#chronic fatigue syndrome surgeries

[69yard]

Chronic fatigue syndrome (CFS): Causes, Symptoms and Treatment

Chronic fatigue syndrome (CFS) Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), is a complex and debilitating condition characterized by extreme fatigue that does not improve with rest and is not caused by any underlying medical condition. The exact cause of CFS/ME is still not fully understood, and there is no specific diagnostic test for the condition. Symptoms of…

[problem-project]

So I found out today that the black spot in my vision is officially permanent and that if my medicine doesn't start working again at a higher dose, then I will need a stent/shunt placed in my head. Brain surgery scares me so much, but it's impossible to function every day if I don't somehow get my head pressure managed 😞 send me positive vibes and well wishes pls, it sounds like I might need it 🖤

[primrosebitch]

Tbh it really is something to have grandmothers (one late 70s other late 80s) who are in better shape than you are, like I go see my grandma and we walk somewhere and i'll be panting before she's even slightly out of breath and it's not like she's in the best of conditions either, and then don't even get me started on my other grandma, she still does sports.

[whatshouldwecallchronicillness]

When the test results look terrible, but my symptoms are pretty ok...

[laprosopicsurgon]

Gynecologist Doctor In Punawale

1. Polycystic Ovary Syndrome (PCOS)

PCOS is a common hormonal disorder among women of reproductive age, causing irregular periods, weight gain, and fertility issues. Dr. Balaji Nalwad Reddy offers a range of treatments, from lifestyle changes to medications, to help manage PCOS symptoms and improve overall health.

2. Heavy Menstrual Bleeding

Heavy menstrual bleeding, also known as menorrhagia, can disrupt daily life and lead to anemia. Dr. Reddy uses advanced techniques like hysteroscopy to identify the cause of heavy bleeding and provide treatments that may include medications or minimally invasive surgeries to control the bleeding.

3. Pelvic Inflammatory Disease (PID)

PID is an infection of the reproductive organs that can cause pain and lead to fertility problems if untreated. Dr. Reddy provides effective antibiotic treatments to control the infection and prevent complications, ensuring women's reproductive health is preserved.

4. Infertility

For couples facing difficulty in conceiving, Dr. Balaji Nalwad Reddy offers infertility evaluations and treatments. He conducts thorough assessments to identify the root cause of infertility, such as ovarian cysts, endometriosis, or hormonal imbalances, and suggests appropriate treatments like fertility medications or assisted reproductive technologies.

5. Contraceptive Counseling and Family Planning

Dr. Reddy provides expert advice on contraceptive methods, helping women and couples choose the best options for their family planning needs. He offers long-term and short-term contraceptive solutions, including IUDs, oral contraceptives, and sterilization procedures, to ensure safe and effective family planning.

Dr. Balaji Nalwad Reddy is dedicated to providing comprehensive gynecological care in Punawale, ensuring that his patients receive the best possible treatment for their reproductive health. If you need expert care for any gynecological concerns, make an appointment with him today.

For More Info-https://gynaeclaproscopicsurgeon.com/blog/2024/10/02/gynecologist-doctor-in-punawale/

[icequeen1371]

I know the sun is only on one side of my face, but when I put the black-and-white filter on, it looks like I have a blackeye. Is that seriously how tired I look all the time? Wow….

[little-pissbaby]

tw it's a medical update. I talk about surgery

it's official! I need brain surgery.

for all the new faces I can't see, I have idiopathic intracranial hypertension. I have since I was 15, but it wasn't diagnosed and treated until I was 25. for a full decade, I had a migraine that did not let up and no one could figure out why. to be fair, what skinny, barely-scraping-100lbs 15 year old develops IIH? I was taking acetazolamide for it, but unfortunately my kidneys are now chicken fried and I currently have Acceptable™ kidney function.

I'm going to have a ventriculoperitoneal shunt placed. I don't have a date yet, but I expect it to be sometime in the first few months of the new year. it will be risky, but better than permabanning my kidneys and taking one from my brother.

I am,,,,, exhausted. every time I feel like I'm finally on top of my health, something goes catastrophically wrong. thank god for friends willing to stick it out with me through the inconsistency <3

[onlyangel4]

pushed too hard. mv1. SMAU + written.

max verstappen x chronically ill! reader

in which max's girlfriend has a very valid reason for not attending the races but the public doesn't know. and when the hate gets too much she pushes herself too hard.

author's note: so i have written this completely from experience, so the reader has elhers danlos syndrome (which i also have) but if you suffer from a different chronic illness please do imagine it as that.

warnings: chronic illness. hate. hospitalisation. injury.

face claim: katie douglas

y/ninsta posted a story tagging maxverstappen

written: y/sister managed to get a picture of me as soon as i woke up to find out that max won the bahrain gp with a twenty second lead. i am such a proud girlfriend rn.

maxverstappen replied to your story: good you are awake i'll facetime you rn. i miss you and the cats.

user1 replied to your story: if you really were a good girlfriend you would have been there supporting him

maxfan: you are such a bad wag you didn't even stay up to watch the race.

you had woken up on a high. you had turned your phone on to see all the messages informing you of your boyfriend's impressive win and you had even managed to facetime max before he went to bed. it felt like a good day. but then you made the mistake of opening social media. people on twitter were doing what people on twitter do best, talk shit. your eyes scanned over the screen as for the millionth time people picked apart your relationship and called you every name under the sun. they saw you as a villain that just did not support her boyfriend and that could not be further from the truth.

