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Must-Have Items This Holiday Season
We know that having a disability like HOD means undoubtedly having to get creative with…
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Navigating the Holidays with HOD: Finding Joy in the Season
With the holiday season upon us, you may be wondering how to handle well-meaning (or…
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We’re in This HOD Life Together
A brief description of Brad’s journey…. by Lauren, Wife (October 5, 2023) The following is an…
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Building Community Isn’t a One-Man Job
By Chris Coates, HODA Founder and Board President I have some things that weigh on…
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What is Hypertrophic Olivary Degeneration?
You’ve been diagnosed with hypertrophic olivary degeneration. Now what? Well, first things first, you probably…
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The Hidden Costs of Brain Disease Diagnosis
By: Christina Coates The costs of these diagnoses are truly immeasurable. Many of us arrive…
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Erin’s HOD Story: Drastic Life Changes After A Stroke
An interview with Erin Loughran Visit Erin’s Instagram @myinvisiblebff for more and to keep up…
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Helen’s Story: The Sacrifices That Changed Her Life Drastically
Helen Busuttil Regenbogen was diagnosed with Hypertrophic Olivary Degeneration (HOD) in 2019. The night before…
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HOD’s Official Greeter, Brad Asher: A Survivor’s Story
By: Brad Asher 12/2021 In mid April 2017 there was a giant non cancerous tumor…
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From “Normal” to “Rare”: Christina Coates’ Story.
My journey with brain disease begins in 2017. I began having daily migraines that were…
