Wow!Thanks for all of the replies,I didn't think anyone would reply,thankyou so much!
I did some physio therapy today,could only manage 20 minutes,but that's progress.I went on the tilt table-that's where you lie flat on this table thing all strapped in and they press a button so that the table goes at a 90 degree angle and you are standing upright.It's always a great feeling to be standing upright but it's scary as well because I just can't feel anything from my waist down so it's like I'm not standing at all,if that makes sense!I also went on the bike today-well,they attached my legs to the pedals while sitting in the wheelchair and the pedals move automatically so it's like I am cycling but I'm actually not doing anything!
One of i.v. antibiotics is going in now,ceftriaxone(rocephin),2g every 12 hours.I'm in hospital at the moment by the way,have been quite sick,but doing much better now.
Maggie Anne(Mary)-I'm from Ireland too-hence the name 'creidim'-irish for 'I believe'
Thanks again everyone for taking the time to reply,I really appreciate it,it's nice to talk to people who have/had lyme disease. 