Open main menu
☰
Health Conditions
Allergies
Alzheimer's Disease
Anxiety & Panic Disorders
Arthritis
Breast Cancer
Chronic Illness
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Irritable Bowel Syndrome
Lupus
Lyme Disease
Migraine Headache
Multiple Sclerosis
Prostate Cancer
Ulcerative Colitis
View Conditions A to Z »
Support Forums
Anxiety & Panic Disorders
Bipolar Disorder
Breast Cancer
Chronic Pain
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Hepatitis
Irritable Bowel Syndrome
Lupus
Lyme Disease
Multiple Sclerosis
Ostomies
Prostate Cancer
Rheumatoid Arthritis
Ulcerative Colitis
View Forums A to Z »
Log In
Join Us
Close main menu
×
Home
Health Conditions
All Conditions
Allergies
Alzheimer's Disease
Anxiety & Panic Disorders
Arthritis
Breast Cancer
Chronic Illness
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Irritable Bowel Syndrome
Lupus
Lyme Disease
Migraine Headache
Multiple Sclerosis
Prostate Cancer
Ulcerative Colitis
Support Forums
All Forums
Anxiety & Panic Disorders
Bipolar Disorder
Breast Cancer
Chronic Pain
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Hepatitis
Irritable Bowel Syndrome
Lupus
Lyme Disease
Multiple Sclerosis
Ostomies
Prostate Cancer
Rheumatoid Arthritis
Ulcerative Colitis
Log In
Join Us
Join Us
☰
Forum Home
|
Forum Rules
|
Moderators
|
Active Topics
|
Help
|
Log In
nothing can be done for L5 nerve compression
Support Forums
>
Chronic Pain
✚ New Topic
✚ Reply
❬ ❬ Previous Thread
|
Next Thread ❭ ❭
beachbumcindylou
Regular Member
Joined : Sep 2014
Posts : 51
Posted 9/30/2014 11:09 AM (GMT 0)
Has anybody been told after a nerve conduction test that they have a nerve compressed but there is nothing that can be done to fix the problem and they have to "learn to live with it?"
nvrthesame98
Veteran Member
Joined : Jun 2008
Posts : 6706
Posted 9/30/2014 12:15 PM (GMT 0)
Welcome Cindy to the chronic pain forum at HW, I read your post on the Monday check in and please let me know if you have trouble with something in the forums. You can click on my name and my email is there in my profile. Feel free to email me with any questions you may have or you can simply start a new post addressed to my or Mod and one of us will help you.
To answer your question though, yes most times there is nothing they can do to alleviate the pressure or pinch on a spinal nerve and doing so would likely cause other issues so we do eventually find anything we can that helps eve just a little and put them all together and learn to live with it!!! I know not what you wanted to hear but sadly the truth.
This is a great forum with some very awesome folks,many who have lived with CP for decades and out of that living comes experience and that is what we try to share here. Support to those who need it and sometimes just a place to rant and vent where others know what you mean!!
Welcome aboard!
Alcie
Veteran Member
Joined : Oct 2009
Posts : 5200
Posted 9/30/2014 10:59 PM (GMT 0)
Can't they even do an ablation to relieve the pain?
beachbumcindylou
Regular Member
Joined : Sep 2014
Posts : 51
Posted 10/1/2014 1:47 AM (GMT 0)
what is that?
straydog
Forum Moderator
Joined : Feb 2003
Posts : 19850
Posted 10/1/2014 2:40 AM (GMT 0)
Hi Cindy & welcome to the chronic pain forum. By chance have you had a second opinion? If you have not seen a neurosurgeon, I would suggest getting an appt with a board certified, fellowship trained neurosurgeon.
You have not given much info as to what kind of drs you are treating with. Perhaps if you provided a little more info it would help.
Take care.
White Beard
Veteran Member
Joined : Feb 2009
Posts : 3740
Posted 10/1/2014 3:48 AM (GMT 0)
Hi Cindylou and Welcome to Healing Well Chronic Pain Forum. Was this a neurologist that told you that there was nothing that could be done and you should just learn to live with it? I had a neurologist do a nerve conduction test on me and told me the same thing! He was dead wrong! I went back to my PM who had also referred me to a neurosurgeon and he was in complete disagreement with the neurologist! Anyway I went to a neurosurgeon and he looked at my MRI as had the Neurologist, and he also looked at the results of the nerve conduction studies that the neurologist done, and he said I had a bad disc and he could help me. So I had surgery, a ACDF ( Anterior Cervical Disc Fusion) at C5/6 and when I woke up from the surgery the pain in my arm was gone! Personally I have never met a neurologist that I liked or trusted! And I have met quite a few of them over the years!
So I strongly suggest you get a second opinion, and preferably by a neurosurgeon! Again I Welcome you to the forum, and I do hope you keep us all informed of your progress! When your here at this forum you are part of our Chronic Pain Family!
Good Luck to You!
