Mr. Speaker, May is Lupus Awareness Month, and I am honoured to raise awareness for the one in every 1,000 Canadians living with this chronic autoimmune disease. Lupus, sometimes called “the disease of a thousand faces”, is characterized by its diverse symptoms, which makes diagnosing it a complex and lengthy process.
Lupus patients struggle with physical and psychological health impediments, impacting daily activities, employment and social relationships. Unforeseen costs, such as home modifications and medical transport, exacerbate financial stress. Access to health care is hindered by long waiting periods for specialists and medication costs. The disease's unpredictability further complicates matters. Often, disability policies do not recognize lupus, leaving patients vulnerable and unsupported.
It is for this reason that we must ensure equitable access to health care, treatment and supports for all Canadians living with lupus.