My Son and Bipolar Disorder: Where is My Casserole?

Last Updated: 19 Jun 2019
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Bipolar disorder is just as serious as many other physical illnesses, so why does society view it so differently?

wheres-my-casserole


When my son was diagnosed with bipolar you could’ve swore I told people he had the plague. No one brought casseroles to my house or offered their support. Yet I got a lot of “I’m sorry” and very pitiful looks, as if my son had been diagnosed with a terminal illness. Mental illness is a lifelong battle but it is treatable and not terminal.

Why does society views it so differently? Why are they so afraid of it? Why are people with mental illness treated like outcasts? Society is definitely afraid of what they do not understand. Just because you can’t see it doesn’t make it any less important. Why is there such a stigma attached to it and how to we dispel it?

If I were to tell those same people my son had cancer I am sure their reaction would’ve been much different. I am sure my neighbors would be dropping off casseroles and offering their support. I am sure I would have a list of doctors I could choose from. I am sure I wouldn’t have to wait weeks or months to see a specialty doctor. I am sure we wouldn’t have to spend hours upon hours in an emergency room waiting to get treatment or find an open bed. I am sure we would have options for hospitals stays and they would cater to sick children. I am sure my insurance company would let my son get treatment and not given me a certain number of days in a calendar year or an expenditure cap. I am sure someone would be throwing me a benefit or a go fund me page to help defer the rising costs of treatment. I am sure there would be lots of funding for research. I am sure there would be fundraising events for research and people would be raising awareness. I am sure the community would be rallying for his recovery. I am sure people would care!

So why don’t people care that my son has bipolar? He was just 10 years old when he was diagnosed. A sweet young innocent boy who had no control over his mood swings. A victim of his own brain. I wasn’t a bad parent, he wasn’t raised in a bad environment, it is NOT a behavior problem and he DOES NOT choose to be this way!!! Just because he looks “normal” doesn’t mean he isn’t sick. You can’t see diabetes or epilepsy, multiple sclerosis, or cancer for that matter and still they don’t get the bad wrap mental illness does.

Is it the name? Mental? Does society view it as something you should have control over? The more I am submerged in this world the more I am noticing the number of people who don’t suffer from some type of mental illness seems to be minimal. If the statistics show that 1 in 4 people suffer from a mental illness it would seem we have an epidemic on our hands and yet we haven’t progressed with education, awareness, or research funding. It’s been 12 years since my son was diagnosed and the struggles parents are going through today hasn’t changed much since he was diagnosed. That is very sad to me.

I want someone to bring me a casserole. I want people to send me well wishes. I want my son to get fair treatment for his illness. I want him to be in a hospital without white walls and bars on the windows. I want him to not have to be strip searched for his stay in the hospital. I want him to have a doctor it doesn’t take weeks to get in when he is sick. I want him to have insurance coverage that doesn’t have a bunch of red tape. I want research funding and fundraisers. I want him not to be afraid to tell people about his illness.

I want fair treatment and recovery.

I want him not to be judged.

I want him to have a fair chance in society without stigma!

code: bphopekids

About the author
Julie Joyce is a dedicated mother to an adult son who lives with bipolar disorder and ADHD. She’s also a former Chigaco Police officer (retired after a 25-year career). Over the years, Julie has been a strong advocate and volunteer with the National Alliance for Mental Illness (NAMI) and the Balanced Mind Parent Network and has assisted with the creation and implementation of the Advanced Juvenile Crisis Intervention Training (CIT) for Chicago Police officers. Julie has been featured on numerous platforms focusing on mental health, such as NPR radio, the Attorney General’s office, and other mainstream media outlets. Julie has also conducted educational presentations for DCFS on interventions for kids with brain-based disorders. Currently, Julie spends her time raising awareness and advocating for people living with mental health conditions through her podcast, Behind Our Door Podcast.
73 Comments
  1. Thank you for this. I am doing a presentation tomorrow entitled “Where’s my casserole?” having to do with the abandonment that happened when my son suffered from the potentially fatal disease of heroin addiction. How my family was treated was very different from a few years earlier when I was diagnosed with cancer.

  2. I didn’t get a casserole either during my last depression. It lasted for 10 months.

  3. Sometimes I think people struggle to deal with bipolar people because the ups and downs of life seem common to us all, but for some reason us “moody” people do stupid things lik refuse to go to work or say things in ways that are way out of step with the long suffering decorum everyone else seems to know glues day to day society together. In short it is impossible for a person who doesn’t love someone desperately to tolerate.

  4. Oh what an awesome article this made me cry. I have a mental health condition myself and yes, some people react as if I have the plague. Thanks for sharing your story!

  5. Wow. I can relate to so much. In 1994 my son was diagnosed at the age of 4 with leukaemia. It was a parents nightmare. You do the best you can with what you know and only want your child to be healthy and happy. Six weeks ago at the age of 27 my son hit the back of a large truck going approximately 60-70mph. Thank the good lord above he was physically uninjured. He was in a phycosis and hospitalized for 3 weeks. He has been diagnosed bipolar. Looking back there were signs of disfunction but he was a adult living far away from us. I have just started to digest this information and you are correct. People treat this diagnosis differently. I’ve always been my sons advocate in the past and I want to be his advocate now and in the future. I really appreciate you sharing your story. God bless

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