Photos of our concert adventures, a couple of months ago that I have only just found these PAs are more than carers or more than just people, that showers and wipe our ass. We do lots of things and it allowed me to access the community in the same way as every body else where my visual impairment and other needs can be managed safely, but whilst still accessing the community which I live in which me and my friends have created for ourselves and allows me to be part of their lives. They need to stop seeing PAs and carers, but especially Carers that are employed by their service users that just go round wiping shit/urine of peoples asses because trust me we do a lot more and sometimes I think even social care underestimate what PAs actually do an actually don’t have any clue about what gets done. About what gets done for and what has to be accomplished with the service users which brokerage and social care fund because I know when my social workers come round they have no idea what my PAs help me with even though you could spend hours and hours telling them and they’re still asking the same question a week later
April 30, 2025
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Same Difference 