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Weather Front On The Way

My phone scared the crap out of me today. I don’t know if it is an iPhone thing or a AT&T thing, but that little sucker has a LOUD buzzer on it for weather alerts.

The powers that be apparently thought that the weather warranted an emergency alert. I wonder how much money goes into these things? How much does it cost to set up the systems that detect the weather conditions? Today’s Weather alert was for dust storms but with that dust I saw a whole lot of roiling black clouds high above the wind blown dust.

I could save them a ton of money.

My body told me yesterday that things were changing. Hours before the first alert came through the pain in my body had reached epic proportions.

I remember as a child hearing my grandma say that it was going to rain because her bursitis was acting up. I had no idea what that meant exactly just that it was some sort of ache that grandma had. Over the years I heard doctors say that people couldn’t predict the weather that way, but now I know they are wrong.

Maybe it is the change in the barometric pressure, but I feel the aches, the chest pains of the costochondritis, the deep chest pain that cannot be alleviated even with my pain meds and the fibromyalgia from head to toe. I am struggling to even type and I’m pretty sure it shows that my brain isn’t 100%.  My fingers shoulders and arms ache and are clumsy on my keyboard where my fingers are usually speeding along.

The fibro fog, the pain, the exhaustion are all kicking in.  I managed to repot a bunch of houseplants to consolidate them for someone to keep an eye on while I am off on my adventure, but I am sure glad I’m not leaving today. Yesterday or the day before I would have been ready, but today, no today I could not handle it. As I can no longer handle the pain of typing right now.

So off I go taking my weather predicting body to bed where I can rest and sleep and fight again tomorrow.

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Foggy, Foggy Day

Fog followed my every step today. Living in the desert there is rarely a day that involves the heavy grey mist that blocks your vision and forces you to slow your every move lest you run into something else. Today was no different as far as the desert surroundings go. The skies outside are clear and blue. The fog is inside my house, in my head.

It is called Fibro Fog and it is the bane of fibromyalgia sufferers everywhere. Everyone has those moments where you walk into a room and can’t remember what you walked in there for, but this is like that amplified. Every step I took felt like I was walking in molasses. Walking to the refrigerator found me standing there staring blankly in… What? Why was I there? This happened all day long. I overdid everything yesterday. I managed to get my creative project done and did a little bit of preparation for another project that I planned on starting today, but when today started it was all I could do to get the blog posted about my project from yesterday and I had already composed most of it last night.

My intentions for today was to start the mosaic pot to go inside the little painted chair pot holder from yesterday. I had already used my tile clippers and had separated them into little containers all ready to glue and grout for my little pottery piece. My brain couldn’t follow through. I could barely manage to make breakfast for myself. Wandering around my house to gather my supplies was torture. Room after room puzzling over why I was there, where were my supplies? What the HELL was I doing?

At first when I started having these foggy days I thought it was from the chemo I underwent for breast cancer. There is something I have heard referred to as chemo brain that happens to people that undergo chemo. The information obtained from the women’s center talked about so many possible side effects said that these all went away with time. Well hell, this never went away.

For years now I have struggled and sometimes feared that I had early onset Alzheimer’s or a brain tumor or something equally scary, really it is sometimes that bad. As a child wiz kid my memory was always something I took for granted. Phone numbers, addresses, trivial facts all stuck in my brain for YEARS. Suddenly I was struggling with everything. You know that phrase everyone likes to joke with “Of all the things I have lost I miss my mind the most” well that is me.

I know I am not alone. I belong to several fibromyalgia support groups online and am always looking into studies being done to find a cure. For the record, it is very hard to find a cure for something that they have not even discovered the cause of.  Many people go through this and we all find ourselves wondering if we are doomed to go through this forever.

Daily pain is hard, any chronic condition is difficult for the person going through it. Careful use of pain medications can ease some of the pain but it never goes completely away for me. The chest pains from the costrochondritis is the worst pain ever, it feels like a heart attack and is mostly on the left side of my chest and my shoulder. Toss in the fibromyalgia all over your body pain and the pain meds are a vital part of keeping me relatively sane. The pain medications can make it hard to think sometimes and I am always conscious of the dangers of actually becoming addicted to them and there is controversy over the effectiveness in their use with fibromyalgia. Some studies even say that it may make fibro worse. Personally I find myself unable to think or function when my pain levels are high so I use the meds carefully and walk the tightrope between dependency and addiction.

The fog set in before I had even taken my meds so there was little doubt that I was going to have a foggy, foggy, fibro day from hell. Yesterday between coats of paint on my little painting project I sat and broke down ceramic tiles to smaller pieces to create a mosaic masterpiece from an old terra cotta pot. Normally I don’t eat first thing in the morning, some meds I am supposed to take on a daily basis before eating, others say take with food. Since my brain was not working well I decided it needed some fuel. It didn’t help.

I continued to struggle for a few hours but just could not get myself functional. Every task I started is still sitting waiting to be completed. The only thing I had any success with was taking a nap. My nap lasted 5 hours and I woke up exhausted all over again. The majority of people that have fibro also suffer from sleep disorders. I have a C-pap machine that I have to sleep with and just writing this is agony. My body is aching and I feel as if I have run a marathon….to make matters worse I keep falling asleep while writing this. Yeah, so much for that 5 hour nap. So this is me being human and accepting that for now at least this is my lot in life. The fog will eventually lift for a bit and I will get back on track.

Now it is time for me to give in and take another unwanted break in my quest for creativeness and sleep yet again. Even as I write this I am falling asleep sitting straight up. There is no quick fix for fibro fog you plod through and hope the following day will bring some clarity. Life is a Journey and someone else is holding the map.