Archive of ‘personal’ category

I guess the name of the game is patience.

I am now on day three of “no shampoo (and conditioner)”, only cleaning my hair with water and brushing it.

If I can get through this with my hair intact, I’m only going to wash it before I dye it so that the hair strands are as open and stripped as they can be. Normally I don’t have to wash my hair that often, maybe once or twice a week, but I’m tired of dying my hair and then having the shampoo strip it, no matter what kind it is or how “friendly” it’s said to be to hair that has been colored. I just want my hair to stay as bright as possible, and if that means saving money not buying myself shampoo or conditioner from here on out… that’s great.

Bub’s microSD came in the mail, and so far so good downloading all of his games “from the cloud” onto it. Well, aside from how long this looks like it’s going to take, but I knew that going into this. This is a 400GB microSD, so here’s hoping that it holds all of his games and the ones that he will pick up afterward for… well, at least a year. It seems like we’re getting a new microSD card every year now, but I don’t mind as long as there’s something that I can keep all of his games on. Some of these games are large, so downloading them from the cloud time and time again (which is where they are kept after purchase if they’re not on the actual card itself) can be and is cumbersome… just a bit. And this one is an actual Nintendo microSD card as well!

Here’s hoping that it doesn’t take more than two days to download all of these games, big as some are…

Since I haven’t actually mentioned this here…

At the local pain management clinic, I was put on 2,700mg of Gabapentin to see if it affected my migraines. I titrated up to it over the course of a month. Doctors have people titrate when they’re going up to higher doses to try and minimize the “medicated” effects that the medication is more than happy to provide, but I got there. And as I got there, a numbness began to form in my left hand that I didn’t pay much heed to until I realized that I could only really use my index finger and thumb, that I can not bear weight at all in my left hand, and if I want to type coherently with both hands I need to watch exactly where my left hand is because I hunt and peck by memory. The numbness kind of goes up my arm on that side, and I have milder numbness on the back of my left foot. Since it is helping, the decision was made to leave me on it for as long as is safe and tolerable, and I am adjusting in the meantime. I am also back on Fioricet, and recently had my dose upgraded from one pills to two as needed. If I can get away with it I only take one pill, but I know myself well enough by now. If the side effects from Gabapentin persist or get worse, I will titrate back down.

I was also put back on Olanzapine as needed for migraine abortion, but this medication has made me gain weight. Too much weight gain adversely affects my spirometry, and if it keeps going, my ability to breathe (so then there would be weight gain on top of my already pre-existing asthma). I take it only as I need it…

I am also thinking about having my primary care doctor upgrade my nortryptline from 50mg to 100mg, too.

I should have done this awhile ago…

For the most part, I’ve transferred my neurological care from the neurologist that I was seeing one town over to the local pain management clinic here in my city. My primary care doctor was, and has been, in full support of this and thinks that it was (is? how do I phrase this?) the right thing to do. We discussed Botox when I was seen for the first time, which I am amenable to attempting… we just need to get insurance approval for it, or know that insurance denied the clinic’s attempt to seek approval for it from me so that we can appeal the denial. So far, no one relevant has heard anything back about whether it was denied or approved… so I guess that’s a waiting game, and we’ll see when we see. In the interim, and to have it on hand in the event that I need it, I’ve been prescribed Fioricet again, and we are currently working on getting me the highest dose and frequency of that medication which works, but not go beyond that unless we have to so that I don’t inure to it the same way triptans do in that they no longer work on me at all. “Fioricet is love, Fioricet is life” has become one of my biggest inside jokes, because to be honest, it works decently…

For me, for someone who very often doesn’t get a lot of pain relief other than by waiting it out, this is huge.

I also found out that I am on nearly the largest dose of Gabapentin. That is 3,000mg, and I am currently on 2,700mg. I’m also not sure if I’ve mentioned it here, but I’ve begun to develop peripheral neuropathy on my left side due to it… but as long as it helps migraines, which it does, I am reluctant to give that up unless I am made to give that up. The only major downside to this is that I am left-side dominant. My left ring finger, left pinkie finger, and the area going downward from that to my elbow is numb now. I also can’t bear weight on or with my left hand. But like I’ve said, if it makes a sizable dent in the pain, I am willing to live with all that.

The back of my left foot is also numb, which means that I have to be careful walking, but… see above, heh.

Since I said that I would write about it…

This is not a sponsored product review. These are merely my own opinions on the matter.

I was given Madison Reed as a Christmas present in the shade of rimini garnet (or is it Rimini Garnet?). Initially, I couldn’t choose between that and volterra amethyst (Volterra Amethyst?), but the red shade won out because I’d read reviews on the amethyst one and saw that several people who had dyed their hair that color had the amethyst portion of it wash out really quickly. As an asthmatic, and as someone with… a weird immune system, to put it bluntly, the last time that I actually dyed my hair was probably more than ten years ago. I just gave up on it. But I’d heard a lot of good things about Madison Reed, wanted to try them out for myself at some point, and hoped that I wouldn’t adversely react to any of it. I react to, well, a lot of things.

First of all, there’s no bad smell with this hair dye like there is so many others out there. All you have to do is put on the barrier cream that they give you so the dye doesn’t stain your ears or forehead, put on the gloves, and mix the colorant in the activator bottle that they give you. It’s surprisingly simple. What was not quite as simple was me covering all of my hair with the colorant because I have thick, wavy hair. There is more hair on my head than it looks at first glance. Another thing that I like(d?) about Madison Reed is the fact that it doesn’t stain the shower when you rinse it all out, and it doesn’t even stain your hands that badly. Using Splat, I was guaranteed to stain the shower and my hands for at least a week, and generally longer, heh…

The shampoo and conditioner that they provide also leaves your hair extremely soft, which I really liked.

After this, to maximize how long my hair stays colored, I think I’m going to start on the “no poo” (no shampoo/conditioner, just water to clean it) method. I’ve heard that part of getting over the hurdle until your scalp produces the proper amounts of oil is to brush your hair a lot, which I’ve started doing in advance.

All in all, Madison Reed is a lot better than all of the other dyes that I’ve tried in the past. I like it a lot.

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