The
past two months have being very wonky, don’t know how else to put it. My body
and mind haven’t being feeling up to scratch. I know this because since I’ve
being completely gluten free for the past two years, and have felt fabulous-
seizures brought on by my temporal lobe epilepsy had also been dramatically
reduced to minor incidents. (Incidents caused by eating at friends and family homes
without realizing there was gluten in the food. A rookie mistake….) So what was
wrong now?
I was having episodes while at work with clients, the feeling of things being to real, experiencing déjà-vu, nausea and dizziness. Having a tingling sensation at the back of head going down to the base of my spine. It felts like I was going slightly insane… just slightly.
I was having episodes while at work with clients, the feeling of things being to real, experiencing déjà-vu, nausea and dizziness. Having a tingling sensation at the back of head going down to the base of my spine. It felts like I was going slightly insane… just slightly.
Part of It felt like I was poisoning myself somehow, but I was baffled as to what it was. I eat healthy, drink enough water and most important I watch what I eat… I had to sit down and think about all of this; my eating habits, my life style and stress levels. What have I being eating??? The only thing I could think that has changed is my devouring of packets of liquorice and crisp on the daily bases. I thought nothing of it as I consumed these items that gave me my daily fix. Why would I?
It’s
just liquorice and potato crisp after all, how could they be gluten in it. I decided to google liquorices, to find out
what it is made of. And as I tapped on
the enter button I knew the word wheat or modified starch was one of the
ingredients. I was gutted. As for the crisp, all I had to do was turn over
packet in my hand and behold……gluten. Why hadn’t I read the label. Clearly another rookie mistake…..
So diet had been a factor,
I decided to look at other factors in my life…
Have I been stressing?? I didn’t think so but the more I thought
about it, the more I realize that I have being stressed and I was giving myself
anxiety. I had set myself a personal goal and a time line. And as that time
line came and went, I started panicking because two months after, I was still
some way from reaching this goal. I decide then to go see a neurologist since I let
myself fall of my wagon and I haven’t been for a checkup in over two years.
The challenge for me was which neurologist to see. The last
one I went to I felt was suffering from the “God complex” and had no empathy (and
the fact that he put me on so much medication I was high as a kite and a non
functional human being). I settled on the neurologist that first diagnosed me
five years ago. As I sat in the chair, trying to describe my fit
to the doctor(it’s so hard to explain to someone what happens in my brain when
I get a fit)I knew I made a mistake
coming here. I tried to explained as best I could about how I had been feeling. And even
though my symptoms hadn’t changed, I was told I needed to be re-diagnosed. I
was stumped. On what basis did I need to be re-diagnosed? And If I needed a
re-diagnoses, why was I given a prescription for a new Epilepsy medication. I
couldn’t understand.
I left
the rooms confused and extremely agitated. Two days of over thinking and
chewing at my nails. I decided that the best way forward was to continue to
manage my lifestyle, from my eating habit to exercise. I have learnt not to over think the mundane things life to
and to except life will always throw curve ball at you, it’s just how you deal
with them. And most important was to have fun and enjoy the little gift life
sends your way.
This was not an easy lesson to learn, specially the over thinking part. But doing
this helped me manage my Temporal Lobe Epilepsy and Celiac Disease. Being
diagnosed the Temporal lobe Epilepsy was extremely hard for me to except. The
scariest thing for me was, it was genetic and if I decided to have kids there
was a six percent chance of it being passed on. I didn’t want my kids going
through the same feeling of chaos I did. So having the doctor tell me I had to
be re-diagnosed, after living with this for most of my life and my initial
diagnosis years ago and going through the acceptance process was a definite
blow to my system.
I have now made a conscious decision not to
let this get me down. My mission to find a neurologist and next time I fall off
my wagon to pick myself up……. Because i can, we all can ;-)
SD