Vice grip on both legs with both feet feeling stiff on bottoms.
I have been dealing with a leg, foot and lower back issue for 6 years now. It started with my right foot feeling like I had stepped into glue and it dried on the bottom of my foot. Skin feels very tight. Then about 2 months later, my legs started to get very tight and ache. I seem to have trouble controlling them when I stand or walk. Feel like I walk on outside of or sides of feet. Now both feet stiff and both legs feel like there is a vice being tighten down on them. I have had 3 nerve tests, all ok, a PAD test which was negative, all the Lymes tests that I know exist. I have osteopenia, had a low vit.D count but have found no relieve or a close maybe dx. Anybody else ever experience any thing like this? I have seen 3 Neurologists, a Urologist, a Rheumatoligist, my GYN and 4 General Practice Drs.
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hi, njejhwk - I loved the term "vice-like sensation" you used to describe the sensation in your calf!!! I assume you are not taking a statin? If you are, your symptoms are related. The dark red spots are a mystery though. I am trying compression socks for the swelling in my ankle due to the statin induced Achilles tendon injury. It is helping. The compression socks seem to he helping that nasty stiff crinkle feeling of the feet pads. Go figure! This feet pad and calf discomfort thing is a real mystery. Statins also mess with nerves in calves. Hopefully this
situation passes, but who knows?!!!! 🙁 Guess we will just have to keep chasing doctors to see which one can help. (sigh). d.
Just want to give a bit more information the chiropractor/doctor that I am seeing here has told me that it can be cured or very close to it, but it is not an overnight cure, he told me it could take up to two years, and I have only been in the program for three months but I have noticed a difference, but beware before it eases up, the symptoms or pain gets worse first as the nerves are starting to wake up again, so you wind up feeling a lot of discomfort and unease . I sometimes get firey feelings in my legs--which he is is absolutely normal, means the blood flow is getting back into the parts it should be going through--it is like getting a hot flush. I take something called NOx Synergy which is a source of substrates for Nitric Oxide, which is what gets your blood flowing to the muscles. The best thing is to keep moving without overdoing it. Standing a lot is a bit of a problem, if pain does get too much I do take a pain med called Diclofemex (spelling might not be quite accurate) with an addition to it to protect the stomach as it is hard on the stomach and best taken with food. Told to take it twice a day as needed, but I find one can last for a couple of days and a lot of times I do not take it for a couple of weeks or more. I always check out any pills they try to give me, if too many side effects I refuse them there are always alternatives--I will not take statins, they do more harm than good as far as I am concerned
You name it I have tried it, compression socks foot machines, none of that really worked--the electrical stimulation does help, just make sure you get the right kind, it is a very slow process sad to say.
Oh wow....Appears to be so many sources of feet and leg issues. When I looked up Letrozole, I got this feedback: "According to the Health Canada Summary Safety Review in 2023 , Aromatase inhibitors (like anastrozole, letrozole, and exemestane) have linked these drugs to tendonitis and even tendon rupture. " That's what happened to me, only from statins! WOW Amazing. But what the heck is with the Achilles tendon and these meds?!!!! Of all things to happen. Sounds like it wasn't the EMS, but the Letrozole that caused your issues. Having said the, I am not a doctor, but Letrozole and Statins clearly affect the Achilles tendon and leg/feet issue. Now if we could only find a way to fix our symptoms permanently!! Some of the drugs we use are a blessing and a curse. We have to take them to find out which applies to us. Thank you for posting. I appreciate learning about Letrozole. Best of luck to you Timely. I hope you have a speedy recovery. 🙂 d.
Thank you for that added comment Maremouse. It is helpful to know a realistic timeline for recovery from the effects of statins and their affect on feet, ankles and calves. I figured 6 months, but I see it may take way longer, and that is helpful psychologically to know. 🙂
Well, it is helpful to know Maremouse that electrical stimulation may be helpful for our feet and calf symptoms. My best guess is that the Letrozole you take and the statins I was taking, both cause problems with feet, calves and Achilles tendons :(. I just hope we both recover from the nerve damage, because that's what it sounds like to me has happened. 🙁 d.
I do not take letrozole never have . My doctor cringes when I come in, because I will tell him first off what I will not take and we have to find alternatives, and so far I have been lucky he has worked with me, if he cannot help me then he will tell me, if meds are prescribed he states they are mainly for pain and I reply that I don't want to mask the symptoms I want to cure them and this has taken me on a long road of inquiry plus trial and error, my issue I believe arises from compression in my spine, just got some results today and it is looking promising I have gotten somewhat better and he is agreeable that it is sad that it is going to hurt more before it gets better, but says that is a good thing as it shows the nerve are waking up and not causing the problems. I do keep laughing and saying I am going to cure myself before the doctors do really, GPs a lot of times do not realize what all the issues are I find. For my issues the chiropractor--decompression and the reflexology are working for me.
It is a nerve problem and doctors do not address that for some reason, they just say its a nerve problem and if there is pain they give pain meds which is not helpful. If you have the tightness on the bottom of your feet, like shoe leather that has been wet and is shrinking it is because of deadened nerves which have to be restimulated to work properly and if they do not work the problem gets worse end result would be surgery which is not guaranteed either. nerve and blood stimulation is what helps and to find out where this problem is coming from if it is your spine, then decompression helps, but a slight warning--the problem gets worse before it gets better with the treatment, you start feeling more pain for a while, but that is a good thing as it means the nerves are waking up once again. Your best bet is to find a doctor--or chiropractor--which is what I have--who deals with nerve pain/neuropathy, and sad to say they are not readily available it took me a few years to find one. My last results showed good progress but I will have to continue with it .
Hi, maremouse - Yeah, I'm trying to be patient while my Achilles tendon heals, but I am still shocked that it happened becaue of statins!!! 🙁 Thanks for another great post!! 🙂 d.
Sorry to hear statins caused your problem. I was forced to take them once only took two or three pills and quit because of side effects--my legs were so sore I could barely walk and I worked at a school that had stairs very painful, lasted for a full three months. Maybe I am one of the lucky ones quit the statin completely and have not had any problems for years until now. Hope you can get some answers soon I know it is very frustrating