4.08.2015

Another Seizure

Still waiting for the UCLA MRI results. Haven't been posting much, but wanted to make sure you all know I'm fine. Had another seizure yesterday. A legitimate one, not just an aura. I had forgotten how bad seizures hurt. And today, the day after the seizure, my head feels like it's exploding. Especially if I lower my head down toward my heart (is that normal?). Freaking seizures. I'm exhausted and can't retain much since wires are all fried. It's a nap day. 

Dan took this after I fell asleep. He had rushed home to help me.


It's good that Dan could come home and help me. He found the house in a mess, water everywhere (counter and floor) - I had tried to get ice water to cool me down and stop the seizure's progression. He found my packet of lorazepam (my seizure pills) on the ground crumbled by my fist as I couldn't get the pills out. I was half in and out of my clothes because I was overheating, then freezing, but couldn't get dressed again since my entire right side was paralyzed. My lips were blue and my skin purplish, from chill. It all always happens so fast. I imagine it's similar to a stroke. (Although, perhaps a little less damaging.)

My right side was paralyzed, then numb, the entire rest of the night. It's starting to get better, but shockingly this seizure has had very long-lasting side effects. It's one of the most intense seizure situations yet, without losing conciousness. 

Hope you all are well. I'm off to rest some more. Just thinking hurts. 


3.23.2015

MRI 3/22/15 Results


The MRI results are in: "Findings: 
Compared to multiple previous examinations, contrast enhancement at the site of previous left parietal craniotomy and tumor resection is unchanged. The extent of flair signal abnormality is also unchanged compared to July 20, 2013."
                     
Woo HOO!!!! 

Still have to wait for final UCLA results in a few weeks, but with UW's results like this, I'm going to remain optimistic. Time to dance!!!

And now I can focus more on others, not me! Ha! YES!!! My ultimate goal is manifesting. I like this.

Organizing Patient Data

My butt has been planted on a padded bench at a coffee shop since 7:30 am. I'm down in the city, in the place I love - Seattle - killing time until I can make my way to the records department at Harborview Hospital (the new location to house all of University of Washington patient records) to get my radiology report.

Don't worry seizure monitors, it was a split shot.

I could have walked in there hours ago, they open at 8:30 am, but I'm trying to wait until Dan and I can read it together and I don't trust myself to have the report and not read it. It's too stressful to have that hot ticket in my fidgety little fingers. My plan is to ask for an envelope, and I'll seal it. Then I can't sneak a read before Dan. The thing is that I'm the kinda girl that can't even wait for people's birthdays or Christmas to give gifts. I get too excited. And although this is different, it's essentially the opposite side of the same candle.

I'll have to grab the report before Dan's off work so there will be a period of time where I will have to demonstrate enormous restraint. Ugh. I hate having restraint. It may be my worst - or missing - attribute.

So what am I doing? I'm going through all of my emails, text messages, and phone calls, organizing all of my patient records. I have been helping lots of people over the years, and we've all talked about so much stuff, all these unique cases (as all cases are), and it's a mess. I never had a good system, which I am realizing is a major misstep. Fortunately, Stephen (astrocytoma options) sent me a wonderful spreadsheet for just this purpose, and I'm having a blast entering all of the data. I love me some organizing. It's helping me realize how random my accumulated patient data is. It's making me want to reach out to everyone and see if they can fill out some info about how they're doing now, what they're taking (treatments, supplements, off-labels), how often their MRIs are, what their pathology is, the mutations, who their doctors are, etc. all that good stuff. The more we know about what we're all doing, the more we can start correlating and working together. I keep saying that there's strength in numbers, but the truth is that if we aren't organized, the information is almost useless (not really, but it definitely isn't as helpful). Just so you know, I won't share your private information, I'm just trying to make sure that I can keep up with all of you and make sure you're doing okay. And if you allow me to reference your case to others, it might be helpful for others. An example might be anecdotal information about dosing and side effects of off-label use. (No names would be needed.)

That's what my day is looking like. This is my distraction that makes me happy. I feel best when productive, and I feel best when I'm focusing on other people's needs. I'm excited to beef up my spreadsheet, very hopeful that it could make things easier for all of us. As each of us continue to be successful, or at minimum continue to try new treatments, and new combinations to get healthy, it's a win-win for all. Doctors have a lot on their plates, and I don't expect them to fix everything. As you know I take a lot of responsibility for my health. I don't expect anyone to cure me, but me. That includes choosing the right team to employ (my doctors, and nurses, and experts). But I do the majority of my own work. People rarely give us things in life, not the big stuff anyway. People don't just give great jobs just because, they give jobs because you've earned it by the resume you've built, by the experience you've gained. They don't give away houses just because you want one. You have to save money, or do the research to find supplemental programs that will help you get a roof over your head. All things in life take work, effort, but you don't have to see it as a burden, you can just look at it as a process. Everything is a process. Is it all fun? Nah. Course not. But with the right mindset, and the right people around you, anything can be fun. Hell, I'm even having fun today as I await my fate.

I've been chilling in Green Lake and it's almost time to start the hour long, two bus, trek to Capital Hill to visit Harborview's medical records department. A journey that in a car, if I could drive, would be less than 15 minutes. Thus goes the life of an epileptic.
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