Does anyone have Spinal Stenosis that is extremely bad at wake up?

Posted by mick472 @mick472, Sep 26, 2024

I was just diagnosed a couple months ago with lumbar spinal stenosis. I have good days and uncomfortable days. I am not in severe pain, but very limited on what I can do so I don't aggravate it. But, I am having a terrible time upon wake up for some reason. I have to hold on to doors, wall whatever, as I can hardly walk. It eventually subsides as I take a anti-inflammatory and hang on in a hot shower for about 20 minutes. Does anyone have this problem or better yet a routine at night to help prevent this in the AM?

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Profile picture for heyjoe415 @heyjoe415

Hi Dallas,

Stenosis is a drag. Does it press on your sciatic nerve? You'd notice pain in the back of your legs, buttocks if this is the case. Sounds like you have pretty typical morning stiffness but no leg pain.

Take a look at my comment to jtw on exercises to strengthen the core. These will help your back.

My stenosis got so bad that I had laminotomies on S1/L5/L4 - the surgeon drilled a hole in the back of each vertebra, allowing more space for the sciatic nerve. Simple surgery, doesn't compromise the integrity of the vertebrae. It was either this or fusion, and I didn't want fusion. That was over 10 years ago and still feels good (although my lower back is stiff and sore after sitting too long). There are stretches you can do for the lower back and can just search for them on Google. Ice, not heat, helps as well. I never put heat on my lower back. Feels good but increases inflammation in its wake.

All the best to you!

Joe

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@heyjoe415 the sciatica starts each evening and both legs ache like toothaches. I have brittle bones so my exercised are with my physical therapist

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Profile picture for kmfdallas @kmfdallas

@heyjoe415 the sciatica starts each evening and both legs ache like toothaches. I have brittle bones so my exercised are with my physical therapist

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Thanks Dallas, and I'm so sorry for what you're going through.

I've had two bouts of sciatica - the first one resolved after about a month, but it was awful. Felt like an icepick in my calf.

The second bout was many years later. The disc at S1/L5 had partially ruptured. A surgeon used a minimally-invasive surgery (is that an oxymoron?) to remove the disc fragment and create room for the sciatic nerve via lamintomy. Still haven't need fusion, and that's why I keep my core strong.

Is surgery an option for you, probably fusion, but maybe something less intense? What does your back surgeon think? I imagine having osteoporosis (brittle bones) also plays a factor.

I dread fusion surgery. I've had four joints replaced - both knees, one hip, one shoulder - and got almost immediate pain relief. But if sciatica came back and the pain was chronic, I guess I'd do the fusion.

In the meantime, I suggest icing your lower back to reduce inflammation around the sciatic nerve. Never use heat as it results in inflammation and more pain.

All the best to you Dallas, and I sincerely hope you find some relief.

Joe

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I experience the same. Have you had any physical therapy? They can help with your mobility and stiffness. I have severe stenosis L4-L5 and it has made a difference along with a steroid injection. I am not perfect but am moving better. I am also focusing on stretching and moving as much as possible.

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I have lumbar stenois getting going in the morning is a ritual I'm and early morning gym person it seems when I get out of bed and my body settles and realizes it's upright some days it's like OMG so I have to get up early enough so I can do what needs to be done before I can get out of the house walking you might want to say "half way normal" hot rag compresses on my lower back (oh how I don't want to stop it feels so good) stretching is a must before I leave the house, I down a yogurt and take 2 Tylenol. I was reading in another health community site on this subject someone suggested the patches(Bio-Freeze)what I first used but they are good but expensive before bed with Tylenol so I tried it one weekend boy did it help no more hot compresses. My husband shared a couple of his lidocaine patches with me, He said he didn't like that cold feeling when applying them, I didn't care they worked for me I got a script from my the Dr. for Lidocaine patches 5%(can only be gotten through Insurance) and it makes things for me more manageable in the mornings, may drop a couple of Tylenol during the day. I'm to the point I skip some nights with the patches. Hope this can help you in some way.

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Profile picture for heyjoe415 @heyjoe415

Thanks Dallas, and I'm so sorry for what you're going through.

