Hello again, just a note to say I’ve had an article published on Independent Australia. It’s in reference to Australia’s Chief Medical Officer, Paul Kelly, referring to the deaths of the vulnerable from COVID-19 as a “reaping”.
Last post, I wrote about my experience having COVID in January and not being able to access an at-home PCR test (or any other useful support). Recovering from COVID was a slow and arduous process, but in March I felt I had maybe regained 80% of my pre-C function – that’s still not great, considering how little functionality I had to begin with, but probably as good as it was going to get.
In January, I came down with what felt like the worst virus of my life. I was weak, feverish, shivering and shaking, delirious and had a sore throat and splitting headaches. My first thought was to ring the COVID hotline, only to find the at home testing service for Disabled people had ceased to exist.
I spent hours on the phone, trying to reach someone who could help me. Alternating with lying exhausted and breathless on the couch. I was finally told to get a GP referral to ‘prove’ my need for the service. How? I asked. Just go to a GP clinic!