Hi everyone,
Thank you so much for sharing & signing this petition. Please don’t stop! We need as many people to see this as possible until it gets into the right hands.
I have been in touch with my local superintendent, district principal, MLA, nursing support services directors, PCQO and the office of the ombudsman and everyone blames everyone else.
I have been told directly by Nursing Support Services that this decision was made by the Nursing Professional Body and that our neurologists don’t have a say in this decision. Apparently nurses trump doctors?
However the “honourable” Adrian Dix is quoted as saying, “We have a plan, an approach that’s founded on the advice we get from the neurology group at BC Childrens Hospital … I’m not going to be changing that over that advice.”
Wait, what? Read it yourself in this CTV news clip:
He is lying. I am not surprised but I’m sad and disgusted.
Our neurologist who is the head of BC Children’s hospital has said that as long as Noah carries a prescription for rescue medication he should have a care plan and support from Nursing Support Services and someone trained in the school setting to administer rescue medication.
His life depends on this rescue medication if he has a seizure.
Please share this with anyone you know. I’ll continue to post updates as well you can follow us at @ourlittlefamilyofthree on IG.
Thank you. ❤️