May is ME Awareness Month and once again I am participating in the virtual campaigns online to help raise awareness of this life-destroying illness called Myalgic Encephalomyelitis. Today I'm sharing my story. How did I become so terribly ill and housebound? When did it happen? And how long did I have to wait for a diagnosis? Here's my ME story:
Ironically my life was super busy and active during the weeks and months before the onset of what lead to my Chronic Fatigue Syndrome diagnosis. There seems to be the general belief that we are tired or lazy or that we have some sort of unhealthy aversion or fear of exercise, but nothing could be further from the truth!
As we move towards ME Awareness Month (May), I wanted to share some of my health and fitness memories from the week before I fell ill. I hope that this will help to dispell the idea that we are lazy and afraid of exercise and help people understand that the opposite is actually true. Now I know that healthy eating and exercise simply doesn't cure everything.
One of my favourite things about the blogging community are the seasonal tagging events. These blog tags are like a game of "20 Questions" and "Tag - You're It!" rolled into one.
You generally answer a bunch of themed questions or write a post based on a theme or prompt and then tag a few people to take part. It's a wonderful way to get to know each other better and a fun escape from the usual topics we write about. This one is all about Summer favourites!
April is a very special month for me. Many of my great life changes seem to have happened in April. This particular celebration is very special to me: on 7 April 2012 I was baptised in the sea at Brighton beach in the UK!
I was 30 years old at the time. Baptism was something I had been thinking about doing for years, but I never really understood what living a life in Christ really meant and how baptism fit into it all, so I kept putting it off. In 2012 everything changed and I finally understood what Jesus' sacrifice meant for me.
It might surprise you how often people with chronic illness are asked what they do with all the free time they have at home. I think many healthy people have no idea how difficult it is to deal with unrelenting symptoms on a daily basis. I hope to shed some light on this by sharing with you what a day in the life of Severe ME is like.