if you could attend every race you would but that just was not plausible. you suffered from elhers danlos syndrome and on top of that you had chronic fatigue. the elhers danlos effected your joints making every day painful to some degree. yes there were good and bad days but there were never pain free days. both of your knees had been operated on and you were awaiting surgery on your ankle due to frequent dislocations. the simple description of elhers danlos is that you had fault collagen, this collagen is what makes your connective tissue so your connective tissue was faulty and therefore your joints had a habit of dislocating and causing you a hell of a lot of pain. it was a domino effect the constant pain that you were in made you incredibly tired and that is where the chronic fatigue came in. max often called you his sleepy girl because you needed at least one nap per day to function properly.

you knew the problems you were having with max's fans could be solved by you telling them what you suffered with medically but they did not deserve an explanation from you. you should be allowed to live your life how you want to without thousands of strangers telling you that you were doing it wrong or that you were a bad girlfriend. you wanted to keep your medical issues private and max completely understood and supported your decision to do so. so instead you had to deal with all the hate. you just had to remind yourself that these people did not know the real you and if they did they, hopefully, would not treat you like this.

y/sister posted a story tagging y/ninsta

written: y/n finally left the house for the first time in five days and it was just for a snack run.

maxverstappen replied: is she having a bad week, she only eats reese's when she is a lot of pain

y/sister: i didn't tell you this but she is not doing well at all, she slept all of yesterday and then today the internet hates her because she wasn't at the race.

as the saudi arabian gp came and went max was busy with stragety meetings and such this meant that instead of coming home for a few days like he had previously planned he stayed out there and was going to go straight from there to australia and at this point you were really missing your boyfriend. the hate had not subsided either. it was just a very difficult time for you. one night where you had just been scrolling through twitter reading through the cruel things that people had been saying about you, you hit your limit. there was no way that you could deal with this for the rest of the season. so insteadyou decided to do something about it.

the morning you needed to fly to australia was when you realised that this was a bad idea. you had woken up in enough pain to down a horse, joints aching and head spinning. but danny had pulled strings for you. he had arranged everything just so that you could surprise your boyfriend and there was no way you were going to cancel when the plan was already in motion. so instead you just grinned and bared it. the flight was okay, luckily daniel had booked you a first class seat.. but sleep was hard to come by due to your body not being used to sleeping while being in flight. you were already tired when you landed in australia. due to the lack of notice the only flight daniel could arrange got in late on the saturday night. so you had booked a hotel next to the airport and arranged for a car to pick you up in the morning.

it had been so fucking hot in your hotel room and that meant that sleep was incredibly difficult to find. you tossed and turned all night only getting five hours of low quality sleep. in the morning you had pulled on a comfortable outfit and made your way out to the car that daniel had arranged for you.

y/ninsta posted a story

written: fit check

f1wags

liked by user30, user31, user32 and 89,172 others

f1wags: y/n y/ln has arrived to her first ever grand prix. y/n has been dating max verstappen for 18 months and had never been to a race before. but today that changes. she is not dressed in usual wag attire instead in an oversized shirt and bike shorts with a red bull cap. she may not be dressed like the others but we are happy to see her in the paddock

view all 628 comments

user30: we wait for her to show up and she comes wearing that. what an awful wag

user31: go on girl. give us nothing.

user32: i'm actually so happy she is here. i love y/n and have never understood the hate i think she is the cutest

the red bull garage was incredibly easy to spot. your eyes found danny loitering outside having a meaningless conversation with your boyfriend, "i got you a present mate. as it is my home gp i decided to spoil you", danny spoke and max raised an eyebrow.

"whatever it is i am sure that i don't want it", max responded

"i wouldn't be so sure", you cut in and max turned around instantly at the sound of your voice a wide smile gracing his features.

"oh my god, y/n", he spoke as his arms engulfed you in a tight hug. "what are you doing here love?"

"i wanted to surprise you"

"well consider me surprised"

you laughed softly as you followed your boyfriend into the red bull garage he gave you a tour of the garage and you followed him clinging onto his arm. he was used to having to hold you up so leaning on him did relieve your aching joints. max knew all about your medical issues he had helped you with them for over a year. he knew that coming to australia was pushing your body past its limits so every so often he made sure to check in on you. make sure that you sat for a little bit before interacting with the rest of the team. however when he left to go and race there was no longer anyone in the garage that knew about your medical issues. and this is what led to you being stood all of the race. stragestists and other people who you gathered were important to the team took the seats, while you stood towards the back of the garage.

it was around lap twenty when your left ankle began to properly hurt and your eyes felt heavy. a clear indicator of fatigue and your body telling you that you needed to rest. but your boyfriend was racing so well and you wanted to be able to watch him. the race continued for a few more laps however just as max started the thirty first lap your ankle gave way, dislocating from the strain of you being stood on it when it was already under pressure. you crumpled onto the floor a yelp leaving your lips as you fell but you were unable to put your hands out to soften your fall so you ended up hitting your head on the hard ground. this was enough to knock you out. first aiders ran over and called the ambulance into the paddock but you next regained consciousness inside the ambulance, on the way to hospital. alone.

f1updates

liked by user35, user36, user37 and 54,092 others

f1updates: as the drivers go into the 4oth lap of the australian gp an ambulance was spotted leaving the paddock with full lights. sources say the ambulance was parked outside of the red bull garage, but no one knows who was inside of it when it left the paddock

view all 554 comments

user35: the stress finally got to horner

user36: shit i hope whoever it is is okay

user37: the red bull garage do look rather stressed

"well done max you have just won the australian grand prix", christian had called over the radio. he felt guilt twinge at him. his girlfriend had been rushed to the hospital thirty laps ago but christian had made the decision to not tell max until the end of the race. he knew that the dutch driver was going to be mad when he heard the news. christian decided he needed someone else to tell max what had happened. "daniel can you come find me as soon as you are out of the car", he had intercepted the racing bulls radio just to give daniel the message, christian knew it would be better to have bad news coming from him rather than himself.

