Loneliness

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Just remember.

If you cry,
feel alone,
feel lonely,
feel nobody understands you,
feel like giving up,
feel like hope has faded,
feel like what’s the point of trying,
feel like it’s too tough,
feel stressed
feel lost,
and feel you can’t,
then remember, Danny believes in you, is always cheering you on, and no matter how many times you feel like quitting, he will never give up on you, will always stand by you, and for you.❤️.
-Danny Gautama

#MentalHealth #Depression #Anxiety

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I’m new here!

Hi, my name is AnneD. I'm here because I have Long Covid, ME/CFS. Basically, I’m just sick and at home all the time. I’m an artist who doesn’t have much energy to make art, but I still love it, and I love art history. I have empathy for all of us who are dealing with grief, loneliness, and isolation

#MightyTogether

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I have no family #PTSD #BorderlinePersonalityDisorder #SocialAnxiety #MajorDepressiveDisorder

I haven't tell anyone this, I live in El Salvador and all my family is either in United States or Canada. The last one to leave was my father, he was the love of my life, I wanted him to be proud of me, I was a nerd and won lots of competitions when I was a teenager. I'm a failure now, I had made so many mistakes that my entire family hates me. When he left, we didn't say goodbye, and as soon as he got there he became estranged, no calls, just the repetitive messages whenever I text him. I know that I have done so many wrong things in my life. So I'm an outcast, I have no one to go to, my mother was abusive since I was a little girl. I realized how lonely I am, because a friend just got out of jail and his family loves him so much and they were so happy to see him.
I've never been in jail, but I'm always sick.
My dad and my sister say that I'm faking my mental issues, my daughter's health conditions and that I am the worst.
I hate weekends... They just remind me when I used to be happy with my dad and my sister...Now they both hate me.
#Salvadoran #MyJourney #MentalHealth

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Chronic pain is so unfair

When I first started getting sick four years ago, it started with stomach pain. I thought no bother just an upset stomach I'll live. Then a week passed then two weeks then three. I thought huh that's odd but I'll get over it soon. After two months passed I thought right okay I'll go to the doctor I probably just need antibiotics or something.

I was prescribed buscopan and lansoprazole. Sent for blood tests and handed in a few samples for testing for like helicobacter. But everything came back clear. After another two months went passed and I wasn't any better I went back to the doctor. A few more tests got told there wasn't anything wrong with me probably because of my weight and mental health. Got told to loose some weight and put on anti depressants.

I lost a bit of weight took the antidepressants and got on with my life. I silently got on with it and ignored the pain as best I could. Four months went passed and I was exhausted. I'm pretty sure the GP thought I was wasting his time. I mean 20 year old females who are overweight and have a history of depression and anxiety don't have any other issues? Right?

A year came and went I was still dealing with the pain and fatigue. My joints were hurting on top of it all too. I didn't go out with friends I didn't drink I had tried every diet I could come up with. Nothing so I found a different doctor. I was switched from paroxitine to fluoxetine. I also switched the lansoprazole to omeprazole. My pain didn't get any better so I stopped going to the doctor I mean you heard them? There is nothing wrong with you. It's been a tough few years, your just depressed.

A year and a half came so I thought here let's give the GP another go. Benefit of the doubt, this time I saw a female doctor she up my antidepressants, gave me propanol, switch omeprazole to famotodine and then esomeprozle. Finally she did something else that no other doctor did, I was referred to a gastroenterologist. They then did a endoscopy and found a few things but nothing serious. Things were looking up I was being taken seriously

Then I moved from Scotland to England I registered with a new GP and I was back at square one. The doctor thought it was my mental health so he referred me. On my last appointment with him I faked being happy and put a big smile on it was like I was trying to prove to him "hey look at me I'm happy but still in pain please help" he finally referred me back to gastroenterology.

For four years I've been living with this stomach pain, joint pain and more I do have bpd, depression, anxiety, PTSD autism and ADHD but apart from that no firm answers on what causes my pain. The worst part I've done this all alone when I had my endoscopy? My parents thought I went to a job interview. Like the doctors they think there is nothing wrong with me. Since I moved to England four months ago we haven't spoken.

