Finding new "normal" and the right pace could be hard. Those focal seizures and auras sometimes feels like invisible punches-sometimes even invisible machine gun bullets-to brain. Take a time off to resettle. I hope you're feeling better soon, Carlos. 💜💜💜💜
We're constantly learning how far we can push our brains before we hit burnout and we're tweaking the work we do. We've become scientists for our bodies lol That's such an accurate explanation when it comes to auras/seizures. Although we may look "normal" on the outside, we are going through a battle inside. This little break has really helped a lot. I feel more centerted now and everything has a time limit to it. Thank you for your kind words
I'm so sorry for what happened to you last week😔. In my case I have focal seizures and every time I am on the computer for a long time and I do not rest because I want to advance university work, my head starts to hurt, my hands go numb and sometimes I have tremor on my lips and my arm. This happens to me for the simple fact of not accepting that I have a condition that other people I know do not have it. I also always pretend to be fine when I'm not with the simple fact that people do not think that I am weak and I let my condition prevent me from doing normal things. Thanks for this video.✌️🙌
Your comment is incredibly relatable. When it comes to epilepsy, like I said in the video, we push ourselves because we want to PROVE to ourselves that we can do something. We don't want our ailment to stop us, but when it comes to doing a lot of work in one sitting, our minds can't handle it at times. Have you talked to your university about your epilepsy, so you are able to get accommodations? One of my friends has epilepsy accommodations for epilepsy and they get more time to finish assignments I understand your thought-process with not wanting people to think you're weak, but your health will always be the most important thing in your life. Although it's easier said than done, it's best to be upfront with your family/friends about your epilepsy and how you're feeling. I understand how difficult it may be because it took me over two years to share when I was having auras with my family. You can do this, Josefa! Stay Strong, Warrior!
Finding new "normal" and the right pace could be hard.
Those focal seizures and auras sometimes feels like invisible punches-sometimes even invisible machine gun bullets-to brain.
Take a time off to resettle. I hope you're feeling better soon, Carlos. 💜💜💜💜
We're constantly learning how far we can push our brains before we hit burnout and we're tweaking the work we do. We've become scientists for our bodies lol
That's such an accurate explanation when it comes to auras/seizures. Although we may look "normal" on the outside, we are going through a battle inside.
This little break has really helped a lot. I feel more centerted now and everything has a time limit to it. Thank you for your kind words
I'm so sorry for what happened to you last week😔. In my case I have focal seizures and every time I am on the computer for a long time and I do not rest because I want to advance university work, my head starts to hurt, my hands go numb and sometimes I have tremor on my lips and my arm. This happens to me for the simple fact of not accepting that I have a condition that other people I know do not have it. I also always pretend to be fine when I'm not with the simple fact that people do not think that I am weak and I let my condition prevent me from doing normal things. Thanks for this video.✌️🙌
Your comment is incredibly relatable. When it comes to epilepsy, like I said in the video, we push ourselves because we want to PROVE to ourselves that we can do something. We don't want our ailment to stop us, but when it comes to doing a lot of work in one sitting, our minds can't handle it at times. Have you talked to your university about your epilepsy, so you are able to get accommodations? One of my friends has epilepsy accommodations for epilepsy and they get more time to finish assignments
I understand your thought-process with not wanting people to think you're weak, but your health will always be the most important thing in your life. Although it's easier said than done, it's best to be upfront with your family/friends about your epilepsy and how you're feeling. I understand how difficult it may be because it took me over two years to share when I was having auras with my family. You can do this, Josefa! Stay Strong, Warrior!
Hello cuh
Mr. Default wassup mate