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I hate cold weather

30-10-2021
2 min read
living with chronic pain
Daily Hell
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Cold temperatures arrived in Portugal. With them came an increase in the pain level. What was already bad just became worst.

I was never a big fan of cold, except when I could spend the day in bed, all cosied up. Since fibromyalgia came into my life, it’s different: I can’t spend a whole day laying down because it will make my body hurt even more, and the cold makes the pain even worst.

An average pain level of 6, on a 0 to 10 scale, is now a 7.5. Bear in mind this is a revised scale. Using the previous one, the numbers would be 8 and 9.

The only thing that has helped me decrease the pain temporarily is water bottles. They are only palliative because I only get a slight relief when they are against my body. If I take them or they cool down, the fucking pain comes rushing in.

What can one do in a situation like this? Dress in warm clothes, do a ton of water bottles every day and hope for the best.

What’s worse, however, is being forced to do even less stuff. Cooking? Only after a hot water bottle, and the cooking has to be fast or I’m forced to take a few brakes for - you guessed - more hot water bottles. Cleaning the apartment? Delegate and forget about it. Taking the trash out? Delegate again. Think with clarity? The brain fog is even worse and more frequent.

The list goes on, and on, and on…

I can’t wait for the warm weather to return.

photo by Pavel Lozovikov

#living with chronic pain #weather
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Bruno Suffering from fibromyalgia since July 2020
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Series of Posts

Third anniversary of my living hell
Animal companionship in the context of chronic pain - my personal experience
Driven to desperation
I feel defeated
The holidays
How a cat made me feel excited again
I'm terrified about my future
Vacations and the toll on the body
Types of pain
Cannabis and pain
Covid, Fibromyalgia, and an increase in fatigue
A walk in the park
Fifth appointment - quick notes
Fourth appointment
Finding purpose
I had a chronic pain appointment that made me feel even more pain
Messed up sleep continues
Medical board to me: fuck you very much
High level, non-stopping
How it felt after the third appointment
Tracking the therapy progress
Third appointment done
Better on the surface
Multiple regions of my body with maximum pain intensity at the same time
Farto desta merda
To coma or not to coma
Things have gone downhill again
The pain relief didn't last long
Still feeling the treatment effects
Second transcranial magnetic stimulation appointment
Starting 2022 worst than I ended 2021
Looking back to 2021
No pain, no what!?
The Hellidays were like a beaten to my body
My arms hurt as much as my back
Maybe it's all bad luck
The third day after the first therapy session
I had my first transcranial neurostimulation appointment
Another very, very bad day
Things I do to "distract" myself from the pain
Transcranial magnetic stimulation medical appointment scheduled
How I keep an increase of pain at bay on family days
A Christmas pain song
O Christmas tree, O Christmas tree, how painful are your cold days
Another sleepless night
Round and round it goes
Things you should not say to someone with chronic pain
Worst pain level so far
Presented myself before a medical board and left the facilities feeling like shit
Building a good support network is essential
My experience with Social Security's medical boards
How I started cooking after fibromyalgia
I wake up feeling like I ran a marathon
A week of waking up around 8h like a fucking clock
WhY aRe YoU iN pAiN iF yOuR eXaMs ShOw NoThInG wRoNg?
Another sleepless night
I hate cold weather
HaVe YoU tRiEd (insert random stuff)?
Sleep and fibromyalgia

See Also

HaVe YoU tRiEd (insert random stuff)?

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