They
did not give Morphine due to Mom being allergic to Codeine, but
Dilaudid instead and since I know more about that medication, I am glad
they chose it. They also gave me "Ativan" that I can give her, and then a
combination of meds in a "cream" that goes at the pulse points for
nausea, agitation, and to assist in breathing... so far, Mom has been
able to swallow just fine, but they gave me the Atropine because it may
get to where she does have problems swallowing, and that is what is
another part of the "comfort medications". I am able to give her the
Norco just as before, she now has really stopped eating all together,
which as they said was "normal"... and she still gets a dry mouth of
course the medications themselves can do that, so she will drink of all
things it is so funny, Mom never drank any type of "Cola's", or
carbonated drinks... but when this first began, she wanted nothing but
Diet Dr. Pepper, Sprite Zero, and sometimes Diet Pepsi....
so if she
does tell me she wants a drink it is usually the Sprite Zero, with some
water in it, so it is not so "strong" with the carbonation. I changed
her a couple of hours ago, and got her all on clean and dry sheets, and a
dry night shirt, and her diapers on, then they gave me some cream I put
on the heels where the blisters were... actually the nurse told me
unless they are "weeping", to allow them to "dry"... rather than put
anything on them... so really the one heel is the only one needing much
care...
most of the other places where her skin is so thin, and like me,
she has very huge places that appear almost like "blood blisters" but
flat, and not blisters, just more broken blood vessels... and the Lupus
causes me to have those... I told her that I had to look at those "new"
types of diapers, because it has been so long since I used diapers on my
2 kids I was out of practice... LOL... and I told her that I wished we
were at the Casino, and that everyone here online, and around town that
knows tells me to say hello and tell her they are praying for her... but
I try my best NOT to disturb her...
I realize she "hurts" all over...
and just even trying to roll her gently from one side to the other to
change a sheet, diaper etc.. just plain hurts... so I give her the pain
drops, and meds, and then I try to clean her good, but not put her
through any more misery of being tossed and turned in the bed... and
today she said "ouch" a few times, but I would tell her it was me, and
that I was trying to do a "better job" that the aide as far as not
making her hurt worse... and by the time I had her dry, cleaned up and
gave her meds, she was asleep and peaceful again.... I don't know
whether I should be "posting" this stuff or not, BUT it "helps" me
honestly... have some way to "say" the feelings and emotions.... and
then I am not so "frazzled" - thus the posts help.... my back is so
messed up, I could sit in my floor, scream, cry, and gripe due to the
intense burning in my hips and down both legs....
I may have to go to my
pain doctor if I can next week and have him "up" my pain pump meds
until I can get into surgery.... but we shall see.... As I said in
another post, I continue to "learn" a great deal from those from
Hospice, and I have a high and new found respect for the people that I
have been in contact with so far.... they are definitely Angels... what a
difficult "job"... that has to be.... Anyway, back to the sofa for
me... I have to try and get my back to calm down a bit... I did not
sleep well at all last night, and had severe nightmares all night
long... so I am drained......
"Through my heart's work of writing, I share with you my complex journey a top the mountain, sliding down, crawling up, & living through the realms of Autoimmune Arthritic Illnesses. Taming "The Wolf" Thru each Day... One Step at a Time … Together We Are Learning to Survive. Please follow along, to New Beginnings - looking Thru the Window Pane of Pain in life where we shall find our journey leading us to - New Perspectives
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