"thirty fucking laps ago", max spoke pacing back and forth in front of one of his closest friends. "you are trying to tell me my girlfriend had an ambulance called on her thirty laps ago and no one told me. she is in a foreign hospital. alone and probably scared shitless", max ranted to danny.

"i know man, christian just asked me to tell you. we can go to the hospital after the podium ceremony"

"oh fuck that i'm going now"

"you aren't driving", daniel knew better than to argue with max in that moment. yes christian would be pissed to find out that max was skipping the podium ceremony but daniel was not going to stop him from leaving. instead the two man snuck out the back of the paddock and to danny's car. the two racecar drivers got to the hospital in record speed with max running up to the front desk asking the nurse where he could find you. he was ushered through the hospital to a ward.

you were sat in a private ward you ankle elevated, an ice pack on your head and fluid iv in your arm. "max. you won.", you spoke softly. you had the television on and the grand prix on, you had just watched footage of a frantic christian looking for the driver that was now in your room.

"that does no matter my love, what happened?"

"i just pushed myself too far max. i forced myself to stand the whole time and my ankle dislocated, the doctors want to operate on it soon. and when i fell i gave myself a nasty concussion", you explained and the look on max's face could only be described as broken.

"oh my love", he spoke softly pressing a kiss to your forehead.

"i just didn't want the fans to think i was a bad girlfriend. that you deserve more than me", you spoke quietly, "they all hate me because i can't go to races", you spoke tears forming in your eyes but max's thumb quickly wiped them away.

"they don't hate you. they just don't know you honey."

"we should put out a statement, tell them what has been going on with me"

"you just read my mind my love"

maxverstappen posted a story tagging y/ninsta

y/ninsta

liked by maxverstappen, landonorris, daniel ricciardo and 830,121 others

tagged maxverstappen

y/ninsta: a long awaited health update. after a week in hospital i am now finally back home from australia. i am expected to have surgery on my ankle in the next couple of weeks. and i am on a strict diet of hourly lollipops because my blood sugar was low. i just wanted to say a massive thank you to max who literally ditched his own podium ceremony (sorry christian) to be with me. i am so incredibly lucky to have you and i love you with all of my heart, even if i am pissing you off while i'm on bedrest.

view all 28,001 comments

maxverstappen: you could never annoy me

y/ninsta: even when i try to walk when i'm not supposed to

maxverstappen: y/n sit tf down

danielricciardo: so glad to hear you are doing better

y/insta: thank you for bringing me take out every day i was in australia

user40: the world owes this girl an apology. you all bitching and moaning about her not being present just to find out that she has a chronic illness. some of you should be really embarrassed rn

[arandomao3user]

As an Ao3 author, I love giving headcanons that'd probably anger a certain side of the Batman fandom, but I personally don't care because it makes great angst and, again, I'm an Ao3 author and chronically ill!

First up! Dick Grayson, I like the idea of him having ADHD, of course, BUT... joint hypermobility syndrome.

(Joint Hypermobility Syndrome: Joint hypermobility syndrome is a connective tissue disorder. Thick bands of tissue (ligaments) hold your joints together and keep them from moving too much or too far out of range. In people with joint hypermobility syndrome, those ligaments are loose or weak. If you have joints that are more flexible than normal and it causes you pain, you may have joint hypermobility syndrome.)

Chronic pain fits him, don't ask, because as the eldest child with chronic pain and hypermobiltiy syndrome, trust, he has that look in his eye that he's been walking on swollen knees for the past twelve hours, had three mental breakdowns, and is still pushing through because SOMEBODY has to deal with this bull.

That's also the reason he wears freakin' spandex-- only, it's for compression! He wears compression items to help with swelling and pain TRUST, and let me have this because the math maths (it probably doesn't, but let me have this.)

He's got chronic fatigue, he's gotten used to popping dislocated joints back into place, Bruce was so confused how he dislocated and sprained so many bones so quickly when out as Robin. It's genetic, of course, Bruce finds. But he has money, and Dick powers through it all! Till he develops arthritis in his early thirties/ late twenties and actually hates everything because WHAT AND WHY--

---

Next up! JASON TODD! I have no proof, evidence, and it doesn't have to make sense but I like giving him asthma sometimes for the angst potential of if he didn't have it, he wouldn't have died in the explosion.

He didn't die from said explosion, nor JUST the smoke inhalation, but because he had an asthma attack, on the ground, bones broken, unable to breath because his inhaler did NOT survive the blast, if he even had it on him.

And that's why he wears helmet with so, so many filters in it now...

Also, being a street kid who struggles to even get his medication that keeps him alive? Peak angst, being to poor to afford your medication because the American healthcare system is actually trashy garbage.

R.I.P. Jason Todd, you would've loved clean air--

---

ANEMIC TIM DRAKE! But I up you, Tim Drake with Postural Orthostatic Tachycardia Syndrome (POTS)

(POTS: Postural orthostatic tachycardia syndrome (POTS) is a condition that causes your heart to beat faster than normal when you transition from sitting or lying down to standing up. It’s a type of orthostatic intolerance.)

Read ONE SINGLE FIC/ SERIES with this and I've loved it since because what do you mean he randomly falls asleep anywhere? No, forget your canon, he passed out and people think he just fell asleep... NOpe, he passed out, sorry random lady he was on a date with!

(The majority of people are AFAM but we aren't ready for my trans Tim headcanons yet either.)

(You’re at a higher risk of developing POTS after experiencing the following stressors:

Significant illnesses, such as viral illnesses like mononucleosis or serious infections.

