That was my thought. I don't know where I would be without the faith my team has in me recovering. Without them cheerleading me to give life a chance despite the length/duration/severity of my illness, who knows where I would be.

As a patient, when I am underweight, I talk endlessly and seriously about wanting to die. Those feelings are very real when in the depths of my illness, and i feel i do have capacity at these times. This coversation was very thoughtful, but I do fear such discussions about palliative care and EDs.

Significant conflict of interest.
Vile propaganda

www.thecanary.co/uk/analysis/...

Even having a window in my bedroom door that anyone can look through was enough to trigger my ptsd, we need to be treated with dignity, not constant observations and restrictions. It instils a sense of fear that makes me more dependent on maladaptive behaviours

I am in favour of assisted dying but im extremely wary until society accepts, appreciates and supports the sick & disabled to live. I don’t trust a society who forever calls us a burden or scroungers to make decisions in our best interests. The article was genius

I saw this art and I really don't think people understand how much disabled people like me are framed as "burdens" as it is - maybe it would be better for everyone if we were to end our suffering. It saves our families money & time caring for us. The taxpayer money.

So, as seen in Canada...