Tag: EDS

Ehlers Danlos Syndrome Type 3: What to expect at your first physiotherapy appointment

Hello everyone, For a long time, and I mean a long time I put off physiotherapy. Why? – I hear … More

I Think I have EDS. What Happens Next? The Ehlers Danlos Series

You have been feeling sick for a very long time.  Had many routine tests come back clear. Yet, you have … More

Go Fund Me: Morgan’s EDS Mobility Aids

Hello everyone, Some of you may or may not know that I am suffering from an incurable connective tissue disorder … More

Confessions of a Zebra #4 Hypermobility Ehlers Danlos Syndrome and Me – Ansley

Hello everyone, One of my conditions I write about a lot on my blog, is Ehlers Danlos Syndrome (EDS). I … More

23 Ehlers Danlos Syndromes Life Hacks: The Ehlers Danlos Series

  Although, being diagnosed with Ehlers Danlos Syndrome, has given me slightly more sanity. Living with this illness, like many … More

Interview with an Invisible Illness Warrior

Hey Guys, I was asked to be a contributor in an educational film to present to medical professionals by Troy … More

The chronically ill student’s quick-guide to success

It is hard enough for University students to balance their coursework and exams with their social life. So, when a … More

PoTs – The Invisible Demon.

PoTs Explained and my Symptoms Postural Orthostatic Tachycardia Syndrome also known as Dysautonomia (PoTs). That’s one a hell of mouthful, … More