#chronic health condition
Explore tagged Tumblr posts
Text
Biden Administration Proposes Enhanced Coverage for Obesity Medications
Biden Administration Proposes Coverage for Obesity Medications The Biden administration is set to unveil a significant policy initiative that aims to expand Medicare and Medicaid coverage for obesity medications. This ambitious move, likely to be met with both enthusiasm and scrutiny, has the potential to provide millions of Americans with access to essential treatments that are currently not…
#Biden administration#Chiquita Brooks-LaSure#chronic health condition#health complications#healthcare policy#Medicaid coverage#Medicaid program#Medicare coverage#obesity epidemic#obesity medications#obesity treatment#Wegovy#Zepbound
0 notes
Text
Day 573
Despite the fact I had enough time in my day yesterday to play video games, do my cleaning for the week and even do some journal set-ups, I had forgotten to write anything. I blame it partly on being distracted by the problem of what to bring to my specialist appointment.
Even though it has been four years since Covid first surfaced, not everything has returned to the way it was. Granted, that will never happen, like I am probably never going to go back to working on site full time, but there were also things I hadn’t gotten around to restoring.
Going back to my specialist for maintenance on my condition happens to be one of those things. For those who are perfectly healthy (and may you continue to be perfectly healthy), when you have a chronic condition maintenance appointments are important. They ensure that if or when a complication happens, it is caught early. Specialist appointments, where I live, require a referral from a physician and referrals, even once you’re in service only last about a year or two. This means if I go an extended period of time without seeing my specialist (like four years due to Covid) I need a new referral.
Which is kind of hard, when you have to physically see your family physician, because Covid. So it made things a bit complicated. I could have actually done this last year, but frankly I don’t know if I had the organizational skills last year to even consider doing this. Calling my family doctor to set up an annual appointment actually had been one of my monthly focus tasks last year, and the lead up to the appointment was writing a list of things I wanted to ask and get done. It was a lot.
Unfortunately the catch up isn’t quite done yet. I have at least one test I need to do (because it has been four years). Once that test is done, I can go back to a regular schedule. More or less, I did realize as I sat with my parents over dinner that I am going to have to figure out how to take myself to this appointment. My parents cannot be helping me do this forever, but that is a problem for future me.
1 note
·
View note
Text
Gentle reminder that disabilities are disabling.
You're not some awful, bad person for not doing things that able-bodied people can do without negative consequences.
Sometimes, you haven't showered in a while.
Sometimes, your room is a mess.
Sometimes, the dishes pile up.
That doesn't make you a failure or deserving of less respect, support, and kindness.
Being disabled, having disabilities, and things that result from said disabilities, don't change the fact you deserve to exist. You deserve peace, and love.
#shitpost#screaming into the void#disabled#disabilties#disability#physical disability#invisible disability#visible disability#disability positivity#positivity#spread positivity#mental health shit#physical health shit#disabled positivity#disabled system#chronic condition#chronic illness#chronically ill
3K notes
·
View notes
Text
this poor woman ended up in hospital because she ate cayenne + cinnamon coated orange (unpeeled) because there’s a health and wellness influencer with millions of views who recommends it for digestion - she burned her oesophagus
i always saw a few really good other additions of similar things on the comments
please be so, so careful taking advice from these people online, as many of them are not formally trained or educated, brand ambassadors, deep in pseudoscientific rabbit holes and unfortunately, there are many out there who struggle with disordered eating habits
(not mentioned here but another one worth noting: i have personally known people who have burned their oesophagus with viral apple cider vinegar shots and drinks. don’t do that. a burned oesophagus is not fun)
#also tbh I’ve had this before this previous posts: please don’t make fun of people who fall victim to these kinds of things#lots of them have chronic health conditions and feel unlistened to and are desperate for remedies for their conditions#and nobody is ever fully immune to the effects of social media#katie rambles#ask 2 tag#wellness culture#<- tag for this kinda shit
5K notes
·
View notes
Link
0 notes
Text
Diabetes is a chronic health condition that affects how the body turns food into energy. When the body gets sore and difficult to treat, there might be a need for amputation and Disability Care in Gainesville, Florida. And for us, this is not a good sign as the damages are permanent.
0 notes
Text
I think it would really benefit people to internalize that mental illnesses are often chronic and not acute. Some of us will never be able to jump the hurdle of managing illness, much less sustaining a sense of normalcy. Many of us will never "recover," will never manage symptoms, will never even come close to appearing normal - and this is for any condition, even the ones labeled as "simple" disorders or "easy-to-manage" disorders.
