Skip to main content

A new way of life.

With Maisie now receiving her chemotherapy we had to adopt a new way of life. A life where sterilising every surface, every toy, and every inch of the house became a daily ritual. A life where we could no longer go shopping, go for coffee, go for play dates or attend baby classes, go swimming or play in the park. A life where visitors were restricted and only allowed in if they had no coughs or colds and they used the hand sanitisers that we had installed in the house. This may sound a tad over protective to some but with a suppressed immune system the risk of infection is seriously high and could hinder her treatment. We knew that we couldn't take her cancer away and we couldn't change anything for her, so the best we could do was to protect her and keep her free from infection, no matter what that meant.

Over the next few mornings when I woke my heart was heavy with worry about how Maisie would be. Worried that her little face would be lacking all colour, her beautiful ginger hair falling out bit by bit, her girly eyelashes not being able to hold on and her tiny body wrenching with sickness. But every morning when I lifted her from her cot she surprised me. She was just her usual little self and to any onlooker she was just a 'normal', happy and healthy 8 month old baby. But we knew better. I kept looking at her thinking this is just the calm before the storm.

The weekend following her first cycle of chemotherapy was Easter. We had originally planned to go to the caravan for the weekend, be surrounded by family and do a little egg hunt but we knew this was not going to happen. We quickly realised that all the plans that we had previously made, (including our first family holiday to Spain and Keith's 30th birthday celebrations), would now have to be cancelled. Life was going to have be lived one day at a time and inside our little 'chemo bubble'.





Easter for us was a morning spent playing with Maisie's new teddies and an afternoon having dinner at granny and granda's house, (they too had been busy with the Detol). It may not have been what we had planned for but I was so thankful that Maisie was feeling well and showing unbelievable resilience to her treatment and was able to smile her way through her first Easter. Our girl just amazes me. However, going to bed that night after having seen other peoples fun filled Easter celebrations over social media, a part of me felt robbed. It became clear to me that living life this way, inside the bubble that we needed to in order to protect Maisie, we were all going to miss out on so much of her childhood and it was so unfair. This new way of life was going to be difficult and painful but it was also necessary.


Wendy.












Comments

Post a Comment

Popular posts from this blog

Confirming suspicions.

At 4.AM the next morning after a few hours of restless and uncomfortable sleep, I woke to the unfamiliar sounds of the hospital ward. I looked across and saw my beautiful little girl fast asleep with her mouth open and her wee legs hanging through the gaps in the cot. For a second it actually made me giggle and then the realisation of why she was lying there came back. I then felt guilty for having a giggle, I felt guilty for not being able to protect her from this, and I felt guilty that I hadn't noticed. What kind of mother was I? The guilt swamped my body in an unbearable physical weight and unable to move by it, I lay there crying silently to myself until my head felt like it was going to burst and my throat was sore from trying to contain my sobs. I lifted my phone and frantically scrolled through every picture I had of Maisie desperately looking to see if I could find the lump in any of them. Even though we had been informed that with the type of tumour they suspected Maisi...

Hoping for four and not any more!!

Driving to Belfast the next morning to start a new round of chemotherapy was a heart breaking reminder that this nightmare was not over. That even after all the challenges and battles Maisie has fought and won so far, the cancer war was still going on. Today was not only a trip for chemotherapy either, today was the day we were expecting to hear the pathology report and the anxiety could be felt amongst us all. Apart from Maisie who was still smiling. Up until now we had no indicator as to what stage Maisie's cancer was at and we only had a vague idea of the type of cancer cells that were present thanks to the biopsy. So until the tumour was removed and went to the pathologists we had no solid idea of what type of treatment plan Maisie was going to have to endure following surgery. The very best outcome we could hear today was that the tumour would be completely dead of all cancer cells but that was a tad optimistic and a bit too much to ...

The results are in!!!

Waiting.....  Nobody really likes it do they? Waiting for a bus, waiting in a queue, waiting for exam results, waiting for your husband to empty the dishwasher; they all suck right?  Well waiting for the biopsy results of your 8 month old baby's tumour is a whole different ball game. After 5 days of waiting, where one minute felt like an hour, an hour felt like a day, and a day felt like forever, my head was in overdrive heading to Belfast to hear what the consultant had to say. All that waiting had made every possible scenario and outcome to become blurred and overthought. I couldn't see past this. I couldn't see any light. I couldn't see a future. The word cancer does that to you. All that my eyes, my head and my heart could see and feel was pain, fear and uncertainty. The smile of being blissfully unaware of what was ahead. On the drive up I kept saying to myself please let it be benign. If its not, and it is cancer, please let it be a Wilms. Isn't tha...