This year I was diagnosed with severe combined ADHD.
It's been a journey, and a tough one. It was a light bulb moment for me, it was like a missing puzzle piece for me. It made me understand myself more. But I was also left grieving for the support I wish could have received back then. However, it's not a surprise that women are tested late for ADHD.
Studies have been prioritised to focus primarily on ADHD in men, and women have created coping mechanisms to hide these symptoms, which is known as 'masking'. To add there is also the societal pressure of expectations on how a woman should act.
Before researching about this neurological disorder, I too thought it was just being hyperactive, or being immediately distracted. But this is further from the truth. It affects every part of your life, whether you are, or are not aware of it.
ADHD is more commonly known as Attention Deficit Hyperactivity Disorder. The irony is that this definition is outdated. It's nothing to do with having less concentration or hyperactivity, but more known as a neurological disorder. This is also known as executive dysfunction, if you Google the word, it is defined as a "behavioural symptom that disrupts a persons ability to regulate, control or manage their thoughts, emotions and processes."
I have been living life on the edge for 28 years without knowing I had ADHD, and this was due to masking since I was a kid.
In my culture openly discussing ADHD is a taboo. Majority of the time you rarely hear about any Nepali who has ADHD, Autism, BPD, or even Bipolar disorder. The reason for this is people find it hard to accept their diagnosis, or they aren't educated on this.
I want to clarify ADHD is inherited, and not caused by taking pain relief, or external factors. ADHD doesn't suddenly appear during adulthood. It became evident to me as I got older that I was struggling, I often found it difficult to process information, and sometimes I had to ask for sentences to be repeated. Moreover, I could also relate my experiences to others who have ADHD.
This blog post was something I was planning to publish, and although I was hesitant at first, I realise that talking about it might encourage the BAME community and the Nepali community to speak more openly about neurodivergence, and normalise these conversations. I want to highlight that everyone has their own experiences, but it is particularly evident that those in the BAME community face extra struggles due to the lack of support systems and services. This also includes the lack of representation online reflecting the community's limited voice.
I hope we help those who are ashamed to talk about their diagnosis, or even those who might think they have ADHD.