Physical trauma, such as a head injury.)

Ngl, my dude gets a LOT of physical trauma (and mental--) also, losing a spleen? Surgery and at risk of viral illnesses? I'm sorry, but I need him to suffer more because I like when Tim Drake suffers horribly.

Now, despite having this condition, I am no expert, but also his caffiene/ energy drink addiction is from chronic fatigue, he shouldn't drink it, it's not healthy or good for him, but he stopped caring between the spleen loss and whatever the "Drake" run he did was because what even was that name?--

---

Damian is autistic and I will DIE ON THAT HILL--

No, I won't explain and you can't make me.

---

[auntie-doom]

We gotta find out if looking for holes in the heart would help more of us, the dysautonomia and connective tissue disorder and long covid sufferers. (and more, and more)

This congenitally incomplete heart ("atrial septal defect," in my case), with just a little, diffificult-to-detect hole in it ("heart shunt"), is frequently comorbid with/possibly caused by connective tissue disorders.

(hmmmm, so is dysautonomia)

We all get our hearts thoroughly checked during diagnostics because heart damage could cause some of these symptoms. But they NEVER LOOK for this particular issue ("bubble test" during echocardiogram), because surely if you had a heart defect, it would have been found before now.

(I'm 45, by the way. This is the first year anyone has ever checked if I have a heart shunt. My POTS diagnosis was over a decade ago; they all assured me that my heart was completely normal.)

Even if you have a heart shunt, where blood leaks between heart chambers, well "20% of people have one, this isn't causing your (symptoms of heart damage)"

(how many of those 20% are *US*? Or people who could be US, if they had a virus hit just wrong, like Epstein-Barr/mono, flu, or.... *drumroll* covid?)

And how many times have you tried to get more fit, got to where you thought you could really do some of the activities you desperately wanted to do, and suddenly crashed? ... and then could never get to that level of fitness again? Like something was damaged further, like something inside broke a little more and your very best is now less than it was a week ago.

Or you had a physically difficult activity like moving house, and afterwards you were never as able as before the move, because maybe the extra bodily stress really did add a tiny tear to a tiny, minor, miniscule existing injury in just the wrong place.

Or you just suddenly couldn't do the same amount of activity any more, out of the blue, because something damaged your heart a touch more but they assured you your heart was solid, it's just the dysautonomia.

More than one hole. I've been walking around with more than one hole in the inner walls of my heart. ToShredsYouSay.jpg

Before surgery on Oct 2, I was walking 3 steps at a time then resting for hours. Yesterday, Oct 13, my fitbit recorded 4221 steps. How far will I improve? How much of my dysautonomia symptoms, how much of my fatigue and pain, was

A FUCKENING HOLE IN MY HEART??

Cardiac surgeon: "There was more than one hole."

strongly recommend against dislocating additional rib when getting open heart surgery

recommend against having rib re-locate by having unadjusted bipap mask pressed to face and inflating lungs too much

also recommend against discovering new vomit-level meds allergies when coping with open heart surgery and rib trying to re-dislocate

Tristan's Fetch and Tug Buddy: "You went through open heart surgery on hard mode."

There's no place like home.

[covid-safer-hotties]

What is POTS? This strange disorder has doubled since the pandemic - Published July 23, 2024

Unpaywalled at our covid archive!

Millions of people now live with the debilitating disorder, which can be triggered by viral illnesses like COVID-19. And many say the recommended treatment—exercise—has backfired.

In late 2021, after 18 months of long COVID symptoms, Oonagh Cousins, a member of Great Britain rowing team, was ready to resume training. She’d contracted COVID-19 in early 2020, and although her initial case was mild, Cousins spent the next year and a half experiencing a fatigue that went far beyond just feeling tired. “It was like a deep sickness,” she says, a “sludgy, deep weakness” that flared up after even mild exertion.

After that lengthy recovery period, Cousins’ only remaining symptom was a very mild case of postural orthostatic tachycardia syndrome—POTS—which is a type of dysautonomia characterized by an abnormal rise in heart rate after changing position, like sitting to standing. Patients with POTS report a variety of symptoms, including dizziness, fatigue, brain fog, and gastrointestinal disturbances.

Cousins is among millions of people living with POTS, a number that is estimated to have doubled since the beginning of the pandemic. Some of the known triggers include pregnancy, surgery, or a viral illness, such as COVID-19. A subset of these POTS patients also has a condition called myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), which is characterized by post-exertional malaise (PEM)—a situation in which symptoms worsen after exercise.

For patients with PEM, pushing past their physical limits—often encouraged in POTS recovery exercise protocols—can lead to major crashes. As a result, many patients with POTS and ME/CFS report being given inappropriate guidance on exercise, the consequences of which can be severe.

“They don’t teach us about ME/CFS or POTS in medical school,” says Sujana Reddy, a resident physician at East Alabama Medical Center, who developed both conditions after a COVID-19 infection in 2020.

Read the rest at the link above!

[autmnsun]

my best friend layla made a gofundme for her boyfriend, who suffers from very severe me/cfs (myalgic encephalomyelitis / chronic fatigue syndrome) and cci (craniocervical instability).

because of these illnesses, he might die. only two doctors in europe do surgery on me/cfs patients, who also suffer from cci, and they are located in spain. he will have to pay a special flight from italy, somewhere to stay and the surgery itself, and none of that is covered by insurance.

he is suffering so much. layla listed a few of his symptoms in his gofundme already, but the only thing he can (or is forced to) do is lie in a dark room with no stimuli AT ALL. no music, no light, no touch, not even being on the phone for too long, accompanied with tons of physical suffering as in pain or seizure-like symptoms. his suffering is not imaginable for people who don‘t have very severe me/cfs.

please read, share and donate. it‘s so very very urgent and a reblog would mean the world and could save his life.

