A day at the beach
When I first realised how ill L was, I constantly wanted to know how long it would be before she got treatment, then how long before she was better. A […]
When I first realised how ill L was, I constantly wanted to know how long it would be before she got treatment, then how long before she was better. A […]
L’s sister, K, reads this blog. I told her about it, partly because I thought it would be a good place for her to understand how I feel and how […]
A quiet week on the blog, but a manic one in real life as we get ready to go away to Spain. Until Monday, it wasn’t clear if L’s doctor […]
There is a picture/poster doing the rounds on Facebook at the moment – which bears the slogan “I’m thinking of starting an OCD support group at my house. I don’t […]
If L goes into hospital she will be put on bed rest for most of the day, which means that outside of supervised mealtimes or therapy sessions she will have […]
*with apologies to Laura Collins for the plagiarism. L and I have had a good couple of days. Yesterday I was off work and had to rush into town, and […]
I’ve written before how the comments on this blog and Twitter have really sustained me over the last few months. To know that people have been through this and come […]
After no posts for a while, I think some rants have built up inside my head. These are just a few. This post will probably be deleted once I have […]
No posts for a while. L and I have been away for a couple of days and now she is with her father while I am still away. She lost […]
It is impossible to describe what living with an ED is like. I can only tell you what it is like to experience watching a loved one with a disorder. […]