Category Archives: relationships with medical professionals

Toilet talk

I’m interested in linguistics and communication in general, so it makes sense that I spend a certain amount of time thinking about the kinds of things that Crohn’s makes it imperative to discuss. At the same time, I didn’t grow … Continue reading

Posted in coping skills, fatigue, friendship, gut problems, partners, relationships, relationships with colleagues, relationships with medical professionals | Leave a comment

New stats!

The Crohn’s and Colitis Foundation of Canada just released a report on the Impact of Inflammatory Disease in Canada. Pages 47-49 in particular, which deal with the costs of medications and their burden for patients with Crohn’s, and pages 53-57 … Continue reading

Posted in accommodations, disability, fatigue, finances, government policy, gut problems, insurance, relationships with colleagues, relationships with medical professionals, Remicade, treatment, work | Comments Off on New stats!

My diagnosis story

I mentioned in an earlier post that it took 4 years between when I first had (what I now know are) Crohn’s symptoms and when I got diagnosed. The on-again, off-again, unpredictable gut and arthritis symptoms I was having during … Continue reading

Posted in arthritis, bias, diagnosis, diagnostic tests, disability, evidence-based medicine, food, frustration, gut problems, hidden disability, immune suppression, mania, misdiagnosis, mobility impairment, prednisone, rash, relationships, relationships with medical professionals, side effects, steroids, symptoms, treatment, ulcers | Comments Off on My diagnosis story