Well we made it there and back and for sure a draining day. I have pics and will post as i can i have had a total of 2 hours sleep in 2 days so not sure how long i can prop myself up..lol
From what i got from doctors his count is at 300 but they still wanna keep him a few days more not make sure all is still going well
Hey all we are leaving tonight to go and gonna be there by 6 am hope to be back by tomorrow night and then will have pics to show hope everyone enjoys there holidays
More and more its looking like Micah will be in the hospital. For 3 days his white count been at 0 , not really understanding how but with chemo theres is alot i dont understand. I will have pictures depending whether i go tomorrow or Monday. I want to wish you all a very Merry Christmas
looks like we are going to see Micah one way or the other, Doc restricted visits to Family only but its been strictly family anyway. I want to really thank all who have been thinking of micah and sending out prayers because when things seemed at the worse things seem to happen for the better. I hope each and everyone one of you have the best holiday and hope you all have the joy you have brought to mine
Well got up early today and made my usual call and he was having yet another transfusion and fever hasnt broke yet but he seems to be getting better so maybe he can be home for Christmas
Well everyone seems to have got sick all at once so unless a miracle we wont be able to make the trip to see Micah for Christmas, we just can't take that chance making him sick.I have my moments and i start to cry. I know it all sounds so selfish but its all i ask for the holidays
So far His Dad tells me he is doing ok a little hair loss and still not much of an appetite and he takes a shot daily to boost his T-cells . Right now my biggest concern is getting well cause noone can go around him sick and i cant even have a cold..:-(
My son Mike called me today he got to come home briefly to do some things, he told me they are doing 14 months of cemo.3 days this month, 5 days next month and 5 days the next and then from there gonna slow days down a bit. It did spread to the bones but they seem to be hope full after 14 months of cemo whatever is left will be removed through surgery.
So much like a dream my life has become
each day let you get close hoping I dont get burned, can you promise me forever can you promise me i wont get hurt can you say you wont make me cry.... No none of these even you can give.. but each day I go on
