I’d always wanted to become a mum but was anxious about whether it was possible with Crohn's, especially after trying to conceive for 18 months.
So, I focused on staying well and seeking answers as to why I hadn't been able to conceive yet. After an ultrasound and blood tests came back clear, we knew there was no medical reason and within a month I was pregnant! I believe the relief after the scans helped me to feel calmer and stay more positive about getting pregnant.
In late 2019, our son Oliver was born. I was very fortunate to have a straightforward pregnancy, and whilst his journey into the world was less straightforward, my Crohn’s remained stable throughout.
Being a mother with a chronic and unpredictable condition is tough and has a huge impact on our daily lives. But the joy we bring each other every day more than makes up for it. It has forced me to evaluate what's important in life and ensure that I take time to look after me.
So, what living with a chronic illness has taught me?
You’re not a failure or a bad parent if you don’t do everything yourself
I have limited energy due to fatigue and want to use that energy to spend time with my family so I’m fortunate to have help. When my husband works away, I order homemade meals on a subscription service, and we have a regular cleaner. These days energy is like gold-dust, and fatigue can make the simplest of tasks a huge challenge, so be gentle with yourself.
Getting the right balance is key
We can’t be everything for everyone, even if we’d like to be!
I work 3 days a week and have a day to myself when Oliver is in nursery. At first, I felt extremely guilty for choosing that time for myself but I know I’m a calmer and happier parent for taking that time to recharge.
Qigong, Yin yoga, reading and a good nap are my go-to activities for recharging my batteries. Or they at least stop my battery from draining so quickly.
Prioritise your own health – both mental and physical
For years after my diagnosis, I focused on being physically well to stay in remission. However, I was neglecting the emotional and psychological impact of the diagnosis and life with Crohn’s.
So, I started to write. It was a release for the mix of emotions I was feeling, and I hoped that it would help others with Crohn’s.