#fibromyalgia Doctor
Explore tagged Tumblr posts
Text
Discover how a fibromyalgia doctor can help manage your symptoms and improve quality of life. Learn more about specialized care for fibromyalgia at Elite Medical Fitness.
0 notes
Text
Breaking Free from Fibromyalgia: Meet Our Specialist in Bhubaneswar
Fibromyalgia: a complex and often misunderstood condition affecting millions of people globally. Its widespread musculoskeletal pain, fatigue, and tenderness can significantly impact one's quality of life. If you're grappling with fibromyalgia in Bhubaneswar, finding a dedicated specialist is essential. At Neuron Pain Clinic, we offer specialized fibromyalgia treatment in Bhubaneswar to help you manage and improve your symptoms effectively.
Understanding Fibromyalgia
Fibromyalgia is a chronic disorder characterized by heightened pain sensitivity, chronic fatigue, and sleep disturbances. The pain associated with fibromyalgia often involves tender points across the body, causing discomfort and limited mobility. Individuals with fibromyalgia may experience mood swings, memory issues, and cognitive challenges, further adding to the burden of this condition.
Seeking a Fibromyalgia Specialist in Bhubaneswar
In your journey to manage fibromyalgia, seeking a specialized fibromyalgia doctor in Bhubaneswar is crucial. At Neuron Pain Clinic, we understand the unique challenges that fibromyalgia poses and offer tailored treatment plans to address your specific needs. Our team of experienced fibromyalgia specialists in Bhubaneswar is dedicated to providing comprehensive care and support throughout your treatment.
Our Approach to Fibromyalgia Treatment
Our fibromyalgia treatment in Bhubaneswar focuses on a multidisciplinary approach, combining various therapies to alleviate pain and improve your overall well-being. Here's a glimpse of our approach:
Personalized Treatment Plans: Our fibromyalgia specialists in Bhubaneswar create customized treatment plans based on your unique symptoms, medical history, and lifestyle.
Pain Management: We employ advanced pain management techniques to mitigate the discomfort associated with fibromyalgia, helping you regain control over your life.
Physical Therapy: Physical exercises and therapies are integrated to enhance mobility, flexibility, and strength, ultimately reducing the impact of fibromyalgia on your daily activities.
Medication Management: Our specialists carefully prescribe medications to alleviate pain, improve sleep, and manage other symptoms associated with fibromyalgia.
Mind-Body Techniques: Techniques such as relaxation exercises, meditation, and mindfulness are incorporated to manage stress and enhance mental well-being.
Your Path to Relief Starts Here
At Neuron Pain Clinic, we strive to empower individuals living with fibromyalgia in Bhubaneswar. Our fibromyalgia specialists are committed to providing compassionate care, ensuring you receive the best possible treatment to improve your quality of life.
If you're seeking a fibromyalgia specialist in Bhubaneswar who understands the unique challenges posed by this condition, visit our Fibromyalgia page to learn more about our specialized treatments and book an appointment today.
Don't let fibromyalgia control your life. Take the first step towards a more comfortable and fulfilling life with Neuron Pain Clinic. Your path to relief awaits.
More Info Get in Touch with our Social Media Profiles Facebook, Twitter, YouTube & Instagram
0 notes
Text
How can chronic pain patients be “addicted to pain meds?” That’s like telling someone with a prosthetic that they’re addicted to their prosthetic. Or a cardio patient that they’re addicted to their pacemaker. Or a diabetic that they’re addicted to insulin. What is the thought process here?
#how does this make sense in their mind#oh wait they’re fucking stupid that’s why#chronic pain#cripple punk#cfs#cpunk#cripple#cripplepunk#crip#crip punk#crippled#tagging cpunk bc fuck doctors fuck abled people etc etc#fibro#fibromyalgia#chronic fatigue#chronic fatigue syndrome#chronic illness#chronically ill#disabled#disability#abled ppl can talk about their mental health experiences here#bc ik people with adhd get told they’re addicted to adderall#or us schizos getting told we’re addicted to antipsychotics#just don’t talk over us crips#bc this is specifically about physical illness
2K notes
·
View notes
Text
This can be a huge source of medical trauma and it's so cruel that it's being imposed on people by the medical establishment itself. How can they help but feel anything but helpless? There's no fighting that.
