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-   -   Burning feet (https://www.neurotalk.org/peripheral-neuropathy/214552-burning-feet.html)

razzle51 01-09-2015 03:35 PM

Burning feet
 
Please help my feet have been burning a lot here latly a kind of a swirling motion
I have read about it don't now which way to turn . Has anybody else had this

bluesfan 01-09-2015 11:29 PM

burning feet also
 
Hi razzle51
Burning feet here also - currently middle of summer where I am so at its worst. Can't tell you too much about it as I'm still trying to find out myself. I have an endocrine disorder (cause: auto-immune) which causes all sorts of symptoms so it may be part of that.
Burning feet as a symptom has also been linked to: Sjogrens Disease, Peripheral Neuropathy and Vitamin B deficiencies (amongst other things), so there could be any number of reasons.
Getting relief: medically so far I have found no solutions (I don't think the doc's really get how bad it is) but I get some temporary relief from basic things like sitting with feet in a bucket of cold water. To sleep at night I wrap a freezer block (like you put in a "cooler, ice chest, chilly bin" - depending on where you're from) in a hand towel and put it between my feet - will last most of the night.
Good luck finding relief - appreciate anyone with more info re diagnosis or treatment if they could post it please.

Stacy2012 01-10-2015 09:07 AM

I thought I had neuropathy for a long time, turns out I have erythromelalgia. Burning feet. Biggest thing that has helped me is a specific laser treatment that uses the avicenna laser. I tried Klaser and others but they did not work. I think many people are misdiagnosed with neuropathy since many doctors do not know what EM is. My neurologist doesn't know what it is but admits after reading my papers that it sounds like I have it. I quit using her.

Laser has been my life line.

Stacy2012 01-10-2015 09:22 AM

bluesfan, I wanted to add that if you put your feet in water,use plastic bags to cover your feet or the water will eventually break down your skin, get infections, cellulitis, and so much worse things.

I also have auto immune hashimoto and believe it caused my EM.

zkrp01 01-10-2015 01:07 PM

I know you have heard of
 
Quote:

Originally Posted by razzle51 (Post 1117262)
Please help my feet have been burning a lot here latly a kind of a swirling motion
I have read about it don't now which way to turn . Has anybody else had this

Morton's Epsom Salt Lotion. It helped me w/ burning, tenderness.

Rosie33 01-10-2015 06:32 PM

Just some thoughts!
 
Quote:

Originally Posted by bluesfan (Post 1117324)
Hi razzle51
Burning feet here also - currently middle of summer where I am so at its worst. Can't tell you too much about it as I'm still trying to find out myself. I have an endocrine disorder (cause: auto-immune) which causes all sorts of symptoms so it may be part of that.
Burning feet as a symptom has also been linked to: Sjogrens Disease, Peripheral Neuropathy and Vitamin B deficiencies (amongst other things), so there could be any number of reasons.
Getting relief: medically so far I have found no solutions (I don't think the doc's really get how bad it is) but I get some temporary relief from basic things like sitting with feet in a bucket of cold water. To sleep at night I wrap a freezer block (like you put in a "cooler, ice chest, chilly bin" - depending on where you're from) in a hand towel and put it between my feet - will last most of the night.
Good luck finding relief - appreciate anyone with more info re diagnosis or treatment if they could post it please.

I don't think it's a good idea to use a freezer block because the cold would stop the blood flow to your feet. I use a small fan beside my bed, and have it blowing directly on my feet. It really helps with the burning. I use Topricin lotion which I add a few drops of peppermint oil, and it helps with the pain and burning at night....good luck! :hug:

bluesfan 01-10-2015 07:39 PM

Great info thanks
 
Hi razzle51 - after my first reply to you I did further reading on the PN threads and you may already have found this one: "Anyone with Anti-MAG Neuropathy?" It's been running for a few years but has some discussion about burning feet in relation to this unusual neuropathy. You may find some useful info - sorry not sure how to put the direct link in here.
Thanks Stacy2012 for the info on erythromelalgia. I hadn't heard of that so looked it up. I don't have any of the redness typically associated with EM but I do have persistent numbness in the toe & ball area of both feet and in my left hand - slowly increasing. You're right about the confusing diagnosis with PN etc. - it's important to get as accurate assessment as possible. It took more than 10 years of misdiagnosis and treatment before I was given a definite diagnosis for Addison's Disease during a near fatal crisis. Will ask the neurologist about EM (when I finally get an appt. that is).
In regard to soaking skin in water - mine is so dry/hard that it probably does it some good. I usually only leave it in for 10-15 minutes at a time for quick relief. I also use an aqueous cream fortified with Vit E and Emu oil, twice daily as a moisturising/soothing balm.
To zkrp01 and Rosie33 thanks for the suggestions - will try some of those. I have no problem with the ice block re cold restricting circulation - having it wrapped in a couple of layers of toweling reduces the chill impact - discussed it with podiatrist who said it shouldn't be a problem. Unfortunately a fan would only add to the tinnitus and insomnia.
Good luck to all in the quest for relief. Hearing others solutions is a great motivator to try something new.

razzle51 01-18-2015 10:17 AM

thanks for the responses , dr did diag me with Neuropathy .... not perifical kind ... gave me keppra and lorazapam and benedryl woring quite well ..

Jon_sparky 01-18-2015 10:40 PM

Quote:

Originally Posted by razzle51 (Post 1118962)
thanks for the responses , dr did diag me with Neuropathy .... not perifical kind ... gave me keppra and lorazapam and benedryl woring quite well ..

So we're your feet hot to the touch? How they discribed PN, they said a sensation of hot, but I realized later that this is real hot!
I just did a experiment with my Exergen infrared thermometer, my feet are real cold right now, the Ambian temp in the room is about 76 deg. The soles of feet measured 69 degrees, my palms are 84 degrees, and I am running a temperature 99.5 deg. My feet will heat up and get painful, then cool off and be cold to the touch.
My Rheumy thinks it is the micro capilaries misfiring, cutting off the blood flow, then when they heat up it has to much blood flow to the feet, she thinks it is a part of the neurological misfiring from SLE Lupus.
Hope they are helping you out with it!

briley7333 09-30-2018 11:45 AM

Quote:

Originally Posted by Rosie33 (Post 1117476)
I don't think it's a good idea to use a freezer block because the cold would stop the blood flow to your feet. I use a small fan beside my bed, and have it blowing directly on my feet. It really helps with the burning. I use Topricin lotion which I add a few drops of peppermint oil, and it helps with the pain and burning at night....good luck! :hug:

GM Razzle51-

My PN started with numbness on soles of both feet. Over 5 yrs advanced to Severe Neuropathy, confirmed with Conductivity testing 4 times.
Take 3200 mg gabapentin and 6 mg ropiniole daily. Couldn't deal the manner in which Antidepressants interefered with my sleep. Stopped opiiates. Sedation and other common side effects became intolerable.

PN pain and periodic epidsodes of severe cramping are a daily challenge.
Consultations and testing with the best neurologists repeatedly confirmed PN and kSpinal Stenosis but without effective treatments or remediation of pain.

Moved from Detroit area where I was patient of U of M Dept of Neutology that did intervene with epidurals when crises occurred but now live in Tennessee where I'm continuing to search for a neurologist to provide ongoing PN care and pain mgmt.

I take the std supplements, Magnesium, B-12, alpha liproic acid, prescibed Vitamin-D.

Accupuncture was $70 / visit w/o noticeable benefit

My primary care is a DO that performs "Manipulation", that seems to be only non-drug therapy that's proven effective for me.
Could be worth investigating for your situation.

All the best,
Briley7333


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