When I was 16 I was diagnosed with crohns disease. I had 6 years of hell with it. I came out the other side but no medical professional or my parents offered any kind of mental health support. I'm much older now and reflecting on those years. I don't really know how bad it was in relation to other people's trauma. To summarise:
-I had 12 months undiagnosed where I lost so much weight I was skeletal. No one suggested IBD to me, I thought I was dying
-I could eat or even swallow food without being sick
-I had an endoscopy and colonoscopy at 16 without sedation
-I started to have accidents. I was doing my a levels at the time and would have to change my underwear before college started
-constant pain and nausea
-my bowels would make the most horrendous noises, I would have to sit through lectures/exams with the noise and people sniggering
-I started to lose my hair. I remember sitting in the hair dressers and it was coming out in handfuls as the hairdressers brushed it.
-the medication made my face balloon, I didn't recognise myself at all
-meds also made me flush, I would go puce/scarlet, people would comment
-rumours in college started that I was anorexic
-I developed a blood clot and glandular fever due to low immune system
-was in hospital on an adults ward at 17, very very poorly with parents only allowed regular visiting hours.
There's more but that's the worst of it.