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

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

Morgan’s Ehlers Danlos Support U.K Fundraiser

Hello Guys, I am asking for kind donations of art materials from my Amazon wish list to make animal drawings … 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

#EDSBlogChallenge (Part 2)

Hi Guys, If you are just tuning in and missed my initial post or want to get involved in the … More

5 Ways to have a Productive Day with a Chronic Illness

“Having a productive day is very subjective; what is productive for one person is not for another”. Some days, I … More

5 Challenges Blogging with a Chronic Illness…

 with a sprinkle of advice. Hello, there 🙂 If you haven’t read my other posts, welcome. It’s not a secret … More