HiTBI carer here
I'm so angry all the time. I'm struggling with my husband's changes after his TBI but it's other arm chair neurologists telling me what to do etc. I know they're trying to help but it overloads me. How can they know what's best when they're not living with it? Always making arrangements behind my back and never considering the risks. I've had no follow up appointments with the neuro team, just left to navigate my way through all these changes without any professional support.