It isn't a failure if you cannot manage your symptoms. It isn't a moral failure, and you aren't an awful person. You are human. There's only so much you can do before recognizing that you cannot lift the world. Give yourself the space to be ill because, functionally, you are.
#mental health#mental health advocacy#like... anxiety and depression are often concieved of as simple and easy to manage...#...but that isn't the case for so many of us. anxiety and depression just have a lot more research invested into them...#...and while i wish this were the case for literally every other condition it does alter people's perception of you to some extent...#...so while this is NOT solely about anxiety or depression it includes us...#...my anxiety and depression and PTSD have *destroyed* my life. this is chronic and will probably be life-long...#...and that isn't my fault. i've done the fucking work but guess what? that doesn't account for the fact that I Am Just ILL#the least we can do for each other is to be compassionate#be compassionate to those who cannot heal. be compassionate to the people who can't manage their lives. this world is scary enough#recognize that management of symptoms is something not all of us can do - even IF their condition is labeled as 'easy to manage'#i allowed myself to feel angry that i can't heal 'normally' and that was unfair as fuck toward myself#and i NEED people to internalize this so that MAYBE this could help somebody else who is where i was#i NEED them to understand that it's okay that they are where they are - sometimes shit just doesn't turn out how you expect or want#don't beat yourself over you being a person. you are struggling enough. you deserve to rest. just rest please#and just... give yourself space
2K notes
·
View notes
Text
My E-niversary is later today!! Yay!! Yippie!!!!
I'm glad to have made so much progress and found so much more joy and happiness and community!
Unfortunately I'm probably not going to make it to my next one due to chronic health issues that look like they'll be taking a turn for the fatal or worse over the next month if I don't get the medication I need for that, but I'm not going to stress about it. If I survive, I'll have a massive breakdown about it later, but for now, I'm a happy little kitty!
Love all my frens <3
#trans#transgender#transfem#trans joy#queer#lgbtqia+#kittyposting#eniversary#estradiol#estrogen#catgirlthing#intersex#trans hrt#the intersex condition causing my current t blockers to fail and causing swelling in my spine is the current threat btw#i'm 3 inches taller than I should be due to spinal inflammation! 🫠#chronic health issues#and the medication is approved by insurance (FINALLY. Only took 4.5 months) and my clinic will be using it on me the second they get it#the issues is that it's being shipped very slowly. and the logistics for transporting it are buried in legalese#soo. if I get it too late I die fairly painlessly. if I get it SLIGHTLY before then I get paralyzed from the neck down and die.#if I get it soon I live tho!!! and if I don't get it my spine just sort of splinters and crunches in on itself. and I stop having a CNS#which would suck. but i can only hope it arrives soon!#nonbinary
99 notes
·
View notes
Text
62 notes
·
View notes
Text
#bindi irwin#feminism#feminist#ecology#endometriosis#endo safe#women's health#chronic fatigue#disability#disabilities#chronic conditions#health#medicine#women's rights#women in science#women in stem#reproductive rights
1K notes
·
View notes
Text
me stubbornly forcing myself to drink green tea and rest from my THIRD COLD THIS MONTH
#i am so fucking tired of being ill#is it not enough that i have a chronic illness and chronic pain condition all the time anyway???#ughhh#i'm grateful because i at least managed to get to (most) of the gigs i wanted to this month#but other than that i've literally just been stuck in bed unable to do anything and my brain is starting to melt with boredom#idk how i can still not be well enough to write or absorb myself in reading a good book or fanfic or even be on here properly#but my brain feels like MUSH and it's so frustrating#i miss my little four walls men so much 😩#i miss being able to see the sky and see my friends and taste the food i eat#sorry i know i'm complaining#i just needed to vent for a moment#it's been such a shit few months anyway and i was already in a really rough spot with my mental/physical health for a number of reasons#so this just feels like the last straw#universe please let me feel a little better soon#i have things i want to do and people i want to talk to and fics i want to write#oh how nice it must be to live in a body that isn't constantly impaired in some way 🤦♀️#lulu posts
41 notes
·
View notes
Text
to be, or not to be (romanticization of the inevitable)
