Hello all...It has been a few months since I've posted, I do apologize...Meg went back for her 6 mo check in May and her curve had gotten worse and is now 55, so we are going to do the spinal fusion. We meet, with the surgeon on Wed to iron out all the questions and stuff, but the nurse called today, saying the schedule is filling up and we have Meg down for July 19th....Now that we have a date I am really nervous and going thru a whole new gammit of emotions...If any of you have any advise for me to ask the surgeon or any questions? I have pages of questions but you have been there.....I would really like to know of anyone whose child had this who is non mobile/non verbal...My Meggie has CP, is non mobile, non verbal... Just curious.....Thanks in advance.....I am just ready to get this over with. I am literally sick over this.....I know God is driving the bus and I need to sit back and let him steer, but sometimes that darn old human nature kicks in and that is hard to do....
Thanks
Tracy
Thanks
Tracy
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