Unique Eunice

This is unique Eunice's journey here is this beautiful little girls story, taken of her facebook page (unique Eunice - her journey) with permission from her mummy and daddy.  So here's a little about unique Eunice, Eunice was born august 2018 and everything was fine with her, daddy noticed beginning of december 2019 when she was 16 months old that her "back looked odd" and from then it snowballed, to the point  where she had an MRI 18th February 2020 and a growth was discovered on her spine which is so rare that it's only seen once every couple of years in addenbrooks, and never in someone so young. At addenbrooks Eunice has since had a 9 hour spine operation 5th march 2020, in the hope that they can obtain a biopsy as the growth is inoperable and currently untreatable, which against the odds they have achieved. Since this Eunice has had the results that she has low grade giloma and it's called spinal pilocytic astrocytoma, these are normally found in the brain, and when they are they are an easy to fix, and not even referred to as cancer, but the oncologist said due to location, symptoms and treatment (Eunice's walking has been affected due to a spinal injury the tumour has caused, she has secondary severe scoliosis and exsperces a lot of pain) that's why they are calling it cancerous inner case. Treatment plan is for a Hickman line to be fitted. Since then Eunice has had her Hickman line fitted, and started chemo this also hasnt gone to plan, Eunice  has got neutropenia ( she is less likely to be able to fight infection) so chemo has had to be persponed until her levels are a little better and they decided her base level of chemo has had to be reduced to try and stop this happening again. This is where I have made the decision to set up this go fund me to make this beautiful familys journey as comfortable and stress free as possible with less money to think about in this difficult time!!