#EDSBlogChallenge (Part 2)
Hi Guys, If you are just tuning in and missed my initial post or want to get involved in the … More
View Article16 Things A Doctor Won’t Tell You When You Are First Diagnosed with EDS: The...
As it is coming up to my 2 year EDS diagnosis anniversary (if we can even call it that), I … More
View ArticleMisfortunate: A Poem about Ehlers Danlos Syndrome
A short poem about living with Ehlers Danlos Syndrome.
View ArticleMorgan’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
View Article15 Things Medical Zebras have Learnt to Love about their Incurable Illness:...
If you haven’t heard of Ehlers Danlos Syndrome – you are not alone. Ehlers Danlos Syndrome is a rare, incurable … More
View Article23 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
View ArticleConfessions 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
View ArticleGo 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
View ArticleI 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
View ArticleEhlers Danlos Syndrome Type 3: What to expect at your first physiotherapy...
Hello everyone, For a long time, and I mean a long time I put off physiotherapy. Why? – I hear you ask, well I believed it was extremely painful. Each morning, I was getting physically exhausted just...
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