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About lianne cawood

I am a woman, a daughter, a wife, a mother and a friend. I am married to B and have two wonderful daughters Kate and Jem. I have some new worlds to explore, those of being a cancer survivor, an immigrant, and a stay at home mom. I still struggle to say all of those words, let alone accept them. I have so much to be thankful for, yet I don't always see it. None of us do. So, inspired by Hailey of 365Grateful I started this blog. The goal, to find one thing every day to be grateful for. Not always the obvious. But sometimes. And to write about it. To put myself out there. And now it has become more. Not sure what yet, but I'll let you know when I know.

two hundred and seventy five

 

I needed to feed my soul today. I am grateful I have the perfect place to do just that. And friends who feel exactly the same way. Who understand how it takes my breath away. Every time.

two hundred and seventy four

 

My last Zoladex implant and my oncologist is in Canada on conference. Really? I am so over needles and some barbaric sans local implants which my sister in law can attest to, all of which have made me a little tense, and so in need of my gentle caring compassionate doctor who so gets me. The fact that the locum oncologist was not comfortable doing the implants and deferred to the oncology nurses didn’t help. Yikes. So, today I am grateful not only for my last implant but also for yet another angel with a kind heart and a fabulous sense of humour.

fuck yeah

I woke up with a feeling of anticipation today. And I know why. Because today feels like the day I finally start to take my power back. I had my last Zoladex implant today. I have had one every three months for the last nearly five years. This keeps me in menopause, which is essential for the aromatase inhibitor, Femara I take every night and have for nearly five years. My cancer was oestrogen receptive, so all production needs to be suppressed and blocked. I have three more months of Femara and then nothing. Nothing. Then I will become me again. A different me, but a me free of anything but what should be. I can’t wait. I am in awe of my doctors and of the courage I have gained through the efforts of others. I was just too fearful to go it alone. I together with my doctors and my family chose a course of action. A course of action me and my family needed me to take. To do everything I could to make sure I was here January 2013. The ultimate goal. Being here 5 years after chemo. Then we hit the down curve in the bell curve of efficacy of treatment. So no more. I am excited. Especially to discover what the medication has masked. Because I am different. Everything changed the day I was diagnosed and will never be the same again. In many ways it is better, way better, but in other ways not. I feel I’ve also let my cancer control me the last five years. I have been in varying stages of disease, surgery, treatment and recovery. But I know it’s also been a process of acceptance. And growth. Only now can I start to feel a frisson of a personal victory. I am seeing that whilst it occupied a lot of me, and changed me, it hasn’t defined me. I willingly handed me over for a bit. Now I’m ready to reclaim me. But I am proud of how I fought for my life. And I’ll do it again if I have to. So for now, all I can say is yay me.

two hundred and seventy three

 

 

I had two little extra companions on the beach today. And as delightful as they were I had to be more alert today than I have been for a very long while. So whilst those who know me know I wax lyrical about every age and stage and do not wish any of it away, today I was a little bit grateful my girls are not quite so young anymore. It means I get to drift off from time to time. Bliss. And how cool are the sand circles. I watched three young girls spend ages making them. I loved how everyone walked around them for the rest of the day. Well, everyone that is, except my two young companions.

two hundred and seventy two

 

Kate was never very still as a young child, except when she wasn’t well, and then B was her best to cuddle. Which he loved. I am grateful that some things just don’t change.

 

two hundred and seventy one

12 October. I am grateful for unusual mom and daughter bonding moments. Me waxing and plucking Kate, in the usual areas that need attention, brings much hilarity and genuine appreciation from my teenager. I was taken aback by her commenting how lucky she is I do it. It seems not all mums do. I just wish it wasn’t always last minute. Then again, she is my daughter.

two hundred and seventy

 

I am grateful for the making of memories. And for little girls wanting to capture them. And for a polaroid camera that reminds me of way back when.

two hundred and sixty nine

 

Kate gave herself and me a big fright today. She had a fainting episode, or syncope, apparently. It was quite terrifying for her to experience. And me to witness. So today I am grateful for my daughter’s resilience in the face of a day of tests, for her growth, for our shared smiles as our eyes met in the various doctor’s rooms and for her pride at her ‘firsts’. I grateful for that little voice as I kissed her goodnight that stopped me at the door, saying, thank you mommy for driving me around today. Because whilst it was young and vulnerable, the choice of words weren’t. And the gratitude was sincere.

two hundred and sixty eight

 

Today I am grateful I got to spend the day with brave caring just bloody get on with it women. Women who inspire me with their guts, their vulnerability, their honesty and their strength.