Even though what I went through almost two weeks ago wasn’t as traumatic as my rupture in 2006, it was still stressful on my brain. Coiling was attempted and then a stent was employed, so some things out of the norm still occurred.
Even though I know fatigue is a major after-effect of any brain issue, it can still be very frustrating and cause one to feel out of sorts and un-effective when all you want to do is sleep. Reading that it’s OK to feel fatigue and that it’s normal again has helped. It’s getting everyone else to understand that fatigue is a part of this that’s difficult some times.
People at work have been great and Dave is always understanding, but those who are outside of the realm may not get it and explaining it in depth just isn’t something I like to do with every person. Oh, well….it is what it is!!
And I’ll probably JUST get to feeling back to normal and I’ll get to do it all over again for the coiling at the end of April. Goody!
I was back at work on Friday. Dave offered to take me in and pick me up, so I took him up on that offer. I could have done the drive in, but not the 30 mile drive back home after working all day.
The different setting took some getting used to and my office had been cleaned, so many things weren’t in the same place, but it felt good to get back to some kind of normalcy. It turned out to be a busier day than I was expecting, which was good and bad. It made the day go by very quickly, but I didn’t give myself enough breaks, so by mid-afternoon I was wiped out. I forget I need to pace myself and listen to my body after any
kind of a brain procedure. Simple things will take a lot of out of me for a time yet.
Dave arrived about a half an hour early and I promptly left. I kept yawning about every 30 seconds on the drive home. Poor Dave. Not much fun for him.
I was a zombie when we got home. I had planned on making dinner, but Dave talked me into laying down and resting. Of course I immediately fell asleep, which I knew I would. I woke up at 7:00 then was back into bed around 9 or so. Yep….the fatigue is alive and well. Frustrating, but it’s all a part of it.
Saturday I felt okay, but was still tired. I took two naps throughout the day, but that’s okay. I needed them….my mind and body needed them. I took a big step on Friday flying right back into work full-time like that. We’ll see how I do next week.
I want to sow some seeds, but just don’t have the energy right now. And I keep forgetting I have to do this all over again the end of April when I have the coiling done. Yippee!
Although the diagram below isn’t exact, it’s a decent representation of how things are currently looking in my brain,
with regards to the larger aneurysm.
The one that ruptured in 2006 is approx. 1/2” in diameter. 16 platinum coils were inserted into the aneurysm. Since then, either the aneurysm has grown or the coils have compact resulting in a small pocket of blood to leak back into the aneurysm.
Last week, my neurointerventional radiologist attempted to add more coils to the aneurysm, but was uncomfortable doing that with the current conditions of my arteries and the wide neck of the aneurysm remnant, so a Neuform
Microdelivery Stent was implanted across the neck of the
The stent will allow more control and easier delivery of coils to the aneurysm, which we will go back and try again
at the end of April.
According to the information I was given the size of the stent is a little less than 1/8” of an inch wide and a little over 3/4” of an inch long. The stent will allow blood to flow through that artery better and keep the artery open and clear for coil implants.
It’s pretty amazing to think of all this “metal” in my head now, but it’s saving my life.
Hey, I actually slept all night and didn’t have to do it sitting up. Although i think I DID sleep in the same position all night. Neck is very sore. I have the bean bag heated up and wrapped snugly around it.
My job today is to see how the of ALL of my new meds act together. I am now taking 5 pills a day. 3 of which are relatively new (Plavix, Aspirin & Cymbalta). I have discovered this morning that if I’m going to take that many at the same time, I need to eat a lot more at breakfast. I’m shaky and a tad disoriented…..but then I guess I’ve been that way the last six days anyway. Just still not sure how all of this is going to effect me and for how long. I felt pretty good last evening, but had a bad headache right before I went to bed.
I’m not in horrible pain this morning either, so that’s a good sign. My head feels woozy, but not pounding or throbbing and I’m just wicked tired…what else is new. Let’s hope these meds kick in quick, I can get everything regulated and get on with my life as it will be for now. I’m trying to get up and walk through the house as much as I can to keep things moving, but when I’m dizzy…probably not the wisest thing to do. LOL
It feels good to know that a lot of “stuff” I’ve been going through truly WAS withdrawel from taking the Provac cold turkey. Not the wisest thing to do I know, but none of the so-called medical professionals could give me a straight answer…or they could, but they chose not to respond to any of my calls. Better late than never, so I now have a script for Cymbalta and my system will now have to get used to that now. I only take those pills for PMS and for work stress, but without it, all hell could break loose!
At least my appetite has come back and I’m able to KEEP things down now. That was horrible and so exhausting. It’s been seven days, and I don’t think I’m doing too bad considering, but I’m not quite there yet.