#Neurology Medical Billing
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Neurology Coding Challenges
Providers in neurology often encounter obstacles like claim denials, payment delays, insurance coverage disputes, and regulatory compliance issues. To navigate these challenges effectively, leveraging specialized neurology medical coding services is essential.
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I have become so anxious about having enough to get by. I work with up to 9 clinicians on a regular basis, have a dental treatment plan of $4700 and am left with $500 a fortnight from disability after my rent is paid and haven’t had the physical ability to work for years now. I would be so grateful for any assistance 🙏🏻
Hi, I’m Hannah.
I am trying to build my life after 49 hospital admissions in 8 years. After 20+ years of trauma, an eating disorder etc. I have diagnoses of cPTSD, Anorexia, Fibromyalgia, Functional Neurological Disorder and my large bowel no longer works. I have been on the disability pension since 2019 but have increasing medical costs, increase in rent, more and more specialists and appointments weekly, fortnightly and monthly. I currently have 11 people on my team but can only afford to see 2 regularly.
I am needing help financially that I can’t find elsewhere. I am doing all that I can and am also currently studying at university but have become so overwhelmed, in thousands of dollars debt and am always behind in bills. I would be so grateful for any donations. Thank you
#medical expenses#medical bills#treatment#healthcare#disability#actually disabled#mental health#mental illness#physical health#reblog#signal boost#urgent#actually cptsd#cptsd#living with cptsd#prayer request#prayer#faith#send help#help needed#pls help#donate#donations#functional neurological disorder#fibromyalgia#spoonie#chronic illness#chronic pain#chronic fatigue#chronically ill
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Struggling with complex billing and collections? Let Instapay Healthcare Services take the headache out of your neurology billing! 💼 We specialize in maximizing revenue and streamlining your billing process, so you can focus on what truly matters—caring for your patients.
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#Neurology Billing Services#Neurology Billing Services in US#outsourced Neurology Billing Services#neurology billing company#neurology medical billing Services#Neurology Billing specialist#neurology billing codes#neurology coding and billing#neurology medical coding
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#Neurology Billing Services#Neurology Billing Services in US#outsourced Neurology Billing Services#neurology billing company#neurology medical billing Services#Neurology Billing specialist#neurology billing codes#neurology coding and billing#neurology medical coding
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Neurology Billing and Coding: A Step-by-Step Guide
Navigate neurology billing and coding effortlessly with our step-by-step guide. Ensure accuracy and compliance in your practice's financial processes.
#neurology billing and coding services#us medical billing#medical billing services#medical billing services florida#medical billing services usa#medical coding company florida#medical coding company usa
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EDIT: CRISIS AVERTED, THANK YOU!
Interracial US family w/ disabled autistic dad and toddler needs to get to the US for medical treatment
(New post because the old one was getting LONG with the updates. Details are under the "read more" to save your dash, with updates in the notes.)
TL;DR: If I'm going to live long enough to watch our daughter grow up, we need to get back to the US and get set up in a disability-friendly place where I can use my medical benefits.
Although I was already disabled (autism, adhd, and spine, joint, and head injuries), my health was stable--until four bouts of COVID left me immunocompromised, and utterly destroyed my health (including damage to my heart, blood clots that damaged one eye, neurological and joint issues, etc.), and although we started off fine, we've been hammered with one crisis after another, both medical and financial, that no one could have predicted.
Until we have enough to get back to the US, a chunk of whatever comes in has to go towards medical care that can't be put off, so the sooner we can reach critical mass on that, the better.
If you can help, or reblog, or share the links on other platforms, we'd be grateful!
The "Donate to Little or None" Paypal donation link takes the lowest fees, I think. (Kept the same link from when we were fighting to get our daughter's birth certificate fixed so we could get her citizenship affirmed.)
Then there's Ko-Fi:
And my little sister started a GoFundMe for us!
EDIT: The donation links above still work, but I removed the GoFundMe link.
IF YOU WANT ALL THE DETAILS SEE THE "READ MORE."
(There's more in my "rob gets medical" tag if you want a blow by blow account of how we got to this point over the past few years, but this is the gist.)