I hate how lonely all of this is. I'm on 13 medications and I am exhausted. I spend most of my weekends sleeping. I don't drink, I'm vegan, I exercise when I can and I work full time. I do everything right everything I'm supposed to so I can be healthy and yet I'm not. Chronic pain is so unfair. #ChronicPain #ChronicIllness #Depression #Anxiety #PTSD #BPD #medications #Doctors #lonley

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Rage is Survival

You feel it building, simmering beneath your skin like a storm gathering in the distance, dark clouds heavy with the weight of everything you’ve endured. You are the thunder in the distance, the crackle of lightning that splits the sky. Your body, this body that you once called home, now feels like a battlefield. You live inside it, but you no longer have control. Every joint, every nerve, every cell rebels, not with the grace of a revolution but with the cruelty of a slow, unyielding siege.

They say rage is unproductive, but they’ve never been trapped inside a body that betrays them. They’ve never fought to get basic care, clawing through layers of red tape, begging for relief that never seems to come. They don’t know what it is to scream silently in sterile rooms, your voice swallowed by the suffocating indifference of the system. You sit under harsh fluorescent lights, recounting your symptoms to another blank face, another doctor who listens but doesn’t hear. "It’s in your head," they tell you. "You’re too young to be this sick."

Gaslit into doubting your own pain, you leave those rooms with a smoldering fury that you carry like a second skin. It clings to you, a mantle you never wanted to wear. You want to set it down, but it’s fused to you now, a permanent reminder of every time your reality was dismissed, your suffering waved away like an inconvenience.

The rage is not just yours, though. It belongs to every disabled person denied the right to live fully in this world. Every curb too high, every door too narrow, every public space designed without a thought for those who navigate life differently than the rest. The world is a labyrinth, designed to exclude you, to make you feel like you’re asking for too much when all you want is the basic dignity of accessibility.

You are told to be patient. Be gracious. Be inspiring, even, as though your suffering is a gift for others to learn from. As though your exhaustion, your pain, your very life is meant to be a lesson in perseverance for the able-bodied. But why should you have to teach this lesson when your body is already an education in endurance?

There’s rage in that too—rage at being made into a spectacle, at being reduced to an object of pity or admiration, rather than seen as a whole person. Rage at the endless bureaucracy, the phone calls to insurance companies that stretch into hours, the denials that come with no explanation. Rage at the ticking clock of your body’s limitations, knowing that time is not on your side, and yet still being forced to wait for the care that could sustain you.

Your rage is a fire, yes, but it’s not a wildfire meant to destroy. It’s the hearth that keeps you alive, the flame that burns bright when everything else is dark. It is the only constant in a world that denies you consistency, a world that starves you of safety, of care, of connection.

And yet, rage does not save you from the loneliness. The isolation that comes when you can’t leave the house for days, when your friends stop calling because you’re never well enough to join them. You live in the gap between their world and yours, a no-man’s-land where the silence is so thick you could scream and still not hear your own voice. Depression creeps in like a slow, cold fog, wrapping itself around your mind until you can’t see past it. The deprivation isn’t just physical—it’s the absence of life outside your body, the missed opportunities, the stolen experiences. Your world narrows to the size of a room, a bed, a wheelchair, and that shrinking feels like suffocation.

You work twice as hard for half as much, and the unfairness of it all gnaws at you. You see people breeze through life, unaware of the invisible hurdles you leap just to stay alive. They take for granted what you would give anything to have: a body that moves freely, a mind that is not consumed by survival. They don’t understand that your life is a negotiation with time, with energy, with pain, every day a calculation of what you can afford to give.

But still, that fire—the rage that courses through your veins, the heat that keeps you moving—burns. It will not be extinguished. It is your strength, your refusal to disappear quietly. It fuels your will to fight, even when the battle feels endless. You are not fragile; you are molten, reshaping yourself every day in the furnace of your fury.

The world tries to tell you that rage is dangerous, that it will consume you from the inside out. But you know better. Rage, for you, is survival. Rage is what keeps you alive in a world that would rather you fade away. You are not here to inspire. You are here to exist, to take up space, to demand what is rightfully yours. And that, above all else, is the power of your rage—it is your reminder that you are still here. You are still fighting. You are still alive.

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The Clinic

In January 2021, I became ill in ways that defied explanation. My body, which had always been a mess and a mystery, turned into a battlefield where everything seemed to go wrong at once. My symptoms were baffling to local doctors, and despite countless tests and evaluations, no one could provide answers. It was then that I made the decision to seek care at the Cleveland Clinic—a place known for its focus on complex medical cases.

