April 6th 2019 (Twitter Thread on Disability and Consent)

This entry is part 5 of 5 in the series Heavy Content

CW: Disability, Consent, Ableism, PTSD A thread I read yesterday got me to thinking about my interactions with people in the outside world – especially on the bad days. Specifically, to the different ways people respond to various mobility aids and my particular flavour of broken. See, there are good Continue Reading →

Chronic Illness as a Caregiver: Don’t Burn the Whole Candle

This entry is part 3 of 5 in the series Heavy Content

  Being a caregiver for someone with a chronic illness sucks. There, I said it. Watching someone you know and love live in constant pain, or watching them slip away from themselves and who they’ve always been is a battle in and of itself. Nothing can prepare you for watching Continue Reading →

Chronic Illness: Lacking a Manual (Part 1)

This entry is part 2 of 5 in the series Heavy Content

Chronic illness is hard. Strangely enough, that is actually something that needs to be said. In the first world we are trained to expect answers.  Honestly, I think that this training is part of why chronic illness is so hard to deal with – both by the people living with Continue Reading →