This website has been put together to provide support for people suffering from Peripheral Neuropathy.

Well – a quick introduction is always polite:

I’m Pat, I’m a bit closer to the age of retirement than I’d like, I live in the UK, and have been diagnosed with peripheral neuropathy for about 4 years. Like most people suffering from peripheral neuropathy, it was a gradual onset – chances are it has been about 15 years since it began.
Like most people unfortunate to be diagnosed with pn, I don’t have any idea of the cause. While I always try to be interesting, it is possible I’ve outdone myself with my ailments – to date, those which (I think) may have caused my p.n. are:
B12 deficiency
Lower spine problems
Central sleep apnoea which caused, over a very long time, severe oxygen deprivation

Unfortunately, the above have not yet been sufficiently corrected, so this website is as much for me to get help from you, as I am going to try to help you, by sharing information.

Please share hints about how to get referrals to specialists, feedback on treatments, how to get access to treatments, ways of coping, or just swap your war stories – anything you think might help someone else. If you have had problems getting answers, the chances are other people have too. Maybe you guessed it from the website title, but I am officially down to MY LAST NERVE!!!!!!!!!