I FEEL VALIDATED. The Minnesota Department of Health now recognizes long haul COVID as an official, diagnosable illness (even with its own insurance code), according to media reports citing the MDH. I am thankful. This has been a long time coming for someone like me who lives with this illness.
I have often felt that people don’t necessarily understand the severity of long COVID, how it impacts the lives of those of us affected. It’s real. Not in our heads. Debilitating. Long-lasting. Results of a survey by MDH confirm that.
Thankfully, my primary care doctor listened to me, showing great care and compassion when we were trying to figure out what was going on with my body in early 2023. My many symptoms followed an illness that was assuredly COVID, even though I never tested positive for the illness. COVID tests, if not done at the right time or done incorrectly, can give inaccurate results.
When I look at the MDH’s long COVID check list, I see many of the long-lasting symptoms I experienced: fatigue, brain fog, trouble sleeping, headaches, heart palpitations, tightness in chest, dizziness (balance issues) upon standing, skin issues, hair loss, mood changes, and changes in taste and smell (for me intensified). And in the “other” category, I experienced sensory overload, which continues to plague me.
After many tests to rule out a tumor or other health issues, my doctor settled on long haul COVID as my diagnosis, although that’s not in my official health records. I need to get that changed with this new MDH determination.

I will feel forever grateful to Dr. Todd Sykora of Allina Health for listening to me, for his persistence, for prescribing a medication that eased some symptoms and for his suggestion that I try physical therapy.
I’ve written numerous times about my long COVID experience and treatment in an effort to raise awareness, educate and offer hope to those dealing with the illness. For me, the “help” was six months of vestibular rehab therapy to retrain my brain. My therapist treated me like I’d experienced a traumatic brain injury. He was spot on with that approach. I will feel forever grateful to Ryan Iverson at Courage Kenny Rehabilitation Institute in Faribault for getting me through some really challenging months and helping me reach my goal of “getting my life back.” That also came with lots of hard work on my part and the incredible support of my loving husband.

Today I am using my experience to spread the message about long haul COVID and to also personally support a young man in my community dealing with its devastating affects. J, as I will call him, has been struggling for much longer than me and with much more severe symptoms. I’ve encouraged J (and his mom), offered hope and referred J to my physical therapist. He is making progress.
As for me, I’ve learned to mostly manage the few long haul COVID symptoms that persist, albeit less severe than in 2023. When I got sick with COVID again in December 2024 and then rebound COVID, some symptoms flared. But, for the most part, I’m OK. Like any health issue, you learn to live with it and manage. And when a state agency recognizes your illness as real, it feels validating and empowering.
© Copyright 2025 Audrey Kletscher Helbling




















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