Ehlers-Danlos Blog | CPCF United

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BC EDS

Jun 114 min read

How to Make the Medical Community Take Ehlers-Danlos Pain More Seriously

BC EDS

May 144 min read

The Unpredictable Flare-Ups: Living with EDS and Managing Chronic Pain

BC EDS

Apr 155 min read

Finding the Right Doctor for EDS Patients: A Checklist You Can Trust

BC EDS

Mar 124 min read

5 Foods You Should Avoid If You Have Ehlers-Danlos and Mast Cell Issues

BC EDS

Feb 124 min read

Struggling to Get Pain Medications with EDS? Here’s What You Need to Know

BC EDS

Jan 155 min read

The Challenge of Explaining Ehlers-Danlos Syndrome to New Doctors

BC EDS

Dec 3, 20245 min read

10 Signs Your Doctor Doesn't Understand Ehlers-Danlos Syndrome (and What to Do About It)

BC EDS

Oct 22, 20245 min read

Navigating Healthcare: A Guide for Rare Disease Patients and Families

Living with a rare disease can transform the simplest healthcare challenges into complex mazes. For individuals and families facing the...

BC EDS

Oct 1, 20243 min read

Innovative Therapies and Treatments for EDS: What’s on the Horizon?

BC EDS

Sep 10, 20243 min read

From Diagnosis to Daily Life: Adjusting to Life with EDS

BC EDS

Aug 20, 20243 min read

Breaking the Stigma: Raising Awareness and Understanding of Ehlers-Danlos Syndrome (EDS)

BC EDS

Aug 1, 20243 min read

Navigating EDS as a Family: Coping Strategies for Caregivers

BC EDS

Jul 16, 20243 min read

The Power of Community: How EDS Support Groups Change Lives

BC EDS

Jul 2, 20242 min read

My Journey with Ehlers Danlos Syndrome: Navigating Treatments

BC EDS

Jun 21, 20243 min read

The Role of Pharmacogenomics in EDS Treatment: A Patient's Guide

BC EDS

Jun 18, 20243 min read

Advocating for Yourself: Empowering EDS Patients

BC EDS

Jun 4, 20243 min read

Embracing Your EDS Journey: Coping Strategies for Daily Life

BC EDS

Apr 11, 20243 min read

10 Daily Hacks for Managing Chronic Fatigue

BC EDS

Apr 11, 20243 min read

5 Innovative Pain Management Techniques for Chronic Sufferers

BC EDS

Mar 15, 20243 min read

All Posts

How to Make the Medical Community Take Ehlers-Danlos Pain More Seriously

The Unpredictable Flare-Ups: Living with EDS and Managing Chronic Pain

Finding the Right Doctor for EDS Patients: A Checklist You Can Trust

5 Foods You Should Avoid If You Have Ehlers-Danlos and Mast Cell Issues

Struggling to Get Pain Medications with EDS? Here’s What You Need to Know

The Challenge of Explaining Ehlers-Danlos Syndrome to New Doctors

10 Signs Your Doctor Doesn't Understand Ehlers-Danlos Syndrome (and What to Do About It)

Navigating Healthcare: A Guide for Rare Disease Patients and Families

Innovative Therapies and Treatments for EDS: What’s on the Horizon?

From Diagnosis to Daily Life: Adjusting to Life with EDS

Breaking the Stigma: Raising Awareness and Understanding of Ehlers-Danlos Syndrome (EDS)

Navigating EDS as a Family: Coping Strategies for Caregivers

The Power of Community: How EDS Support Groups Change Lives

My Journey with Ehlers Danlos Syndrome: Navigating Treatments

The Role of Pharmacogenomics in EDS Treatment: A Patient's Guide

Advocating for Yourself: Empowering EDS Patients

Embracing Your EDS Journey: Coping Strategies for Daily Life

10 Daily Hacks for Managing Chronic Fatigue

5 Innovative Pain Management Techniques for Chronic Sufferers

The Prolotherapy Debate in Ehlers-Danlos Syndrome: A Firsthand Account

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