Walking through the Clinic’s halls felt like stepping into a different world. There was a level of expertise and attention to detail I hadn't experienced before at local hospitals, where I often felt like a burden—someone too difficult to treat. Cleveland Clinic is a specialty hospital, attracting some of the best minds in the world, especially in rare diseases and complex conditions. Here, I wasn’t dismissed because my case didn’t fit neatly into a box. Here, I was seen.

From 2021-2023, I would spend hundreds of hours in doctors’ offices, undergoing test after test: MRIs, CT scans, bloodwork, autonomic testing, genetic panels, endoscopies, and more. My appointments bled into each other—GI, vascular, neurology, rheumatology, and cardiology—all working together to put the pieces of my medical puzzle into place. It was at Cleveland Clinic where I was finally diagnosed with a cluster of rare conditions: hypermobile Ehlers-Danlos Syndrome (hEDS), Postural Orthostatic Tachycardia Syndrome (POTS), Mast Cell Activation Syndrome (MCAS), Superior Mesenteric Artery Syndrome (SMAS), Nutcracker Syndrome, and gastrointestinal dysmotility. My body, a connective tissue disaster, was now mapped out with labels that explained why it had been betraying me for so long.

It wasn’t just about the diagnoses, though. It was about the process—the wear and tear of being a full-time patient. Each appointment chipped away at my mental and physical strength. I adopted mobility aids slowly, first a cane, then crutches, and eventually a wheelchair. It wasn’t until then that people started seeing my disability. Before the mobility aids, I existed in that liminal space between visible and invisible disability—a place where I looked “fine” to outsiders, but inside I was constantly battling a body that refused to cooperate.

In the fall of 2023, I went out on Disability. It felt like a loss, but also like a surrender to the reality of my situation. My body could no longer keep up with the demands of the world. And while that decision was incredibly difficult, it was necessary. The transition from the workforce to a life dictated by medical appointments was both jarring and isolating. Being a rare disorder patient is profoundly lonely. Local hospitals often hesitate to treat patients like me because my conditions are so specialized, so misunderstood. Cleveland Clinic, on the other hand, embraced the complexity.

I had multiple extended hospital admissions during that year, and each one felt like a lifetime. The mental toll of lying in a hospital bed for weeks on end, facing yet another abdominal surgery, was crushing. I lost count of how many times I’ve had feeding tubes placed, how many surgeries to repair my gut, how my once active body has been systematically taken apart and pieced back together. It was there that I had a total proctocolectomy—a surgery to remove my colon because its nerves had died and a duodenojejunostomy to relieve my SMA. These surgeries left me with an ileostomy, a permanent bag attached to my abdomen that collects waste. Each surgery came with its own set of physical scars and emotional wounds.

Living as a rare disease patient has taught me more than I ever thought possible about advocacy. The medical system is not designed for people like me—people who have conditions that most doctors have never heard of. There were countless times when I was told, “Your labs are fine,” or “It’s just anxiety,” but my body knew better. I learned to trust myself, to demand better care, to not take “no” for an answer. Every day that I wake up and face this uncooperative body feels like a victory. These are small health victories, yes, but they are victories nonetheless.

I’ve learned to take pride in those victories, even when they feel small. Every successful surgery, every day without a flare-up, every inch gained in physical therapy is something to celebrate. Being a patient—full-time, relentless—has taught me resilience in ways I never imagined. It has also taught me that the best care often means seeking out the right doctors, the right specialists, and not settling for less. Cleveland Clinic has become a lifeline, a place where I can be heard and understood, where I’m not reduced to just my symptoms. The toll of being a rare disease patient is profound, both mentally and physically, but it has also given me an unshakable strength.

Still, the isolation remains. It’s difficult to find others who understand this journey. Most people can't fathom what it’s like to live inside a body like mine—a body that feels like it’s 100 years old when I’m only in my 30s. But through it all, I’ve found a community of others with rare disorders, people who understand the loneliness, the grief, the resilience required to keep going. These connections, though few and far between, are everything.

My journey at Cleveland Clinic is far from over; there will be more surgeries, more admissions, more moments of despair. I’ve had to learn to advocate for myself, to push for answers, and to find strength in a body that continually tries to defeat me. But at the Clinic, I’ve learned to trust doctors again. I’ve learned that there are medical professionals who care if I live and how well I feel. They’ve never stopped fighting for me. More than just saving my body, my doctors have saved me. I’m determined to live a life worthy of what they’ve done for me.

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My 10th attempt of a suicide

I dont know where would I begin so I just gonna say.. I cant,, I am tired Iam lonely.. But I have a child and I wish someone by my side right now

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