I can't help but think of this from my own perspective as a fibromyalgia patient who keeps having to fight being thought of as (or even being labeled as) drug-seeking.
I am literally just trying to live life closer to the standard that 'normal' people have every day.
Why is it in any way fair that most people are mostly pain-free and capable of doing the things they want to do, but I have to suffer with pain on a daily basis that is at minimum, on a very rare, very good day, at level 5?
Why is it when I report that my pain level is at level 7, 8, 9, I only get doctors side-eyeing me and explaining my OTC options?
I have had chronic pain since I was 8. I'm very fucking aware of my OTC options, so no thank you, doc.
And when I spend 20 minutes explaining in detail that my daily pain has noticeably increased and changed in quality since around January 1st, why should I have my PCP giggle at me every time I say that I need help with managing my pain and learning ways to deal with it?
It felt incredibly invalidating and I wish he would have said, look, I don't have the expertise to help you, so here's a referral to a pain specialist.
I only found out there was a such thing by trying to research the topic after this on my own!
So yeah, it's not just the insurance companies, it's the doctors, too.
It's almost like having a profit-motivated medical establishment hurts patients.
#LizMelrath@twitter#twitter#death cw#cancer cw#chronic illness#chronically ill#chronic#fibromyalgia#doctors#microaggressions#reposting everything from my twitter feed#i'm about to delete everything so get it while it's hot#tweet: 2022#marti's mad life
2K notes
·
View notes
Text
"Doing your best" (with chronic illness)
My doctor (bless him) straight up went "don't" when I said "I'll do my best"
Because what I think "my best" is, is completely draining myself for this One Thing and going above and beyond
I guess this goes for people w/o chronic illness as well, but "your best" shouldn't mean you end up hurting yourself in the long run. "Your best" is as much as you are willing to devote to something proportional to how much you care about it within the confines of what is healthy for you AND considering all the other stuff you have to do
Please just- holy heck we're already struggling so much please don't devote your precious energy to something that doesn't deserve it
don't do your best, do whats best for you
#see how much you care and put it on a 1-10 scale and devote that energy to it#if everything is at a 10 throw a logarithmic conversion on that scale to better see the difference between the datapoints#yes i am a stem girlie#please be kind to yourself#yes I am very happy with my doctor thank you for asking#chronic illness#fibromyalgia#chronic fatigue#chronic pain#spoonie#spoonie life#chronically ill#chronically fatigued#chronically disabled
602 notes
·
View notes
Text
Just had a doctor blame me for being in pain??? And she was in shock than when I push myself the pain doesn't go away??? Bruh this fucking medical system
161 notes
·
View notes
Text
this disability pride month, stop making jokes about people in wheelchairs standing up or walking.
can I stand and walk? sure, for a short while and with pain. the consequences for trying to be out all day without a wheelchair are that I'll be in bed for the rest of the week, too tired and in too much pain to move.
but the government won't give me my own wheelchair because they have the same attitude as these jokes - I can stand up, so I don't need one. exercise is good for you, you should walk!
it keeps me trapped in the house, unable to do anything more than short stints anywhere without borrowing or hiring a wheelchair - one that causes me pain to sit in and relies on someone to push me (usually with difficulty), because they're not going to have a high-end chair for that sort of thing.
it's not a miracle that a wheelchair user can stand or walk. it's something we should aspire to see more often.
