Realisation….. it’s a long haul

**** Before you read this, know that I am okay, I’m just trying to be true to myself and blog the reality of my situation ****

If I’m honest with you all, the last month has been really hard. I’ve started to write about four blogs but can’t seem to get out what I am trying to say. I don’t want it to be a poor me post, rather a post about the general aftermath of breast cancer treatment because I am 100% sure I am not alone in how I am feeling at the moment.

For five months, I was in a situation where I was going from one appointment to another, ticking of each box in the treatment cycle. I just wanted to get it done and know I had done everything I possibly could to kick cancer’s arse. I was strong and I was determined.

Then I finished.

I thought….. “right, time to get back to normal”, but it appears that is not how this works.

Apparently it takes time.

I am impatient. I want hair, I want normality, I want to work and I want to exercise. Every time I slightly overdo things, my body kicks me in the butt. Presently it’s with a chest infection.

There are many things about treatment you wouldn’t have even thought about. Like the fact I am now dealing with medically induced menopause. It sucks, my hot flushes are relentless and my brain some days struggles to function. But, the worst has been a clash in medication.

I haven’t been shy in the past about writing about my mental health struggles, so why start now? 🤣 For 15 years I have been treated for anxiety. For 15 years I have taken the same antidepressant. Just weeks after enduring the most difficult thing I have done in my life, I discovered this drug would reduce the effectiveness of Tamoxifen (the hormone blocker I will need to take for at least the next five years to reduce the chance of recurrence). I had to stop.

It took a month to wean off it and I immediately started an alternative. I have had support along the way with regular GP visits, psychologist appointment and other alternative therapies through Solaris Cancer Care. It has been done in a calculated and researched manner, but it has been hard. I have felt quite down and at times alone.

In true Amber style, I thought keeping as busy as possible would be the best way through, my psychologist even agreed. But my body did not. I got sick, and my defences just couldn’t fight it. I took antibiotics and carried on. Today I write this from bed, where I should have stayed a week ago.

Realisation…… I’m not super woman after all.

This week has made me realise, I still have a long way to go to heal from this ordeal both physically and mentally. I am telling myself everything will be there waiting when I am ready, but I have to stop thinking about when that might be. There is no timeline.

My hair is a good indication of slowly, slowly, I should heed its wisdom. It’s now two shades of grey instead of white so things can still change.

There you go, I still have a smile on my dial!!

A dose of sunshine and warmth is on the cards this week, just what the doctor ordered. Andy and I are off to Darwin on Friday to celebrate our 20th wedding anniversary. He needs this as much as I do, my rock throughout, but he is exhausted too.

Yay, https://thetravelbee.blog/ will get a run. Absolutely no talk of cancer on that channel!

Ax

Next tick box

I have had three days to process the next step in my journey. I said the other day, I was shell shocked. That wasn’t quite right, I know enough about this stuff to know chemotherapy was always going to be on the cards. It wasn’t a complete surprise or bolt from the blue.

What I actually was, was deeply disappointed (thanks Dad for giving me the right word) and scared. I was disappointed that I was going to have to walk an unknown road, the road on which I have vast knowledge gaps. And what I don’t understand and am not in control of, makes me scared…….

I don’t know how the drugs will make me feel, I don’t know what will happen to my hair, I don’t know how my children will feel with a mother that will outwardly look sick and I don’t know how I’ll cope with looking and feeling sick. I am not good at sitting still.

But then I reminded myself, I have chosen to undertake chemotherapy because it will give me the best chance of never seeing this thing ever again and living a long and fulfilling life. I also reminded myself, there are plenty of people out there (that I know even) that have done this before as well as plenty that can help me negotiate it.

On Wednesday, I started the day by crying on a friend’s shoulder. Then, I got on with it. I read all of the information from my oncologist, I got on the phone and I started calling for help. I spoke to a McGrath nurse I know through work. After her initial surprise, she was straight onto helping to fill my knowledge gaps. She emailed information specific to my questions and referred me onto Breast Cancer Care WA for counselling support.

I made it my mission to understand as much as I could. A close and very special friend visited and insisted she would be my chemo buddy. This was a great comfort and another thing I don’t need to worry or think about. Others sent messages of support and reminders of how strong I am. I read every one and then I got my big girl pants on and started to flex those ‘strong’ muscles.

Thursday was all about my hair. I still haven’t made a decision about what I will do, but I researched cold cap therapy, debriefed with a friend and called my hairdresser. I talked to my children about what they would feel comfortable with, and I started ordering headwear.

So, that is where I am at….. my knowledge is improving and I am working towards just ticking that next box.

Oh ………………. and I am on a macrame mission.

Ax