Hello everyone, For a long time, and I mean a long time I put off physiotherapy. Why? – I hear … More
Tag: Heds
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
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
Misfortunate: A Poem about Ehlers Danlos Syndrome
A short poem about living with 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
#EDSBlogChallenge (Part 2)
Hi Guys, If you are just tuning in and missed my initial post or want to get involved in the … More
#EDSAwarenessMonth Blog Challenge
Hey Guys, As the sun is shining it is clear summer has started … but for those of you … More
My Invisible Illness ft. Tramadol: The Ehlers Danlos Series
This post was inspired by Invisible Illnesses Awareness Week (15/19/17 – 21/19/17) If you go on my Instagram, you will … More