Kaonarose, to random
@Kaonarose@disabled.social avatar

Positive news for the day: The doctor filled out forms for me to get an accessible parking permit! Fingers crossed that it gets approved. This would be so majorly helpful for me, particularly on high pain days! I don't drive, but sometimes, I get rides places and all the walking can make my pain worse.

LeeFromVT, to music
@LeeFromVT@masto.ai avatar
ahimsa_pdx, to mecfs
@ahimsa_pdx@disabled.social avatar

This amazing embroidered piece (by @lia_pas) is being showcased by Opera Mariposa for this year's "Benefit & Awareness Month"

From their website:

"Until June 1, 2024, you can enter to win art postcards and a book featuring Lia’s exquisite creations – all in support of the ME | FM Society of BC!"

(ME = Myalgic Encephalomyelitis, FM = Fibromyalgia)

https://operamariposa.com/art-showcase/lia-pas/she-breathed/

@mecfs

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
lia_pas, to mecfs
@lia_pas@vis.social avatar

'she breathed' (2018) 🫁
For , Opera Mariposa is showcasing this embroidery by me, a multidisciplinary artist with . Check it out with exclusive insights and enter to win 'she breathed' art postcards til June 1! https://operamariposa.com/art-showcase/lia-pas/she-breathed/

ahimsa_pdx, (edited )
@ahimsa_pdx@disabled.social avatar

@lia_pas That is such a beautiful piece! 😍

It took me a while to figure out that BA Month stands for "Benefit & Awareness Month" so I'm sharing this link with more info.

https://operamariposa.com/benefit-awareness/#calendar

Opera Mariposa is helping to raise money for the ME | FM Society of BC (British Columbia).

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
sfwrtr, to 13thFloor
@sfwrtr@eldritch.cafe avatar

#WordWeavers 2404.29 — Who's feeling shame in your story? Is it justified?

/It's'a [#brainfog #fibromyalgia day, but I'm gonna write this to get something out. Hoping it's coherent. —RS/]

This question made me think hard for quite awhile until I—like an artist or a photographer deciphering how shadow defines volume and dimension—saw /negative space/ in a story... where something wasn't. Emptiness.

Wintereyes /doesn't/ feel #shame, and I'm realizing this is an #emotion with which I can make a #feminist point in my story. Whilst shame is IMHO used more often to control women than it is men, it is both incidious and /learned./ Shame is a combination of built-in emotions programmed into a person to make a person self-punish for "wrong" behavior even if it's secret; it's related to, but not the same as guilt.

Wintereyes was raised by wolves, but not until she was 7 when her "gift" caused her to seek a second set of parents. Her early childhood will require investigation in another story, but I'm pretty sure her human parents didn't teach her the emotion; it's not that she forgot. Forced to live again amongst humans over a decade later, to become more human, people's behavior baffles her. Late in the story, when she's asked to disrobe by stylist at a modeling shoot, and does without a thought, the stylist observes, "You don't feel shame, do you?" This is where Wintereyes will go off like a firecracker, and it should be very interesting.

The stylist may actually feel ashamed...

The author is [#actuallyautistic and retains copyright (c)2024 R..S.]

#BoostingIsSharing and #CommentingIsCool

#fiction #fantasy #sff #writing #writer #writers #author #writingcommunity #writersOfMastodon
#RSdiscussion
#RSstory #RSInklingsStory #psychology

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

New 12-minute video:

"I believe microglia are the primary culprit behind #fibromyalgia, #MECFS, #GulfWarIllness, #LongCOVID, and other #chronicpain & fatigue disorders.

Here is a quick video on what I am trying to do to fix the problem. - Jarred Younger"
https://www.youtube.com/watch?v=XggO__DlALw

@mecfs

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #CFS #PwME @longcovid
#PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #PASC
@chronicpain @fibromyalgia
#Fibro #FMS #FM

Eeyore_Syndrome, (edited ) to cannabis in The Psychology of Getting High—a Lot
@Eeyore_Syndrome@sh.itjust.works avatar

I’m addicted to not being in pain.

I’m addicted to feeling like not wanting to die because of pain 24/7.

Nerve pain just the top of the list of horrible things I feel at random.

Mux, to queer
@Mux@swingset.social avatar

Hello, I'm Mux. I'm a , musician based in and I'm having a bit of financial hardship.