HOW IT STARTED:
I moved to the Philippines six years ago, after the deaths of my adult sons, in part to make my disability payments stretch further. Shortly afterwards, I was joined by my now-wife @thesurestthing (also from the US) for what was supposed to be a visit, but which turned into a permanent arrangement.
After I got a contract to license an old story for a mobile game (which tripled our income*), we found out we were having a baby, which was fine, because despite my disabilities (autism, adhd, two spine injuries, traumatic brain injury, a herniated esophagus, joint issues, etc.), my health was stable, and thanks to the contract, we were fine financially as well.
HOW IT STARTED GOING DOWNHILL:
Zoey's pregnancy was complicated, requiring two hospitalizations, and our daughter's birth was complicated, too--requiring a C-Section--which tripled our hospital bill. A few weeks after our daughter was born, the aforementioned contract was canceled without warning. THEN, when we tried to register our daughter's birth with the US embassy, we discovered an error on her birth certificate that left her stateless, and which took nearly two years, all our savings, and a fundraiser (thank you, generous people!) to resolve. Combined with medical expenses, that left us in a lot of debt.
A brief summary of went else wrong (leaving a lot out for brevity's sake):
I got COVID three four times during all this, became immunocompromised, and developed a slew of other medical issues (heart damage, eye damage and temporary facial paralysis from blood clots, persistent infections, a worsening of my joint issues, neurological issues, etc.) as a result of Long Covid.
I've had to be hospitalized a couple of times, undergo surgery, and was on an oxygen machine twice--once for an entire month, while I was bedridden. As of 24 January, 2024, I'm still recovering from my fourth bout of covid, which started at the beginning of October 2023.
There's a lot more, but you get the idea. COVID has completely wrecked my health, including tearing up my immune system.
And yes, I'm as fully vaxxed against COVID as one can be in the Philippines, with all available boosters, but again--I'm immunocompromised, plus they don't have the vax for the newest variant here yet. Zoey is vaxxed, also, and as a result, her bout with covid was extremely mild. El isn't vaxxed yet because they won't give the covid vaccine to kids under five here, but she's been able to share Zoey's antibodies from breast-feeding--which is apparently a thing.
The only way we can see for me to stay alive long enough to watch Eleanor grow up is to get back to where I can use my Medicare and VA benefits**.
WHY SO MUCH MONEY?
First, while we're still here, we need to pay for whatever medical care can't be put off. Plus, since I'm now immunocompromised, we have to get LOTS of vaccinations before we have to spend 24 hours or so in crowded planes and airports.
Second, we're going to be arriving with only what we can carry with us on the plane, and we'll need to get into a place near a VA hospital that I can easily get around in while I'm recovering from surgeries and getting various treatments. We'll need to pick up some secondhand household goods, and some kind of used transportation (because, you know, it's the US, where you kind of need a vehicle to get around).
We'll also need enough on top of my and El's disability payments to get by for a couple of months while Zoey looks for work. And all this is while we're still paying off the debt from the stuff I mentioned above.
So we're figuring that unless we catch some very lucky breaks, it'll probably cost between 20K and 36K altogether.
(We can't simply stay with friends when we get back, because literally every single close friend we have in the US with extra room and who lives close to a VA hospital has cats--to which I have a severe anaphylactic reaction. As in my entire respiratory system shuts down, and I have to be rushed to the ER to keep from dying; this has happened more than once. The only way I can be around cats is if I'm on immunosuppressants, and my immune system is ALREADY compromised, so I CAN'T do that.)
So again, if you can kick in, or reblog, or post our crowdfunding links (or the link to this post) on whatever other platforms you use, we'd appreciate it.
(*When I told social security about it, they said I could keep getting disability, too, because licensing IP rights didn't count as work income, and since it was a Moldavian company, it also fell under a special tax clause for getting paid by a foreign company while living overseas, so no taxes on it, either. )
(**VA benefits--I was a cold warrior in 1980s Germany. It was less than forty years after WWII, there was a lot of sabre-rattling--some of it nuclear--and we were there as a deterrent to prevent in Germany the kind of thing that's happening in Ukraine right now. Disclaimer because I'm tired of people accusing me of "invading" folks in the early 1980s when I was a dumb, heavily propagandized pre-Internet kid fixing generators in Europe. I wouldn't join today even if I could.)
