, I am a memeber on spine health for a long time and I have passed news about this site. I hope thats ok. Its sad to see what chronic pain can do to some of the people on there . I think this is an invaluable reasource that Ive not seen anywhere else online. Thanks again
Author

Posts

Viewing 3 posts - 1 through 3 (of 3 total)

You must be logged in to reply to this topic.

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.

Submit your review
First Name, Last Initial:
Email:
Review Title:
Rating:	1 2 3 4 5
Review:

Check this box to confirm you are human.
Submit Cancel