Long story short, I got burned out, fired, diagnosed with and , and refused any kind of assistance from the state.

Currently I'm surviving by scavenging my wife's dental fund, but that bill will come due soon enough.

Goal: 527€/3000€

Librapay: https://liberapay.com/mux2000/
Bandcamp: https://mux2000.bandcamp.com/

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
ChronicIllnessHumor, to random
@ChronicIllnessHumor@mastodon.social avatar
UnseenCrafts, to folklore
@UnseenCrafts@mastodon.world avatar

A little progress today, not as much as I would like but I’m still struggling so I’ve had to stop. I know I have a couple of people patiently waiting on commissions, I’m on it as soon as I am less wobbly! #handmade #craft #pyrography #folklore #wood #seals #selkies #artist #art #fibromyalgia #eds

aby, to Autism
@aby@aus.social avatar

Packing for hospital next week.

I have shoulder surgery on Wednesday and it will be an overnight stay (hopefully only one night!), probably in a shared room.

Tips and tricks for preparation and packing would be super helpful, please!

OldAndCranky, to random
@OldAndCranky@sfba.social avatar

people with - do you ever get burning sensations everywhere, rather than the deep muscle pain? I feel like I have a sunburn all over. Gods, I complain a lot. I'd ignore me were I you.

UnseenCrafts, to art
@UnseenCrafts@mastodon.world avatar

It’s a small start to ease back in because I’m still in a lot of pain but it’s nice to be burning.

tomkindlon, to fibromyalgia
@tomkindlon@disabled.social avatar

A cross-sectional study demonstrated significant impairments in attention, memory, and higher cognitive functions among a cohort of patients with and (RA)

https://www.hcplive.com/view/patients-with-fibromyalgia-scored-worse-in-memory-attention-cognitive-function

@fibromyalgia

tomkindlon, to cfs
@tomkindlon@disabled.social avatar

New from Norway:

Exploring levels of TSH and FT4 in patients with (), () and healthy controls did not reveal any associations between fatigue score and level of hormones

Free fulltext:
https://www.tandfonline.com/doi/full/10.1080/08039488.2024.2332442

@mecfs

@fibromyalgia

tomkindlon,
@tomkindlon@disabled.social avatar

2/

Fukuda criteria were used for CFS diagnosis. The authors conclude that, although they found no between group differences, "we suggest future studies to examine the field further by exploring the influence of thyroid receptors and responses of the thyroid hormone cascade".

@mecfs @fibromyalgia

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
nsf001, to transgender
@nsf001@shitpost.cloud avatar

Racism has forced me to resort to eating a Taco Bell bean burrito for lunch. I could really use some prayers for my colon and $1500 to buy a pistol-caliber carbine and a Steam Deck.

@mutual_aid
@mutualaid
@MutualAidVisibility
@mutualaid


aelyaen, to transgender
@aelyaen@mastodon.social avatar

My goal is big: £3170.
My time is short: 18.03.24 deadline.

My landlord has been nothing but an * delaying me moving but I've handed in my 1mnth notice.
I've had a lot of support from Rape Crisis but my support worker is on leave.

paypal.me/aomojikei
£aelyaen
revolut.me/aelyaen
ko-fi.com/aelyaen
Crypto - https://ncwallet.net/pay/aelyaen

@mutual_aid
@mutualaid
@MutualAidVisibility
@mutualaid

#singleparent #transgender #Black #disabledcrowdfund #transcrowdfund #disabled #fibromyalgia #chronicillness

tomkindlon, to Vape
@tomkindlon@disabled.social avatar

Jarred Younger:
A large remote clinical trial grant on low-dose naltrexone ( ) & cannabidiol ( ) for was rejected. If you want to hear a bit about how I feel about rejected grants & how I handle them...

https://www.youtube.com/watch?v=9fkfvFIDyWI

@mecfs
@fibromyalgia

ahimsa_pdx, to mecfs
@ahimsa_pdx@disabled.social avatar

The slides and a recording from the March 17 presentation - Dysautonomias 101: More Than Just POTS - are now available:

https://www.massmecfs.org/news-events/66-sunday-conversations/881-sunday-conversations-mar2024

original post:
https://disabled.social/

@mecfs @pots

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