halcionandon, to chronicillness
@halcionandon@disabled.social avatar

Unsure how common this is in other affecting cognition, but when you have the writing errors you’re almost guaranteed to make are:

  1. Double the same word
    or
  2. Exclude it altogether
    Or do both!

So frustrating & the sicker you are the worse it gets. You simply can’t see mistakes! Other problems too ofc but I’ve found this is the most common error made by

I did both when composing this!

I miss my old brain!
😩

@mecfs @longcovid @chronicillness

britt, to cfs
@britt@mstdn.games avatar

The elusive good night sleep. 😴

I get one of these once every 3 months, maybe?

I shall compound my interest and make today a rest day. Onward to binging Netflix.

Fury, to scifi
@Fury@mastodon.au avatar

Got a new idea for a novel. Pre-industrial society on nameless planet. Disabled people sometimes disappear and come back “fixed”. It’s the aliens. The kicker is they’re purifying the gene pool and replacing the people in synth bodies. I know this might trigger some disabled people, but what I wouldn’t give to be in a non disabled body with the same mind…

ahimsa_pdx, to mecfs
@ahimsa_pdx@disabled.social avatar

"Long COVID advocates hammer Biden over ‘minimal funding’ in budget request"

https://thehill.com/policy/healthcare/4682533-long-covid-advocates-hammer-biden-over-minimal-funding-in-budget-request/

"According to a Centers for Disease Control (CDC) report from September of last year, around 18 million adults reported dealing with long COVID as of 2022."

@longcovid

WillardHerman, to random
@WillardHerman@mastodon.social avatar

My doctor finally figured out what has been wrong with me for seven years.

I felt like saying “I told you so.” But I was just too tired. And why bother saying that?

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
programmablecat, to random
@programmablecat@post.lurk.org avatar

i think the hardest thing about becoming inflicted with a debilitating chronic illness in your 30’s is having to reset your understanding of your own body, your capacity, your energy, and learning to be even more understanding, forgiving, and kind to yourself

and giving yourself time to grieve the person you used to be

i’m still there in that space.

i’m also still convincing myself that my dreams and goals don’t have to change. its the steps i’m taking to achieve them is what has to change.

ahimsa_pdx, to books
@ahimsa_pdx@disabled.social avatar

"Ten new books about Long Covid, chronic illness, and disability"

https://thesicktimes.org/2024/05/21/ten-new-books-about-long-covid-chronic-illness-and-disability/

"Here are ten recently published books on Long Covid, Myalgic Encephalomyelitis (ME), chronic illness, and disability."

britt, to medical
@britt@mstdn.games avatar

#ChronicIllness #Medical

My new med for RA finally arrived by delivery courier. This is after 6 weeks of talking to the drug manufacturer, 2 speciality pharmacists, doing paperwork, intake phone calls, and finally scheduling a delivery.

The med is covered under a provincial ‘compassionate care’ program because it costs $6,200 USD / month out of pocket.

I share because it’s important to know what we go through. We don’t choose to be sick. We don’t want this. We just want to be well. 💜

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar
ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
vlrny, to mentalhealth
@vlrny@disabled.social avatar

Following up on a side chat, what are folks doing for lazy food hacks when yer too tired to cook but don't want to eat junk?

Share yer ideas so others can steal 'em!

ahimsa_pdx, to mecfs
@ahimsa_pdx@disabled.social avatar

As we approach May 12, ME/CFS International Awareness Day, it's important to remember those with severe ME.

Many of them are so sick that they are on social media either very rarely or not at all 😢

This video from Anil van der Zee, The Prison of ME, explains the agony of severe ME:

https://www.youtube.com/watch?v=yLRateIQdzc

About 12 minutes. Subtitles in multiple languages.

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
britt, to random
@britt@mstdn.games avatar

More pokey pokes today … hopefully the last lab tests and vaccines before I get to start on my immunotherapy.

2 week countdown let’s go!

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
tomkindlon, to disabled
@tomkindlon@disabled.social avatar

UK Government Open Consultation
“Modernising support for independent living: the health & disability green paper”

Article with links
https://www.gov.uk/government/consultations/modernising-support-for-independent-living-the-health-and-disability-green-paper

The government has published a series of documents including a Green paper & evidence pack

@disability @disabilityjustice
@chronicillness @spoonies

1/

halcionandon, to mecfs
@halcionandon@aus.social avatar

Please and share to other platforms.

Seems I’m famous (and real!) and desperate enough to go to the media for help. Yes, the trapped woman in the article below is me.

https://www.thecanary.co/global/world-analysis/2024/05/03/me-cfs-anna-australia/

I’ve tried every level of government and they simply won’t help. Ask people in real life if they have somewhere for me to go. Is anybody an ? I need help.

@covid19 @mecfs @chronicillness @auscovid19 @neisvoid @disability @disabilityjustice @socialwork
@dysautonomia
@dysclinic
@mutualaid

horachio, to mecfs
@horachio@aus.social avatar

Super happy to see Jaime Seltzer in the 100 Health List. Used to occasionally interact with her on the bird site about She is always generous with likes, shares & comments. The information she posts is the advice I trust most. One of the first to discuss in 2020. Congratulations Jaime!

https://time.com/6967257/jaime-seltzer/

britt, to medical
@britt@mstdn.games avatar

A fun story from my past week… I’m trying to share the positives.

