After all, they are a health professional and I'm just the kid's mother!
So the children’s hospital near me that my son was at...
Gives parents photo ID on bright orange lanyards that read PARENT CAREGIVER.
The ethos is that the parents are as much a part of the treatment team as the docs and nurses. Right up to being included in
every meeting, consult, reading, decision, etc. after day 1. (Day 1 = normal hospital type experience, unless you’re there a lot, but if you aren’t discharged within 24hours? Welcome aboard!) I went down to the smoke shack on day 2 all “Why are they asking me for my ideas on what antibiotics to use???” :O_o: And the other parents laughed, and said after a week I’d have a strong opinion on the matter! :roflmao:
They were right.
The hospital feels that parents only have 1 patient, and are with their kids 24/7, so if you educate them as to what’s going on medically, and how to perform basic tasks/read the machines, you’ve got someone who is
useful and not just in the way, but even better can be counted on opinion-wise. And they really, reeeeeeeally listen / take you at your word. Whether it’s worded medically because you know exactly what, or “Something just seems off” = the docs drop everything and figure out what.
:inlove: And don’t even get me started on how freaking well educated the entire staff is (from volunteers up). 2 words “sensory issues” and the dynamic immediately shifts. Same is true across the board. Pick a developmental disorder or neurological condition, and wham bam, people do exactly what’s needed, how it’s wanted, shifting gears as smoothly as a sports car. It’s a thing of beauty.
I despair sometimes of ever lessening the stigma and having more understanding of mental health in the general community when we can't even achieve it within the health professions
:sneaky: So there IS hope. It can be done. It has been done.
Now we just need to thump everyone else into line, is all. ;)