The New Normal

Saturday 31 August 2019

Twenty-six-year old-Amy Voaden writes, ‘“It all started one day when…”. That’s how these things are supposed to start, aren’t they? The real truth is that I don’t know when my M.E. journey started because I don’t really remember living without it. What I do remember is being told to get on with it at nine years old when I complained about a stomach ache or not feeling well at school. What I do remember is suffering pain, sickness and fainting every day as I pushed myself to go to school. What I do remember is the confusion and mental health struggles that came alongside a two-year wait for a diagnosis, only to be told that nothing could be done. What I do remember is how hard it was to slot back into the rollercoaster of teenage existence on the days when I felt well enough. I can’t put all of the blame on M.E., there was actually a range of things that made my childhood and adolescence a difficult time, but my journey up and down the M.E. disability scale has by far had the most significant and undeniable impact on my past, present, and future.’ You can read an extract of her article, The New Normal, in this month’s blog post.

Welcome to the real M.E.

By the age of nine I was already aware that I had a reputation for complaining about pain or feeling poorly a lot. I distinctly remember thinking ‘I won’t tell anybody about this pain because they won’t believe me anyway’. I never knew what was wrong or that what I was feeling wasn’t what everybody else was feeling. All I remember is being in pain and feeling horrible and embarrassed. I’m a teacher now, about to begin my first year of teaching year one, so I understand that children complain and fuss. I’ve even had a lovely little girl draw a red dot on her finger in felt tip and ask me for a plaster. I understand. But I also understand my feelings of embarrassment over feeling poorly or weak at just nine years old. Don’t get me wrong, my primary school teachers were really lovely teachers. Fifteen-plus years ago many teachers had no idea what to look for, when or how to help, particularly in a small village school in the Devon countryside. I soon learned that my experience of M.E. would continuously revolve around the fact that people don’t understand. They don’t know what it is or why it happens and they don’t try to learn.

By the time I was twelve things were a different story. My pain, sickness and episodes of fainting had got steadily worse. I passed out every time I did any exercise, slept for hours following physical education lessons, working for any length of time or even if I just walked too far that day. I didn’t have a diagnosis then, so my sickness felt unpredictable and I felt constantly anxious about what I was doing and, more importantly, what I wasn’t able to do any more. I don’t remember too much from this time: the thick haze of brain fog has blurred everything over. What I do remember is being really confused, which had (and continues to have) a monumental impact on my mental health. What I do remember is hating myself and hating my body for failing me every day.

Over the next few years I continued to deteriorate and struggle until I couldn’t go to school anymore. I want to begin by saying that my secondary school were very accommodating. They arranged for me to have tutors come to my home to teach me Maths, English and Science. Without this I wouldn’t have any of the seven GCSEs that I scraped myself through. I would have a maximum of two one-hour lessons at a time, after which I could collapse in bed for the rest of the day and night to recover. However, being proactive and trying to help does not mean they had any understanding of M.E. or what I was going through. On days when I could make it into school, I had to attend all lessons, including P.E. which was always a double lesson. Inevitably this ended badly. Every time I did physical exercise the least painful thing that happened to me would be a fainting episode, after which I would be scooped up, often by other students, and carried into the school reception and fed biscuits as a cure. I have one distinct memory of waking up on the floor, having moved from where I fell, with food already in my mouth and wondering what on earth was going on. I will be forever grateful for my qualifications but forever disappointed in the lack of understanding, even after my diagnosis.

This severe phase in my health lasted for two years and was the lowest point for me. I had reached 80% on the M.E. Disability Scale and was not functioning on a daily basis. I spent almost all of my time stuck in bed, and any other activity would push me further into the exhausted, achy, brain-foggy abyss. Throughout this time my mum was my champion. She took time off work to take me to various medical appointments and fought for me to finally get my M.E. diagnosis at fourteen years old. Then we were told that nothing could be done. That was the last time that I saw a doctor or paediatrician about my M.E. No treatment, no support, no follow-ups or check-ups. I am twenty-six years old now and nobody has checked up on how I am doing.

 

Please continue to The New Normal for part two of this article.

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News

7 Nov 2019
ME/CFS Biomedical Partnership
3 Nov 2019
M.E. Organisations
1 Nov 2019
Badges Back In Stock
31 Oct 2019
M.E. from the Male Perspective
14 Sep 2019
Forward-ME
30 Jul 2019
New ME & FM Article
20 Jul 2019
CMRC Meeting Summary
21 Jun 2019
New Article Published

 
 
 

News

7 Nov 2019
ME/CFS Biomedical Partnership
3 Nov 2019
M.E. Organisations
1 Nov 2019
Badges Back In Stock
31 Oct 2019
M.E. from the Male Perspective
14 Sep 2019
Forward-ME
30 Jul 2019
New ME & FM Article
20 Jul 2019
CMRC Meeting Summary
21 Jun 2019
New Article Published