A new care factor.
In the midst of becoming a semi-carer for my elderly neighbour, I’ve decided I want to change the world. Continue reading A new care factor.
Tag: carer
A new day has come.
Friday the 6th of March marked the day that my Mamma Bear reached the end of her breast cancer journey. On Friday the 6th of March, Mamma walked into the oncology ward for the last time and had her last hit of radiotherapy for breast cancer. After 8 months of treatment, we had finally reached the finish line; 16 blood tests, 16 hits of chemotherapy, 6 stomach injections and 20 hits of radiation were finally, FINALLY, behind us. 8 months later. And let me say, there was joy because it has been a long, hard, heartbreaking journey. On that day, … Continue reading A new day has come.
May we never meet again (in the nicest possible way of course)
Today at 10:30 am, my mamma and I walked into the oncology ward of our local hospital for her fourteenth, and last, chemotherapy session. To say there was mixed emotions would be an understatement! We walked in excited and anxious at the same time. We have been counting down to todays session since August, eagerly looking to the finish line. January 8th, 2015, was a date that was constantly brought up in conversations with mum and I; it was our ‘light at the end of the tunnel’. I used it to encourage her to hang in there, to see her … Continue reading May we never meet again (in the nicest possible way of course)
Today was a gooooood day!
Today. Today was a good day. The sun shone a little brighter. The breeze was a little cooler. The coffee tasted better. Today was a good day. Why? Not because it’s New Years Eve and 2014 is coming to an end. The reason today was, and still is a good day, is because today was mums second last chemotherapy treatment. She has one more chemo session and the chemo part of her treatment is finished. FINISHED!!!! That light at the end of the tunnel is so bright right now and I can’t even tell you how excited I am. I … Continue reading Today was a gooooood day!
Tell me something I don’t know.
I was having a chat to someone a few days ago and we were talking about mums chemo journey and how she’s coping with it. We chatted about how hard it must be for mum to go through and I made the observation that it’s been hard on all of us. Interestingly, my statement was sort of shut down. I was frowned at and got told that “Well, it’s hardest for her because she is going through it.” I smiled and agreed that yes, it is hardest for her and slowly retreated. The comment bugged me for a few reasons: … Continue reading Tell me something I don’t know.
Control freak.
And it begins: the side effects have hit mum in full force and she is struggling. The vomiting, the body aches, the headaches, the loss of hair. It’s all happening and it’s killing me. Bit by bit my heart is breaking as I watch this treatment take over my mum’s body. I’ve repeatedly asked myself if we’re doing the right thing with the chemo and then I remind myself that we need to do it to help prevent it from coming back. I also keep reminding myself that we are not fighting off cancer, we are just trying to prevent … Continue reading Control freak.
Normal.
This week is our treatment free week -woo! Mum doesn’t need to do anything this week: no blood tests, no chemo, no nausea injections. She can just chill out and be. Which is great because her first treatment has knocked her about some. She’s more tired than usual (that’s normal with chemo) and she is feeling nauseous (also normal with chemo but they’ve given her meds for it). But she’s a strong one and is coping well, shaved head and all. The hardest thing has been keeping up all the little things, like staying out of the sun and regularly … Continue reading Normal.
Reflections by Leila 