Before I was diagnosed, I noticed my feet going numb and hurting when I exercised. Now they are hurting other times. When I am up I don't notice it real bad but after I have been sitting and then walk, I feel it - especially in the evening. I am just wondering if it's really MS or something a podiatrist could help with. I have bought lots of shoes to help with no avail!
There are several people in our swim group who talk abut the pain they have in their feet and the problems with the toes curling in painful ways. Some folks here have talked about the foot pain when walking.
Hopefully someone will stop throug here and share their personal experience with you.
I too have foot pain. Like Ren and Wobbly, it feels like walking on rocks, or pebbles, or stones, depending on the day. I also get pain along the tendon of my big toe, and stretching does help but doesn't totally fix it.
Shoes tend to drive me nutz and I change pairs about 5 times a day. Like the others, I have just learned to live with it, using hot, cold packs and a tens units occasionally too. Not comfortable at all, but one of the myriad MS symptoms.
Hang in there. If you find a creative solution, jen, please share it with us.
Thanks for all the advice :) I am hoping that this will not stick around. My symptoms have been mild since being diagnosed last April. To jump to this permanently would be devastating as I am only 38. My worst fear is not being able to walk, UGH! But I will remain possitive and try some of your lovely suggestions, I really appreciate them.
It's possible that your foot pain is MS related but it's also possible it's not. This is the challenge we all face with any chronic disease. Obviously it possible to have more than one thing going on in our bodies especially as we age.
Why don't you discuss with your dr/neuro and see what they say. Perhaps a podiatrist is in order. Shoe inserts helped me tremendously with my on/off foot pain.
I don't have foot pain, but when I get going with exercise, I get numbness (mostly in my L foot) and spasms (bilaterally) in my arches or individual toes, or along the tibial nerve to the top of my foot.
Yeah, I'd see your podiatrist, but I'd see your neuro, too.
The pain that I have just started to happen in the last couple of week's It feel's like the bottom of my foot separate's from my toes.Only when I walk on it. It's like I broke my foot in a straight line that goes from the little toe to the big tow. I know this sound's confusing, but MS to me is confusing. Does anyone have the same feeling
I too have foot pain. I was recently diagnosed with MS after years of going to my neuro and complaining of numbness and tingling on my left side that eventually turned out to be pain on the left side. My foot pain extends out into the toes and is quite severe. Walking on it is always more difficult when I first stand up. My doctor has me on Gabapentin for pain (and Copaxone shots) and it does a pretty good job for me. I am so sorry you are experiencing this but you are not alone.
I would go to a doctor and ask about this.I was diagnosed with plantar fasciitis when I was 28(understand the only a certain age thing)I also have fallen arches and I pronate inwardly.I suffered for many years before I got the right footwear...but needed specially made orthotics(helped soooo much!Unfortunately,I got diagnosed with ms at 35,and always feels like I am walking on rocks...got some tingling and burning with this pain(ms type symtoms (symptoms)...in my hands too)I wonder if having both ms,and feet problems is just working against me.But serioudly, get it checked, because if it is something orthotics can relieve, you will never regret it.I need to go and get some more made,because I lost mine in a house fire,and now walking these days is torture!!!Even AFTER I get off my feet they hurt and burn for hours after I take a walk ,or do my housework!All the best.I hope this was helpful.
Sorry for your pain ,it gets you down I know .
I have had foot pain for over 4 months now and have taken lyrica tablets which has helped slightly but not cured the pain,the best way to describe the pain is thumping and like electric waves running up and down the sole of my feet :( I guess I just need to live with it ..I too wondered if it was related to MS and turns out it is very common.
The origins of this thread are pretty old. Many of the original participants, including jen673 no longer visit. I just didn't want you to think she was ignoring you :-)
About foot pain, mine was pretty bad. My feel felt like someone had dropped a bowling ball on them or like they were being squeezed in a vise. On really fun days it was both!
It took a while to dial in the right med cocktail, but we did. I take 100mg Lyrica 3X/day and 75 mg Elavil (amitriptilyne) once a day. Fore reasons that can't be easily explained anticonvulsants like Lyrica and, or antidepressants like Elavil seem to quiet neuropathic pain.
I'd ask your doc about adding to your Lyrica. My relief is nearly 100%.
I've had pain for several months, always worse on my left side(where most of my MS symptoms are). I finally saw a podiatrist this past Tuesday. My left foot has a fracture and a neuroma! I'm in a boot for 8 weeks! I hope you get some relief soon!
hi i have realy bad foot pain burning and feel like i am walking on stones hands are the same and neck fell over tonight with itseen doctors and a spicalest wbo gave me a sterod injecionand has taken xrays of feet and hands dose any one no what this could be thank you
If you have pain in both hands and both feet it doesn't sound likr typical MS. MS usually effects one place at a time. My foot pain, before the meds, was much worse in my left foot than my right, and I have no pain in my hands.
Xrays will show if there is anything structural, like a ruptured disk, that might be causing your symptoms. To see if there is a nerve related problem you need to have an MRI. When are you seeing your doctor again?
I have just had a brain MRI ( 4/29/15 ) and what the doctors thought was Fibra has turned out to be MS. My sister has had MS fro about 7 - 8 years now. I am 65 and my feet started bothering me. My big toe and the ball of my foot and then the other toes. Feels like electrical shorts. Mostly my left foot but both have pain. My doctor gave me gabapentin and it doesn't seem to do much. I am also taking duloxetine which was prescribed for Fibra.(09/2014) when I had pains in my arms.
I see the nuero next week and can't wait to get something for my feet. I have a cage type device to keep the sheets off my feet because when the sheets touch my toes it feels like someone is trying to pull my nails off.
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