#disability#disability pride month#chronic fatigue#fibromyalgia#cfs/me#post exertional malaise#like fucking hell people we should really be long past this by now#why am I seeing these bullshit jokes on my dash in twenty fucking twenty three#i did a short walk to a cafe yesterday because I thought I was up to it#and my right leg has seized up#my ankle can barely take my weight and my hip won't move properly#also lol I almost certainly have hEDS but cannot persuade a doctor to give me a referral#in summary#stop being fucking dense#i would rather people who don't need mobility aids use them than have people struggle because they don't want to be seen as a faker#or have people think that you have to reach a certain level of severity before you need it#also if I had a wheelchair I would bring my cat with me more places but that's by the by
2K notes
·
View notes
Text
hi so our last post died, and things have gotten kinda worse with the arrival of our other cat, my elder brothers homelessness, and the racial abuse getting hurled my way
we’re two disabled black lesbians trying to navigate employment discrimination and the American healthcare system, and tbh we’re losing. we originally had to split everything between 6 people, but due to my brothers getting evicted, everything we have (and everything we don’t) also goes to them
like last time, I’m still waiting for a doctor but recently they told me to call back in November. I’ve been calling since April. I believe the stress of everything is causing a flare up of something and I have no idea how to manage it, on top of my new seemingly random food sensitivities that keep popping up. I’m exhausted all the time and sometimes can’t even get out of bed.
on a brighter note, my girlfriend applied to five jobs, but their phone was shut off this morning so it’s urgent that they pay their bill.
we were able to get some necessities early last month due to peoples help, but we can’t make it stretch with 8 people. it’s a shitty situation all around and I wish we didn’t have to ask but until my gf can get a job and I can find out exactly what’s wrong with me, this is literally all we have.
I’m not gonna link my PayPal anymore because people are harassing me with my deadname
my cashapp is $silvertheestallion and my gfs is $Peachjammn
my Venmo is cherryadventure2
thank you so much for reading
#this ask isn’t money related but if anyone has fibro or just burning chronic pain can I ask how did you know? I’m trying not to just say#oooh I have this but idk when I look at the symptoms it relates to me. I’ve found help in the fibromyalgia subreddit but I don’t know if it#is it not and I really don’t know if I can get to my doctor#I’ve been in pain for months. and nothing helps long term#and ik I should try and find a differnt doctor but I am trying#and it’s the same radio silence for months only to be told oh try again next month and I feel like going insane#I should prolly make this it’s own post
625 notes
·
View notes
Text
Doctor Beverly Crusher @SpaceDocMom "No pain, no gain," is only said by the health-privileged and they're mostly wrong about it for their own bodies too. For anyone with a chronic illness, more pain is likely to equal less gain. Listen to your body, not ignorant people. emojis: black heart, blue heart, masked 2:31 PM · Sep 21, 2023
#star trek#doctor crusher#star trek the next generation#star trek memes#star trek tng#support#kindness#care#compassion#health care#healthcare#medicine#exercise#me cfs#fibromyalgia#chronic fatigue syndrome#chronic illness#spoonie#disabled#spoons#chronic fatigue#chronic pain#post exertional malaise
565 notes
·
View notes
Text
i’m a medical mystery
#i would simply like ✨competent✨ doctors#credit in pic#possumcore#opossumcore#possum memes#opossum memes#chronically ill#chronic illness#mental illness#mental illness memes#chronic illness memes#rheumatoid arthritis#fibromyalgia#chronic migraine#occipital neuralgia#allodynia#cptsd#posturaltachycardiasyndrome#vasovagal syncope#undiagnosed
732 notes
·
View notes
Text
either people with fibromyalgia need to stop being so relatable or i need to see a doctor
#i am in fact seeing a doctor today#wish me luck#chronic pain#disability#disabled#chronic illness#chronically ill#chronic fatigue#joint pain#fibromyalgia
43 notes
·
View notes
Text
Things about doctor appointments that no one tells you about:
Test results are interpurted differently by different people. I was so excited about a weak positive however my Dr. completely dismissed it.
Sometimes, Dr. will try to say lies that aren't really lies. [like my Dr. said that a medication should last around 48 hours in my body, but it barely lasted 2-3 hours]
Doctors don't expect you to read up after them. Or read more about what they are talking about.