[laprosopicsurgon]

Good Ovarian Cyst Doctor in Nigdi: Dr. Balaji Nalwad Reddy

Ovarian cysts are a common health issue among women that often go unnoticed until they cause discomfort. While many cysts are harmless and resolve on their own, some require medical attention to avoid complications. If you are in Nigdi and looking for an expert gynecologist, Dr. Balaji Nalwad Reddy is a trusted name for the diagnosis and treatment of ovarian cysts and related conditions.

What Are Ovarian Cysts?

Ovarian cysts are fluid-filled sacs that develop on or within an ovary. They are typically classified into two categories:

Functional Cysts: Linked to the menstrual cycle, these are the most common and often resolve naturally.

Pathological Cysts: These include conditions such as dermoid cysts, cystadenomas, and endometriomas, which may require medical or surgical intervention.

While many ovarian cysts are asymptomatic, others may cause symptoms such as:

Pelvic pain or pressure

Bloating or swelling

Irregular menstrual cycles

Pain during intercourse

When to See a Doctor

It’s essential to consult a gynecologist if you experience any of the above symptoms or have a history of ovarian cysts. Early detection is crucial to prevent complications such as cyst rupture, ovarian torsion, or infertility.

Why Choose Dr. Balaji Nalwad Reddy?

Dr. Balaji Nalwad Reddy is a leading gynecologist in Nigdi, known for his expertise in managing ovarian cysts with a patient-focused approach. Here’s why he is the preferred choice for women seeking quality care:

Accurate Diagnosis Dr. Reddy uses advanced diagnostic tools, including ultrasound and endoscopy, to assess ovarian cysts accurately. This ensures a tailored treatment plan suited to each patient’s unique condition.

Minimally Invasive Treatment With extensive experience in laparoscopy, Dr. Reddy offers minimally invasive surgical solutions for ovarian cysts. This approach reduces recovery time, minimizes pain, and ensures better outcomes for patients.

Comprehensive Care Dr. Reddy not only treats ovarian cysts but also addresses associated conditions like fibroids, endometriosis, and ectopic pregnancies. His holistic care approach ensures that all aspects of a woman’s reproductive health are well-managed.

Advanced Treatment Options

Dr. Balaji Nalwad Reddy offers a range of treatment options for ovarian cysts, depending on their type, size, and symptoms:

Observation: Small, asymptomatic cysts are often monitored over time to ensure they resolve naturally.

Medications: Hormonal treatments can prevent the formation of new cysts and alleviate symptoms.

Surgical Intervention: For larger or problematic cysts, Dr. Reddy specializes in laparoscopic procedures, which are safe, effective, and minimally invasive.

Managing Associated Conditions

Ovarian cysts often occur alongside other gynecological issues. Dr. Reddy’s expertise ensures effective management of:

Endometriosis: He provides targeted treatments for endometriomas, helping reduce pain and improve fertility.

Fibroids: His advanced skills in hysteroscopy allow for effective removal of fibroids, enhancing uterine health.

Ectopic Pregnancies: Dr. Reddy’s training in gynecological surgery ensures the safe management of ectopic pregnancies, which can sometimes arise due to cyst-related complications.

Patient-Centered Approach

Dr. Reddy is widely recognized for his compassionate and patient-friendly care. He takes the time to explain medical conditions in simple language, empowering patients to make informed decisions about their treatment. Many women in Nigdi have praised his ability to make them feel comfortable and confident during their healthcare journey.

Why Early Intervention Is Key

While many ovarian cysts are benign, neglecting them can lead to severe complications such as:

Ruptured Cysts: This can cause sudden, intense pain and internal bleeding.

Torsion: A twisted ovary may result in the loss of blood supply, requiring emergency surgery.

Impact on Fertility: Large or untreated cysts can interfere with ovulation and fertility, especially in cases involving endometriosis.

Regular visits to a gynecologist like Dr. Balaji Nalwad Reddy can help detect and address these issues before they escalate.

Book Your Consultation Today

If you’re experiencing symptoms of an ovarian cyst or have concerns about your gynecological health, don’t delay seeking professional care. Dr. Balaji Nalwad Reddy’s clinic in Nigdi offers advanced diagnostic and treatment options tailored to each patient’s needs.

Take control of your health and schedule a consultation with Dr. Reddy today. With his expertise and personalized care, you can confidently address ovarian cysts and ensure optimal reproductive health.

This blog emphasizes the importance of seeking timely and expert care for ovarian cysts. Dr. Balaji Nalwad Reddy’s commitment to excellence makes him a trusted choice for women in Nigdi looking for advanced and compassionate gynecological care.

For More Info-https://gynaeclaproscopicsurgeon.com/blog/2024/12/07/good-ovarian-cyst-doctor-in-nigdi/

[thebluestockingfirefly]

There are a lot of things I could say right now. A lot of emotions roiling and punching and screaming to be vocalized. But I don't have the strength right now to articulate all of that. What I will say is this.

I'm a disabled woman. I've been disabled nearly all of my life. I had severe chronic kidney infections requiring multi-weekly injections from the time I was three months old until I was four and a half, when I had major surgery - without which, I'd be dead by now. I bear scars and an undersized kidney and the gratefulness I didn't almost die from giardia like my sister. I had about a year and a half between recovering from my surgery and starting to get sick again; in that time, I won the Presidential Fitness Award, played soccer, and did gymnastics, and was so skilled at the latter that they wanted to train me privately for competition (terrible at soccer, though. oof). In second grade, the PE teacher called my parents because I was no longer able to participate the way I had before, and she was worried. Took several more years before I was finally diagnosed with what was then called chronic fatigue syndrome. I got progressively sicker from there. My parents didn't think I'd finish fourth grade because I missed so much of the school year due to being sick. No one thought I'd finish high school, and a huge part of the reason I graduated was because I had a 504, and parents who fought for me to get that 504 - and an advisor who dated the expiry date for it past the time I'd graduate, because the administration had nearly refused to grant it to me and she wanted to make sure it wouldn't be taken away.