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All of Bill's stock history and tastes that you mentioned are things he did after Euclydia, but nothing suggests that he had those tastes in Euclydia or there is something that made him a weirdo in Euclydia besides his mutation or his eye fetish.
ok let's break this down.
Nothing suggests he didn't have those tastes in Euclydia. There's no compelling evidence to suggest he was normal for a Euclidean. Take out his mutation and we don't know anything about what he was like in Euclydia except:
he had squeaky shoes (normalcy unknown—although, in humans, squeaky shoes are often used to help children with physical & neurological development issues learn to walk)
he wanted the crusts cut off his sandwiches (normalcy unknown; but the fact he had to remind his mom suggests it wasn't normal)
he could be manipulated into drinking his medicine with curly straws (normalcy unknown; the fact that he's specified as a "picky eater" suggests it's abnormal)
his birth was allegedly celebrated with a best baby award, holiday, and free knives (normalcy unknown, possibly a lie)
he didn't learn to tie his shoes until age 16 and called shoelaces fascist (the fact that his parent(s) apparently recounted this as an amusing anecdote later suggests it's abnormal)
it's heavily implied he murdered his optometrist, and possibly his family at around the same time (i'm just gonna take a leap of faith and assume this is abnormal for Euclideans)
So his normalcy score is "unknown but dubious; might be abnormal; might be abnormal; unknown/untrue; abnormal; abnormal." And that's everything we know.
At any rate, if we want to know what he was like as a Euclidean, it seems a lot less sensible to go "well we know next to zero facts about his childhood, so that must mean he was normal" than to look at what we do know about his personality and assume that... y'know... it came from somewhere. We have no reason to take it as a given that he only developed those personality traits post-massacre.
Plus, saying "he was normal except for his mutation" is sort of like saying "he was an introvert except for what a big fat party-loving attention-hungry extrovert he is." It's like saying "Ford was normal except for his mutation"—okay except Ford isn't normal, his entire life is shaped by being abnormal, everything he's ever done is a response to the tension between pursuing kindred abnormality versus seeking validation from normies, and all that is caused by his mutation. What person are you talking about if you're talking about who Ford is without his mutation? There's no Ford left.
Similarly you can't just excise the trait that made Bill who he is and act like you're still talking about the same character. Like yeah sure I guess he probably would be a lot more normal once you remove the trait that alienated him from everyone else he knew, led to him enduring medical trauma from toddlerhood, and caused his grade school classmates to chant "Cipher, Cipher, he's insane, starting fires with his brain." "Bill's a normal Euclidean once you remove his personality." Sure, that technically isn't a false statement.
"or his eye fetish"—okay, so we're talking about my version of Bill, not canon Bill Cipher? In that case:
he dropped out of school by equivalent-to-age-14 to run a cult (weird)
he claimed the third dimension was real and people who didn't believe in the 3rd D thought he was crazy (this part is kinda normal, and caused by his mutation)...
... and claimed that it was where heaven is, and people who did believe in the 3rd D thought he was crazy (this part is weird and NOT caused by his mutation)
by middle school he was telling his bullies that their moms fucked the family dog (weird) (also, when I rewrite that scene, in honor of the precedent set by TBOB, I'm probably going to change that to Bill telling his bullies he fucked their moms)
he handled all his homework by not doing it, all his tests by cheating on them, and getting caught at cheating by crying to his mom about how his teacher was prejudiced against him so that she'd get mad at the school before the school could tell her he'd been cheating & she'd get mad at him (weird)
he resolved an argument with his mom by murdering her at like 15 and then went right on leading his cult (incredibly weird)
he publicly went on a screaming tantrum that made national news against respectable scientists because he'd told a bunch of lies he KNEW were false and they went "you'd have to be dumb to believe this stuff" (weird & a terrible idea)
he publicly issued a million dollar bet against the entire scientific community as a teenager when he knew full well he didn't have a million dollars (weird & an even worse idea)
he ravenously devoured so much cosmic horror literature that when he met an actual cosmic horror and it acted normal he had a full mental breakdown over it not being horrifying enough (incredibly weird)
by the time of the massacre, he had developed into the kind of person who would respond to the extinction of his entire dimension by pretending he meant to do that, kidnapping a bunch of neighboring people, throwing a nonconsensual zombie party, and declaring himself god-king (unfathomably weird)
These are just the things that have already happened in the fic. I could cheat and tell you all the things that made him a weirdo that haven't come up yet, but I won't.
