I was diagnosed in 2007 when I was 13 with CRPS. One of 6 diagnoses but definitely my most painful.

Most of my health issues I have had since baby and as I get older they just get worse. Or more things come up.

I was diagnosed with my most painful diagnosis late last year. I was still 18 at the time. I've been symptomatic for many years before that though.

I'm 17 and I'm only diagnosed with amplified musculoskeletal pain syndrome but my doctors are almost 99.99% sure I have fibromyalgia but it's hard to get an official diagnosis because I'm still a kid

I was 16 at the time of my diagnosis(I only have two diagnosed at similar times, I suspect others but I don't want to deal with it yet and enjoy my denial at the moment)

I was 20 when I was finally diagnosed with autism. My younger brother was diagnosed when we were children, and I spent my whole life being ignored, and being told that I wasn't like him - I didn't need the kind of supports he needed, I needed to take care of him, to be more patient with him, etc. No one even thought to consider that I might be autistic, too, and now I'm facing burnout and struggling to find supports as an adult 😔 Aside from that, I was JUST diagnosed with fibromyalgia after living with "Amplified Musculoskeletal Pain Syndrome" (A word that would make doctors either question me or roll their eyes due to being unaware of it) for years

A kid, I was about 15-16 when I started getting truly diagnosed but age 4 I already had been diagnosed with ptsd(later, into cptsd) and panic disorder and GAD when I was in a program meant to address these early onset issues

Technically diagnosed as an adult, but suspected when I was a minor

I developed ME at age 12, didnt get diagnosed until age 22

Adult for everything

But had it as a kid

I was diagnosed with POTS and EDS when I was a kid, chiari malformation when I was 18, and gastroparesis at 19

As a kid I was diagnosed with pots iga deficiency and amps

an adult, but to be fair i havent even been an adult for a full year yet. i got my ankylosing spondylitis diagnosis innn march i think? thats the main one

Adult. My parents wrote off all my symptoms as me trying to get out of school/chores as a kid/teen. It wasn’t until I started dating my now husband that I realized (with a lot of his encouragement) something wasn’t right with my body.

I was only diagnosed with ADHD as a kid. As an adult, I've been diagnosed with multiple anxiety disorders, EDS, POTS, and MCAS. We also suspect Endometriosis, but that can only be diagnosed with surgery. My symptoms were always written off as "normal" growing up

As a kid, shortly after I turned 5 when I was diagnosed with ulcerative colitis and some of my other issues that came later (psoriasis, psoriatic arthritis, kidney stones, etc) are suspected to be extraintestinal complications of my UC. I'm grateful my parents believed me enough to seek answers because teachers certainly didn't and thought I was just using it as an excuse to skip school...

an adult. my 21st birthday I found out I am on the verge of liver failure. 21 sucked.

Adult at 24 diagnosed w Fibro