Diagnosis and medication

Sodium Valproate

Week 1- 4

The idea of medicating a small child (Or anyone for that matter) is a daunting one. I read all of the leaflets and researched online. It didn’t help. In fact it made the situation worse. The best thing I did was ask a ‘friend of a friend’ for advice, as her little one had also been diagnosed with Epilepsy. It was a breath of fresh air. I hope to do the same for anyone reading this.

The side effects for any medication can be vast. They can vary depending on the age and gender of the person taking it (Sodium Valproate is particularly risky if there is any chance of pregnancy -it can seriously harm an unborn baby) Everyone will have a different experience of the same brand/medicine. The side effects of Sodium Valproate are frankly scary – hair loss, liver complications, tiredness, hunger, over activity, mood and behavioral change etc. – but remember these are ‘possible’ side effects not definite ones. For us, so far, things haven’t been as bleak as the inside leaflet suggests .

Week one we started with 1ml in the morning and the same again at night. We hardly saw a change in W. There were no tonic clonic seizures, but he did have a cluster of absences. The seizures didn’t stop straight away which we expected.

Week two (2ml/1ml) and week three (2ml/2ml) is where we started to see some side effects. He was starving. I don’t mean a little bit hungry. I mean starving! We had to restock the cupboards mid week with healthy snacks. He was out eating me and then some. I watched him basically swallow a banana whole! I had visions of him turning into a little, toddler sized, bouncy ball. He also went from tired to super energetic on a couple of occasions making him rather grumpy. I do however wonder if this was a side effect at all or the fact he’s 3. In all honesty he was behaving like a toddler and nothing more dramatic than that.

Week four is where we are now (3ml/2ml). This week the hunger has slowed down. He appears tired, but not as grumpy. A couple of times his speech hasn’t been as clear as normal, but this was at night, after a long day at nursery and returned to normal after a rest.

Remember your little one will be monitored. If any unwanted side effects crop up, let your Neurologist/Epilepsy Nurse know. For us it’s going well.

I’ll update you on week five soon,

Lots of love,

Clare xx

Diagnosis and medication

Lets start at the very beginning…

Firstly I am not a medical professional. Just a Mum telling our story so far.

W had two febrile seizures when he was around 18 months old. He had tonsillitis at the time and we were told it was a normal reaction for a child who has a high fever.

Fast forward to this year. W has now had 2 convulsive, tonic clonic seizures and numerous absence/unexplained episodes.

I remember being in the Neurology waiting room. I honestly believed (even after 1 convulsive) they were going to send us home and say ‘come back in 6 months’ but they didn’t. They diagnosed Epilepsy. I cried.

I couldn’t believe it. I still thought they’d made a mistake. I remember speaking to the Epilepsy nurse and considering not putting W on medication. I found the possible side effects of Sodium Valproate daunting. Surely he didn’t need it? Nothing had actually ‘proved’ Epilepsy.

After this we visited hospitals for numerous tests. MRI’s, EEG’s, ECG’s, bloods. Then another convulsive seizure hit 2 days before Christmas. Yet again we were in hospital. It really hit me then. He was Epileptic and this was the start of a new chapter of our lives.

We started his medication on Christmas Eve and so far so good (apart from the tiredness and over eating) he’s only had a cluster of absences.

We are due to attend another EEG next week – but this time sleep deprived. I am anxious but I’ve now developed a little survival kit and grab bag for hospital visits. If you are just starting this journey, like me, it might be helpful (if you’re an experienced pro it would be awesome if you could add any helpful tips in the comment section)

  1. Food (a lot of food, snacks, drinks)
  2. Pj’s and comfortable clothes, as you never know how long you’re going to be there. Dress in layers as it’s so hot in some wards.
  3. Magazines/small toys and DVDs
  4. Wet wipes or similar
  5. Deodorant
  6. Socks/slippers
  7. Phone chargers (depending on length of stay or procedure).
  8. Change for the car park

Wish us luck for next week. I will update you on how it goes,

Love,

Clare xx

Uncategorized

The Journey Begins

 

Hello,

Welcome to my new blog ‘E-word’. I’ve decided to begin writing for my own well-being and after realising that there were not many (if any) support networks in my local area to support children with Epilepsy and their parents/carers.

My son was diagnosed with Epilepsy in October 2018 after having 4 seizures (2 diagnosed as febrile). Since then he has suffered with more seizures and we are now on the journey of medicating and hoping some normality – for us – may return.

This is our journey. I hope it helps to support others, even if it’s realising you are not alone.

Lots of love,

Clare

Good company in a journey makes the way seem shorter. — Izaak Walton

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