So sure, some of the things that currently make him look weird to humans are normal for Euclideans; but no, he wasn't normal for a Euclidean.
And on top of all that, he figured out he had an eyeball fetish after he left Euclydia ¯\_(ツ)_/¯ because he hadn't done any romantic/sexual experimentation by the time of the massacre (slightly abnormal) because—he would subsequently discover—the only thing that gets him going is grotesque higher-dimensional non-euclidean aliens (very abnormal).
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Help a Disabled Friend (and her service dog)
It's day one of Disability Pride Month (literally, july 1st is when Disability Pride Month lol) and I'm already struggling to get things that will make my life easier. The mort important thing on this list is a mobility harness for my service dog.
if you don't know, I have neurological problems, dysautonomia, and ehlers-danlos syndrome, and they are the most problematic for me because of the motor/mobility and digestive issues they cause. While I'm doing all that is medically possible for the digestive issues, the motor and mobility issues are basically not being dealt with.
I have a service dog, and part of what he does is help me with walking/standing/getting up/getting down, and that's lovely, but I do not have an appropriate mobility harness for him-- which would be sturdy and built specifically for differences in weight, pressure, etc, and have a rigid handle. In the past, I have used a secondhand mobility harness but it lacks the correct handle. I would strongly prefer to use a safe, sturdy harness that is built for my needs and my service dog's safety.
I also need guide attachments for this harness so Heathen (my service dog) can do better at guide tasks at night and during very bright parts of the day. The feedback of a pullstrap isn't quite enough.
With all appropriate options, this harness costs $349 USD.
The guide handle I need is $71.
I have $50 in my paypal account to put towards this, and being on SSDI, I only get paid once a month, and not much-- $1311. 500 goes to my mortgage. Most of it goes towards caring for my service dog and paying medical bills, and it really, really is not enough. I have literally tried appealing to SSA to raise my monthly payment, but I've been told that is not a thing they even entertain.
Please, if you can, help me get this mobility harness. It would mean a lot more mobility and freedom for me, considering my wheelchair is still damaged and my insurance will not tell me yet whether they approved the repair or not.
My paypal is [email protected]
My venmo is nikkicantrell96
Please, please help if you can.
#help#mutual aid#fundraising#fundraiser#disabiled#disability#disabled person#service dog#disability pride
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My sweet baby Peppermint passed away on December 8th, 2024 at 2:45 AM. She became sick very suddenly and unexpectedly on the 6th as we noticed she wasn’t eating any food or drinking any water. Believing it was a UTI, we took her to our local vet where they prescribed antibiotics. On the second day she got worse and we took her to the emergency vet where she was diagnosed with pancreatitis. We were told that with treatment she would likely survive, but that unfortunately was not the case. Peppermint had suffered from neurological issues and food wasn’t able to go into her stomach, resulting in her passing. I make this post because me and my family are grieving, and in need of help. The vet wouldn’t have recommended treatment if they thought it was too late for my girl, but now we must pay for the rest of the treatment she received.
Her two vet visits cost us $3000 altogether, and this is $3000 we do not have. But we wanted to do anything we could to save Peppermint. If you have a dollar to spare, please consider donating so my baby can rest peacefully. I am happy to draw anything in return for any amount of donation, I just ask that you message me on Instagram @sundrits with your request and proof of donation. Thank you for your time.
Here are some pictures of my girl. She kept me well in some of my worst moments. From the moment we brought her home, she never stopped purring. She loved to go outside and roll around in the grass, play with her two kitty siblings, and cuddle with her people.
