#free clinics

[cuspidgoddess]

January: The Good Doctor Is In

[clownpulp]

hiii know i havent posted much art here lately but i am once again disabled and very broke, looking for anyone who may want one of these semi-monochrome rendered bust sketches :] $25+ depending on detail, and i can always do larger pieces, color, etc !

dm here or email me clownpulp@gmail.com

ko-fi if you just want to help me out

[stuckinapril]

There will not be a single moment next week in which I’m not running around doing something

[pastaghostt]

Would you jump for the beef?

[eclecticopposition]

seeing personality disorder discussion on the dashboard. the impulse to share all the self-therapy books and tools we have has never been stronger

[beachypeasysandy]

🐈Happy Tails Vet Clinic🐕

Is your pet feeling sick? Then head on over to the Happy Tails Vet Clinic where the amazing staff will fix your furry family member!

Built for my #AYORB challenge #AYORBLtBlue

Gallery ID: BeachyPeasySandy

No CC

Playtested

40x30 lot (Brindleton Bay)

$89,887

Gallery Art: Gothamstrash

[atariaaren]

"aaren where have you been for the past 5 days you havent posted" ive been playing wobbledogs im sorry

[thunderblazz]

Some stuff wooo

[salt-baby]

As someone who is currently working in the healthcare field and looking at attended medical school, can you please elaborate on the ableism and doctors post you made? I’d very much like to avoid inadvertently falling into that category.

Somehow this missed my radar, my bad!

It's a difficult question to answer, although it is the right question to be asking.

You can find my other elaborations here and here, which will likely be helpful.

But to address your specific question, when I think about the ableism of practitioners, in some cases it is just bias, but in many it's just your run of the mill ignorance.

It takes experience to work well with disabled people - both because of the heterogeneity of them, and because the disabled experience is so far removed from the able bodied one.

Some people like myself call themselves disabled as an identity they're proud of, some people call themselves disabled but are uncomfortable with their condition to various degrees, and a lot of people would find it offensive for you to call them disabled because they would call themselves chronically ill or not impaired at all.

In your medical practice, "disabled" is going to be a legal term with a set definition, used to distribute benefits. You'll be taught an impairment model of disability, and your first instinct will likely be to try and fix the problem your patient is experiencing.

In a case like mine, that's not a mindset the patient is going to appreciate, as backwards as it sounds. Yes, I'm in a doctor's office to get treated, but the reality is that expert doctors have already evaluated my conditions and done all they can to help me. There's no quick fix - the fantasy of curing a difficult case is impossible with me, but it doesn't stop some young doctors from trying. My disability isn't one illness, but ten, and often what disables me is the environment around me rather than my actual illness (this is called the social model of disability, and that's where you should start studying).

I'm in a doctor's office to find relief from specific symptoms, or for a new problem (secondary to my existing conditions) that has popped up. Some residents have reviewed my entire medical file, and asked about things that weren't followed up on, and there's only so many times I can say "there's nothing we can do about it". Many premeds, when I mention the medications I'm taking, think that there must be some kind of better medication setup for me. Except there isn't, all of my meds are essential, and at this stage of illness, all medications have nasty side effects. I will never get better and will likely live the rest of my life on immunosuppressants and I'm okay with that, but that's very difficult for able bodied people, esp medical practitioners, to accept.

And in many cases, medical practitioners have put their foot in their mouth by just being ignorant. One person working at a rehab hospital asked if I slept in my orthotics - the answer is no, obviously, orthotics are painful to wear (it's also bad form to ask a disabled person about their disability just because you're curious). Someone told me it'll be okay, they used to wear wrist braces too and they're fine now - in reality, their supervisor just told me to consult surgeons, I was recommended casts, and my wrists remain permanently displaced to this day. I lost most of my ability to write. Our issues were not the same.

On another occasion, a premed picked up my orthotics and moved them away from me without asking - those are expensive (2000$ USD) and irreplaceable, and I need them to walk, I'm vulnerable without them. But to others, they wouldn't be aware that those braces are that valuable. Many disabled people, myself included, view mobility aids as an extension of their own body. For all intents and purposes, my orthotics are my "knees". I often compare it to a phone - it'd be really weird to take someone's phone and move it away from them, or even to touch it unannounced in the first place.

The reality of what a disabled life actually looks like is obscure to the vast majority of able bodied people. Let me be clear, I live a happy and satisfying life, where I enjoy my work and my friends and my family. My existence is not a tragedy, and when it's treated like one, it devalues my hard-won happiness in life and what I have to contribute to the world. But at the same time, every hour of every day is impacted by my disability. I have to change how I cook because I struggle with lifting a pot or standing on my feet for too long, my closet has to be adapted for my orthotics and nerve pain, a number of medications have to be kept basically within ten feet of me at all times, and I have to be very careful anytime I eat something I didn't prepare myself.

You may prescribe a medication which you know can cause nausea, and not realize to your patient, that side effect looks like being sick everyday, skipping meals, wearing a mask so a smell doesn't set you off, and not enjoying eating anymore. You may write a script for the test which is medically the correct option, but your patient may be sensitive to the specifics of the procedure (ie, for religious reasons, it may be difficult to strip down to a gown for some of the more involved imaging procedures). Cystometry and other urological procedures especially. I find this is where doctors sometimes inadvertently do harm. The best option for your patient isn't always the best option medically - it's what fits their priorities and improves their quality of life.

