Has anyone suffered from lumbar spinal stenosis? Did you have surgery?
Has anyone suffered from lumbar spinal stenosis and the severe pain that goes with it? Did you have surgery? Mayo Clinic?
Interested in more discussions like this? Go to the Spine Health Support Group.
Greetings, all. I am a member of "My Chronic Pain Team" website but stumbled on the page as well, so I thought this would be a good place to seek an opinion. Or two.
Here's what i posted there (wondering what you guys think as well):
My surgeon said no surgery. Said he didn't think it was necessary. I got to say, with so many other doctors saying I need surgery, and the pain getting worse, not to mention quality of life, I was a bit taken back, and disappointed.MRI report below, in case some of you haven't seen it:IMPRESSION:
Moderate degenerative canal stenosis and moderate bilateral foraminal
narrowing at L3-L4.
Mild multilevel canal stenosis and foraminal narrowing at L2-L3 and L4-L5.
Disc degeneration from L2 through L5 most significant at L3-L4 with Modic
type I changes.
Thank you.
Welcome @davidstory,
Your concern is certainly understandable. First, I’d like to underline that although we cannot diagnose medical problems on Mayo Clinic Connect, it is Mayo's longstanding history to share information beyond our walls through patient education, shared experiences, expert video, and much more.
You may also notice that I moved your discussion and combined it with this existing discussion on spinal stenosis as I thought it would be beneficial for you to be introduced to the many members who have discussed similar conditions.
If you click on VIEW & REPLY in your email notification, you will see the whole discussion and can join in, meet, and participate with other members talking about their or their loved ones' experiences.
There are quite a few different discussion threads where members talk about spinal stenosis. Here are few that I’d encourage you to view:
– Laser treatment for spinal stenosis? https://connect.mayoclinic.org/discussion/laser-treatment-for-spinal-stenosis/
– T.E.N.S. for spinal stenosis pain https://connect.mayoclinic.org/discussion/t-e-n-s-for-spinal-stenosis-pain/
– Chronic Pain members - Welcome, please introduce yourself https://connect.mayoclinic.org/discussion/welcome-please-introduce-yourself-welcome-to-the-new-chronic-pain-group-im/
In the meantime, I’d also like to invite @barbarn @leslie324, @gailb, @mamie, @shoregal45, @annmerc @trishanna, and @lollypop to share their experiences and the treatments they have found to help them.
@davidstory, how are you managing the pain? Has your doctor explained why they feel that surgery is not necessary?
I have also been diagnosed with Spinal Lumbar Stenosis and I am having an MRI in a couple of weeks! I cannot have Surgery, because I have Epilepsy and am allergic to Anesthesia! I also have Asthma, and Osteoporosis; so my only choice is Physical Therapy and walking! I absolutely sympathize with your pain, and hope you feel some relief soon!
I need some help I can’t find any doctors willing to help me because I am young and Medicaid denied another MRI even though it has been 3 years and I was suppose to have one after 6 months I have cervical spinal stenosis I can’t lift my arms up or I get tingly and lose feeling I’m my arms which I am 25 I have 3 babies which is very hard to manage considering my diagnosis. I have a cyst inside my spinal cord from t7-t9 which wasn’t compressing on my spinal cord at that time I have multiple lateral process transverse fractures on the right side with chronic Pseudarthrosis so they don’t heal themselves and arthritis which I don’t even know what kind I was never told I was just told these diagnosis shouldn’t be causing me as much pain that I am in which I had never taken pain medication at the time and they were the only thing that made it so I could walk and care for my kids at all which I have a lot of addiction in my family and now my body relies on them and I used to lose feelings in my legs and fall all the time which I haven’t fell in almost a year so that is good news but I feel so weak and like my muscles are getting so weak and I don’t know what to do anymore I need help from someone and I feel like they just left me for dead cause everyone is too scared to paralyze me because of the cyst most chiropractors won’t even touch me and now the crack down on medication. I understand it I really do but where do I go from here?
The cure sounds worse than the pain. Is ART very painful?
@chas93 No doctor I, but I was getting to the point of not being able to grasp things, or lift heavy, slippery stuff, or other stuff. Long story short - went to a physical therapist and am getting the help I need. You will need an order from your doctor for insurance to cover, and your doctor will also know if this is a safe activity for you. Well worth a try, please?
I went for 2 months I didn’t help but my dr wants me to try a different physical therapist and see if that works. I want to find someone that will try the nerve block so I can do physical therapy even that is hard on me to do I just feel weak and tired and just not myself anymore I have had these issues for 4 years and I feel like it is really starting to take a toll on my body and every like 6 months I get really sick with 106 temp and horrible stomach pains I don’t know if it is related to the blunt force trauma to the stomach that cause the spine to fracture from the inside because the right colon has asciatic fluid and wall thickening and usually with those injuries you have a internal injury also and I was never told from a dr about some of my diagnoses I went and got my car scans and mri scams on my own cause I felt like not everything was adding up and I have had interest in the Mayo Clinic but I live so far away from there. I know there is someone that can help me just don’t know how to get there?
I feel like all of my mucsles and joints are locked up and it’s extremely hard for me to get going especially in the mornings.
@chas93 Really can't talk about some of your problems, but I would not be walking without my physical therapy. Diagnosed in 2007 with spinal stenosis and told most women with that problem use a cane. Well, this is 11 years later and still no cane. Had to fight to get PT, bit it was worth it. After PT, I feel like the Tin Man in the Wizard of Oz, with all my rusted joints oiled!!!!
@chas93 You mentioned you had or have back fracture Have you gone to an Orthopedic Dr? for this? You do need to be under Dr,s care if your not I hope@ Colleen Young the connect director will reply as she can give you information on the Mayo Clinic in Az,Mn,and Jacksonville Fla also satellite Mayo,s .