"Still adjusting spines and attitudes, even with ALS trying to cut in."
Most of you know Lindsay who could make you laugh even on your worst day. Life, unfortunately, has thrown her the toughest challenge yet: a diagnosis of ALS (Lou Gehrig’s disease).
ALS is brutal. It slowly takes away mobility, independence, and speech — but if you know Lindsay, you know she isn’t going quietly. She’s facing this with courage, wit, and the same sass that made her a beloved chiropractor to her patients and a personality that can shake up any room.
💪 Why We’re Raising Funds
ALS care is expensive. Specialized equipment, home modifications, caregivers, and medical costs pile up fast. Insurance helps, but it doesn’t come close to covering everything she’ll need to stay safe, comfortable, and surrounded by family.
Every dollar raised will go directly toward:
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Home care and caregiving support
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Accessibility equipment (wheelchair, lift, communication devices)
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Medical expenses not covered by insurance
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Giving her as much quality of life — and laughter — as possible
💃 Her Spirit
Even now, she’ll crack a joke before you can, roll her eyes at ALS, and remind you that dancing isn’t only about moving your feet — it’s about joy. We want to make sure that joy stays in her life no matter how much ALS tries to take away.
🙏 How You Can Help
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Donate if you can — any amount truly makes a difference.
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Share this link with friends, family, patients, and anyone whose life she touched.
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Leave a message for her — she loves hearing stories and laughter from everyone.
ALS sucks. But together, we can make sure Lindsay knows she doesn’t face it alone.