#help needed#cat#black cat#peppermint#go fund me#furry art#furry artist#furry#fursona#commissions open#commissions#furry commissions#art trade#queer#transgender art#transgender#help
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Major Medical Coding and Billing Challenges in Neurology
The significant medical coding and billing challenges in Neurology demands experienced neurology billing services to maintain precise and detailed documentation. https://www.outsourcestrategies.com/blog/medical-coding-billing-challenges-neurology/
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whatevr ill post my stupid baby bill poem nonsense on this app
i hold my son close to me. we just went to our first eye doctors appointment. his big round eye is closed as he sleeps. he clings to me as he naps in my arms. i look at the medication they gave me. the bottle doesnt even seem to have proper dosage. i sigh. ever since my son has started his diagnosis journey, i've worried for him. all the doctors flock around him when he starts looking up nobody has ever seen what he calls up, it perplexes the specialists, the teachers at school, his peers. and yet, i feel like there has to be someone who has there has to be more like him, correct? today's my baby billy's first day of second grade hes grown so big from when he was in his baseball sneakers. i measure him from angle to angle, hes grown somewhat taller. he beams. i walk him to school, he tells me about the stars once again. how they glitter and glow. i tell him that even if i can't see what hes talking about, i see him, and always will. he smiles with his eye i tell him he'll have his silly straws clean when he gets home billy has started telling me he can't see. i check his medication. they've upped his dose from 2 sips to 3. i yelled at the doctor for not even giving me a proper dose for him. they told me not to worry, that they know best. i dont believe them. i have stopped giving bill his "eye medication" it turns out that it wasnt helping him at all, the doctor who gave it to us was outed as a fraud he looks at me with that round eye and wonders why ive stopped i tell him he'll be safe this is billy and i's first appointment at a psychologist. billy looks at me with worry in his big round eye. he's never had to have an appointment where he has to talk about himself. i tell him he'll be safe and that i'll hold his hand through the whole thing. they were perplexed to say the least, but they were helpful they told us to come back for an assessment they said they might have the answer the psychologists have a diagnosis its a thing they dont know a lot about, hes the first one to be officially diagnosed the doctors want to name it after him but i insist they don't. i don't need my boy to be the center of his condition he looks at me in the car with fear. i tell him that everyone is still learning, even doctors. he smiles with his eye again . i make him a sandwich with the crust cut off when we come back, he beams years later, the diagnosis has been named silly straw syndrome its considered a neurological conditon that effects the way someone sees the world. people are still scared of my son when he looks up at the stars but we're getting somewhere, the world of shapes is making progress. bill brought home a friend im overjoyed, hes never had a friend over and for once, i see a kid other than my own look up at the stars with him! and i finally see that my son is understood! i tear up, my beautiful boy is finally understood by his peers. i dont have to worry. im at peace. my son will be ok in the world, there IS people like him! i cry, i sob. my son is finally finding a place. hes finally ok.
#worlds most self indulgent piece ever#i finally get those people who wanted to raise the eraserhead baby#baby bill#i dont care that this isnt lore accurate#canon divergent baby bill where he's actually understood by doctors ;;
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Do any of the gang members find out that they have any disorders/mental illnesses/etc. once they get timewarped and if so what are their reactions? Ranging from “oh, I though that was normal” to “NUH UH!”
timewarp was founded on the gang realising they have ptsd and kieran's autism being more obvious and worse in timewarp. but in detail
kieran is autistic
sean might have adhd but he doesn't actually have hyperactivity as a symptom. plot twist he just has that erratic trauma avoiding energy. it is a lot more masking severe c-ptsd and imposter syndrome that is his behind his exaggerated happy personality. see reform school lore
arthur is one of the few diagnosed he definitely had an acquired brain injury which while a physical injury manifests with mostly neurological symptoms. sometimes he gets confused or irritated for seemingly no reason, and this has been a thing since long before timewarp. the gang move on from joking about how dumb he is he does have an intellectual disability as part of his ABI. his response was very "oh I thought that was normal" and "bah i ain't need help".
