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Looking for advice
Hi. I am new here. Female age 64. I've had neuropathy in my feet for several years and currently take Metanx. 2 months ago I had a stroke and now my neuropathy seems to be getting worse. I just saw the information about B12 deficiency and would like thoughts on this. Thank you
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Great to meet you!!
Janicer, :Wave-Hello: It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place. Here is a couple of forum to check on: Peripheral Neuropathy: http://neurotalk.psychcentral.com/forum20.html Vitamins, Nutrients, Herbs and Supplements: http://neurotalk.psychcentral.com/forum49.html Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
One other thing you might consider--
--is Central Pain Syndrome, also known as post-stroke pain or thalamic pain syndrome, which produces neuropathy like symptoms through damage to the thalamus or spinothalamic tracts of the brain and spinal cord (these are important relay centers for the processing of sensation)
See: http://centralpainsyndromefoundation.com/ http://www.centralpain.com/ |
Hi everyone,I'm new 2this site n finding it great.just a question,iv ad a av shunt put in nearly 2weeks ago,all went well.but today I find it hard 2 consentrate and light is really affecting my eyes.just wondering if this is normal,I'm new to shunts n not sure what 2expect after surgery.thanks so much.xx
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Great to meet you!!
Sammy, :Wave-Hello:It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place. Here is a forum you need to check into: Hydrocephalus: http://neurotalk.psychcentral.com/forum14.html Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
B12 shots, pain afterwards
Hi, found this site on the web hoping I can get some insight.
I noticed everytime I get a B12 shot in the rump, I'm out of commission for several days. It's so painful I can't even sleep at night. It's like a knife stabbing me if a move. And it last for about 3 to 4 days. B12 is very low so Dr gave a prescription for shot every week at 5000 units each. It even makes me nauseated and my appetite is low almost like a flu symptom. Has anyone else had similar problem? The pain in the rump is the worst like a knife or pinched nerve. |
Quote:
Do you know what your B12 level is? Are you severely anemic? Severely anemic patients when given injections of B12 may have temporary low potassium, as potassium is grabbed by the bone marrow to make red cells quickly. So eating potassium rich foods is a good idea. You don't really need injections. Studies show oral can work if taken on an empty stomach, daily. 5mg of activated B12 called methylcobalamin works and is not expensive or hurtful and invasive. Here is my B12 thread: http://neurotalk.psychcentral.com/thread85103.html methylcobalamin is now available at Walgreen's, and Costco. You can also buy it online. Pennies a day. |
I have my B12 injections in my arm. Sometimes sting when I get them but don't hurt afterwards. Have you asked for them in your arm?
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B12 & nerve pain
Hello,I am new to this site.11 years ago I had electric shock pains in my left leg,behind the knee.They were severe and I have been left with nerve damage and disability as a result.
While in hospital with this problem they found that I had B12 deficiency and I now have a jab every 3 months to sort that out.There are no side effects from the B12 jab, it does sting for a short while,but that is all.A simple blood test was all that was needed to check. I also went on Gabapentin for about 7 years-.Although left disabled the shock pains subsided,but now suddenly they have returned.I am back on the Gabapentin and am now trying to get the pains under control.:grouphug: It is scary and my heart goes out to others on this site that I have been reading about. :grouphug: |
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