23rd day in rehab and my last full day! (wheelchair drama, walking for miles and surprise visits from friends)

Up bright and early this morning (with both shoulders and a hip out of joint! It’s really hard to pop a hip back in when you can’t feel anything besides pins and needles in either arm!) After yesterday’s emotional meltdown I was up ready for a fight this morning but my morning was a little…Continue reading 23rd day in rehab and my last full day! (wheelchair drama, walking for miles and surprise visits from friends)

21st day in rehab (sneaky visit home to watch Grey's Anatomy, the GF Easter bunny)

I had a layin of a whole half an hour this morning before scrambled egg on toast and getting up and dressed. My back is definitely a lot better when I take diazepam at night so I think I might stick with that for a while. I spent most of the morning reading in bed…Continue reading 21st day in rehab (sneaky visit home to watch Grey's Anatomy, the GF Easter bunny)

14th day in rehab (race horses, the great escape and beading)

Today marks 2 weeks here at Aldeburgh Community Hospital and tomorrow marks week 5 in my hospital admission. (1st ever admission and hopefully my last for a LONG time) I have filled my room with stuff from home, my orchid, my beads, my clothes and it almost feels like home. I started the day with…Continue reading 14th day in rehab (race horses, the great escape and beading)

Phase Change Cooling Vest Review

So I was very excited to get my cooling vests in the post this morning. I was lucky enough to snatch the last 2 of the ‘Junior Cooling Vests’ from DisabledGear. I have been really struggling with heat intolerance, progressively since Christmas when I started developing symptoms of Postural Orthostatic Tachycardia Syndrome (POTS) Basically being…Continue reading Phase Change Cooling Vest Review

EDS Awareness Month Continued!

I Posted this photo as part of EDS Awareness Month to highlight just some of the effects that Hypermobile-EDS has had on me and many others.. well the response was phenomenal! By the time I went to bed yesterday an amazingĀ 41,312 people had seen that photo! There is no way this would have happened without…Continue reading EDS Awareness Month Continued!

May is EDS Awareness month! I have Hypermobile Ehlers Danlos Syndrome

EDS is a part of me, A part of my life and despite all of the problems, the pain, the endless fatigue, the tears, the sleepless nights, and the fact that as soon as I learn to manage one thing another one pops up! I wouldn’t change it for the world. I have met amazing…Continue reading May is EDS Awareness month! I have Hypermobile Ehlers Danlos Syndrome