To begin with, my name is Tarushi Tyagi. I belong to city
name Alwar, India. By profession I am a Chartered Accountant, member of Institute
of Chartered Accountant of India and have been working for a bank for the past
I have wonderful family of 4 including my mother, father and
brother who have been a great support throughout my life. They brought me up
with lots of love, affection and most importantly never made me feel that I was
different from other kids because I had epilepsy. They didn’t ever make me feel
that I wouldn’t be able to do some things in life. I still remember my doctor
telling me that I couldn’t do 2 things in life: fly an aeroplane and drive a
I have had epilepsy for the past 24 years. For as long as I
can remember it has been a part of me and I am part of it. I don’t think of it
like a disease though, rather it’s simply a part of me. The sooner we accept
ourselves the way we are, the sooner we are set free - trust me, it’s the best
thing in world and I love the feeling.
I was 7 years old when I first had a seizure in school. My
doctors told me that this didn’t always mean that a person had epilepsy, but,
after having a cluster of 3 seizures just after lunch one day, I went on to
have an EEG and MRI, the results of which led to my doctors diagnosing me with
epilepsy. They diagnosed me with a rare form of Reflex epilepsy known as Eating
Epilepsy. My uncle is a doctor hence I was lucky to be in the right hands
regarding the diagnosis.
Multiple doctors were consulted all over in North India but
were not able to reach or decide upon the drug or dosage that could suit my
body and stop my seizures. I was referred to another doctor in Delhi8 who was
able give me partial control over my seizures however.
All my life my seizures have occurred between 3 and 4pm,
just after lunch! I used to tell my ma (mother) that I was seeing lots of
flashing lights around my eyes and that I wasn’t feeling well, and I would then
go and lie down.
Both my parents have personally focused and enabled me to
focus on both my studies, and the things that I excel in. Families, relatives,
friends, and schools have the responsibility to support people with epilepsy
just like they would everyone else. They must be treated with equality so that
people don’t feel that they are less than anyone else.
Through the support of loved ones I have been able to
overcome hard times and look forward. Many times that I’ve had seizures it has
been due to stress from my studies. After the seizures I would have a cry, put
the seizure out of my mind and focus on plans for the next day.
It’s very important to be able to find things to look
forward to. What has helped me is to decide upon and lay out my goals in front
After being seizure-free for 7 years (during which I
completed one of the toughest national courses in finance), my doctor told me
that we were going to slowly reduce my epilepsy medication dosage and have me
come off of them over 2 years.
I’d previously had my body tell me to sleep 13-14 hours a
day but my mind conflicted and told me I should be active – they conflicted.
Anyway, after 2 years I was taking only 1 medication and the way I felt was
like nothing I’d ever felt before – I felt so fresh and with so much more
energy that it was like I’d just sobered up from drinking! 😊
This made me realise the psychological and physical impacts that my medication
had been having on me.
Feeling energised was new to me as at age 25. Being on this
one medicine didn’t make me feel sleepy and I’m told that I didn’t look sleepy
to other people anymore either!
Mental health - depression & negative
Negative emotions hit you back even after having greatest
support of loved ones.
Whilst I was enjoying an energised life, I had another
seizure. I’d completed my studies but was jobless and I went into very bad zone
of self-doubt. Some jobs I had to turn down because they’d have stopped me from
getting the sleep I needed (sleep is like a form of medicine!). After a while
though I got some great news: I’d won a job with an amazing organisation!
After 3 months with the new company I had another seizure,
in the office. I’d told my colleagues about my epilepsy though, so they took
good care of me. I was back to the office after 4 days although was feeling
drowsy because I’d had to have my medicine dosage increased.
Increasing the dosage caused a new negative psychological
issue for me as well; I feared that I might have another seizure and was really
doubting myself. I did find some ways of relaxing, but I started distancing
myself from people: I felt that I had no choice but to do so.
It took me few months to get back to “normal” – and life was
really challenging, but I did it and had another wonderful 4.5 years of seizure
In October 2018, my seizure freedom ended again when I had 4
seizures over the period of a few months. The dosages of my medicines were
increased again (!), but this time with different side effects. It’s crazy
stuff: you don’t know how your body will react to the medicines. Again, I had
an issue with coordination between my mind and body, which was so frustrating.
I tried everything to get back to my normal life through routine, but it was
quite a struggle. One day I read a quote:
“There are only two ways to live your life. One is as
though nothing is a miracle. The other is as though everything is miracle.”
It felt like a miracle that I was still alive. Every time I
had a seizure my first thought was: “My parents will be worried, and I am
troubling them again”. Slowly and gradually though, I removed my feelings of
guilt from within and started taking 1 day at a time.
Due to the latest dosage increase I was sleeping 12 hours a
night, but as I got used to it, I felt less tired, and now I’m back to 9.5
hours – it’s a happy moment for me.
My next target is to get back to 9 hours and start
yoga/meditation which is crucial and just like medicine and sleep for me.
What I have learned from my journey to date is that the most
control I have over my epilepsy is to take my medicine on time, keep to my
sleep schedule and try and manage my thoughts (which can play a crucial role in
For families who care for anyone with epilepsy, providing
them with emotional support and confidence can encourage them to lead their
lives with confidence. They might still face negative thoughts and self-doubt
but having a strong family foundation can help them towards overcoming this.
Accepting the diagnosis of epilepsy has helped me to live
with it and how it has influenced much of my life. Acceptance is key. There is
not a specific path; each day brings new beginnings and new struggles.
During these unfortunate times of COVID-19 we
need to take care of ourselves as it is deeply impacting many people mentally.
Take care of yourself and those you care for both mentally and physically.
Wang X, Chen B, Jin L, Zhang W, Liu Y. Eight years follow-up
of a generalized epilepsy patient with eating-induced late-onset epileptic
spasms and atypical absence with myoclonic jerks [published online ahead of
print, 2020 Aug 10]. Brain Dev. 2020;S0387-7604(20)30201-1.
Purpose: Eating epilepsy was previously known as a kind of
focal reflex epilepsy. However, the development of eating-induced multiple
generalized seizures and the associated EEG changes were rarely reported.
Herein, we present a 13-year-old generalized epilepsy patient with
eating-induced generalized seizures since the age of 5.
Conclusion: In conclusion, this case demonstrated the
variability of eating induced multiple generalized seizure types, and eight
years follow-up also indicates that generalized epilepsy progressed with age.
The EEG and clinical changes of our patient contribute to a better
understanding of the electro-clinical features of eating-induced multiple
generalized seizures and the course of generalized epilepsy with such seizures.