Really, the fact they spent thousands trying to cure my DD says different to ME. The fact that state of the art equipment and treatement was available for her treatment without me having to even consider the cost says different to ME. The fact she had regular, safe, blood transfusions says different to ME. The fact that she had physio, OT, wheelchair services, home tutoring and ultimately palliative care so she could die at home says different to ME.
We never got kicked out of a hospital bed because our money ran out. She wasnt denied MRIs because our insurance didnt cover it. She wasnt denied treatment because she was going to die anyway. She got whatever she needed.
I had two homebirths because that is what I wanted and needed. I had two others in hospital without having to work out how much it would cost me.
I have an appointment with a specialist next week because I need the help.
My DS sees an excellent specialist nurse for his skin condition every three months. I can get an appointment with my GP within a week for a non emergency.
My DS has been diagnosed via NHS small.
The battles i have had regarding his LDs and ASD have been with the LEA not the NHS.
NHS is fucking brilliant.
It has faults - they dont include denying children chemotherapy and pain relief because their parents are uninsured or ineligable for medicare.