hey to all my fb friends and net friends and of course my closest ones,
im just dropping few notes to you guys as you all knew i was emailing dr richard walker to see if i could use links from his pages on here with a huge smile on my face now he has said yes. the ones who know me well know i really respect this guy and was totally gutted that he retired. i would have told any of you guys to look him up.
i have put a link o his pain site wich has a lot of very helpfull information and links to other things in the uk.
i know from talking to you all there is so little out there in the uk so when there is a site as good as this one its well worth its weight in gold.
im going to post a further couple of the information leaflets of that site to here too as i know a few of you have been asking about certain proceedures they are for the uk but the information on how the proceedure is done and what to expect i would imagine would be pretty much the same
wishing you all a pain free day and night
aj
hi this hopefully is the start of helping others and somewhere for people to go that have come across, live with , care for someone or just want to learn about crps/rsd this is just my own experiance living with crps a small voice in a sea of many 1000s that have this and still a lot of those voices are unheard and are suffering every day
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