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
To say I am angry is an understatement. Yesterday when I arrived home, fully of optimism about our country and its desire to put the patient (I am writing a post about this too), to find a letter from Social Welfare. Readers of my blog know I have Multiple Sclerosis, Continue Reading
There are times in life where you see a massive difference in the way two similar organisations approach a situation. Last week I had an experience which both angers me, and saddens me, at the same time. The contrast was stark. People with disabilities travel. We use cars, trains, boats, Continue Reading
When living when a disability or chronic illness, getting active can sometimes be a challenge. Whether it’s managing pain or mobility problems, finding an appropriate exercise regime can take a little trial and error. Rest assured, there are a number of exercises out there that can be achieved and adjusted 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!!
I have been sharing my experience of using Sativex for spasticity in Multiple Sclerosis in Multiple Sclerosis. This post links to all the videos I have posted live on Facebook.