At some point, the Dr. will say it's anxiety, but it doesn't mean that it's not a real symptom. Even if it's anxiety, it is valid.
Most of the time, you'll leave them disappointed.
Doctors don't know how we feel and they struggle to think the way patients think. If that makes any sense.
Doctors aren't necessarily against you as a patient. If they dismiss something it's not because of you as a person. But more likely something they truly don't think it affects you.
93 notes
·
View notes
Text
So I went to the rheumatologist the other day and can I just say how obnoxious it is to have a doctor who never listens to what you say. I had a whole list ready bc she didn’t listen to my list last time so I was going to make it a point right. And she still didn’t listen. And then when I asked about if mobility aids would help me she told me that I didn’t need them because I don’t have any issues with balance. Like huh. I was telling you how I was so weak and unstable in michaels one time and ever since then I’ve been super weak and shaky since. How my knees are in incredible pain that makes my legs numb. But yeah I don’t need any help. So guys help me pick out a cane!!!
#spoonie#chronic illness#chronic pain#pots#potsie#hypermobile ehlers danlos#fibromyalgia#fibro problems#doctors don’t listen#cpunk#I’m don’t trying to explain my pain to doctors who don’t care#canes#mobility aid
118 notes
·
View notes
Text
Fucking hate it when I tell people I have a chronic pain/fatigue illness and so when I tell them I'm tired they're like "really?? You should try this, this and/or this!"
Im not telling you I'm tired because i want your help, I'm telling you so you don't wonder why I don't (cant) do much.
I've tried a lot of things, trust me. I just want your understanding.
#unless youre a doctor#then please#give me all the drugs#disabled#disability#chronic illness#chronic pain#chronic fatigue#fibromyalgia#tired#im so tired
38 notes
·
View notes
Text
spent 3 hours last night panic searching for doctors to help me with my fibromyalgia. They are all either scams, extremely expensive boutique options (but are actually good apparently, if you have the money), extremely expensive scams, or have never heard of fibromyalgia and kick you out after 15 minutes.
#wrenfea.exe#apparently theres a thing called direct cost now#where the doctors spend like 2 hours with you and do all this testing and only take on a limited amount of patients#but they dont take insurance and are expensive#so you still need insurance for like. hospital stuff#but also have to pay out of pocket hundreds of dollars#if i had the money id do it since i already spend a ton of money on doctors that dont give a fuck about me#so might as well spend them on doctors that do#all the holistic care around me is scams for rich old ladies#my fibromyalgia symptoms are really holding me back#im so tired and achy and foggy and im so frustrated#i want to do things#i want to do my job well#but all the searching was fruitless#ive already seen a rheumatologist and she sucked#and none near me work with fibro patients#no neurologists do either#chronic disability#chronic pain#spoonie#fibromyalgia#disability
24 notes
·
View notes
Text
Just had the big appointment™️ with my GP where I basically beg for alternative pain relief for my fibro and he told me he can't do a thing. I'm already on 2 anti depressants that are supposed to help. I'm already in therapy. Reducing the level of stress I'm under while being as poor as I am is just not possible and I know I need to go to physio but I'm in so much pain I can barely leave the house. I was just hoping for something to allow me to have some kind of quality of life back but all he could offer are opiates and we both said that wasn't a good idea with my drug history and like I'm fucking 27, I absolutely don't need to spend the rest of my hopefully long life dealing with that.
I guess the one good thing is he said the likelihood of paracetamol causing the ulcers over stress was pretty low so I'm allowed my sexy over the counter, don't do anything pills again ⁽⁽ଘ( ˊᵕˋ )ଓ⁾⁾
I guess that's what I get for having an illness that everyone thought was hysteria with a fancy name until a few years ago
#i joke but im genuinely fucking devastated#i really thought he could help but he cant#then i texted my mum to vent and she bailed to make dinner for my 24 year old brother (her favourite kid)#fibromyalgia#chronic illness#cw doctors#cw medication#cw opiates
21 notes
·
View notes