Yet again it's been a long time between blog posts, yet again I feel I have to apologise. I've been getting a lot of writers block recently and my mental health has taken a bit of a nose dive, these two things have clubbed together to make me feel very disillusioned with blogging. I've felt … Continue reading How a thoughtless act can ruin a trip out
Firstly I yet again have to start with an apology for the lack of posts. I had a couple of posts ready to go but without photo's before I went into hospital, but didn't want to just find photo's to use I wanted to have taken them myself (the found photos weren't quite right for … Continue reading When your body is shouting stop, what would you do?
Having a chronic illness or long term condition usually comes with the need to have many hospital and doctors appointments. You can sometimes get to know the staff so well that they know its you on the phone before you identify yourself, and treat you like a friend when you walk into the surgery etc. … Continue reading Medical overload and operation stress!
No one said that having a catheter was easy, and I've been under no illusion that this was the case. However my bendy body doesn't seem to think that having a catheter is bad enough on it's own, and so this past week and a bit I have had to call the nurses out four … Continue reading Catheter woes and what is a supra-pubic catheter??!!
May in my EDS world is awareness month. As I've explained to you before I have got a bit of awareness month fatigue, there are so many of them and so many different days. However for me awareness month is how I found out about EDS and how I finally got some of my answers. … Continue reading EDS Awareness Month……….and what you need to know about my condition!
I decided about half way through my previous post that not only was the post getting incredibly long, but it was also going to make everyone switch off!! 31 questions would be fine if they were really short answers, but they aren't! So I apologise for what might be two really long and tedious posts, … Continue reading Awareness month and What you need to know about my EDS part 2!!
I haven't managed to write a blog post for a bit now and thought I better give you an explanation. There are two reasons, firstly it's the Easter holidays so I've not got the space or time to concentrate on writing. Secondly I had planned to have a number of finished posts ready so that … Continue reading Having a break!!
So I've been writing a number of posts recently, however it's not that I've got writers block more that I've got too many thoughts that I can't actually finish one off. I've not been out in pretty much 2 weeks which is one of the posts I've got in the pipelines, but it seems that … Continue reading Too many thoughts and none of them finished!!
A friend of mine noted on her Facebook page today that two friends had asked her about how she was feeling. She gave two different answers because of their relationship to her and the conditions they had. To one friend she had replied that she was "fine" and to another who shared her condition she … Continue reading The many faces of chronic illness!
One thing that a lot of non-disabled people don't understand is the sheer panic, annoyance, anger, inconvenience and, or upset moving a disabled person's mobility aid can cause. It's almost difficult to explain just how we feel when it happens because you have very little to compare it to, but what it pretty much equates … Continue reading Moving my legs!!