dr. elizabeth leroux, a neurologist and founder of migraine canada, sees the constant battle people living with migraine have to fight and the lack of current awareness and support from employers regarding this debilitating disease.
she said in a press release that “people with migraine often work through their debilitating episodes. raising awareness among employers and hr departments could lead to a cultural and structural change in canadian workplaces.”
“stigma and skepticism should be replaced by support, adapted environments, and access to medical care. this campaign marks a significant step forward in addressing an area of high unmet need.”
gerhart hopes that the campaign can act as a much-needed catalyst for change. “what we’re really trying to do is have the conversation, get people talking about it, get people asking questions,” she said.
dr. pim echoes the same sentiments as gerhart and dr. leroux. “ultimately, i hope employers, insurance companies and government officials better realize the impact this disease has on young members of our society and improve environmental and work conditions and access to health care and treatment for migraine sufferers,” dr. pim said.
changing the lives of migraine sufferers for the better
at the end of the day, people living with migraines deserve to have their disease recognized and destigmatized so that they can take suitable precautions and avoid added stress that can end up triggering episodes.
for that to happen, people must first understand that migraine is not just a headache. it is a neurological disease that can be highly disabling.
when people become aware of migraine, what it entails, and how canadians are affected, employers, colleagues, and social connections can all understand the disease better, which can foster a supportive collective that helps people with migraines feel safer to take time off when they experience an attack or use their time to seek out proper treatment.