hi i have posted before when i thought i had ms but been told its my nerv syst thats closing waited 5 years to be told and the last neroman i seen was really nippy when he told me he said i had been widly talked about and that was it there me n hubby sitting looking like 2 numptys saying what is it so told me and said still the same nothing they can do some of the things i have are really along the lines of ms the bladder for a start if anyone is getting the botox please dont worry i have had it done and im due again to have it done no pain and worked bout 70% they might give me more this time will know in october for the dont know but i really ill ask bout nerv systm my own local doctor didnt know either that i was supposed to be told i know i forget things but i would have rememberd what was making me feel so ill i always take hubby into room so i dont forget it was a woman and all she kept going on about was how much i drank (not touched a drop for 17yrs) and what happend when i did harry just sits there and takes it all in what they say but i remember that day when he came out he was blazing mad and we went right to doctors and seen a locum and said i wanted to go to edinburgh n repeated the story feel really let down by them over this the nero that is the bladder men are really nice well thats my rany lol but well i know some of you out there dont no either and gives you another roaad to go down karen
