I grew up knowing only about a bad leg and foot. That much was obvious because it was something you could see. Wearing skirts made it more obvious, because you could see me walk toe heel, and because I walked with a limp.

I Was Led to Believe I was 'Normal'

Growing up and throughout my life, I was led to believe I was 'normal', but it would eventually become clear, I was far from normal.

Functioning in my Own 'Normal' was Difficult

Fast forward to leaving home and functioning in my own normal began to get more difficult. Believing I was normal, is further from what I am or what I've had to deal with over the years. I was never 'normal.' It's not fine, but better if you're not in a partnership. I have spent the best part of 61 years trying to work around symptoms I didn't know I had, while trying to conduct myself normally.

My Disability Has Caused Me Unnecessary Stress

There is no excuse for what I was made to live through. Not knowing about my disability has caused years of unnecessary stress and anxiety. That's not the same as going into a relationship and the other person knowing exactly what you deal with.

It takes a certain personality, allowing their child who they know deals with a disability to go through their life, knowing nothing about their disability and what they may have to deal with, and think it okay. That is what happened to me.

Ilana Estelle is a mental health and wellbeing advocate who combines educational insight with her personal experience of living with physical, mental, and emotional disabilities. She holds diplomas in Counselling, Diet and Nutrition, Nutritional Therapy, Psychotherapy and Counselling, and Stress Management. Through her writing, Ilana supports others in navigating their emotional, mental, and physical health challenges. In addition to writing for The CP Diary, her work has appeared in healthy lifestyle magazines. Ilana is also the author of three books: Cerebral Palsy: A Story – Finding the Calm After the Storm, Spirituality, Healing and Me, and Survival: The Covid Years – Time for Change.

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4 comments on “Believing I was Normal”

  1. Believe you're normal, because you are. So abolish your distinction between normal and not normal until you show me a standard that is more normal than you.

    It's normal to be a good person, excellent writer, author and awesome mother and have a disability. In fact, diversity is very normal.

    If you're not normal I must be a monster.

    1. Awww that's kind. Thanks Tim. The hard part was having to behave normally with no allowances, when my brain damage, was telling a completely different story.

      But as they say, 'what is normal to the spider is chaos to the fly.' My normal may not sit well with others, but being able to live with my disability with relative ease, makes me normal.

      So I'm normal and you're not a monster.

  2. It boggles my mind that any parent would expect their children to think of themselves as normal when they're anything but.

    They should have at least been able to let you know about your conditions, so that you would have been more equipped to deal with your life.

    I would find it very hard to live with myself if I had done something like pretending that my daughter didn't have cerebral palsy and watch her struggle with life.

    I'm sure it's heartbreaking and devastating when you think back on your childhood, as it does for me; seeing as I know that things could have been so much better for both of us.

    I'm thinking that is why I've been having such a hard time even contemplating writing about my childhood and life, seeing as it dredges up so much pain and suffering.

    I know it needs to be done, so I can finally move on with my life.

    1. Thanks Randy. I've had a hard time digesting it myself. My writing helps bring understanding, but I'm not sure I'll ever come to terms with it fully.

      Both of our experiences have shaped us. I agree with you about the past dredging up so much pain, but speaking from my own experiences, it is well worth the effort if you can do it.

      I feel vindicated now. It doesn't feel like my responsibility. It doesn't change the experience, but it does change how we get to view those experiences and the people behind our experiences.

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