BIG NEWS!! The Return of ‘Everything Sci-Fi’

I very excited to announce that I’m returning to Eat Sleep Write, hosted by Adam Scull.

After a long hiatus, Adam has returned with the eatsleepwrite.org site that hosts various author blogs and their backstories. Adam is a long time photographer that was involved with Studio 54 back in the eighties. Now, he’s back hosting podcasts and author blogs.

This is a VERY strange story. A story that I’ve not even shared with Adam as yet. Last week my wife and I were just talking about Adam, wondering whatever happened to him and where he is today? The very next morning, Adam popped in on my instant messenger, inviting me to return to his web as a blogger. About six years ago, I was highly active on his blog, writing a weekly article titled Everything Sci-Fi. I had also done some podcast interviews on my writing journey. Unfortunately, I had to take a break from this due to my physical issues going on. Now that I have a handle on them, I was more than ready to accept. So, effective immediately, I’m now a part of the Eat Sleep Write community one again and have committed to writing my weekly blog.

Yeah, I was hesitant at first since I do have these physical limitations… Well, I decided to do this regardless of my issues. I told Adam, “I can’t let these issues control me. I have to control them.” This will also be one of my blogs in the coming weeks.

You can find my first story, with updates, which was originally posted here, over there on my own blog page. Click this link to find me there.

Pirates Trilogy is on sale all week!!

Greetings to all you pirate lovers. Today, starting at 8am, Pirates of the Galactic Empire: The Trilogy, will be on a Kindle Countdown Deal!!

Yes, that’s right, starting today in just a couple hours from this post, this three volume eBook will be discounted from $7.99 to a miniscule $3.99 for two days. Then $5.99 until Saturday, March 12th at 8am. Don’t miss this fantastic discount. It’s three books in one volume and of course, if you have Kindle Unlimited, you can always read the entire work for free.

I think I’ve lost my mind, but we already know this.

Happy Reading…

The diagnosis is in

Well, I’ve been officially diagnosed with Keratoconus (pronounced keh-ruh-tow-kow-nuhs) in my left eye.

A condition in which the clear tissue on the front of the eye (cornea) bulges outward. With keratoconus, the clear, dome-shaped tissue that covers the eye (cornea) thins and bulges outward into a cone shape. Its cause is unknown.

This usually shows up in puberty or late teens, so, they’re mystified as to why now?

But the good news is, I can get this special contact and new glasses to see better.

I go in on the 7th for the fitting and then again to get it. But then, I’ll have to get the new glasses, so it’s a process.

They want to see me every six months to check it it’s changing. It it is changing significantly, there’s another procedure that will help.

I’m hoping I can tolerate the thing in my eye. Time will tell.

Getting a sclera contact fitting today

Wish me luck. It’s been a challenge finding a provider that does these sclera contacts and takes my insurance.

I’ll let you all know how this went later today as my appointment is at noon my time today. Once they take all the needed measurements, it’ll take a week to 10 days for it to come in. I also have to order a new set of glasses and get those to come in so I can try it all out.

Here’s to hoping all goes well.

Brian

Summoning the dead for Jury Duty

So, you may already know that my mom passed away last month on the 8th. Yesterday, and I kid you not, she received a summons for Jury Duty. I called and left a message at the clerk’s office. This morning, they called me to let me know she was excused. Wasn’t that nice of them? I wanted to kid with him that I could bring her ashes, but thought twice about that.

I’m wondering how random this really is as everyone in our household has been summoned for Jury Duty, most of us in the last 3 months.

On top of all that, I got a call yesterday from Visiting Physicians asking if mom still resided at the nursing home. I told them she passed last month. Her answer to me was the nursing home told them she was discharged. ‘??’ Well, I suppose that is accurate.

I don’t know what’s going on in this world we live in, but jeez! I’m tellin’ ya’ you really can’t make this stuff up.

Finally, a diagnosis for my eye

Well, after almost 3 hours at the eye clinic yesterday, I have a diagnosis on my blurry and double vision.

Apparently, the cornea in my left eye is warped. No explanation as to why and why all of a sudden. It’s very odd, he says. So, I told him it matches my personality of oddness and warped.

It’s called Monocular Diplopia caused by corneal ectasia which is a weakling of the cornea. Basically, the cornea becomes excessively thin and weak, and isn’t able to hold the normal eye pressure. Thus, it starts bulging out. The doctor explained it like pressing in on a balloon changing the shape. This causes the light to not reflect properly making the visual distortions of blurry and double vision.

Fortunately, there is a solution that might work. This is aside from a chemical a procedure that’s not guaranteed, or a cornea transplant; which is one idea really don’t want.

I’m going to schedule an appointment with my optometrist to fit me with one gas permeable ridged contact. Wearing this one hard contact lens will reshape the cornea when wearing. Then I have to have a new left lens made for my glasses so I can were them over the contact to correct the vision. He says since I have astigmatism, the contact will correct for that, so the left lens can’t correct for that, together.

The ophthalmologist doesn’t know why this has happened as this typically occurs earlier in life or after LASIK surgery. He also says rubbing your eyes can cause the cornea to warp. I’m not an eye rubber, but a word of caution if you do. Don’t do it.

For now, I’m going to get scheduled for this special contact fitting. I’m hoping I will adapt to this. I used to wear soft contacts years ago, but stopped because I needed readers and didn’t like taking them on and off. I even tried mono vision contacts, but it was not real good at the time. But now, since I’ll be wearing glasses to correct my vision over the contact, I just have to get used to putting them in.

