One Family's Journey with Vascular Dementia
I am trying desperately to find the positive in our current situation. Having always been a bit of a dreamer – a girl with her nose in a book, carried along through life trusting in fate and goodness – I am now wracking my brain to try and decipher what positive I can take from it. Continue reading “Time To Make Time Count”
It’s only when you look back at photos of a year ago or a few months ago that you notice the decline. If you dare to look, then the difference – the decline – is face-slappingly obvious. Continue reading “Singing for Dementia. Singing to cope.”
My youngest daughter has just seen a picture of herself from around two years ago. In the photo, she is sitting between her brother and sister and is around 18 months old and other than looking a little younger, she looks exactly like she does now. Soft blond curls framing her small, angelic face. So, I was a little stumped that she didn’t recognise herself. Continue reading “Dementia: In Her Shoes”
By my dad…
I haven’t been in touch recently because Jane has been quite settled over the last few months. All the family and children have been up to see us over half term which has been very nice for me, but perhaps a bit confusing for Mrs T. Continue reading ““I Don’t Know””
It’s been an exciting week in our house: Martha was in the local paper yesterday as she’s raising money for Alzheimer’s UK (more on that in another post), which made her feel like a bit of a celebrity and of course, it was Valentine’s Day on Tuesday, which meant my eldest two got a bit giddy and unnecessary for a couple of days. Continue reading “Young Love”
 | Sarah Stoner on The Final Curtain |
 | melissajanisin on The Final Curtain |
 | Vicky Laidlaw on The Final Curtain |
| Sarah Stoner on The Final Curtain |
 | Loretta Ward on The Final Curtain |
My Crazy Mum 
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