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

8 Body Language Mistakes you Might Be Making due to your Chronic Illness & How to Fix Them

8 Body Language Mistakes you Might Be Making due to your Chronic Illness & How to Fix Them Body language … More

10 Tips to Live Your Best Life with a Chronic Illness

If you live with a chronic illness, it is easy to be resentful and feel sorry for yourself – and … More

When Chronic Illness becomes a Competition and you are Left Feeling ‘Not Sick Enough’

I came across many blog posts that say chronic illness is NOT a competition. I believe that no one should … 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

10 Must Read Chronic Illness Blogs in 2019

Hello everyone, Although, it is my birthday today *yay I survived another year*  I have curated my Top 10 chronic … 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

15 Things Medical Zebras have Learnt to Love about their Incurable Illness

15 Things Medical Zebras have Learnt to Love about their Incurable Illness: The Ehlers Danlos Series

If you haven’t heard of Ehlers Danlos Syndrome – you are not alone. Ehlers Danlos Syndrome is a rare, incurable … More

Ehlers Danlos Syndrome

16 Things A Doctor Won’t Tell You When You Are First Diagnosed with EDS: The Ehlers Danlos Series

As it is coming up to my 2 year EDS diagnosis anniversary (if we can even call it that), I … 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