Epilepsy and work

 my daughter is studying beauty, please god if she applys for a job should she tell them she has epilepsy as I feel if they know they wont employ her

I had my first seizure. At work.So they have known about it From the start. Took about 6 months to get my first diagnosis. They couldn’t have been any more supportive. My manager is always there if I need a word. There always accommodating to any hospital appointments or anything relating to my epilepsy’s. I do feel a bit judged when it comes to overtime. For a time they would avoid asking me. I like doing overtime. So I had a word with my team leaders and managers. And they were only trying to be nice! Much appreciated. But mostly they have been great especially since my full diagnosis with my second seizure and September 

I am a a good plasterer my journeyman was a great guy but needed a driver at the end so I was quickly  dropped when my apprenticeship was complete  I did manage after almost 40 job applications to get a job this was almost 30 years ago  it was just a packing job in a meat factory so many employer's are bias towards our condition and only think of us as a liability and are often left last 

I work from home, but the one thing I find is that I get very depressed and find it hard to be with lots of people epilepsy has changed me.