Danielle Russell

Hi my name is Danielle. I'm 21 years old and have done two years in a Bachelor of Early Years Teaching Degree. I was born with a rare brain tumour called a Germinoma which has affected all my hormones. It took until my 21st birthday to finally be diagnosed with cancer.

The previous 3 years my health had taken a downward spiral. The effects my cancer experience had on my friends, family and community were enormous and I'd like to share these with you.

I had a 21st party the weekend before my actual birthday date which was the day of my biopsy. The whole community was there to wish me luck, support and celebrate my night with me. The support from the community was fantastic. I even received cards from the pupils at the local primary school while I was receiving my radiation treatment. This is very special as I attended this school too and am also training to be a teacher.

My family was affected immensely by this journey. My mother had thought (like all mothers do) that she could bring me home from university and make me better. However this was not to be and soon put considerable strain on the family as I just got sicker. My biopsy in Auckland City hospital turned into a 3 month stint in hospital at both Auckland City and Waikato hospital which meant trying to run a farm on the East Coast and be there for support was difficult for Mum and Dad. Living in a city for this long soon started to get to my family as we are country bumpkins and have issues with huge crowds of people, cars and large cities. My sister and my best friend quit her job milking cows in Opotiki and moved home to help run the farm which also meant I got an occasional visit from her. Her twin brother started making frequent phone calls to my cell phone while I was in hospital to check up on me. Phone calls had previously been ghost of the past as both my brother and sister hate the telephone. My older brother who was living in Australia at the time came home for my 21st and about 3 weeks later moved back to New Zealand for good. Although the reasons why he moved back to New Zealand have not been discussed. I am secretly glad he did move back to New Zealand even if he was at Mount Maunganui.  Consoling a distraught Grandmother on the telephone while you are been wheeled around the hospital in a wheel chair is not on my list of to dos. I found this extremely hard thinking, 'It's no big deal. I'm ok .Why is my grandmother more upset than me?'

Although on a positive note I got to catch up with my mother's side of the family who live in the Waikato. We had lost contact with most of them when we moved to the East Coast 11 years ago. I was even let out on day leave from the hospital to attend their family reunion. I learnt I have a fantastic supportive family and it was great they were close by for my mother especially. This also meant there was never a shortage of visits, flowers and hugs while in hospital. It also makes follow up appointments almost fun knowing that I can catch up with some of the family and always have a place to stay. This experience had brought both my immediate family and my extended family very close. I never imagined me being sick could do so much damage and affect so many people in so many ways.

CanTeen had been fantastic in my later part of this journey. It is a safe place with a great support network that had helped me deal with my ordeal and the guilt I have surrounding it. CanTeen also helped me overcome the anxious feelings I had after not being in the social scene for a long time.

I also think it is fantastic that not only does CanTeen support patients but their siblings as well. I think this is awesome as siblings suffer just as badly as the patients. However my sister and I do not talk about our feeling surrounding this event and I have yet to get her to become a member of CanTeen.

Cancer is tough, it's a life experience and a journey but with the help of my family and CanTeen it has just become a small blip in the radar.