Ashleigh: 'I was told my daughter would have dwarfism - they were wrong'
I wanted to share my story about traumatic births - though, truthfully, it started long before my daughter was born and has never really ended.
In 2015, aged 20, I became pregnant. From early on, I was seriously unwell with hyperemesis gravidarum, vomiting 30+ times a day for the full nine months. I was hospitalised repeatedly and was collapsing from dehydration and exhaustion.
But I wasn't believed. I was told "everyone gets sick in pregnancy". Even when I was lying on the toilet floor in A&E, passing out from vomiting and exhaustion, I was left for six hours before anyone helped me. I was eventually admitted to hospital.
Later in pregnancy, during a routine scan, the stenographer told me - unprompted - that my baby would be born with dwarfism, possibly Down's syndrome, and be abnormally small. No emotional support followed. Just fear and silence.
When labour came, it lasted for 36 hours - with sickness every couple of minutes throughout.
I begged for an epidural after hours left in a room with my mum and husband. My epidural didn't work properly. I could only feel it in one leg. They attempted it seven times before switching to a spinal block later in labour.
A student doctor was brought in while I was mid-labour and in unimaginable distress.
Hours later my daughter became stuck and both our heart rates dropped. I was rushed into emergency theatre for forceps and ventouse, which I had previously begged not to have. I had the spinal block at this point.
When in theatre they sounded alarms and everyone ran to the theatre. My mum collapsed in the hallway thinking we were dying, my mother-in-law was trying to be strong and support my mum. My husband was crying. I was lifted and tilted by multiple nurses in a panic. I was losing consciousness.
My daughter came out purple, bruised and silent. She was 9lb 1oz - not small, not with dwarfism, not a child with Down's syndrome.
I later learned that I should have been offered trauma therapy - and never was. Not a single person followed up with me about what had happened.
After we got home, I noticed my baby was yellow/tanned but again, I was dismissed. It wasn't until a community midwife visited and said she had jaundice that anything done.
It didn't stop there. As a newborn, she refused milk. I knew something was wrong, but when I reached out to specialists, I was blamed. I was made to feel like a bad or inexperienced mum.
I was told it was me. Then we were told it was me and my husband. Then when my daughter was three and we still had no answers, they said it was because I was pregnant with my son. Then they blamed the fact we had a new baby.
Now, nearly 11 years later, I am still fighting. She has since been diagnosed with a severe eating disorder. She was like this since birth. She barely eats, she is constantly exhausted and she struggles every single day with emotional regulation, sleep and pain.
We've been passed between services with no proper care plan in place. We've been ignored, dropped discharged and re-referred for over a decade. The trauma of her birth was not just a one-off event. It became the foundation of how we were treated in the healthcare system.