Hi, this is my first post...I would like to know if anyone has experienced what I have been experiencing which is excruciating pain from my ankles to the bottom of both feet??? Unfortunately , I haven't been able to stand on my feet at all.
Pain on bottom of feet: Hi, this is my... - My MSAA Community
Pain on bottom of feet
I have had pins and needles with pain in both feet and hands for twenty three years 🤬 Off and on in left thigh 🤷🏼♂️🐾🐩🙏 Ken
I have pain in both my feet everyday. My legs, thighs and hips at times. I usually just keep myself moving. If I just try to rest it feels like it hurts worst. I know it is very painful but if therapy taught me anything it's to keep it moving. I'm sorry your in pain.
My feet to my knees feel frost bitten most days.
Heat helps some. Likely meds for neuropathy would help but I don't want the side effects.
Oh what a great analogy! I had terrible frostbite from a Mt Rainier climb years ago, and my feet and toes feel just like that.
My feet burn every night as I go to bed. It feels like I've walked a ten K marathon on hot blacktop. It's not bad in the daytime but I really struggle to get to sleep. Can't have my feet touching anything, I just hang them over the bed. Gabapentin helps some.
Yehealth, it's Fancy1959 and I would like to welcome you to our extended family. You have found an incredible chat room where it is safe to ask questions, like you just did, voice concerns, or simply speak to others who truly understand what you're going through. This chat room is full of some of the kindest, most caring, and compassionate people I have ever met. What would help us if you told us more about your MS and what you are currently doing about it. Do you have a neurologist? What type of therapies or MS medicines are you on?
I have tingling in both my feet. It starts about ankle high and goes down to my toes. My arms tingle and are numb from the elbow down through my fingers. The dexterity is pretty much gone for my hands and I have no tactical sensation left in my fingers. I have had it for several years now. And I take neurontin to control the intensity of the tingling. Now do not go out and get a prescription for Neurontin and try it yourself. We are not doctors we just are simply sharing what works for us. Make sure you go to an MS specialist neurologist if you don't have one and if you do have one get in and ask questions. Keep a journal of symptoms you have in questions you have so when you go to see your doctor you don't forget to ask everything you wanted to.
Since walking is kind is important to most all of us it is pertinent you get in to see your doctor as soon as possible. Please keep us informed of what is going on. I am glad you have found this chat room! The more you post and answer post the quicker we will get to know you and you will get to know us! There is much we can learn from each other! Until we speak again please take care and remember together we are stronger!
Oh, yeah. Off and on for more than thirty years. I have found that keeping them moving helps...
I take pregabalin zentive love them they not only stop my feet from feeling like there stuck in a bucket of ice but help me get a good nights sleep 💤 💤💤 as well TTFN