I've fought every step of the way to achieve what I have, but I absolutely wouldn't have got there if it weren't for the fact that disability rights legislation exists - and it exists because of hard-fought battles by disability rights activists. Disability rights are still a relatively recent thing - the ADA was only passed in 1990 - and people with disabilities are still regularly left out of rights conversations. And, lest you think 'oh, well, I'm not disabled' - guess what? You're going to get old. A split second might change your life. Disability is the one demographic literally anyone could find themselves in at any time, and are increasinbly likely to become a member of as they age. People with disabilities are uniquely vulnerable to the whims of governments, and looking forward, it is an absolute surety that our rights - our very value as human beings deserving of life and respect and love - will be in danger. Our lives will be in danger. Medicaid and Medicare are both at extreme risk. Health insurance coverage in general is almost certainly going to contract and exclude a hell of a lot of us. (I lived in the UK during the 2016 election knowing I was moving back to America in 2017 and sobbed at the results because I was terrified.) Access to care in general is also likely to seep away like toxins into groundwater, leaving far too many without access to vital and necessary means to survive.

To sum up: people with disabilities are going to die. And if you don't care about that, if you can't be bothered, I have only this to say to you: go fucking trip in a pothole and break your neck on the way down.

Moving on to a different topic.

Two of my closest, dearest friends are queer. Very different identities, very different people, both people without whom I'm not sure I'd have survived the last decade. You know who not only doesn't give a shit about people with queer identities but is actively advocating to relegate them to statuses less than human? Yeah. The shithead America just elected as president. It's made trans identities a pointed, specific point of attack, demonizing people who literally only want to be seen as normal so they can carry on with life. The vitriol spewed at trans individuals, at anyone who isn't cis-het, is horrific and disgusting and now has an even greater platform to not only continue to demonize perfectly normal people but also actively legislate to remove their rights, along with those of anyone who doesn't happen to identify with their assigned gender at birth or a strictly heterosexual attraction to others.

As my last futile shriek into the night, for now, I return to the fact that I'm a woman. I've been on birth control since I was 18. I currently have an IUD. I used to have the arm implant thing. For most of the time that I've been using birth control, the goal has been to control, minimize, or largely eliminate my period, but I'm gonna be honest here: I've also used it to keep from getting pregnant (gasp, shock, horror, go fuck yourself if you think this is somehow unacceptable). But guess what? Birth control is a vitally important way in which people are able to exercise autonomy over their bodies. How we are able to choose to be intimate with men without being terrified that doing so will irrevocably alter our lives in a way over which we have no say. How we're able to avoid having to face the decision to have an abortion. When my mother was a young woman, abortion was illegal. Didn't matter the circumstances, didn't matter the timeline; you got pregnant, no matter how, you had almost no options. If you decided to end your pregnancy and were lucky, you might visit a doctor who knew what they were doing and provided competent care without risking your life, and survive to one day have a family, if you wanted. If you weren't, you might end up with permanent damage to your reproductive organs that meant you could never have children. Or dead.

We started a return to this reality several years ago, when Roe v. Wade was repealed by the Supreme Court and states across the country instituted extreme abortion bans that basically said a hearty Fuck You to every woman in this country. Women have died as a result, women who should be alive right now. Children are living without their mothers because doctors are scared to provide necessary care. And now even more women are going to die. I live in a blue state with no restrictions on abortion and I'm fucking terrified because my rights, my autonomy, my ability to make my own fucking decisions about myself, my body, my own damn life are in question despite where I live. I'm a person. Every fucking woman is a person. We deserve to be able to decide what the fuck we want to do with our bodies, without anyone else's input.

[aitadjcrazytimes]

Hi, I saw your tags:

I was wondering. Um. Would you be comfortable sharing what other symptoms you have?

I've had memory problems for years but every time I look them up I just get stuff like alzheimers and car crashes and stuff, which doesnt apply. Idk

I was wondering if this might be me also. I'll talk to a doctor, of course, but. Just wondering what the general vibe is

Sure! Though, be aware, if you Can get evaluated for your symptoms you probably should, at least to make sure it isn't degenerative.

Via-a-vis the ABI (That's Acquired Brain Injury), part of the reason it took so long to diagnose is because

I already have a different diagnosis of cEDS (Classical Ehlers Danlos Syndrome) that explained several of my other symptoms

I have GAD and PTSD due to living in a very abusive and dangerous environment up until about 5 months ago, and

At least two of my family members are autistic, so it was just kind of vaguely assumed that any weirdness regarding my sensory processing and so on was because of that.

So! To summarize (and I put this below a cut because it gets Long).

Chiari Malformation is when you have a defect in the base of your skull that puts pressure on your cerebellum, causing part of it to go into your spinal column. Many people with this condition don't experience any symptoms, but that is not always the case, and even with no symptoms, it does place you at a much higher risk for a brain injury. With a Chiari Malformation, even a mild concussion can cause serious damage.

I have had several concussions, with one of them knocking me out for several minutes when I was very young. So. Here we are.

