This Month is Epilepsy Awareness Month. My youngest child has had it since his teens so I would like to add it to my lineup of this to post about.
Epilepsy Awareness Month
Purple Day: A Young Girl's Campaign for Epilepsy Awareness
On November 9th, 2008, Cassidy Megan of Nova Scotia, Canada, launched the first Purple Day for Epilepsy Awareness.
At just nine years old, Cassidy, who lives with epilepsy herself, took a bold step to raise awareness about the neurological condition and dispel the stigma surrounding it. She chose purple, the internationally recognized color for epilepsy, as a symbol of hope and understanding.
Cassidy's initiative was remarkable not only for her young age but also for challenging the traditional notion that children should be passive recipients of care.
Cassidy's initiative empowered countless individuals to speak openly about their experiences, fostering a sense of community and reducing the isolation often felt by those affected by epilepsy.
Her efforts challenged the prevailing narrative that epilepsy is something to be hidden or ashamed of. Instead, she promoted a message of acceptance and understanding, encouraging people to see beyond the diagnosis and recognize the individual.
Cassidy Megan's actions on that November 9th demonstrate the power of youth advocacy and the impact a single individual can have in raising awareness about a critical health issue. Purple Day continues to be observed annually, serving as a reminder of the importance of education, support, and inclusivity for people with epilepsy.
@TheNewsOwl This was inspiring to read, Owlie. I have shared it in its entirety. ππ
Great read π Thanks for sharing π
@JulesofJoy No problem at all. π€
She defied this expectation by becoming an active advocate for herself and others living with epilepsy. With the support of the Epilepsy Association of Nova Scotia, she encouraged people to wear purple and learn more about the condition.
Purple Day quickly gained momentum, spreading across Canada and internationally. It became a platform for people with epilepsy, their families, and supporters to come together, share their stories, and educate the public.