As May is EDS Awareness Month, I decided to do what I have never really done before – I signed up for a conference to learn a little more about EDS. EDS UK hosted the medical team from the Royal National Orthopaedic Hospital at Stanmore to present a day symposium on “Managing Your EDS” – […]
You know that feeling when you comment on something, and then the original post is then deleted? That feeling of “hey, I thought my comment was insightful, and now the whole discussion has just vanished”? Well, this weekend I had that feeling. Without revealing too many details, I had reacted to a discussion about feeling […]
This post was originally published on Baseline Physiotherapy to raise awareness of Ehlers Danlos Syndrome. May is EDS Awareness Month. To learn more about EDS Hypermobility type (the type of EDS I have been diagnosed with) please visit the Hypermobility Syndromes Association. Growing up I knew that I was double jointed. I used to think it […]
That’s Felix. After sending him to The Dog House in Wales for ten weeks earlier this year (following his “look at me I’m chasing a herd of cows” incident), he’s been back at home with us for just over a month. Ten weeks was a long time without that face. What I learned when Felix was […]
This is the face. The face of someone who just realised they had to cycle up a short sharp hill not once but nine times. And the face of someone who then realised that the same hill needed to be tackled twice again while running. Oof. On Sunday I did the Crystal Palace Triathlon. This […]