I also saw an opthalmologist since birth.
In terms of my development, I was slow to talk and walk (I didn't talk or walk until I was 3) and my language development was also slow making doctors think that I had a learning disability (it was later confirmed that I didn't). Doctors also blamed my total blindness since it was difficult for me to be mobile and explore my environment due to the fact that I couldn't see.
Because of my slow language development and inability to talk or walk until I was 3, my mother placed me in an early intervention program with a psychologist who worked with me on speech and language starting when I was 4 years old.
After that time, I was put into an early childhood program when I was 5 and held back a year.
My mother decided to hold me back so my slow speech and language development wouldn't have a negative impact on my ability to learn thereby making school more difficult for me in the future. In looking back, I think she made the right decision.
At aged 2 i still wasnt able to sit up or walk so i had regular physio
i didnt talk properly till i was in nursery school i think because thats why i started getting proper teaching etc. every child in ma school had speech and language therapy from the deputy head every week or so. after receiving my implant at 10, when i started secondary at 11 i started receiving Speech and Language Therapy from a speech therapist till i was 14 years old which i absolutely hated cos i had to miss Phys Ed swimming lessons. Till i was around 13 years old i didnt kno the full extent of ma hearing loss, i did not know that i was profoundly deaf(my mum and my audiologist notes usually writes im profound which is confusing as some say severe-profound)
At aged 2 i still wasnt able to sit up or walk so i had regular physio
i didnt talk properly till i was in nursery school i think because thats why i started getting proper teaching etc. every child in ma school had speech and language therapy from the deputy head every week or so. after receiving my implant at 10, when i started secondary at 11 i started receiving Speech and Language Therapy from a speech therapist till i was 14 years old which i absolutely hated cos i had to miss Phys Ed swimming lessons. Till i was around 13 years old i didnt kno the full extent of ma hearing loss, i did not know that i was profoundly deaf(my mum and my audiologist notes usually writes im profound which is confusing as some say severe-profound)
How do i find out which one i am? severe or profound?
How do i find out which one i am? severe or profound?
To Hear again, we are similiar!
I was only 2lb 1oz just a bit bigger than the other poster
I had severe respiratory syndrome also, many blood transfusions was on a ventilator, had mild ROP, lots of infections, fits at a day old, blood poisioning, my lungs kept collapsing so needed lots of chest drains etc. but im now perfectly healthy and just deaf.
I was born at 28 weeks, my mum went into premature labour with me and my sisters. we were triplets but my sis Emily died at 5 months old.
I dont know as i dont have any recent audiograms
Well when i was 15
my right ear was
0.25- 90
0.5-95
1-115
2-120
so my right ear is profound?
that was done when i was 15 i am now 18
I have had hearing tests since then but dont have the results. the last hearing test i went for, i didnt evenget the results.