new to the site but not to hms was diagnosed when i was 18 now 37. since i had my daughter in 2007 my hms has got worse constant back ache & fateigue. I was in a real bad place at christmas dont think i could of got any lower. Went to see profesor G & he has refered me for the re- hab program in London all though i live in the north west. He also thinks i could have pots as well so going to see yet another doctor in london regarding this. Could anyone tell me wot to expect at re- hab at stanmore london. I am alittle aprehensive about going as it`s a 3 week stay with out coming home leaving my daughter & husband at home.
would love to hear from anyone who is awaiting an appointmant at stanmore
Ann
) Actually the ward is closed at the weekends, so you are only there from Monday Morning 'til Friday morning/lunchtime. Because you have to be there early on the Monday, I travel down on the Sunday evening and stay at a hotel nearby, although the hospital has accommodation that they can put you up in if needed (I'm not sure if you need to pay for that, it is for family members of patients usually). I've stayed at the premier inns at Watford and Borehamwood which are both a short drive away. You can see the RNOH Stanmore website about transport, hospital transport or how to get there if making your own way.