When in doubt always ask your doctors about it.

So frustrating can take weeks to get an appointment so by the time I do I’m all better and as my memory is not the best I forget what I went there for 🤦‍♀️😂😉 x

I feel like my doctor is writing down my prescription before my bum hits the seat. I always have loads of concerns In my head when I manage to get an appointment but I just seem to get the same palm off of aw well and gives me another copy of my prescription. I’m not good at talking about personal problems in person. I’m not confident in my medical after care or update records at all. I feel just as lost and vunerable as the day I was diagnosed. I hate it. I’ve lost so much weight and confidence that I’ve resorted to this.....a cry for help on social media health advice chat pages 😔 why can’t I find support to stop me hitting the point of no dispare rather than cleaning up what bits and pieces Ieft behind. If I don’t get help to keep myself housed I’ve lost everything due to epilepsy. I can’t bare to think of the effect of becoming homeless would do!