There's a new smartwatch on the market called Embrace smart watch. The thing that makes this watch different from other smart watches and caught my attention is that it tracks seizures. This new watch which has just been cleared by the FDA, has been tested on patients and collected over 6530 hours of data, during … Continue reading Embrace smart watch: seizure tracking and epilepsy management
Tag: epilepsy
I just realized today that I have an appointment with my neurologist in two weeks. My first thought was "this is great, I'm still seizure free", but then I remembered that last time I saw my neurologist he asked me why I wasn't driving yet and seemed disappointed in me. That was back in August … Continue reading Reminders
I try to stay active everyday, working out in the morning before doing anything else during the week. This just helps wake me up, at least it does some days. Other days, like today, I wake up tired; I sleep nine hours and I wake up tired. Then I wash my face, have breakfast, workout, … Continue reading Side effects
When my neurologist prescribed the epilepsy medicine I should take he also spoke to us about me taking some supplements. At the moment I didn't remember the reasons for which I had to take the supplements but my mother agreed with the doctor and I had no reason to doubt my neurologist. They told me … Continue reading Folic Acid Awareness
I keep saying I am so open about my brain injury and I usually am but lately I feel like I don't have to give everyone so many details. Like telling the kids I tutor; I don't really need to tell them, they're kids and I feel like that's just too much information. Today I … Continue reading They don’t need to know
The best part of the holiday season is, for many of us, spending time with our family and friends. This time full of parties and other gatherings with friends and family may be difficult for TBI survivors, I mean so many people and so much noise can get a little difficult, at least for me. … Continue reading Tips for the holidays
Having epilepsy is not easy, but I have learned that I have to be brave when talking about it, I have to bring it up and I have to tell people. I bring it up and I'm not afraid to because that's just a part of my new normal, living with epilepsy. I know people … Continue reading Start the conversation
"My Shot at Epilepsy" is this year's challenge to raise money for Epilepsy Awareness month. Participants are asked to take a picture or video of themselves in "My shot pose" (arm raised in the air, index finger pointing up), making a donation to MyShotAtEpilepsy .org and sharing it on social media, tagging friends to donate … Continue reading My Shot at Epilepsy
My bad, I didn’t give November the welcome it deserves being a very important month. No, I’m not talking about thanksgiving, I’m talking about Epilepsy Awareness Month. This doesn’t mean that we need to take extra care of our epilepsy, we have to do that all year, but share our knowledge and news about epilepsy. … Continue reading Epilepsy Awareness Month 2017
So look at what I found today: I think it was just sitting around in that Hobby Lobby waiting for me to find it and of course I had to have it. The only thing better than that was finding another one that said María but that's asking for too much. Finding that just made … Continue reading We are unstoppable
I stopped my monthly count once I reached 2 years of being seizure free but today marks two and a half years seizure free and I think that deserves a recognition. It's not just two years anymore, it's over two years and I am so proud of that. There have been challenges since April like … Continue reading Two years and a half
This morning I had an appointment with my neurologist to discuss those episodes I have had and the result of the EEG. I'll be honest with you, I was terrified that he would say they found something weird in my brain activity meaning he would need to increase the epilepsy medication dose and I was … Continue reading EEG results are in
My electroencephalogram was removed today. This process, just like gluing it to my head yesterday, didn't hurt one bit but it was a lot faster. I'm not sure what the technician put on my hair to make it all come out, but my head was really sticky, like I had way too much hair gel. … Continue reading After the EEG
Like I said yesterday, today I was getting an EEG. I had 24 electrodes glued and taped to my head. These are all connected to a recorder that I'm have to carry around like a purse, except it's not really that cute. Each of the cables from the electrodes is a different color and that's … Continue reading Electroencephalogram
Tomorrow I will have electrodes placed on my scalp to read electrical signals in my brain. It sounds weird and it is, but it's for a good cause. It's an EEG to find out if those weird episodes I had when I couldn't find the right word are seizures. I had this done before in … Continue reading Another EEG
Unstoppable María 