Support Sonya's cancer treatment costs
Dunedin, Otago
Wow, this is what has happened in the past 18 months.
The life of Sonya Boereboom from August 2022.
Starting with pain in my back, thought I had a pinched nerve, then started having numbness and tingles in my legs. Within two days got admitted to hospital and ended up paralysed from the waist down. After extensive hospital investigations, I was diagnosed with an autoimmune disease called MOGAD which is a rare inflammatory disease that affects the central nervous system. Months of intensive treatment to manage it followed.
Unfortunately then I slipped on wet tiles at work, fell over and broke my left femur at my hip joint in January 2023. And so began twelve weeks in a wheelchair while still getting used to MOGAD.
However, just when things couldn’t possibly get any worse, in March 2023, I was diagnosed with an aggressive breast cancer and again a very rare one. Next came the first round of chemo, then radiation and then the second round of a different chemo, all of which had little success in slowing the cancer progression. Now I am on an unfunded option in the private hospital sector. This unfunded drug - Sacituzumab govitecan - is extremely expensive and is not covered by any form of insurance, so I am funding it myself. After two cycles of this, my latest CT scan has shown some improvement which is a positive, so, the plan is to continue with more cycles and hope for the best.
I am a colleague of Sonya's, and co-ordinating this for her while she focuses on her treatment
Medical treatment (Sacituzumab govitecan) and support for family
Page closing 15 August 2024
Hi all - with Sonya's passing earlier this month, we will close the page. Thank you so much for each and every dollar donated to support Sonya's treatment.
We will all miss Sonya, but are thankful we had her in our lives.
thank you Bipin
Thank you Edwin, Claudine & Roman!
thank you Rennae
thank you!
thank you!
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