the gang have subconsciously been aware of this long before they had the medical knowledge to understand it and are all pretty used to quickly explaining things or reminding arthur of stuff he forgets. lowkey consider this canon ever notice how the gang talk to arthur sometimes not entirely condescending but explaining things on his level eg sean being the one to point out the grays will definitely recognise him and he should hide in the wagon, grimshaw almost playfully reminding a grown man to wash because he straight up forgets, gentle reminders of what they're doing through heists even beyond game mechanics a lot of heist cut scenes are super repetitive like charles very much breaking down we're blowing a hole in the bank. take the spool and connect it to the detonator. the detonator is over there. it just feels like they know arthur isn't always entirely there and are v supportive. arthur is so curious and asks so many questions and the gang just roll with it and answer most of the time it feels so kind and positive.
arthur also definitely has adhd. hyper-fixates on new interesting thing for a month and then completely forgets everything he ever learned about it
almost the entire gang acknowledge they have ptsd/c-ptsd and varying levels of trauma as a response their lives/childhoods/relationships with parents/being a VDL. acknowledging it doesn't mean they do anything to move towards recovery because they are still mostly men raised with 19th century values who hang shit on each other for flinching at loud noises or being 'is someone shooting at us' alert
lenny and isaac as the most aware begging their friends/family to take their mental health seriously and are constantly met with 'lmao no' 'that's?? normal?? what do you mean' and 'NUH'. lenny cries 'please this is re-traumatising you are actively upsetting yourselves' while the gang go 'boo grow a pair' despite experiencing varying levels of anxiety attack in response to triggers.
john will only bring up 'hey stop making wolf jokes about me it is Actually a Trigger' to stop the gang bullying him. very genuine trigger and phobia of wolves and wolf-like dogs but still doesn't take it seriously himself
bill has recognized anger management issues and is in therapy. alcoholism is a definite concern. he's also just got a lot of internalised homophobia and complex feelings about the gang and his own childhood to unpack and learn how to articulate and express his feelings in a healthier way. only one of the adult gang who is actively trying to improve his mental health through therapy go king
the d in dsm-5 stands for dutch and he is thriving in in-patient care. not even the doctors know entirely what to diagnose him because he seems to have symptoms of everything but is responding best to medications traditionally used to support bi-polar
special acknowledgement to karen who is very very depressed but is a thriving with anti-depressants because trying to get the gang to go to actual psychologists and therapy is Hell. her and sean send each zoloft memes constantly
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I have now lost access to crucial and necessary psychologist appointments that I have weekly due to no funding from the government or otherwise, am completely wheelchair dependent because I can’t afford physiotherapy, am trying to study, pay rent and weekly medical bills such as dietitian etc.
Am in desperate need of immediate help and can’t say how grateful I would be. I have tried every avenue for funding and support and can’t attain it. I am in crisis and desperate need of help. Please 🙏🏻
11 months ago I was diagnosed with Functional Neurological Disorder and with Fibromyalgia earlier this year.I have also dealt with cPTSD and an eating disorder for the last 20 years.
I have been mostly bed bound for 12 months and have spent 6 months of this year in hospital. I cannot currently walk more than 20 metres without needing a wheelchair to mobilise. I have been unable to drive for the last 12 months due to continued non-epileptic seizures.
I am needing continued help to manage all of my medical bills, specialist appointments, medication, transport etc.
I am attaching a PayPal link if you feel at all inclined to donate to help me manage week to week as the pension I’m on doesn’t even cover basic expenses for each fortnight after rent and each of my medical team appointments.
I would be so grateful for any donations, reblog etc. Thank you in advance x
#fnd#christian#paypal#donations#donate#help#help needed#reblog#please send help#prayer request#prayer#chronic illness#spoonie#functional neurological disorder#fibromyalgia#wheelchair user#mobility aid#therapy#cptsd#actually cptsd#disability#actually disabled#fundraising#medical expenses#medical bills#medical costs#appointments#physiotherapy#dietitian
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https://handyclassified.com/neurology-billing-made-easy-increase-your-earnings-today
#Neurology Billing Services#Neurology Billing Services in US#outsourced Neurology Billing Services#Neurology revenue cycle management#neurology billing company#neurology medical billing Services#Neurology Billing specialist#neurology billing codes#neurology coding and billing#neurology medical coding
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