I was 23 when I contracted Viral Encephalitis on the other side of the world miles
away from home in a strange city. I had been doing the back packing thing and had
like many other young New Zealanders come to England for a look around. I had meet
my partner 6 months previously and at the time this illness hit we had just booked a
six month trip via India, Bangkok and Bali. Ironically all the places you expect to
contract encephalitis not in the United Kingdom.
It was a Monday morning when this illness struck me and it all happened in the space of
fifteen minutes. One minute I was fine then the numbness started, then the feeling
light in the head. Next thing I knew I was in our office foyer looking at two ambulance of
ficers and had apparently suffered a seizure. I was admitted to St Thomas Hospital that
day and was released from King College Hospital almost two months later. My partner rushed
to hospital from the middle of London to be told after a mountain of tests that they had
no idea what was wrong with me. I had a very high temperature and continuous seizures.
The strangest thing at this time was that I was so alert that when friends would come to
visit I would go and have a cigarette with them only to return to my room and suffer
serious seizures again.
The first diagnosis for my illness was ecstasy related illness which would have been fine but I hadn't touched and ecstasy tablet in almost over a year.
The next diagnosis was Epilepsy as there is a history of it in my family but it's purely trauma related. Then it was Malaria that I had contracted
over 7 months earlier on my way to the U.K. in Indonesia on a 2-day stopover. Mmmm. By this time my partner was beside himself and was watching
a girlfriend he had only had 5 months slowly die in front of his eyes and the scariest things for him was that nobody could tell him what was wrong
with me and this was meant to be a hospital. After 2 or 3 days he was called back to the hospital at 3 in the morning and on arrival was told that
there was nothing they could do and they didn't think I was going to last the night. But I did.
The following day I was booked in for a Brain Biopsy. I had been extremely uncooperative
up until this point and at times extremely violent with the staff and the only person
who could calm me down was my partner. Then a doctor who had been training in New
Zealand came in to visit me and I became his long lost friend. It was this man that
saved my life and diagnosed me with Encephalitis of the viral kind.
I was moved to Kings College Hospital to recover and put on a rigorous course of anti-biotic's and Acyclovir (not sure of the spelling sorry)
the encephalitis drug. I have very little to no memory of around that time but do know that I underwent over 10 Lumber Punches and 15 MRI scans
during that period. The hospital staff were brilliant hospital I would need constant care and he had to continue working to support us as neither
or our families could really afford it. The day my memory started to return I began to see people I went to school with in the hallway of my ward
and was extremely frightened. When I asked the doctors they said this was normal and a good sign.
I left hospital after almost two months of which I remember very little. I spent hours
picking up all our ornaments and belongings trying to remember where they came from and
the event that they belonged to. Slowly my memory came back and my mother returned to
New Zealand over which I cried for almost two days and then a friend that is one in a
million took over the job of caring for me while my partner battled on for us.
We left London for South Africa to my partners parents a month later and for six months
I concentrated on recovering and didn't work. In October of that year I went home
for nine months. After nine months at home in New Zealand and finally being able to
work again I returned to London to face my demons and prove to myself that I could make
it out there again. And I have! Since then I have been back to South Africa and am
now working in London again but will be going home to New Zealand for family reasons
in two days. My partner and I are getting married in January of next year in South
Africa and he is the most important person in my life and my allie in the entire
emotional backlog we both have had to deal with due to this ugly illness.
I have a very strong character anyway but I remember the turning point in my illness
being that I would never see my little brother and sister again and there was no way
in this lifetime someone was going to cheat me of that! So I fought and I won and
apart from having to take one tablet a day and a few eye twitches I have recovered
100% and will never ever look back. For anyone reading this who has contracted this
illness my advice is this. Don't stop fighting, read all you can to understand the
illness and surround you sick loved one with as many friends and family as possible
because it counts more then you could know.
Good luck and keep Fighting