Do you have specific questions about the B vitamins?

rose

Daniella
 

I have no advice at all. I just want you to know your thought of,it's
so hard when you don't know what's wrong and sometimes scary when
you do. You are in my thoughts and prayers. Just keep posting and
when you get your Neuro report give us a chance at it. Now a days
they rush you though everything and make you wait far to long for those
blasted reports. Take care honey :hug: :hug: Sue

Thanks. I'm just so nervous about another med. I hate how I feel overall with that spacy and dizzy. Has anyone went med free not pain meds but like neurontin etc and still see progress in recovery or are meds really essential. Maybe I just need to keep trying till I find the right one. I guess for the b I'm just nervous making things worse and the side effects of added things making me dizzy/spacy even supplements. Yesterday I did take my b complex and magnesium,multi,glucosamine.I guess I will try the b12 I bought 1000. I had another set of blood work but just got the written and have to discuss but they said though some off no real concern in the report. My b12 is now 1500. I have high liver enzymes that I knew in the past,low white blood count and bun. Like I said in the past my blood work though never shows even when I ended up in the cardiac unit for a week it was pretty good so I'm not that trusting. Especially I'm dizzy,nausea,so thirsty,always stomach problems,and then this. I had tests of diseases of all kind auto,systemic,blood sugar,celiec. So frustrated. For long time I thought I had celiec but in these blood results no. I have the high liver,bloating but constipation but when I do go its explosion,nerve issues. Sorry to go off so long but thank you again.

Lots and lots of B12 is a very good thing when trying to heal. The only danger is in having too little.

rose

Thank you. I really read all about the b12 and am going to take them. I know I asked this in the past but has anyone seen any other natural things that help like diet or supplements other? I'm going to start my neurontin but still wonder is everyone on a med like this or alternative? Is it practically a must for pn relief?Does sometimes the pain just stop or go away like an injury with time?

The vitamin forum has lots of information about supportive supplements.

rose

idiopathic peripheral neuropathy
 

I was diagnosed this disorder abut 3 years ago. Initially my symptoms presented as a more serious disorder as the peripheral nerve in my left arm and hand had been destroyed by the disorder. It grew back about two years ago and now I am left with this disorder all over my entire body which according to my neurologist is an unusual presentation. I am currently on a reduced dose of cymbalta as the usual dose affected my thinking. I find that at any dose it will work providing you live in a geographical area where the barometric pressure remains above 1005 and is rising. If it gets beyond 1040 bp then 60 mg of Cymbalta will work to the degree where I was able to snow shoe about two miles without symptoms. When the pressure falls I prefer to do as little as possible. Has anyone else had this experience with barometric pressure and Cymbalta.

I react to barometric pressure with increased pain too.

But I don't take Cymbalta or any other antidepressant or Neurontin.

I get more misery with rapid changes esp to LOW.

Wow this is a post from me from a long time ago. Anyhow I am on Cymbalta increasing to 120 and on neurontin. I am impacted greatly by the weather when it is cold,snow,etc I am in such high pain but this was before I started these meds as well. I don't see the connection between the meds though with myself but that is not saying it is not with you. I have been told though the pain dose of cymbalta is 120. I used to be on 60 and it did nothing and then was told that it was the depression dose. Feel better

I react to pressure changes as well. No medication involved. I'm not sure the Cymbalta would have anything to do with that. What does your doc think?