A member of our board of directors who has lived experience with MS has agreed to share a bit of her story to raise awareness.
Nim got diagnosed in 2019, and it came as quite a shock at the time. She experienced stigma and stereotypes from her community and even her family. This is something she believes needs to change. People can and should openly discuss how they are feeling without any judgement. She chose to join a support group for people with MS, through MS society of Canada. This is something she would recommend to anyone else out there who could use the support.
Additionally, Nim highlights the importance of managing symptoms. For her, this is done with prioritizing a healthy lifestyle, and movement. Keeping stress at a minimum is pertinent for those with MS, as it can cause a flare-up of symptoms.
This month, consider sharing your story if you have lived experienced and connect with others in the community. Read below for some local events.
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