So, as a funny side note, I told them that at least I got to wear steampunk glasses. I also noticed after, that I’m waring R2-D2…

Now, it’s time to get back into writing today. Finishing chapter 6 in Return to Revein’sev.

Been a challenging year already

Some of you might have wondered why I’ve been MIA, again. Well, I have a few health concerns that I’ve been dealing with. Some of which, I’ve already explained that I’ve got a pretty messed up neck and back. So bad, apparently, that the crushed and pinched nerves in my neck, has created several neurological symptoms. All of which, mimic Multiple Sclerosis or MS.

Late October, I got a new pair of glasses. I got through the eye test and was corrected to 20/10 in both eyes. I had a prism in my last prescription to correct a slight issue with double vision. Well, after my exam, we discovered I wasn’t having that issue, so it was taken out. A few weeks after seeing great in my new glasses, things began looking odd to me. It was like wearing the wrong prescription. I covered my left eye and everything was cleared up. Covering my right eye makes everything blurry and that double vision issue is back. But it’s only in one eye.

I went in for a recheck and the doctor is only able to correct my left eye to 20/70 and no matter what combination of prim the doctor tried, it was no longer correcting that issue. So, I was referred to an eye specialist. Even the digital image of my eyes have not revealed any underlying cause.

I’ve waited nearly a month to get in to a specialist. They’re first available appointment was 3 1/2 weeks out. So, tomorrow it it. I go in to, hopefully find out what the heck is going on now.

The ophthalmologist says it’s neurological if it’s only one eye. My neurologist says no, it’s not neurological if it’s only one eye. So, who do you believe, anyway?

So, there you have it. I’ve been taking lots of breaks to rest my eyes and my back and that’s why things are progressing on the slow side these days. Wish me luck tomorrow. I’ll be offline due to my eyes being dilated, but I’ll keep y’all updated.

Why I’ve Been MIA – Part 3

You know, sometimes life’s not fair. But, through our daily struggles, we learn to grow. We learn to accept the unacceptable. Some struggles seem tougher that others. The only thing we can do, often times, is count the blessings we do have. I know, it’s very hard to find good things, when being surrounded by unfortunate circumstances. But, the key is to know that there’s always something to be thankful for. There’s always something to be grateful for. Find it. That’s all you need to dispel that darkness. Let me tell you, there’s been darkness. There’s been bleak times that no one or nothing seems to help. Find that spot of light. Focus on it and once you start to feel grateful for that one miniscule thing, it begins to grow. It grows. Nourish that speck of light and it will flourish. It may not seem worth the effort. But if you do, it will chase that darkness away.

I say all this to focus on the positive. Sure, I’m talking about negative things that happened to me.

But, it’s a story I must share if it will help someone else find that flake of hope. Yes, I’ve been in dark times over it. But I want to tell you, I began to see that small glimmer of light. I began to focus on just that one thing. Maybe I don’t have MS after all. Maybe there is a diagnosis after all these years. Well, last Thursday was a day that I will remember for the rest of my life. It’s a day that changed my perspective and provided me with that, ever so, small glint of hope.

You see, back in 2017/2018, I was told by a neurologist and after seeing their associate movement disorder specialist, that everyone of my symptoms where all in my head. I was making it all up. Not intentionally, they say, but I was told my symptoms where Functional. That is to say, Functional Neurological Disorder or FND and Conversion Disorder. My brain is creating every symptom which mimics Multiple Sclerosis. But, the neurologist, who was also a phycologist, says, motioning with balled up fists, “I’m confidant, you can get better!”

I gave up all hope that they didn’t find anything. Even thought my nerve conduction study showed abnormal results. Results this doctor says doesn’t make sense to him. He didn’t understand the readings and what they meant. So, obviously, since this doesn’t make sense, it’s all in my head.

Jumping ahead to last Thursday, if took this neurologist five minutes to identify what was going on with me. Why am I tipping backwards when standing? Why do I get these electrical sparks in my legs, arms and feet? Why do my hips and back ache constantly? Why do I constantly drop things, or miss when grabbing things? Why is it difficult to chew food without biting my cheeks or swallow simple solids without choking? Why do I get swollen glands in my neck all the time? All these questions are being answered. Prior to my appointment, the doctor reviewed all my MRI’s, lab tests and X-Rays of my back and neck and after a few simple tests in his office, he knew what it was. You could see the excitement building as he began to understand what was going on.

The first thing he said, and I nearly cried, is, “You’re not making this up, but you don’t have MS. You have Lumbar Spinal Stenosis with Cervical Spondylosis and it’s caused by a narrowing of my spinal canal and herniated disks in my back and neck.

He said this is a degenerative disease. It won’t get better, but we can help slow down it’s progression by strengthening and anti-inflammatory injections. This condition can and does cause neurological dysfunction in all these area, so it explains where everyone of my symptoms come from.

Now, I’m waiting for more MRI’s and X-rays to be scheduled so we can pinpoint areas that need injections to help stop the nerves from being crushed.

I am looking forward to having my symptoms reduce. I know they’re not going to vanish, but I have hope. That small glimmer of a spark, that I can return to semi-normal lifestyle. I can enjoy the simple things in life, like sitting here and writing. I can focus on the important things in life. The good things. The positive things. They are out there, you just gotta look for them. Will there still be depression and anxiety? Will I still have dark days? Yes, I’m sure of that. But, don’t let it rule you. If you ever face a situation that seems utterly dark., reach out and talk to someone. There are those out there that do care. Just ask.

I hope this message brings you hope. We’re right in the middle of the Holidays. It’s a time where many suffer from dark days and depression. Turn it around for the good. I know it can be done. I did it.

Until next time, this is Author Brian K. Larson, off to spark your imaginations.