December 2020 archive

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.

This song is nice, but the finale still sucked.

Once I rose above the noise and confusion
Just to get a glimpse beyond this illusion
I was soaring ever higher
But I flew too high
Though my eyes could see, I still was a blind man
Though my mind could think, I still was a mad man
I hear the voices when I’m dreaming
I can hear them say

Carry on, my wayward son
There’ll be peace when you are done
Lay your weary head to rest
Don’t you cry no more

Masquerading as a man with a reason
My charade is the event of the season
And if I claim to be a wise man
It surely means that I don’t know
On a stormy sea of moving emotion
Tossed about, I’m like a ship on the ocean
I set a course for winds of fortune
But I hear the voices say

Carry on my wayward son
There’ll be peace when you are done
Lay your weary head to rest
Don’t you cry no more, no
Carry on, you will always remember
Carry on, nothing equals the splendor
Now your life’s no longer empty
Surely heaven waits for you

Carry on, my wayward son
There’ll be peace when you are done
Lay your weary head to rest
Don’t you cry, don’t you cry no more

I can’t believe that I haven’t mentioned this.

One of the reasons that I see myself so readily in Dean Winchester, and one of the reasons that he is my favorite Winchester brother and one of my all-time favorite characters in the show, is because I can see why someone might get it into their head “oh, I’ll die young anyway”. Some of my disabilities come with the price tag of a possibly shortened life because they are ones that I could actually die of. For the longest time, I used to joke off-handedly about that, and I had “made my peace” with a shortened lifespan. In very large part, Dean Winchester’s character changed that for me, and I decided that I wanted to live as long as I possibly could. In doing so, I didn’t want to actively worry about potentially having a shortened lifespan. And then Dean, who always said that he knew that he would die on the job or during a hunt, does exactly that… owing to a very rookie mistake and Sam’s refusal to summon aid for him, which could have saved his life had he done so. Our lives, no matter what we struggle with, are worth living. Shame Andrew Dabb disagrees…

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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