Multiple Sclerosis

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 and bad. For now, we do not know what further impact it will have, but I know its impact on me. In this post, I am going to share how it has helped shape …

2021 Patient Advocacy & Me, what an amazing year Read More »

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

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 some exercise, head outside for a scooter ‘walk’ and yesterday we went to Galway to collect my new glasses. Everything happened with much less pressure, …

A positive week after making a difficult decision Read More »

How I make a difficult decision because of chronic illness

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 21 posts, missing two days. One of which was yesterday. I have really enjoyed the process of having to write, share the content, and then …

How I make a difficult decision because of chronic illness Read More »

Pain is expensive: A day in my life

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 to be very careful about pacing, which I am succeeding in, mainly. Yesterday, I decided to write a very short post, so I would not …

Pain is expensive: A day in my life Read More »

Scroll to Top
Verified by ExactMetrics
Verified by MonsterInsights