Understand that the current culture in medicine, for doctors, is often very callous and frustrated towards their patients. Recently I heard someone express that their patient needed to just accept their disability already and start being compliant with treatment - they had been disabled for three months. It took me a year to feel even remotely settled with becoming disabled, and my disability isn't nearly as severe as that patient's. Do not follow in your colleagues' footsteps.

If you spend the time trying to understand your patients (which may look like reading disability theory papers, memoirs, watching documentaries, possibly even volunteering, talking to some of your seniors with more experience, etc) then you're already miles better than most of your coworkers. Take the time to consider it from your patients point of view, and even though it's not what's in your textbook, appreciate the value of the information your patient brings to the table (their experience, their concerns, their gut feelings), and you've already done what most disabled people are desperately searching for in a practitioner.

The reality of a minority identity, is that for adults who have become accustomed to something like being disabled, it matters a lot more where your heart is than what you actually say. I don't care if someone is politically correct - I care if they're trying. Even if they're not quite there, that effort will pretty much always be seen and appreciated. I'd far rather someone call me "handicapped" but never view me as lesser, rather than someone who falls over themselves to "accommodate my limitations" and never actually intends to accommodate anything. Be sincere, and you can make mistakes, we'll know what the intention was.

Best of luck, my friend.

[confusedhostage]

Which dilemma (and its outcomes) made you the most emotional?

[amethystsnow]

i often see it mentioned how for transfems estrogen increases happiness obviously, and also how it is easier to cry. these make sense, and i am definitely feeling those. however, something i dont see mentioned nearly as much is how it increases other emotions and feelings as well.

i feel more enjoyment in things. i have found multiple shows and games to be "one of the best i have watched/played in my life", which used to be a much more rare occurrence. along with this, i also laugh more. i find myself laughing out loud so much more than i used to, even if its something ive found funny before (i cant watch snapcube videos when my parents are asleep because i always laugh too loud lmao).

i feel more passionate about things. when a character i care about was revealed to be canonically queer, i literally cheered out loud, something i never actually did before. i also decided to make a source mod, and actually started by installing blender addons to allow for exporting those models, and started learning the source sdk and hammer, rather than just wanting to do something and not doing anything until i just forgot like i have done many times before.

i feel more pride. like queer pride obviously, but in this i mean being proud of myself. when i drew that little cat that i used for my little talking dude on streams, i was like "heh, thats a funny little guy (neutral)", but didnt really care about it because i felt it was bad, but when i drew what is now my pfp, which is basically the same drawing but its my fursona rather than my warriors oc, i felt so happy with it, even if it looks like it could be drawn by an 8 year old. it was something i made myself in a medium that i am very inexperienced in, and i feel more pride over that than really anything else i have made myself in my life. i am working on making a 3d version of the drawing, and it looks terrible and very simple, but its my first time ever trying 3d modeling, and i am very proud of my minimal progress.

i feel so much more confident in myself than i ever have. i have been posting pictures of my boobs online. i wore a crop top in public for the first time. im actually making progress on voice training rather than giving up like two days in because of thinking i sound like shit.

all of this is only three months into taking it. hrt is such a wonderful thing. i hope everyone who wants/needs it is able to get it, it has literally saved my life and i hope it can save more.

if you have similar feelings you would like to share, please feel free to on this post, i love hearing fellow queer peoples experiences (this goes for people on testosterone as well, i would love to hear your stories as well)

[trivialbob]

House windows - shut Air conditioning - set to high Fans - also set to high Curtains - closed Dog blanket - in the basement Doggie downers - administered

I hid the pills in wet dog food. Ella and Oliver know what Pill Pocket "treats" mean and won't eat those anymore. They didn't know pills were in the wet food and each one wolfed it down in two gulps. So that worked.

And… the first firecracker just went off. Not perfect timing, because the drugs take a while to kick in. The noise of the fans though does a pretty good job of masking booms that aren't close to the house.

[the-lonelyshepherd]

versez le sang, mes beaux amis

[zatdummesmadchen]

Hello there, 👋

I am Tamer Aldeeb, a dentist from Gaza.

We have suffered greatly from fear, displacement, and the destruction of our home and my clinic, and everything we literally own...

We want to save ourselves from what seems like an inevitable death.

I hope you can take a look at my campaign on the pinned post on my profile ,and help us by donating or sharing our campaign to reach the largest number of supporters.🌹🌹

Our campaign is verified by @90-ghost , @ibtisams , @el-shab-hussein , @nabulsi and @fairuzfan 🇵🇸🇵🇸🇵🇸

Thanks a lot in advance ❤️❤️❤️

🍉🍉🍉🍉🍉🍉🍉🍉

HELLO EVERYONE !!!

PLEASE SHARE THIS CAMPAIGN AND REBLOG THEIR POST TO HELP THEM !!!

🔻🔻🔻

AND PLEASE TRY TO DONATE WHATEVER YOU CAN. THEY ARE IN DIRE NEED OF HELP !!!

🫒

Tagging: @battlebabebeulah @nomoresympathy-eh @lemedstudent2021 @abla-soso @timetravellingkitty @importals99 @redpinejo @kuch-toh-garbad-hai-daya

[oldshowbiz]

1967.

James Coburn helped fund the Hollywood Free Clinic, a place that still exists, which provides free health care to the poor and uninsured.

[podcastsagainstapartheid]

We're honored to have @vestaclinicpod join the Podcasts Against Apartheid list.

Want to join the AFZ podcast list? Let us know.