If you've recently been diagnosed with or suspect you have HCM and are looking for additional support, there are Canadian patient organizations ready to help you.
Finding answers to unexplained symptoms can be difficult. These personal stories from others who’ve navigated similar journeys are a reminder that you’re not alone in yours.
Carmine shares his personal journey with HCM. From years of unexplained symptoms attributed to being out of shape and aging to receiving a life-changing diagnosis, Carmine opens up about the challenges he faced, the impact on his health and lifestyle, and the vital role his family’s support played. Carmine’s story is one of resilience and hope, offering a powerful perspective on living with a heart condition and the power of support and determination.
Linda openly shares her experience of living with unexplained symptoms for years, including constant shortness of breath that made even everyday activities feel like a struggle. Linda never suspected that her breathlessness was linked to a heart issue, but her diagnosis of HCM changed everything. Now, she urges anyone experiencing similar symptoms to take them seriously and seek further evaluation so they too can embrace life to its fullest as she does today.
In addition to talking to a specialist medical team, you can visit the websites of patient organizations for more information about HCM and additional support.
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