Amalia the Princess Warrior
Spende geschützt
October 2015, Amalia was diagnosed with multi system Langerhan's Cell Histiocytosis, with involvement to her liver, spleen & skin. After 10 months of chemo and steroid treatment, unfortunately she is in a worse position now than where she was in 2015.
She had scans on 29th August 2016.
The results of the scans identified that the LCH has spread to her skull, brain, pelvis and still in her skin, liver and spleen. Also probably in her bone marrow.
So where to from here?
Amalia will need intensive high dose chemotherapy and she will more than likely need a stem cell transplant which will happen in Sydney. Naomi with Amalia and her two other children, Tommy and Henry will need to move to Sydney for 3-6 months for Amalia's treatment.
If Amalia's treatment is stopped she would only have a few months left but they are going to fight this, do what ever they can and kick it on its arse so it will be a story to tell Amalia's kids one day.
Thank you so much for your financial support in helping Naomi move her family to Sydney so Amalia can receive the essential medical treatment she needs!!
She had scans on 29th August 2016.
The results of the scans identified that the LCH has spread to her skull, brain, pelvis and still in her skin, liver and spleen. Also probably in her bone marrow.
So where to from here?
Amalia will need intensive high dose chemotherapy and she will more than likely need a stem cell transplant which will happen in Sydney. Naomi with Amalia and her two other children, Tommy and Henry will need to move to Sydney for 3-6 months for Amalia's treatment.
If Amalia's treatment is stopped she would only have a few months left but they are going to fight this, do what ever they can and kick it on its arse so it will be a story to tell Amalia's kids one day.
Thank you so much for your financial support in helping Naomi move her family to Sydney so Amalia can receive the essential medical treatment she needs!!
Organisator
Kate Clarke
Organisator
Wistow SA