Surrounded by terrible news. On the TV the presenters are asking when will this lockdown stop, can we survive this, or the world is in crisis. The economists are predicting global recession, and some are talking about a depression. There are websites counting the deaths, YouTube has channels urging us Continue Reading
My legs are a disaster. In the last year I have started using an FES device for my right leg, and my left one is now like my right was a year and a half ago. Sativex helps with my mobility, but its cost is prohibitive, and now I only Continue Reading
In this post I reflect on 2019 and the obstacles I faced, how I dealt with these, and what I learned in the process. Now, more resilient, I look forward to the New Year!!
Living with a chronic illness can be tough, very tough. For me the sickness is Secondary Progressive Multiple Sclerosis, and the key word there is Progressive. This means no matter what I do it will get steadily worse, and there is no treatment, just various pills and potions which mask, Continue Reading
Mornings are the best part of my day, when the realisation of my physical state has not registered. Eating a leisurely breakfast, followed by coffee, brewed from just ground coffee. The morning is full of promise, and my day is undecided. After this meal, I put my dishes in the Continue Reading
(As we enter the new year, it’s time to think about your resolutions, with goals that will both empower your life, and possibly even empower the lives of others. As we enter the new year, it’s time to think about your resolutions, with goals that will both empower your life, Continue Reading