Women of Color
Beyond the Myths: Four People Talk About the Reality of Living With EDS & HSD
We wanted to end EDS Awareness Month by spotlighting the lived experiences of four individuals with Ehlers-Danlos Syndrome (EDS) or Hypermobility Spectrum Disorder (HSD). Through these perspectives, we aimed to tackle a few of the many myths surrounding these conditions. We also wanted to offer a glimpse into the reality of living with EDS/HSD, including […]
Brianna Cardenas, PA-C, ATC, on challenges as a queer woman of color with EDS
CW: Discussion of suicidal thoughts and depression. [None of the information provided in this Q&A is to be taken as medical advice; please consult a doctor if you have questions about your medical condition.] For our June newsletter, the Chronic Pain Partners media team interviewed a diverse group of people […]
Adrienne Ferron on challenges as a woman of color with EDS
For our June newsletter, the Chronic Pain Partners media team interviewed a diverse group of people to highlight the diversity of our community and emphasize the challenges that arise when one belongs to more than one minority. In this interview, journalist Karina Sturm speaks with Adrienne Ferron, an EDS advocate, podcaster, and social media influencer […]
Popular Posts
Ehlers-Danlos Syndrome May Increase Susceptibility to Infections
EDS, POTS and MCAS Linked by One Gene Mutation
Popular People With Ehlers-Danlos Syndrome
In memory of John Ferman, Founder and President of Chronic Pain Partners / EDS Awareness
EDS Physical Therapy Book & Free Webinar: “Living Life to the Fullest with Ehlers-Danlos Syndrome”