Regarding treatments for Chiari, most of what can be done is simply treating the symptoms. Unless there is concern about the condition getting worse (more memory loss, paralysis, etc.), patients will likely be referred elsewhere to discuss pain management, because from my understanding, the only effective treatment for Chiari is a decompression surgery, which will remove part of your skull to take pressure off the brain. It's not terribly risky as brain surgeries go, but the best brain surgery is, of course, no brain surgery.

Re my Physical symptoms:

I get headaches very frequently, and often very severely. They have been categorized as migraines in the past, because they come with severe light and sound sensitivity, and they tend to knock me out for hours. That said, they don't meet all the criteria for a migraine, including having no aura to speak of. They are often triggered by strain and jostling my head--by coughing, sneezing, vomiting, jumping, or anything that would cause motion sickness.

I have poor balance. I have found that walking with a cane helps, but physical therapy doesn't do all that much (because it's in my brain and not my muscles).

I also struggle with chronic fatigue. Getting out of bed is a real struggle most days, as is getting anything done outside of simply going to work and then coming home--although I recently went on an antidepressant, which has helped a bit.

Insomnia! I have trouble sleeping. It comes and goes, sometimes I get several days worth of restful sleep, but sometimes I get only a few hours worth of sleep over the course of a week.

Shooting and burning pain in back of skull, neck, spine, shoulders, and chest. Be careful with this one, because this can also be a result of a heart issue. That said, I've had my heart checked out, and that's all good, which is why they checked the brain in the first place.

As for my cognitive symptoms, it's a bit fuzzier, because like I said before, I have PTSD, I have the ABI, I have GAD, several of my family members are somewhere on the autism spectrum, and now my therapist is also having me evaluated for OSDD. So, your mileage may vary. But essentially:

Memory loss. Some of it is retrograde, and I have found that I'll forget significant events and people. Most of it is anterograde, or short term--so, forgetting what a conversation is about while I'm in the middle of a sentence, and either having to improvise and try to make a guess as to what I was talking about, or having to have my conversation partner walk back what we were talking about to explain what we were doing. I have to have a very detailed and elaborate task tracker at work in order to stay on top of things, or I would simply forget it all. I also have the experience of feeling like all of my memories are stories that were told to me. So, I rarely experience a memory as a thing that happened to me, complete with sights and sounds and feelings and sensations and so on, but more like a story that someone told to me once. So, a vague recollection of events and the order in which they happened. This makes it difficult to differentiate between my own memories and stories that other people have told me. It has happened a few times that I have told a story of something that happened to me, only to find out that it actually happened to the person I was talking to instead, and I just got confused.

I'm not sure what to call this one, but I get EXTREMELY easily distracted from processing audio, especially in an environment with more than one thing happening. If I am having a verbal conversation with someone in a restaurant, and someone comes and sits at the table next to us and starts talking, I become almost incapable of conversation. If I'm talking to someone and someone turns on the TV in the next room, I become almost incapable of conversation. If music is playing, I lose track of the conversation. I forget everything I was saying. I won't be able to understand what other people are saying. Spending time in loud, busy, or crowded environments is not that distressing by itself, but I will not be able to hold a conversation.

Aphasia and Verbal Processing. It is incredibly difficult for me to put words together in a way that is coherent. It is significantly easier through writing, because I can look things up and take my time with it. But in vocal conversation, I will frequently have verbal shutdowns where I cannot find a word, and all of my language processing shuts down while I try to comprehend what I was talking about. This often leads to...

Fuzziness/Blurriness. I typically call this "going fuzzy". Generally it involves a verbal shutdown to an extent, where my brain has reached capacity with processing information, and is deciding to simply wipe everything and start over. Think of it like restarting a really old computer. Sometimes it doesn't take too terribly long--a few moments. Sometimes it takes more than half an hour. It depends. This is often accompanied by...

The Buzzing™--It happens for me at the base of the skull, where the injury is. It feels like a tuning fork fused to the inside of my skull. It is completely maddening. My ears ring, and it sounds like a high pitched whining noise. I become very on edge, it's incredibly anxiety inducing, and very overwhelming. I don't know if this is a common symptom you will be able to find under brain injuries, but it's Extremely not fun! I have found that it can be lessened somewhat with massaging the area.

The Voices™: I have heard voices ever since I was a kid. (Schizophrenia has already been ruled out.) Sometimes, it Is an actual auditory hallucination. I recently had an experience where I was grocery shopping and kept flinching because it sounded like someone was shouting my name directly into my ear. Other times, I've heard people whispering or knocking on my walls. These typically occur during or following a stressful situation. HOWEVER, I also experience The Voices™ in my daily life outside of stressful situations. In these situations, it is never auditory, more just a thing that occurs in my own head. I have, in the past, had the experience of talking more or less constantly to one or several distinct people in my head. Nowadays, it feels more like experiencing multiple trains of thought or multiple sets of emotions which feel distinct from "mine". Or feeling like a background voice in my head while someone else does things for me.

Per my therapist, I have recently begun categorizing them as different people to see if that helps. And it does sometimes! And sometimes it does not. It is a process. But that's where I am with that.

There's more to it, but I don't really have the capacity to talk about it much more than I have at the moment.

If you want to see what my experience with this is like... I mean. I did write an entire fanfiction about a character with several of my symptoms recently. You likely won't have the context for what is going on re the character and the situation unless you are into Red vs. Blue, but just in case it helps to see a recounting of it, here:

The Fanfiction That Helped Me Realize I Had Brain Damage™. Have fun!

