LIVING WITH LUPUS | Jolene C.

LIVING WITH LUPUS | Jolene C.

My name is Jolene Clark. When I was 6 and my sister was 12, our mother was diagnosed with lupus after being sick for more than a decade. Although I had been dealing with symptoms since around 2001, I was officially diagnosed with lupus in 2009. Not quite a year later...

Stress Management During the Holidays

On November 30, 2023 Lupus Canada was joined by Jodie Nimigon-Young, fellow lupus warrior for 29 years, who presented ‘Stress Management During the Holidays’. A video recording of the webinar is available below for viewing. Despite dealing with multiple problems with...
Lupus Canada Recipient of Community Services Recovery Fund

Lupus Canada Recipient of Community Services Recovery Fund

November 1, 2023 – We are pleased to announce that Lupus Canada has been selected as a funding recipient of the Government of Canada’s Community Services Recovery Fund which supports Community Service Organizations as they adapt for the long-term impacts of the...

Vaccines

On October 17, 2023 Lupus Canada was joined by Dr. Pope who discussed vaccines and their importance for people living with lupus. Janet Pope is a Professor of Medicine and Rheumatologist at the University of Western Ontario, Schulich School of Medicine.  She has...

Lupus & Indigenous Populations of Canada

On September 27th Lupus Canada was joined by Dr. Barnabe who discussed Lupus & Indigenous Populations of Canada. Dr. Cheryl Barnabe is a Métis rheumatologist and a Canada Research Chair in Rheumatoid Arthritis and Autoimmune Diseases. She is a Professor in the...