I've had two bouts of sciatica - the first one resolved after about a month, but it was awful. Felt like an icepick in my calf.

The second bout was many years later. The disc at S1/L5 had partially ruptured. A surgeon used a minimally-invasive surgery (is that an oxymoron?) to remove the disc fragment and create room for the sciatic nerve via lamintomy. Still haven't need fusion, and that's why I keep my core strong.

Is surgery an option for you, probably fusion, but maybe something less intense? What does your back surgeon think? I imagine having osteoporosis (brittle bones) also plays a factor.

I dread fusion surgery. I've had four joints replaced - both knees, one hip, one shoulder - and got almost immediate pain relief. But if sciatica came back and the pain was chronic, I guess I'd do the fusion.

In the meantime, I suggest icing your lower back to reduce inflammation around the sciatic nerve. Never use heat as it results in inflammation and more pain.

All the best to you Dallas, and I sincerely hope you find some relief.

Joe

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@heyjoe415 Thank Joe. This has been going on for a number of years. Rehab Drs have said surgery is not an option for me with osteo and being a DES Daughter. Physican therapy, pain meds and now my new recliner - from Relax the Back - had helped soooo much. Do not need my canes like I was relying on. I use ice.. so helpful. I have had a back week of night pain. I use Ralph's secret sauce to help with the pain.

Being a DES Daughter has been rough my entire life..especially the past couple of years.

Karen

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try sleeping on a gentle heating pad.

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Profile picture for kmfdallas @kmfdallas

@heyjoe415 Thank Joe. This has been going on for a number of years. Rehab Drs have said surgery is not an option for me with osteo and being a DES Daughter. Physican therapy, pain meds and now my new recliner - from Relax the Back - had helped soooo much. Do not need my canes like I was relying on. I use ice.. so helpful. I have had a back week of night pain. I use Ralph's secret sauce to help with the pain.

Being a DES Daughter has been rough my entire life..especially the past couple of years.

Karen

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Hi Dallas,

Well I'm glad you've been able to reduce reliance on a cane. And icing really works wonders. Too many people choose heat because it feels good immediately. Ice is an acquired taste. But heat draws in blood, white blood cells, and inflammation - increasing pain ultimately.

What does DES stand for?

All the best, friend.

Joe

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Profile picture for heyjoe415 @heyjoe415

Hi Dallas,

Well I'm glad you've been able to reduce reliance on a cane. And icing really works wonders. Too many people choose heat because it feels good immediately. Ice is an acquired taste. But heat draws in blood, white blood cells, and inflammation - increasing pain ultimately.

What does DES stand for?

All the best, friend.

Joe

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@heyjoe415 DES = Diethylstilbestrol

It was prescribed to pregnant women between the late 1940s and late 1970s. It is a powerful synthetic hormone that was also a carcinogen and teratogen. It affected my reproductive organs and my spine.

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Profile picture for kmfdallas @kmfdallas

@heyjoe415 DES = Diethylstilbestrol

It was prescribed to pregnant women between the late 1940s and late 1970s. It is a powerful synthetic hormone that was also a carcinogen and teratogen. It affected my reproductive organs and my spine.

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Thanks for the info Dallas and I am so sorry for what happened to you.

Medical science does make progress, but it is slow and measured, and even then, mistakes are made.

In the early 70s I suffered my first panic attack and chronic depression at age 18. I had no idea what was happening, and neither did my frustrated parents, or our "family" doctor whose advice was - "You need to grow up and paddle your own canoe Joe." Geez, thanks doc.

That was before anti-depressants became available, so I've somewhat forgiven the Dr. My parents shunned me though, thinking me mentally ill, and that was taboo around our house. I finally got the help I needed in 2002, almost 30 years later. I also started talk therapy then and continue to this day.

And I am in no way comparing what I went through with your situation. Bad medicine and stigma affects a lot of people.

I wish you the best Dallas. You deserve some good karma.

Joe

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I have same issue... I've been setting an alarm in mornings to wake up an hour before I need to get up, so I can take my Meds, go back to lying down or sleeping more, until I get out of bed an hour later when the meds have kicked-in.

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