White Beard
beachbumcindylou
Regular Member
Joined : Sep 2014
Posts : 51
Posted 10/1/2014 4:27 AM (GMT 0)
2010 Began seeing an orthopedic dr after having sciatic to my toes and low back pain on the right. He did a couple rounds of shots in to L4-L5 region. First shot gave some relief. Second shot did not. Did not have insurance so could not get MRI or physical therapy. Since 2010, symptoms have grown into constant low back pain on the right, Sciatic kicking into right buttock sometimes down to the toes, heaviness in right leg, started out as just numbness in med thigh but now complete right leg except back of thigh is numb, tingling and burning in right leg and right foot. New symptom just developed in past 3 days of feeling like I'm walking on daggers when I put my right foot down. Also, right leg and foot feel like it is in a vice grip.
After getting insurance, had an MRI in April of 2014. (Old orthopedic dr left practice to go back to Ohio) New Orthopedic dr literally spent 5 mins with me after MRI; said nothing wrong with my back and he can't help me. Referred me to Neurologist. Couldn't get in with him until end of June 2014. He did a Nerve Conduction Test. Immediately after the test, he told me that the nerve at L5 was compressed and that because I had the numbness, tingling, pain and burning for a couple of years that it is most likely permanent nerve damage. He also said there was nothing he could do for me and that I was not a candidate for surgery. Here is where I should have asked a lot of questions but long story short, I was so upset that his answer was nothing could be done and maybe I should try yoga and meditation, that I just lost it and cried like a baby. He did order Physical Therapy and put me on low does of Lyrica.
At PT, I learned some new exercises, bought myself the moist heating pad and found a TENS unit. I have started doing yoga and the stretches seem to help. But at physical therapy one day she decided to do "traction." She had something like a thick belt and had me lie down on my back on a tall table. She placed the "belt" under my hips. She pulled the "belt" while another therapist pullled my arms. It was not fun and I did not like it! lol Anyway, by the end of the day, my back on the left side began hurting. I have NEVER hurt on my left side!! Since then, I have low back pain across my back at all times instead of just my right. I quit PT shortly after that. The main reason being that I can't physically do the 35 min drive twice a week and the $60 a week copay.
I went back to my primary doctor and asked for his opinion and he has referred me to Wake Forest and he very cautiously increased my Lyrica to 100mg twice a day. And he's the one that has been prescribing my Norco all these years. Since the new symptoms appeared a few days ago, nothing is completely helping my pain.
Anyway, I assume I will be seeing a neurologist as they haven't called me yet to make the appointment. Wake Forest is a teaching hospital in North Carolina.
That's the point that I'm at now.
beachbumcindylou
Regular Member
Joined : Sep 2014
Posts : 51
Posted 10/1/2014 4:27 AM (GMT 0)
Alcie said...
Can't they even do an ablation to relieve the pain?
What is an ablation?
beachbumcindylou
Regular Member
Joined : Sep 2014
Posts : 51
Posted 10/1/2014 4:31 AM (GMT 0)
White Beard:
Both the Orthopedic and Neurologist told me nothing can be done and hopefully with this new referral to Wake Forest, I will find some answers!!!
Alcie
Veteran Member
Joined : Oct 2009
Posts : 5200
Posted 10/1/2014 1:18 PM (GMT 0)
Cindy
Ablation is radiofrequency ablation (RFA) - heating the pain sensing nerve until it stops working.
It often relieves things like sciatica and low back pain. My experience is relief for over a year, and it can be repeated. It's not a cure, but it's worth asking about
.
I won't go farther than 5 miles for physical therapy (PT). I did find that aqua therapy helped, but it was too far away to keep going and my insurance cut me off after 10 visits.
Lyrica works for some people with conditions like diabetic neuropathy, where the peripheral nerves are the problem. I had absolutely no benefit from it for nerve pain caused by nerves pinched at the spine. But I had no benefit from gabapentin or any of the other "nerve medicines."
I've got nerve pain from all sorts of spinal injuries and degeneration, particularly in the lumbar area, plus central cord syndrome from falling and breaking a bone spur and crushing 6 vertebrae, 2 in my neck. So my case may not have anything to do with yours.
Look up all your diagnosis words in the search box at the top of the page. You'll find many threads that might give you information.
Merrida
Veteran Member
Joined : Jul 2013
Posts : 4771
Posted 10/1/2014 3:25 PM (GMT 0)
Has a decompression been ruled out?
M.
White Beard
Veteran Member
Joined : Feb 2009
Posts : 3740
Posted 10/1/2014 7:18 PM (GMT 0)
Hi Cindylou I hope this referral helps you! I think it is just to easy for doctors to "blow off" their patients with saying there is nothing they can do! A really "good" neurosurgeon can do allot of things, granted surgery is not the answer for everything, but I have had some pretty good results from mine! Even with MRI's allot of stuff just doesn't present its self, till the surgeon actually gets in there and looks at it! It happens all the time! But to just blatantly say that nothing can be done, well I just don't buy that, at least till I am told that by a good neurosurgeon that has looked at all the test! After all they are the ones who deal with the actual nerves, and the physical structures of the nervous system! They know what can and cannot be done with surgery to help the patient.
I do wish you well and hope they can help you!
White Beard
beachbumcindylou
Regular Member
Joined : Sep 2014
Posts : 51
Posted 10/1/2014 11:22 PM (GMT 0)
Thank you everyone for your help and suggestions. It is so nice to talk to people that understand!! I will definately let you know how things go at Wake Forest.
✚ New Topic
✚ Reply