- Leigh-Ann
- Jul 30
- 3 min read
Updated: Aug 1

When I was finally diagnosed with bipolar I was at a point where I couldn’t leave my bed, I was having episode after episode until I finally had a full breakdown and nearly killed myself. My husband called and informed some family of what I was dealing with because it was serious, and it wasn’t taken seriously by family at all. My husband often says he can’t believe how family disregards me, it didn’t surprise me, I’ve always had to be my own support because family hasn’t been reliable most of my life. Recently I saw a video online of a brother who took time to clean his sisters room after she went through a bout of deep depression and I cried, I cannot imagine getting that kind of unconditional support. I’m not sure my family understands what actual support is, and this has made recovery difficult and lonely.
Most of my recovery has been me and partner trudging though the tough stuff together. It is a very long very hard journey. Bipolar doesn’t go away, it’s neurodivergence, it is how my brain functions so recovery means once I’m stable maintaining a low stress life to keep me stable, and that’s not easy. It’s been 5 years and I’m just now reaching a point where I can get out and walk and set small goals again. Nobody tells you that a break down and burnout can take years to recover from but that’s the reality, it takes year’s especially if you’ve spent years pushing yourself past your capacity while living undiagnosed.
Mental illness is in fact illness, like any other part of the human body brains can get sick and can take you out , and if you don’t treat it for years it can take years to recover enough to function, which is what I have experienced. I’m just getting to a point where I can manage a small self care and house work routine. I think people think you take meds and it’s all better but recovery from burnout takes much, much longer then most people realize. I had this pattern of feeling better and pushing myself and ending up unwell again, I don’t do that anymore. I have slowly created a small daily routine I stick to, I make small changes when I feel I can do more. My illness changed my life, it also changed my spouse as well. He’s been my rock and he’s taken on a lot, also with very little support himself.
We live in a world where people still don’t believe in things like mentall illness and neurodivergence, because they are not physically visible. I find the older generation would prefer people just suffer in silence then address the reality of things like mental illness, adhd and autism. Can you imagine telling someone with Alzheimer’s that because you can’t see their illness it’s not real and leaving them to suffer alone? Alzheimer’s is an invisible illness we can only see the symptoms through behaviour, you can’t see Alzheimer’s physically only behaviourally, invisible illnesses are just that… invisible that doesn’t mean they are not real and it doesn’t mean it’s not having a serious impact on those who suffer from them. ADHD, autism, mental illness have real symptoms you can see behaviourally and left undiagnosed can upend your life. Many people 40+ have never been treated or diagnosed because our parents didn’t have the information to understand these things in the way we do now, but they are very real and denying their reality is damaging. When untreated these things disrupt life, and create unhealthy patterns to cope, and some people end up where I did, nearly dead or taking years to recover as I have.
Mental illness needs to be taken as seriously as physical illness, those who struggle need understanding and support, and if you can’t give those things then you need to look internally, those who are ill deserve support and care and actually require it in order to recover.

