day16 08.18.14
Hello all,
Grandma had her nurse introduced to her on day 16, monday. The nurse seems to be a professional one as she wears her hospital dress at home, she's very disciplined, does not want more than 2 visitors at a time and only for 10mins, she said she will speak to my grandma most of the time,etc... Mom is at home now, she's arranging her own house routines, laundry, food,etc for dad and herself.
I've been through Sandy's message referencing Bob, been through the photos, videos. Amazed to see 2 PTs helping Bob to move his right leg, etc...hope grandma can get to those level of physiotherapy.
Well grandma can not swallow and that's why she is using the NG feed pipe through her nose, but we don't have a clue when it's going to be removed. Got to convince grandma to try and swallow more fruit juice, jam,etc... in order for her to get rid of this NG tube. I guess the reason the bloody hospital had discharged my grandma is that she can not swallow, and they had nothing to do...Guess we have to wait for grandma to get her swallowing to improve. What the nurse said is "if your grandma can not swallow the trial puree given to her, she can then have that food block her airway to her lungs, and then she can have a hard time breathing"...it sounds sensible...but the big question is, when is she going to be able to swallow ? and that can we keep trying to give her some table spoons of juice or yoghurt to see if she can improve her swallowing urge...
I guess the real PT can start after she can be fed by spoon? I will also get the MRIs on day 18 from the hospital and have a look at them myself. I have a feeling inside that the hospital did not give us enough information while they were discharging us...and that *beep* me off a little...
Anyway, patience...patience...little steps each day...
Healthy and happy days to you all,
Cheers,
Cagin
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