Brandon Deen 9/15/25 Brandon Deen 9/15/25

When “Just a Cold” Isn’t Just a Cold: What You Might Not Know About Autoimmune Disease and Immune Suppression

Brandon Deen

Brandon Deen 8/18/25 Brandon Deen 8/18/25

When Pain Looks Normal: Living with Chronic Pain in a World That Doesn’t See It

Brandon Deen

Brandon Deen 8/11/25 Brandon Deen 8/11/25

Unapologetically Me: Life with Multiple Sclerosis (MS) Doesn’t Come with an Apology

Brandon Deen

Brandon Deen 8/4/25 Brandon Deen 8/4/25

“You Don’t Look Disabled”: The Stare, the Judgement, and the Reality Behind the Parking Spot

Brandon Deen

Chelsea Hardesty 7/30/25 Chelsea Hardesty 7/30/25

Tariffs, Venmo, and Crypto Dreams: America’s Economy Is Starting to Feel Like a Meme

Chelsea BreeAnn Hardesty

Brandon Deen 7/28/25 Brandon Deen 7/28/25

Living Past the Diagnosis: The Story Behind the Age I Still Claim, Before MS Took Hold

Brandon Deen

Brandon Deen 7/23/25 Brandon Deen 7/23/25

The Person Behind Words: Why I Write for The Invisible Voice

Brandon Deen

Casey Howell 7/23/25 Casey Howell 7/23/25

From Social Feeds to Hospital Beds: The Impact of Wellness Misinformation & Medication Shaming

Casey Howell RN,BSN

Brandon Deen 7/16/25 Brandon Deen 7/16/25

From Isolation to Beyond the Invisible Diagnosis: A Story of Loss, Resilience, and Finding “My Person”

Brandon Deen

Brandon Deen 7/4/25 Brandon Deen 7/4/25

Not All Pain Is Visible: Living with Invisible Illness and MS Behind the Mask

Brandon Deen

Chelsea Hardesty 7/3/25 Chelsea Hardesty 7/3/25

One Big Bill, Many Big Consequences: House Passes Trump’s $4.5 Trillion Package, Leaving Millions Behind

Chelsea Hardesty

Brandon Deen 6/30/25 Brandon Deen 6/30/25

Invisible, Not Imaginary: How MS Took My Energy but Gave Me a Voice

Brandon Deen

Casey Howell 6/18/25 Casey Howell 6/18/25

Sausage Fingers, Biologics, and The (EULAR) European Alliance of Associations Conference: A Reflection.

Casey Howell

Chelsea Hardesty 6/15/25 Chelsea Hardesty 6/15/25

Reclaiming the Narrative: Misdiagnosis, Misinformation, and Misogyny

Chelsea Hardesty

Casey Howell 5/27/25 Casey Howell 5/27/25

Your Brain on Fire: Why Chronic Pain is Rewiring Your Reality (And Why No One Wants You To Know)

Casey Howell

Casey Howell 5/14/25 Casey Howell 5/14/25

When Your Immune System Throws a Tantrum: My Psoriatic Arthritis Saga

Casey Howell

Chelsea Hardesty 1/15/25 Chelsea Hardesty 1/15/25

The Evidence Paradox: Healthcare Reformers Ignore Evidence Based Data

A crucial look into medical research, that’s failing to translate into better patient care, exposing the gaps between science, policy, and real-world treatment.

Chelsea Hardesty 12/8/24 Chelsea Hardesty 12/8/24

Separating Facts from Fiction in Endometriosis Care

Revealing the reality behind the “revolutionary treatment” claims making waves online.

Chelsea Hardesty 12/2/24 Chelsea Hardesty 12/2/24

Deck the Halls with Awareness and Education - What is Endometriosis?

A quick reference guide to endometriosis, how to get diagnosed, and what questions to ask your doctor.

Emmanuel Sessegnon 11/25/24 Emmanuel Sessegnon 11/25/24

PBMs Are An Unnecessary Barrier to Affordable Care

What are Pharmacy Benefit Managers? And what should be done to make sure the industry focuses on people instead of profits?

When “Just a Cold” Isn’t Just a Cold: What You Might Not Know About Autoimmune Disease and Immune Suppression

When Pain Looks Normal: Living with Chronic Pain in a World That Doesn’t See It

Unapologetically Me: Life with Multiple Sclerosis (MS) Doesn’t Come with an Apology

“You Don’t Look Disabled”: The Stare, the Judgement, and the Reality Behind the Parking Spot

Tariffs, Venmo, and Crypto Dreams: America’s Economy Is Starting to Feel Like a Meme

Living Past the Diagnosis: The Story Behind the Age I Still Claim, Before MS Took Hold

The Person Behind Words: Why I Write for The Invisible Voice

From Social Feeds to Hospital Beds: The Impact of Wellness Misinformation & Medication Shaming

From Isolation to Beyond the Invisible Diagnosis: A Story of Loss, Resilience, and Finding “My Person”

Not All Pain Is Visible: Living with Invisible Illness and MS Behind the Mask

One Big Bill, Many Big Consequences: House Passes Trump’s $4.5 Trillion Package, Leaving Millions Behind

Invisible, Not Imaginary: How MS Took My Energy but Gave Me a Voice

Sausage Fingers, Biologics, and The (EULAR) European Alliance of Associations Conference: A Reflection.

Reclaiming the Narrative: Misdiagnosis, Misinformation, and Misogyny

Your Brain on Fire: Why Chronic Pain is Rewiring Your Reality (And Why No One Wants You To Know)

When Your Immune System Throws a Tantrum: My Psoriatic Arthritis Saga

The Evidence Paradox: Healthcare Reformers Ignore Evidence Based Data

Separating Facts from Fiction in Endometriosis Care

Deck the Halls with Awareness and Education - What is Endometriosis?

PBMs Are An Unnecessary Barrier to Affordable Care

The Invisible Voice

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