Anyone else have a problem with the new LE... - Epilepsy Action

Epilepsy Action

3,016 members1,129 posts

Anyone else have a problem with the new LED light panels?

Hermanm profile image
1 Reply

Hi , I was working in my shed on Tuesday,

when out of the blue,

I suddenly felt dizzy and fell down/passed out ,

I woke up a little bit later ( seconds I think) in a bit of a state ,

cuts all over my head, damaged nose, resulting in 2 black eyes,

I'm currently waiting for a consultation with an epilepsy specialist due to having a fit in my sleep back in January ,

(I think that was caused by a leaking exhaust on my "Chinese diesel heater " but that another story! )

anyway my shed is lit by those new , led panels , very bright , and really cheap to run,

But I have heard that they can affect people's vision/eyes,

Anyone else had problems?

Cheers

Written by
Hermanm profile image
Hermanm
To view profiles and participate in discussions please or .
1 Reply
EpilepsyAction1 profile image
EpilepsyAction1PartnerEpilepsy Action

Hi

I hope you hear from others on this platform, as sharing information and experiences can be a good idea. Can I just check you also know about our other services?

We have lots of information on our website epilepsy.org.uk that you might find useful, such as information about diagnosis, treatment, seizure types, first aid and daily living.

We also have information on photosensitive epilepsy epilepsy.org.uk/info/photosensitive-epilepsy. Photosensitive epilepsy is where someone has seizures that are triggered by flashing or flickering lights, or patterns. This affects around 3 out of every 100 people with epilepsy. Light bulbs of any kind are usually only a possible seizure trigger if they faulty. Otherwise, they shouldn’t flash or flicker and so shouldn't cause a problem for people with photosensitive epilepsy.

We're not sure if LED panels can cause any other issues, such as with vision.

We have our virtual support groups epilepsy.org.uk/virtual-groups. We have our forum4e online community forum.epilepsy.org.uk, and we are on facebook facebook.com/epilepsyaction and twitter twitter.com/epilepsyaction.

Finally, please feel free to contact our helpline team. You can either email helpline@epilepsy.org.uk or phone the Epilepsy Action Helpline freephone 0808 800 5050. Our helpline is open Monday to Tuesday 8.30am until 700pm, Wednesday to Friday 8.30am until 4.30pm and Saturday 10.00am until 4.00pm.

Regards

Jess

Epilepsy Action Helpline Team

You may also like...

Anyone else experiencing seizure onset for first time after having Covid 19

fibromyalgia and severe asthma but no previous epilepsy or seizures and no family history of it.

Does anyone have a constant rushing noise in their head? Could stress have caused my epilepsy & is menopause/diet making it worse?

I was diagnosed with generalised idiopathic epilepsy aged 43 in 2013 after having 2 tonic clinic...

Alcohol induced seizures

job where I need to travel, nice car etc and I think if I take it to the next stage I.e seeing a...

Nighttime seizures advice required

seizures Hi all, I’ve not been diagnosed with epilepsy despite having various tests (ECG, EEG and...

Night time awakenings

wife has been diagnosed with epilepsy. She started with focal epilepsy that Levetiracetam sorted...