Burning |
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11/24/2017 17:44
atterz
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11/24/2017 17:44
atterz
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Burning
Anyone with Ledderhose have the feeling that their feet are burning?
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11/24/2017 18:57
Breakaway65
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11/24/2017 18:57
Breakaway65
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Re: Burning
Half the time burning the other half freezing. I sleep with 4 pairs of heavy socks on, otherwise I cannot get to sleep.
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11/25/2017 16:47
atterz
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11/25/2017 16:47
atterz
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Re: Burning
I've always had cold feet. New symptom is the burning. Wakes me up and nothing I do can seem to cool them. Had steroid injection back in September that seems to have made things worse. Can't wait until I see consultant again December 19th. Can't continue with this amount of pain.
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02/13/2018 15:23
Debbw2bees
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02/13/2018 15:23
Debbw2bees
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Re: Burning
I have LARGE nodes on my right foot and smaller ones on my left. Because the right foot nodule is SO Large, it always has pressure. This node "burns" ALL THE TIME! This "burning" is much different than being a burning "hot" feeling. My feet also "tingle". I have never experienced "cold" feet
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03/13/2018 10:14
crt
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03/13/2018 10:14
crt
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Re: Burning
May, or may not, have any significance but I noticed my ledderhose foot appeared to get hot and itchy when I was taking glucosamine.
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03/13/2018 10:23
wach Administrator
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03/13/2018 10:23
wach Administrator
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Re: Burning
Have you seen the paragraph on glucosamine on https://www.dupuytren-online.info/dupuyt...therapies.html?
Wolfgang
crt: May, or may not, have any significance but I noticed my ledderhose foot appeared to get hot and itchy when I was taking glucosamine.
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03/13/2018 11:30
Seph
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03/13/2018 11:30
Seph
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Re: Burning
atterz: Anyone with Ledderhose have the feeling that their feet are burning?
My feet often, but not always, have a burning feeling. I have Ledderhose in both feet. I take no supplements or other regular medication.
Having said that I have had Ledderhose for more than 40 years and the burning feeling is new. My wife thinks that I might finally be succumbing to diabetes. Time will tell.
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03/13/2018 21:34
crt
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03/13/2018 21:34
crt
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Re: Burning
wach: Have you seen the paragraph on glucosamine on https://www.dupuytren-online.info/dupuyt...therapies.html?
Wolfgang
crt: May, or may not, have any significance but I noticed my ledderhose foot appeared to get hot and itchy when I was taking glucosamine.
Thanks Wolfgang - yes I am aware of it. I was just trying to be cautious with asserting causality. It is another anecdote to add to the body of evidence! My experience was that I had been taking glucosamine for a while but came across a study that was questioning the efficacy. So I upped the dose to see if I could detect any difference, which was the time when my foot became irritated. I then stopped taking glucosamine and the irritation stopped. I haven't taken it since and my foot hasn't been irritated since.
Regards, Chris.
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04/17/2018 05:02
morgain
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04/17/2018 05:02
morgain
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Re: Burning
I am new to this site and new to Ledderhose, diagnosed in January of this year and have three nodules on left foot. I am suffering the burning symptom now and then they can be freezing cold. Still trying to find shoes for comfort, nodules still small. Getting orthotics made hope they will help. Wondering if this is a symptom of LD, the ball and toes and heel of my left foot go purple on standing or walking, not sure if this is LD related or due to very bad varicose veins in that leg and foot and currently the vein is leaking and the blood will be gathering in foot, goes away on resting the leg up. Getting that sorted next month, Would welcome any feedback from group. I live in UK and am on the Dupuytren facebook there. Thank goodness for these groups, so much more information gained than from the doctors. Hope to have radiation treatment eventually depending if my vein situation will let me. Thanks, Brenda
Edited 04/17/18 08:03
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04/17/2018 05:46
spanishbuddha Administrator
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04/17/2018 05:46
spanishbuddha Administrator
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Re: Burning
Hi morgain. It does sound like you have a circulation problem with your leg or foot, and hopefully you will get diagnosed with some recommendations to alleviate it. If you are already on the BDS group I assume you also know about Gary’s blog and forum for LD, one of the best resources http://ledderhose.blogspot.co.uk/.
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