#ray's tag#keys' art#undescribed#skeletons#ok to reblog#the skeleton model that i traced for this was provided by the incredible kiku @kikunai whom you can find right here on tumblr!#so uh. This is a piece about chronic fatigue although the original idea i had for it drifted a bit as soon as I started coloring the linear#(i really enjoy shading and lighting things and got a bit carried away here but i stand by my choice because this is my favorite thing#that i've ever drawn)#anyways. i often feel especially lately with school being back in season that my bones are leaden with this sort of. weariness. theyre heav#it weighs on our mental health and energy a lot and although there's a couple of reasons we have been given for it#that doesn't remove the fact that this is still a thing that affects us in a very real way day to day although we are good at masking it.#often i come home to find that i do not have the physical mental or creative energy to work on things i really want to#especially project: nexus which i feel extra bad about even though i can't help it because i just started it so recently#it is a mild to moderate struggle to make it day to day and i just. wanted to represent this somehow#my original concept for this was a skeleton with some black goop gunk whatever leaking from its joints#but as i started adding the cracks and coloring them gold (a personal touch; kintsugi is a concept that is very dear to us)#i realized that the focus here was less on the condition itself and more on the body that it afflicts.#so i put it into a spotlight.#ironic i know since very little people acknowledge this irl or even know it exists at all but i added rim lighting. I added color gradients#I colored the lineart and made it all fancy and even added a flare for the head to get the point across that even at its core; disability i#a performance. this is not implying that disabilities are fake in fact this is the opposite of that. i wanted to show that with disabilitie#especially i think in my personal opinion the invisible ones#we are all masking at least a little bit during the vast majority of the day. humans are social creatures and it is only when we are alone#or with someone we deeply trust where we allow ourselves to be who we truly are without fear and even then that can be rare#so i wanted to show this bit of the soul in as broad a limelight as i could. idk this is a really abstract piece and i dont know if anyone#will even get it but it matters to me at least. and even though we've been largely bedridden for the past week i think that's okay#we will get it figured out. all of us. okay? okay. i love you. i fucking love you. we are going to fucking make it#(also the xes over the eyes are because i thought they looked cool they have no deeper meaning at least i think they dont#actually i think they do but i cant put it into words idk. Art is subjective assign your own meaning i'm gonna go get a shower)
345 notes
·
View notes
Text
Can we go ahead and normalize medicine? Taking pills in front of people? Taking pills in public and not getting weird looks? Using alternative medicines or anything other than pills and not being treated like a novelty? Fucking please because first of all literally everyone takes medicine of some kind at some point in life okay and second of all people need medicine to live it’s a thing it’s pretty common and people need to be in public for a lot of reasons actually so can we please
#disability culture#disability advocacy#chronic illness vent#undiagnosed chronic illness#chronic illness#chronic pain rant#undiagnosed chronic pain#chronic illness rant#chronic pain#chronic pain problems#chronic pain treatment#medical trauma#disability community#disabled community#neurological disability#physical disability#spoonies#dysautonomia#neurodiversity#mental health stigma#undiagnosed disability#fuck society#healthcare reform#normalize it#normalize this#did osdd#disability trauma#autistic thoughts#autistic borderline#comorbid conditions
78 notes
·
View notes
Link
#creda#credahealth#crohn's disease and pregnancy#crohn's management app#chronicdisease#chronic health condition
0 notes
Text
Oh my god for the last time
DO NOT USE AI FOR RESEARCH. DON'T TRUST ANYTHING IT TELLS YOU.
Do not use AI for research even if it cites its sources. Have you verified the credibility of those sources?
Do not use AI for research even if its sources are credible. Have you checked to make sure they have the most up-to-date information?
Do not use AI for research even if the sources are recent. Is this information generally accepted by experts in the field, or is it a controversial stance? Did AI source the 9/10 dentists or the 1/10? You don't know. You have no way of knowing unless you do your own fucking research!
DO NOT USE AI FOR RESEARCH. for the love of god people
"But I'm just doing research for my novel. It's okay if it's not 100% accurate."
ChatGPT told a person to glue the cheese on their pizza to make it stick. It told someone else a poisonous mushroom was safe to eat. It told another kid that Greek was a combination of four different languages. It thought there were 2 r's in strawberry.
Your information will probably not be 100% accurate. It might not be 50% accurate. It might be so completely and utterly false it would make a flat eather look informed. Just use Wikipedia of you want something quick and dirty. It might not be 100% accurate either, but it won't tell you to eat glue.
#the worst was actually seeing a self-proclaimed disability advocate recommend chatgpt as a tool#to help people research their symptoms to see if they correspond to an underlying chronic health conditions#which isn't writing related but for the love of god we have to stop it with the myth that chatgpt is okay for research
40 notes
·
View notes
Text
one of the most annoying things about chronic illness and having multiple conditions is that neither you nor your doctor know when to take a new symptom seriously or not. Is it a side-effect from all the meds? is it just a new thing that your body is going to do from now on? is it a new/unrecognised condition that has gone undiagnosed? Is it serious or just a one-off? is it stress? or is it just a Thing That Happens Once In A While with no good reason?
61 notes
·
View notes