As many of you know, it was cerebral palsy awareness day yesterday, and I did a lot of work for that.
What I didn't tell you though was my story, which started 31 years ago in Kingston-upon-Thames, UK. My parents Anne and Paul Hayward had married a few years before and they decided they really wanted a baby. I was born one of undiagnosed twins, and I was the "surprise" baby, being that Mum had been reassured by her gynecologist that the pregnancy was going ok and there was no need to worry. Mum's due date was in march 1982. At the time, her sister Debby was pregnant with my cousin Michael who was born full term and isn't disabled, who's less than a month younger than me the way things actually worked out, but I'll leave that for my book which I'd also like to share with you once the first chapter is done (soon I hope! ), OK, I'm rambling a bit , so I'll stick to the title of this blogpost.
Mum felt unwell and went to the gynecologist who said she was in labour.
My sister Natalie Jane Hayward was born on 22/12/81 shortly before me.Mum's labour was difficult and the Doctors thought she was done when they noticed I was coming. We weren't breathing at all when we were born, and were taken to the NICU. We weighted 2lb 6oz each and were born 3 months early. Despite her fight, Natalie passed away at 9 days old. We both almost did when we were 3 days old and had an emergency baptism by Hospital staff and a priest.
I was still in the NICU. The doctors were worried about my head size which was growing and growing. I was diagnosed with hydrocephalus, which literally means "water on the brain". This isn't water but cerebrospinal fluid which surrounds the brain and protects it. I can't re absorb or control the amount of CSF, so the doctors put a shunt inside my head when I was 2 weeks old. The shunt drains the CSF from my brain to my stomach. The doctors also noticed I wasn't moving much at all and diagnosed me with spastic quadriplegia cerebral palsy . In total I was in hospital for 3 months. All my disabilities were caused by a grade IV brain hemorrhage (brain bleed) .
When I came home the doctors saw I was developmentally delayed and I couldn't see at all until I was 1 and a half years old. I use an electric wheelchair and wear glasses, although they don't correct my severe visual difficulties and I'm registered blind. I have astigmatism, hemianopsia (blindness in one half of both eyes) , squint in both eyes nystagmus involuntary eye movements (my eyes constantly wobble from side to side) no lateral vision and spatial awareness difficulties meaning I can't judge distance, speed or depth. I require help in everything.
My shunt was changed 4 times between birth and 11 years of age, as I had symptoms of vomiting, severe headaches and dizziness plus visual disturbances.
I went to a special school in Sussex and then onto Mainstream school in Oxfordshire where I had full time one to one assistance. I noticed I was different from other kids when I was 7 and I was mostly ignored by them.
I'm really proud that despite my disabilities I finished secondary (high) school and went onto University (College) twice, but graduated from one of them. I'm fluent in Spanish and engaged to my lovely fiancée Alfredo. I have had good times and bad in my life and wouldn't change any of it or the fact I'm disabled for the world, as I know no different.
Please feel free to see my YouTube videos "Introducing ....ME! " and " my education as a person with complex multiple disabilities" as well as the rest I've made since last Christmas (subscribe if you like). My Channel username is cpchick. .
My identical twin sister and I were born 3 months premature weighing 2lbs 6 ounces. Lack of oxygen caused a grade 4 bilateral brain bleed. I had cardiac arrests and multiple lung collapses. I have Spastic Quadriplegia Cerebral Palsy and Hydrocephalus. I was on life support in the NICU for my first two weeks of life. Everyone thought we'd die. . My sister did. I have a shunt inside my brain for my hydrocephalus . I survived when no one thought I would. This is my story
Tuesday, 26 March 2013
Monday, 25 March 2013
A couple of days ago, I found out that today is cerebral palsy awareness day in the USA.I'm not from the USA (I'm from the UK), but this was the day that I felt I wanted to mark as important because I have been doing disability and cerebral palsy awareness
work now since October last year which was when I started my Katherine Hayward my life with cerebral palsy Facebook page the link to which you can find here
http://www.facebook.com/KatherineHaywardMyLifeWithCerebralPalsy?ref=hl
I started my awareness work, I have got to know a fair amount of people from the USA with cerebral palsy either through Facebook or YouTube.
As a person with cerebral palsy myself I have many life experiences to tell. In my case I don't just have cerebral palsy, but
have hydrocephalus and severe eyesight difficulties which are registered as blindness.
So the question is this: why did I get into awareness work? Well, the answer for me is simple. Cerebral palsy is one of the most common childhood disabilities, yet it is largely misunderstood by people. Hydrocephalus is even less understood from my experience, but that's another story and one I'll blog about separately and also during Hydrocephalus Awareness Week. . I guess from an early age , I got fed up with all of this ignorance
from people regarding my cerebral palsy and hydrocephalus and in particular cerebral palsy and I was always eager to educate them about it. I was the first person in my primary school with complex
physical disabilities, I have never liked society 's attitude towards disabled people. I suppose that was something I always wanted to try and change, no matter how small my efforts seemed to people. Looking back, I kind of wish that I started the awareness work I do earlier in my life, as I'm really enjoying it and I like the fact that people respond positively to it and are interested in my story and
what I have to say it based on what I live due to my disability as it's easy for them to maybe imagine what it's like to live as a person
with multiple complex disabilities, one of them being CP, but I realise that the only people who actually know what it's like living with disabilities are the people who have them I spent a while preparing for today, and I have done a variety of awareness related tasks during the day. I made a YouTube video and also posted different pictures related to cerebral palsy awareness on my Facebook page.Alfredo also painted my nails green and I wore green eyeshadow for the video, as I don't have green clothes, and I love makeup. All in all it was a very enjoyable day, and some of my Facebook posts today are some of my most "viral" yet! :)
It's all in a good cause and that's CP!
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