
Multiple Sclerosis (MS) is a chronic autoimmune condition that affects 2.8 million people around the world. MS is where the immune system attacks the myelin around the nerves in the Central Nervous System (CNS), affecting the brain, spinal cord, and optic nerves. Canada continues to have the highest rates in the world where 1 in every 400 people are diagnosed with the illness, commonly found in more women than men. The MS Society of Canada utilizes donations not only for research but to also assist those living with MS with medical equipment and supports to help with quality of life.
MS is described by people living with it as an illness that is unseen. Even though the person looks perfectly healthy it can be a war zone inside the body. From nerve pain, to numbness, to chronic fatigue.
I’m supporting the MS Society as it reaches close to my heart as I was diagnosed with relapsing-remitting MS back in October of 2016. The MS Society has not only helped me by providing medical equipment that I needed for my everyday life, but they have also made accessible support groups, which has helped me significantly over the years. By supporting the MS Society, it will not only continue to help with research but provide a better quality of life to those living with MS. My heart goes out to those living with MS, we are in this together.









