Originally Posted by jshire

Hi, here's what's been happening for me:

I've been going to my gp for at least 2 years with symptoms. Mine are fatigue & vague sensations in the feet / lower legs. They're not painful - more 'odd'. I'm not sure i'd even use the term tingling - its more like a buzz that some days is worse than others. If I manage to walk a fair bit then they tend to buzz even more & the sensation goes further up my legs (always below the knee though). So, I told my doctor I work with certain chemicals but after repeat visit trying to get something done he arranged blood tests & then liver / kidney scans - testing for diabetes etc. All that was found was I needed B12 injections & more recently he advised that I need Vitamin D supplements. After doing a lot of research on my own re: the various chemicals & links to PN I went back to him & mentioned it. He said it might be that (why didn't he mention this himself earlier ! I could have stopped using the chemicals sooner). It then took some effort to get him to refer me to a neurologist & i'm now waiting to see if one will see me. I'm not sure what i'm asking here - I think i'm simply feeling a bit unsure of things & what I can expect now. Perhaps i'm over worrying but I still think about whether I might have or get diabetes. I know advice says exercise etc. but whatever it is I have means I have no energy & currently spend a lot of time resting. My doc has also prescribed anti-dp's but i'm not sure I should take them as i've read that some folks think it best to wait until one sees a neurologist + the ones i've been prescribed are known to increase weight & if anything I really need to lose some weight. I'm not massively over weight but i'm not at my ideal weight for my height / age etc.

I'm 50 years old & in the UK by the way.

I guess i'm 'at the start' of all this & lots of you on here have been through all this already, but it seems there's such a lot of hassle even getting the tests let alone a diagnosis & as for any treatment !

So, i'd welcome any feedback on what i've said above & if there are any folks in here who've also had PN because of chemical exposure i'd appreciate hearing about that. Also anyone in the UK who has experience of the NHS way of dealing with all this.

ta,


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