2021 Patient Advocacy & Me, what an amazing year
2021 Patient Advocacy & Me What an amazing year 2021 has been an eventful year. The COVID pandemic is still around and it has changed so many lives, for good...
More pain and fatigue, because I did not pace myself
Pacing is very important when you live with MS. Over the last week my illnesses punished me with more pain and fatigue, because I forgot this rule.
A positive week after making a difficult decision
The last week has been much easier since I stopped writing a post every day (you can read why I made this decision here). Suddenly I had time to do...
How I make a difficult decision because of chronic illness
On the 24th April I decided to embark on a massive challenge, to write a blog post every day for 100 days. Over the last 23 days I have written...
Pain is expensive: A day in my life
The last week has been very busy for me. I have had three trips to Galway and I am up against deadlines on a few projects. So I have had...
Fatigue: Conserving energy
Last night I slept 10.5 hours. Fatigue has raised its ugly head, so I must listen and adapt. So today, this will be my post. Very short.