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#1 | ||
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Newly Joined
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A year ago I was golfing and it felt like my sock was rolled up on the bottom of my right foot. It got worse over a couple months as it progressed to outright pain on the ball of my foot when I walked (especially on hard floors) Fast forward a year. Same symptoms in both feet. Can't were socks and only certain sandals allow me to walk fairly comfortably. This month random pin prick sensations began over all body and severe itching on top of left arm. At night toes 2 and 3 curl down. I've seen many doctors including neurologist who said no MS or ALS but beyond that he jsut said you have idopathic neuropathy. Had blood test for know causes-all neg. EMG of right leg abnormal but not awful.
Anyone have a similar start to their neropathy ?? What other tests should I ask for ? I'm 67 and was in very ggod shape until this started Thanks Bob |
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#2 | ||
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#3 | ||
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Newly Joined
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No diabetes. Vit B 480. I still don't trust the negative Lyme test. Thanks for your reply
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#4 | ||
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If all the usual suspects have been rounded up and eliminated, many here DX as Idiopathic. That means no known source or causal factor. If you have lurked around and read, you know that PN can be triggered by many things. Vaccine shots, Industrial solvents, Chemotherapy, Spine & Joint trauma, Floroquinilone Antibiotics,environmental contaminants plus Tick bites. Lyme testing, as I recall, is not the most foolproof thing. Good Luck, Ken in Texas. P.S. These are not all the things that bring PN, just the ones that jumped to the front of my mind.
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#5 | ||
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Ken I read your list of neuropathy causes like the secretary in Ferris Beuller's Day Off listed the types of people who liked Ferris.
Sadly, this is not a righteous illness, does seem to afflict some nice people, though. It brought a smile to my face, thought I'd share.
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I urge you to please notice when you are happy, and exclaim or murmur or think at some point, "If this isn't nice, I don't know what is." - Kurt Vonnegut "It's an art to live with pain, mix the light into grey"- Eddie Vedder Just because I cannot see it, doesn't mean I can't believe it! - Jack Skellington |
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"Thanks for this!" says: | zkrp01 (09-09-2015) |
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#6 | |||
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Wisest Elder Ever
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We keep out B12 at around 1000 here. If you have the methylation mutations, which are common, then your reading may not reflect ACTIVE form of B12. So you might consider 5mg of methylcobalamin daily on an empty stomach and see if you notice improvements...3 months should be long enough a test to see. Methyl form is the active form and best to use. It is only pennies a day. This is our B12 thread... http://neurotalk.psychcentral.com/thread85103.html Methyl form is now at Costco, and some stores like Walgreen's. Online also at Amazon or iherb. It works out to pennies a day for most brands now.
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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