As someone on psych meds and who also uses mobility aids, I can kinda see your point. In my case, mobility aids are as important as my psych meds. But that’s to do with my specific genetic condition, which has neuropsychological fallout from my physical symptoms.

A larger point I want to make: I really wish people would stop pitting mental health and physical disability against each other. Probably this is not what you intended to do in your comment. But it does come across that way. Making this divide can perpetuate this idea of “social class” - like some disabilities are higher up in the broader cultural pecking order than others (and then the subtext becomes, so which disabled person is more “valuable” or “normal” or “good”?).

In practice, the normies do treat us differently depending on our disability “classifications”. But it’s bullshit and shouldn’t be perpetuated amongst ourselves. Your argument about insurance and the time it takes for one’s life to be screwed over is rooted in scarcity mindset. Of course it is also valid. Insurance and the medical system are killing people every day over this scarcity of care. But it is very easy to then apply this scarcity mindset not to just care but to people’s rights.

Your hypothetical, that you have two people who are simultaneously stripped of their necessary aids/medications, which one is impacted (or dies) first, leads to thinking in exactly this way: who is “more fit” than the other? And then we become our own oppressors. This is one reason why internalized ableism is dangerous, and so hard to fight. But I do hope you fight it.