[onlyangel4]

life of pain. LL30. final part. smau + written.

liam lawson x chronically ill reader

reader has dealt with pain for as long as she can remember but what she did not respect was for her pain to be the reason she met her soulmate.

author's note: i shall be writing this from experience so reader suffers from elher's danlos syndrome, chronic pain syndrome and chronic fatigue syndrome. but if you have a different chronic illness please do imagine it as that

faceclaim: kristine froseth

part one

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sleeping most of the day helped you greatly, you were able to get all that rest that you truly desired and your joints ached a lot less when you woke up from your second nap of the day. you flicked your phone all and checked the time. shit, liam was going to be at your hotel within an hour.

you reluctantly peeled the bedsheets back and climbed out of the warm abyss and began digging through your suitcase but nothing seemed good enough. you were about to have a racing driver in your room, you needed to look good, but you had never been really good at this shit. so you quickly grabbed your phone a face timed your best friend.

to say that she was shocked to find out you were going to be hanging out with one of the drivers was a little bit of an understatement "holy fucking shit y/n, how do you always get yourself in these situations", you just laughed her off and you guys go to work on picking an outfit that screamed casual, i did not try too hard while also not looking lazy. and once you had finally done that and promised your best friend she was going to get the full run down on your time with liam you hung up and began cleaning the room ready for him to come over.

y/ninsta posted a story

written: today's fit

once your hotel room was finally to your liking you took a moment to breathe. it was difficult to wrap your head around what was about to happen. in mere moments a f1 driver was going to be in your hotel room to just hang.

growing up you watched f1 every race weekend with your father, it was one of the main things that you were able to bond on. you would set up the tv in your hospital room after surgeries just so you could watch it together but as you got older and moved out of your family home. you kind of just stopped watching. yes you kept up with the teams just so you could talk to your father about it on your weekly phone calls but you were no longer the little super fan that you had been.

being able to surprise your father with paddock tickets was a way for you to force yourself back into the world of formula one, you knew that after seeing a race in person you would be hooked for good, who knew that you were also going to get to spend some personal time with one of the drivers.

you had been so caught up in your thoughts that you had not heard the first knock at the door, but the second one pulled you from your whirlwind of thoughts, "coming", you called out taking one last look in the mirror before going to the door, a smile plastered on your lips.

as the door opened you were met with liam standing there, he had two bags in his arms and he returned your smile. "hey y/n", he spoke as he walked inside.

"so i brought you a burger and some fries, i hope you like it", he spoke and you smiled at his thoughtfulness

"you already know me too well mister lawson", you teased playfully as he handed you the bag of food.

liam explained that he was on his race weekend meal plan so he was unable to partake in the fast food and instead pulled out a carefully curated meal that had been made for him. you both took a seat on the floor of your hotel room and just ate and spoke. it was really nice, liam was refreshing. yes he talked about racing and his life but he was more interested in wanting to get to know about you and what your life was like. as you spoke about your family and friends, you caught liam looking at you like you were the only person in the world. it was enough to make your heart jump in your chest and cause you to stumble over a few of your words but you powered on.

it unsurprising that you and liam both caught up in each other's company it was only when liam's watch buzzed to alert him that he had a meeting in fifteen minutes that you realised you had been sat yapping for over an hour.

"you have no idea how much i want to skip this meeting right now, but i think i'll lose my seat", liam spoke making you laugh as you stood up to walk to the door.

"it was lovely talking to you y/n, i'm glad you are feeling a bit better. i for one am really looking forward to seeing you tomorrow.", he spoke softly, "and maybe carry on seeing you after the race", he spoke carefully as if he was testing the water between you.

your cheeks flushed softly at the thought of continuing seeing him after this whirlwind of a weekend, "I would like that liam", you spoke softly.

that was when liam reached down and took the unbranded baseball cap off your head putting it on the ground, he removed the rb hat from his head and gently placed it on your head, "much better", he whispered lowly before pressing a soft kiss to your lips. one that you quickly reciprocated. it was gentle and loving as if you had forever.

"goodnight liam", you whispered softly when he pulled away.

"goodnight darling", he spoke before making his way down the hall leaving you to shut the door behind him smiling like the cheshire cat.

y/ninsta posted a story tagging liamlawson

written: someone hustled us garage tickets

y/ninsta posted a story

written: all celebrations in the rb garage DOUBLE POINTS BABY!!

liamlawson

liked by y/ninsta, oscarpiastri, alexalbon and 638,283 others

liamlawson: finally relaxing after a whirlwind of a season

view all 23,485 comments

user1: A SOFT LAUNCH

alexalbon: does the baby finally have a girlfriend

liamlawson: finally

user2: really was not expecting a soft launch from liam, he has not be pictured with any girls at all

oscarpiastri: idc about you, what is the dog called

liamlawson: glad you have your priorities straight mate that is marshmallow

y/ninsta

liked by liamlawson, y/bff, user3 and 643 others

y/ninsta: life lately

view all 23 comments

y/bff: a man???!!1

y/ninsta: babe you have met my man let's not act surprised

friend1: pretty girlll

liamlawson: the prettiest

user3: i was stalking to try and find liam's new girlfriend and i swear i saw him comment here

y/ninsta: who is liam, i don't know anyone called liam

liamlawson posted a story

written: as someone who loves somebody that has a chronic illness i wanted to highlight chronic illness visibility day. people living with these conditions are warriors and we as a society need to treat them as such, please just be empathetic to the strong people in your life that suffer every single day.

liamlawson

liked by y/ninsta, lilymhe, alexalbon and 728,371 others

tagged: y/ninsta

liamlawson: obsessed with you

view all 34,283 comments

y/ninsta: i am so in love with you

liamlawson: i love you more pretty girl

user4: not liam hard launching on a random wednesday

user5: i just stalked her and she has the same medical condition as me, i feel so seen

user6: she seems so down to earth and normal, i love her already

alexalbon: so does this mean i can meet marshmallow this season

liamlawson: yes, yes it does

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