Cassie Day had just taken on a leadership role within her human resources team when she fell pregnant with her first child.
The plan was for the then 23-year-old to take six months off work before returning to the state government department she worked in, when her husband would take over primary parenting duties.
But when their son Matthew was four weeks old, Cassie learned something that would change her career, her relationship and her life forever.
Matthew was diagnosed with cystic fibrosis in 2002 – the first of many complications the family would face – and immediately Cassie’s world began to alter as she became a full time carer to her son.
“Everything changed from there,” the 37-year-old told Mamamia. “We didn’t even know what cystic fibrosis was.”
Matthew required different medications and a form of physiotherapy known as chest percussions, which involves lightly hitting your child's chest for 20 minutes at a time, several times a day.
"Emotionally that was gruelling. I think I cried a lot. That first year was incredibly tough," she said.
While the South Australian mum was able to go back to work, it was just 10 hours a week and not in the same leadership role she had left.
"My career stopped in its tracks. I was just not reliable and able to lead a team, because of my caring responsibilities," the now mum-of-two explained.
"My organisation was fantastic, but the absolute guilt that riddles through you for letting people down is crippling, you feel like a failure.
Top Comments
There is a shortage of carer support for those with ADHD children. This disorder also breaks up parents, and families.
It sure does - I support may in my community who are living with ADHD x
Things have changed since my oldest was born and more help is now available. It can be a lonely life being a full time carer for your child, trying to get help even after you have been told what is wrong. My family would not help putting my oldest and then later my youngest problems to how I was bringing them up, their home life. There is only so much outside help you can get and having to beg for help can get you down. Some call you a super mum, they are your children so you do what you can. A pity they are not willing to help you out with the care or extra things eg: taking my middle child to let him know that his brother's treatment are helping them and he can have fun doing other things. Asking specialist if the program for your children can involve all the children, so the others do not feel like they are missing out. Otherwise you are having to find extra time to deal with "why do they get extra time with you". Making you fill like guilty because you can not get the same time to all.
I absolutely hear you Tracey. Next year we will be running/piloting programs for the entire family in my local council area exactly because of the exclusion issues. It most certainly can be a lonely time. xx