Brainless Blogger – Featured Blogger of the Week February 14, 2020

This week I chose Brainless Blogger as this week’s Featured Blogger of the Week https://brainlessblogger.net/. Looks like I started Following her around late May 2019.

About: https://brainlessblogger.net/about-2/

This blog is about chronic illness, chronic pain, and invisible disability awareness. I myself have chronic migraines, Fibromyalgia, asthma, hypothyroidism, depression, and hypermobility syndrome. I introspect about the experience of living with chronic illness and chronic pain. I also will post research and articles. Occasionally you will see book reviews or item reviews of things I have found. I write around average three posts a week, it is a fundamental pain distraction for me.

So why is the blog called the Brainless Blogger? I named it after the infamous symptom brain fog and fibro fog. A symptom that really bothered me when I was younger. I used to say pain would affect me physically but never mentally. And I was wrong. There are a lot of symptoms of FM and chronic pain. Cognitive dysfunction included. I have always preferred writing over talking but that is magnified now with chronic pain. I can organize my thoughts. I can edit. I don’t have to worry about words just falling out of my brain because I can use different words or use the mighty power of Google. Anyway, that is how I became the Brainless Blogger. Named after a symptom that frustrates me to no end.

On my Header menu, you will see a Favorite Post and in there you can check out some of the favourite viewer posts. There is also a running favourite post along the sidebar as well.  Feel free to explore. There is Stuff I Use, which is basically stuff I have reviewed and continue to use.

BIO

I have been chronically ill in one way or another since I was a child starting with hypermobility syndrome that gave me joint pain and insomnia. It wasn’t until I was a teen though that the joint pain, fatigue, and insomnia picked up the pace and I was having difficulties. Skipping school to sleep and so forth. However, it took until I was 20 to be officially diagnosed with Fibromyalgia. I received no treatment for it though. I was told I was too ‘young for it’. Not sure if that was ageism or some gender bias thrown in there as well. Either way, it took until I was in my thirties to be put on Lyrica. I began to get migraines with aura when I was 20 as well. These progressively got more frequent as time passed. I developed persistent migraine auras. And migraine associated vertigo. Somewhere around 2000 they became daily and have been there since. Migraines they did, however, treat quite a bit or attempted to. I haven’t really responded to preventatives except mildly to Topamax.

The impact of all this has taken a toll on my life and career. Or what career more like. I was on an academic path when the migraines gained severity. I was finishing my Masters. It became clear I wouldn’t be able to go for my Ph.D. until I had some sort of effective treatment. I didn’t know at the time the most effective possible outcome for a preventative was 50% and I’d never see it. So I took time off to find more effective treatment. Which I never found, but did discover rapidly that working was much worse due to painsomnia and sleep deprivation issues. So I had a hard time just finding a job to maintain. I did eventually give up on the idea of even attaining my Ph.D. and just finding a career. To that end, I found a job at a bank as a lending/investment officer. However, the untreated pain was far too intense. Unmanaged pain and full-time work had the best of me. I tried to push through it and did for years. But in the end, it led to a suicide attempt. Then another. Things changed for the better when I changed doctors, was sent to the pain clinic and a new neuro as well as put on depression medication that didn’t have the side effect of suicidal ideation for me. The pain clinic told me straight up I could only work part-time so I changed roles to a teller at the bank to reduce my hours. And even this is difficult to maintain but far less stressful.

My coping strategies have improved and evolved over time. However, I still deal with depression associated with chronic pain that compromises my coping at times. It is a difficult road we travel. I don’t always cope well with it.

 

Posts I re-blogged:

Brainless Blogger Blathering: The worst lesson I learned from pain – YouTube Video Original post/video: https://www.youtube.com/GdtCZtj-uwY

Vlog: The worst lesson I learned from pain — Brainless Blogger. Original post: https://brainlessblogger.net/2019/12/12/vlog-the-worst-lesson-i-learned-from-pain/

To the healthy: This could be you — Brainless Blogger. Original post: https://brainlessblogger.net/2019/06/24/to-the-healthy-this-could-be-you/

#shadesformigraine to support those with migraines — Brainless Blogger. Original post: https://brainlessblogger.net/2019/06/21/shadesformigraine-to-support-those-with-migraines/

The measure we use for life — Brainless Blogger. Original post: https://brainlessblogger.net/2019/05/27/the-measure-we-use-for-life/

Social media links:

Facebook: https://www.facebook.com/BrainlessBlogger/

Instagram: https://www.instagram.com/brainless_blogger/

My Book: https://brainlessblogger.net/my-book/

Pinterest: https://www.pinterest.ca/brainlessblogger/

Twitter: https://twitter.com/Nikki_Albert

YouTube: https://www.youtube.com/channel/UCJ_OOBcdjO1eYhDUHj9MHEAhttps://www.youtube.com/playlist?list=PL5V35sqZtAl4iCp2eH3s8NfiAlcxHf96V

Other Featured Bloggers of the Week: https://upsdownsfamilyhistory.wordpress.com/tag/featured-blogger-of-the-week/

About ICT Genealogist

Originally from Gulfport, Mississippi. Live in Wichita, Kansas now. I suffer Bipolar I, ultra-ultra rapid cycling, mixed episodes. Blog on a variety of topics - genealogy, DNA, mental health, among others. Let's collaborateDealspotr.com
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