I had a surgical procedure Monday and had 4 nurses involved during various steps. My 2 surgical nurses knew what POTS was and treated me so well - they gave me extra fluids. :)

My last nurse in recovery… her 16 year old daughter has . What did I do? Of course I talked to her and answered questions and was an advocate… on my surgical bed… because that’s what I do. 💜☺️

We exchanged emails 🤘🏻

ChronicIllnessHumor, to mecfs
@ChronicIllnessHumor@mastodon.social avatar
drandrewv2, to cfs
@drandrewv2@freeradical.zone avatar

So, here’s some personal and professional news… I’m going to be leaving my job pretty soon. 😬

It’s a bit of a wrench, because this job has been a big and exciting thing, for lots of reasons. But, you know, I have been having a shit of a time with the old and lately, and…

📢 🚨

If you can’t do the job and preserve your health, there will come a point when you just can’t do the job.

That’s not a choice.

It’s an inescapable law of nature.

britt, to medical
@britt@mstdn.games avatar

Going to be a bit quiet here for a few days … I’ve got a surgical procedure in the morning and will have lots of doctor follow up appts to manage.

Good vibes are always appreciated. Imma come back from this stronger, no doubt! I never give up hope 💙💙

brianvastag, to mecfs
@brianvastag@sciencemastodon.com avatar

The Writers Guild Initiative is offering workshops for people with ME/CFS an related conditions.

May 17th deadline for applications.

https://mailchi.mp/meaction/writers-guild-initiative-writing-workshops-apply-today?e=70638fc8c9

Anxious_Agender, to trans
@Anxious_Agender@cooltrans.men avatar

Hey Fedi friends! It's the end of the month again which means it's time for a new mutual aid request. (This ended up being a little longer than I expected but bare with me! CashApp & PayPal links at the end! :floof_Heart:)

To try and keep this short and since many of the folks who have known me or seen me around the Fediverse know or have an idea of what the current situation is like.

I'm a minor with no source of income outside of coding which does not bring nearly enough in for me to even buy lunch most months so I have to resort to mutual aids or theft (Which got me in a lot of legal trouble, but fuck the corporates.). I need at least enough fundings to support me (Age 16, turning 17 this year) and my younger sibling (age 15).

I am a high school student living in a crappy situation with divorced parents. Where one house, the main house, I am refused basic needs such as, but not limited to, food, water, hygiene, clothing, proper medical care, etc. While the other house, my mothers, is a hoarder mess with little to no food, and when there is non expired food that has not been gotten into by animals, months, mold, maggots, etc, it is often times one of the following: Chocolate, cookies, Twinkies, hostess foods, etc. My mother hoards much more than just garbage but indeed, animals also. (With over 70 animals in the house and dogs who are not potty trained along with more animals, outside of the house).

Neither houses include proper medical care. I have a chronic skin disease that causes me severe pain and if it gets bad enough, it becomes an open wound that tunnels often times on my chest or on my legs. My parents do not supply the proper medications I need for these, and when asked or mentioned needing the medications, I get told "Get a job". (Which I am also not allowed to have.)

I'm constantly at risk of being kicked out of the house at any time without warning, a couple of months ago I was locked out of the house in regards to being trans and using my chosen name tho thankfully this was after a school play and I had a safe place at the time.

CPS does not listen. The cops do not listen. I cannot speak up about any of these issues even to trusted adults as this causes more issues at home and gets CPS involved.

Cost breakdowns for the month! Any extra fundings will be put towards getting my parrot a new urn (His last one unfortunately broke).

FOOD: $400

HYGIENE: $30 (Feminine products, shampoo, conditioner, deodorant, etc)

MEDICATIONS: $50 (4x meds for chronic disease (3 prescription + 1 one reg), anxiety/insomnia meds, pain killers)

CAT FOOD: $20

TOTAL: $500


NOT URGENT BUT STILL NEEDED: I will be doing commissions in regards to funding for this stuff, it might take a little bit but I'll do it o7

URN REPLACEMENT: $160 (I know this is expensive but it was the cheapest urn I could find that was made with a decent quality that would work better for traveling with him, as this bird means a lot to me, even in death. If you've known or seen me around within my past year and a half ish on Fedi you'd know how much my beloved Leo was worth to me<3)

(We attempted to fix the urn but it didn't work very well as it proceeded to keep breaking and at this point it's cheaper just to replace it)

LAPTOP FIX: $20

(Keyboard had an incident where one of the keys broke and need to be replaced, this was a rough estimate on the price it should cost from a friend. - The laptop doesn't have a warranty 😹 but I need this for personal use + school + studies)

CASHAPP: $LynxPunk
PAYPAL: https://paypal.me/LynxPunk?country.x=US&locale.x=en_US

@mutualaid

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