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  • Describing Sensory Issues
    Life with MS | My MS Journey | Newly Diagnosed

    Describing Sensory Issues

    ByKB March 16, 2025

    How do you describe a physical feeling that no one can see or experience but you? I deal with a lot of sensory issues in my new MS life. These “invisible symptoms” bother me every day in some capacity, but the severity isn’t always the same. I’ve talked a lot about the unpredictability of my…

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  • I Pre-Board Now
    Life with MS

    I Pre-Board Now

    ByKB January 15, 2025January 16, 2025

    A few months and plane rides after being diagnosed with MS, I realized I was missing out on an essential accommodation I could take advantage of at the airport: pre-boarding for disabled passengers. Over time since my diagnosis, I’ve learned that, depending on my energy levels that day, standing in one place for extended amounts…

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  • I Can Still Rock Out Sitting Down
    Life with MS | Newly Diagnosed

    I Can Still Rock Out Sitting Down

    ByKB December 4, 2024

    I love going to shows and watching live music. There is something about experiencing live music that brings me so much joy and makes me feel truly present (now that I think about it, was I practicing mindfulness all this time??). Whether in a small venue, an arena, a coffee shop, or outside in a…

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  • Lean on Your Support Network
    Life with MS | My MS Journey | Newly Diagnosed

    Lean on Your Support Network

    ByKB November 15, 2024November 15, 2024

    My husband and I recently celebrated our seventh wedding anniversary. After enjoying a delicious dinner, we looked at all the photos from our wedding and went through the awesome playlist made by our DJ. Listening to these songs and conjuring up the moment they were played, I thought about how lucky I am to have…

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  • The Mask We Wear
    Life with MS | My MS Journey

    The Mask We Wear

    ByKB October 31, 2024November 15, 2024

    In the spirit of Halloween, the theme of today’s post is wearing a mask. We all have to put on a mask sometimes in our daily lives – whether it’s to get through a frustrating work meeting while maintaining professionalism or pretending to enjoy an activity to be polite. Perhaps your mask only needs to…

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  • The Many Paths to Patient Advocacy: Interview with Trishna Bharadia
    Community | Life with MS

    The Many Paths to Patient Advocacy: Interview with Trishna Bharadia

    ByKB October 21, 2024October 21, 2024

    In November 2023, I attended the Healthcare Businesswomen’s Association (HBA) Annual Meeting in Chicago. I went to network and learn from inspiring women in the healthcare industry, but it was also a bit of a personal experiment: it was going to be the first time I went “public” with my multiple sclerosis diagnosis among strangers….

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  • Cooking as a Mindfulness Exercise
    Life with MS | My MS Journey | Newly Diagnosed

    Cooking as a Mindfulness Exercise

    ByKB October 16, 2024October 17, 2024

    Food has always been an important part of my life. Growing up Italian American, most of my family time was spent in the kitchen or around a table. Many of my core memories involve a meal. I love cooking, but I don’t pretend I’m a professional chef. I don’t have knife skills or tons of…

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  • Moving Sucks
    Life with MS | My MS Journey

    Moving Sucks

    ByKB October 3, 2024October 3, 2024

    I think there is a universal truth that everyone can agree on: Moving sucks. Moving sucks for everyone. There’s something so stressful about the entire process of moving, whether the move was expected or unexpected; whether you’re in a small apartment or a big house; if you’re going cross-country or to a different apartment in…

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  • The Best Exercise is the Kind You Enjoy
    Life with MS

    The Best Exercise is the Kind You Enjoy

    ByKB September 29, 2024

    At a recent appointment with my neurologist, exercise came up. Not surprising as exercising is extremely important in managing multiple sclerosis. I asked, “What is the best kind of exercise for MS?” He said, “The best exercise is the one you enjoy doing and that you’ll do consistently.” I’ve heard and read this advice before,…

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  • My MRI Spaceship
    Life with MS | My MS Journey | Newly Diagnosed

    My MRI Spaceship

    ByKB September 20, 2024September 18, 2024

    Last week, I had another MRI. Getting an MRI is really weird. I am not claustrophobic, so I am not scared of MRIs. Well, actually, I am scared of them…but not of going in the machine. I’m always a little scared of the results of the MRI, because what the test says determines what damage…

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