Portage la Prairie's Mayor, Sharilyn Knox, officially proclaimed September 9, 2025, as Fetal Alcohol Spectrum Disorder (FASD) Day in the City of Portage la Prairie, drawing attention to a lifelong disability and raising awareness for prevention and support.
The proclamation highlights the city's commitment to supporting individuals and families affected by FASD and educating the public about the disorder. It’s a significant step in recognizing the importance of awareness and providing resources to the community.
A common and underdiagnosed disorder
Fetal Alcohol Spectrum Disorder is a lifelong disability caused by prenatal alcohol exposure. It affects the development of the brain and body, leading to a range of challenges for those living with it. Although it is a very common disability, it's also often underdiagnosed.
According to Shannon Tomalin, Chair of the Portage and Area FASD Coalition, about 4% of the population is living with FASD.
"It's a higher rate than autism and other intellectual disorders as well," she states.
Living with FASD can present a variety of challenges, including issues with impulsiveness, learning, attention, memory, communication, and emotional regulation. However, it's not a hereditary condition; it's a direct result of a mother consuming alcohol during pregnancy.
Tomalin emphasizes that with the right support, individuals with FASD can live healthy and successful lives.
"It's had an impact on how people are going to develop and take in the information required to live a healthy life. That being said, those with FASD can be quite successful with supports and understanding of their strengths and their challenges in life," she says.
How to get involved
The Portage and Area FASD Coalition is a dedicated group working to raise public awareness and provide support.
The coalition, which includes members like Barry Redd, Crystal Bruinooge, and Darcy Anderson, meets monthly and is always seeking new members. They focus on prevention, support services, and offering guidance on obtaining a formal diagnosis for those who are curious.
The best way for people to get involved is by contacting the coalition through their Facebook page, as it is checked regularly.
Tomalin notes they are always happy to meet with new people who are interested in supporting the cause, sharing her personal experience, "It's very fulfilling. We're always happy to meet people and talk with them. Every interaction kind of leads to a little bit more digging into how we can support our community."
You can find a link to their Facebook page by clicking here.
