If you follow me on Twitter (@A30MinuteLife) you will know that I have had difficulty in writing this New Year post. 4 days ago I sat down at my laptop thinking that I would write something about 2017, its ups and downs. As those of you with Chronic Illnesses know we often make plans to do something and our diseases decide that they want to be the main decider of what will happen in our day, not us.
This is what has happened to me over the last 4 days. I would sit down, again, and again, and my headache would assert itself, and stop me from being creative. Over the years I have learned not to try to win a battle with this beast, as I will surely lose. It is better to withdraw, and wait until the beast is sleeping.
Today is a good day, and I can write, and even though the monster in my head is snoring, it is not awake.
Thank you to all those people on my Twitter feed that have liked my post, and written supportive messages. I would especially like to mention Gina Sutton (@KlskTrvlr) for her post.
Five months ago I started writing this blog, hoping that my experiences of how I live with my illnesses could help others that also have a chronic condition. Over this period I have interacted on my blog, Facebook, Twitter and on video with many people, all with various challenges in their lives. This one Tweet has crystallised all the positive words and messages that I have received at this time.
Thank you to everyone that has been a part of ‘A 30 Minute Life’.
I never expected that someone living on the furthest edge of the westernmost island of Europe, by writing a blog about my experiences, could help anyone. 2017 has been a mixed year for me. This blog has been a highlight, and I have also resolved a few personal issues, which have taken a burden off my shoulders.
These positives have been tempered by the worsening of my MS and the impact of my MS and headaches on my ability to work. This has been a challenge for me, and I have, I think, been able to find a new direction in life that has a different focus. By finding a different way of putting purpose in my life I have removed a source of negativity that could push me into a negative tailspin. Thankfully 2017 has been a big step forward.
There are several people that contribute to my life, they accept and tolerate my various bad moods and restrictions that arise from how I cope with my headaches and MS. My partner, deserves a Gold Medal, as she is always at my side and often she is the undeserving focus of these negative emotions, I love her very much.
Also, my family has been a huge support over the year, they offer that constructive critique that only family can give, I need that in my life. It is true that I am not always right, and I need to be pushed back onto the correct path.
Now I am really looking forward to 2018, and all that it will bring. This blog will be a major part of this, I am sure of that.
40 SHARES Share on Facebook Tweet Follow us Save Share Share Share Share Share Share Share Share Custom Custom Custom Custom Custom This post was going to be an information piece about disabled toilets, and the way we should build them. However, in my research, and chatting on Twitter, I have found there are standards […]
40 SHARES Share on Facebook Tweet Follow us Save Share Share Share Share Share Share Share Share Custom Custom Custom Custom Custom Rhiann from My Brain Lesion and Me, Jordyn from The Chronically Unimaginable and Heather from Dinosaurs, Donkey’s and MS have nominated me for the Chronically Hopeful Award. I am sorry it has taken […]