Cadense shoes for balance issues: good or bad experiences?

Posted by brotherchuckles80 @brotherchuckles80, Apr 14, 2024

I am researching shoes for balance issues due to my neuropathy and drop foot. I have read great reviews and then precautions because they will slide on wooden o tile floor. Anyone out there in neuropathy and drop foot land had any experience with Cadense shoes; good or bad?
Thank you,
Charles aka brotherchuckles80

Interested in more discussions like this? Go to the Neuropathy Support Group.

Hey , I wear Brooks shoes too , they have Ghost on them for specific shoe . I had hip trouble with the On Vlouds. I loved them when I played pickleball too ! Bon

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I had a stroke and have PN too. My left side doesn't work very well and I have balance issues. I tried Bozo the Clown stability shoes without good results. Tried my Brooks running shoes and they were stable with good traction. Pricey but at my pace they will last a long time. It took hard work and many attempts to tie the laces, but you know? The laces are great daily OT. Hint: laces of a contrasting color are helpful. my laces are white on black shoes and extra long so I can double knot.

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Profile picture for christina58 @christina58

Hi, I bought a pair of Cadense trainers recently. I have MS and minor foot drop. However I found my usual size was too small so returned for exchange. I believe others have found they run small. I tried out the exchange pair and I’m returning them. I found they felt too unsafe on slippery floors, like tiles. I would be worried about wearing them in wet weather and given their cost I don’t feel they’re right for me.

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@christina58.
I had no luck with Cadence also. They run small and too slippery. It was disappointing. I would never recommend them.

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Profile picture for christina58 @christina58

Hi, I bought a pair of Cadense trainers recently. I have MS and minor foot drop. However I found my usual size was too small so returned for exchange. I believe others have found they run small. I tried out the exchange pair and I’m returning them. I found they felt too unsafe on slippery floors, like tiles. I would be worried about wearing them in wet weather and given their cost I don’t feel they’re right for me.

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@christina58 I hear you Cristina. I have had had them now for over six months. I too had to exchange for a bigger pair resulting in an an uneasy feeling. I solved that by wearing two pair of socks or one thick pair. solved the slickness of the teflon soles, I have sanded them down a bit but I am still very cautious when wearing them.

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Hi, I bought a pair of Cadense trainers recently. I have MS and minor foot drop. However I found my usual size was too small so returned for exchange. I believe others have found they run small. I tried out the exchange pair and I’m returning them. I found they felt too unsafe on slippery floors, like tiles. I would be worried about wearing them in wet weather and given their cost I don’t feel they’re right for me.

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Profile picture for hdrake @hdrake

I was diagnosed with Parkinson's a few years ago and have taken two unusual falls. I say "unusual" because in both cases I suddenly found myself face down on the pavement with no idea how it happened. I have had one or two falls where I was out of balance and could tell that I was falling with enough of a warning that I could make adjustments to the fall to minimize the impact. But these two falls were sudden, unexpected, and a complete surprise ending to a normal walk. I am now convinced that's the Cadense shoe people have correctly traced this type of fall to a difficulty in lifting the foot forward at the beginning of a new step and creating a shoe that is friction-free in the front of the sole. I walk about a mile a day and have been using their shoe for about 6 months with no falls and am increasingly developing confidence in their design. I realize that not all PD patients have this type of fall, but I believe those that do will find relief in the Cadense product.

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Thank you for your comment! I, too, had a sudden fall and experience as you described; fractured some bones in my face, etc. I don't have Parkinson's or drop foot. Saw a neurologist a month ago after that fall, had a number of tests including EMG. So far haven't heard results other than that it was an abnormal test. Neurologist gave me appt for late November. Was not familiar with Cadense products but will look into those shoes. Also looking into Medical Alert devices.

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Profile picture for domiha @domiha

I had laminectomy in 2022. I could walk again but began to notice the numbness and tingling in feet. Balance was a problem. Surgeon suggested I let him check my neck. Found a disc pressing into my spinal cord at C-4/C-5, so I had a fusion of that disc in my neck. Balance issues did not improve after that surgery. Surgeon says he could go back in and do a lumbar fusion and that might rid me of the numbness and tingling in my feet... but he thinks the balance issues are still residual from my neck. The word "might" causes me to hesitate to have the fusion. It's a HUGE surgery .... and at 73, I'm just not sure I want to go through that. I hate the numbness and tingling... but the worst issue is the balance and weakness in my calves ... so I can't walk as far. Anyone had a fusion and found it improved balance? As for shoes, I have some "Grand Attack" barefoot shoes that I got on Amazon... and they have been a huge help to me. They give room for my toes to spead out in the toe box. Best to all. Mike

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Hi Mike - I had cervical stenosis and had a laminoplasty, which was very successful, but I got to the doctor too late and have some spinal cord damage = balance issues. Also have scoliosis and fusion from T-10 to S1 was suggested. I have a hard time walking and standing, but I will not do this surgery *primarily* because I don't think they have taken sufficient account of the balance issues -- which are as your doctor noted in the C-spine, and which the fusion will not address at all. In my case, anyhow. And if I fall down and break any of that hardware, it's back to the OR and a more extensive surgery. I'm 69 and I really do not want to spend the rest of my life in and out of surgery and in constant pain, which depending on what happens with Medicare may not even be available to me. Final note about the fusion: the recovery is extremely painful and takes at least a year. Check out the Facebook groups on spinal fusion for some real-life stories. Good luck to us all!

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Profile picture for brotherchuckles80 @brotherchuckles80

I got them from a drop foot and they work beautifully for that. For me nothing helps me with my balance. I am attached to my Walker in the house and outside the house. If you find something that will correct my neuropathy therefore my balance issues please let me know. Thank you God bless you, Charles AKA brother chuckles80

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For my drop foot not from my drop foot.

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I got them from a drop foot and they work beautifully for that. For me nothing helps me with my balance. I am attached to my Walker in the house and outside the house. If you find something that will correct my neuropathy therefore my balance issues please let me know. Thank you God bless you, Charles AKA brother chuckles80

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