Four months ago, Claudia Burkill’s family announced that her terminal brain cancer was in remission and she was no longer classed as terminally ill. Their happy news was shared around the world
But last night, only a few short months after celebrating a miracle, Claudia’s family announced that she had passed away in her sleep, aged 8.
The announcement was made on the family’s Facebook page, Claudia’s Cause:
Claudia, of Mount Rasen in England, was told by doctors that she had metastatic pineoblastoma, a malignant brain tumour, at the age of five. Three years to the day of her diagnosis, Claudia’s parents were told that she was miraculously cancer-free after an experimental treatment called the Milan Protocol.
Since being given the all-clear, Claudia had been suffering from pneumonia and lung issues, which are believed to have caused her death. A few days ago, Claudia’s mother posted a picture of Claudia surrounded by her pets, noting “I swear that animals understand”.
The Burkill family, including parents David and Andrea and Claudia’s siblings Abigail, Esme and Zachery have asked for privacy while they grieve this beautiful and brave little girl.
Top Comments
I am saddened that this poor little girl didn't have a chance. That brutal medical regime was never going to offer that child a cure and is a cruel and sadistic treatment. The Burzynski method of using anti-neoplaston treatment may have offered hope in this circumstance, we should all be rallying to ensure that this treatment is available to all children with brain cancer. It is a not a guarantee, but if certainly offers a substantial improvement on the horrific regime this poor child was subjected to.
What a stupid thing to say. It DID rid her of the cancer. She died of lung issues because she had been sick for so long. It is not
cruel and sadistic treatment' - it is a desperate attempt to save a loved ones life.
Ummmm... The intense treatment would have left her with these health issues. She died of the treatment, not the cancer.
In this case, that is what they're saying, so yes, I agree. And as someone who has watched her girlfriend die 2.5 years after being diagnosed with terminal brain cancer, the treatment has many harsh side effects. It doesn't necessarily improve the quality of life, although it can prolong it, as it did in my poor gf's case. I felt a mix of devastation and relief for her, when she finally passed.
As the mother of a child with brain cancer who is told we are both terminal and not terminal, who has watched so many incredible children with brain cancer die, stories like this are sad but affirming. They affirm the hard truth that no matter how hard you fight, no matter how long you out run it, in most cases the doggedness of brain cancer or the side effects of the brutal treatment catch up with you.
The survival rate is too low. I hope soon it really makes its mark on the national agenda and our children in a practical way become our priority. New research conducted by Cure Brain Cancer Foundation has found nine out of ten Australians are unaware that brain cancer kills more children than any other disease
I'm sorry if this post sounds hopeless. There is always hope. Hope that each day is lived better than the last, that there is joy in the present moment, that mini miracles of bliss will be delivered along the way and further hope to be found in the light of their faces.
The reality remains uncompromising.
claudia and family you will be in our prayers tonight.
I didn't read it as hopeless - I read it as the reality that you know and live with. I'm sorry for what your child and family are going through. Sending you some prayers too.