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Anybody else in here due to health problems?
Thread starterpeacefulexit
Start date
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Wondering how many people are like me and have multiple health problems that make life unlivable. They also give me 24/7 anxiety and make me feel not good enough for this world. So, I'm out.
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katyusha_kat, _Minsk, RinneOfAragon and 11 others
Wondering how many people are like me and have multiple health problems that make life unlivable. They also give me 24/7 anxiety and make me feel not good enough for this world. So, I'm out.
Thanks for sharing. I'm also in pain due to injuries. However, feeling absolutely too broken for life due to health problems is the main reason for me CTB asap. To make matters worse, some of my health problems are of the extremely embarrassing type that I can't even share with anybody. So, I'm choosing not to continue life now I'm no longer a man.
That's a bit of a list. Mine however are mainly physical - which then triggers intense anxiety. Cancer, colon issues, getting tested for heart problems, a disease that causes a bend that makes sex impossible among a whole heap of others. So yeah, I'm done.
I would say the majority of people here is here because of physical/mental pain.
But yeah there are also some ppl here because of money issues/homelessness of course
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RinneOfAragon, Mateira, SMmetalhead36 and 1 other person
I would say the majority of people here is here because of physical/mental pain.
But yeah there are also some ppl here because of money issues/homelessness of course
Yes, many health issues that have taken so many things from my life. I am so exhausted from fighting and seriously just don't know how much longer I can fight.
I am here because of degenerative neurological and chronic pain issues but I am probably in a different place than most. I don't want to CTB, as long as I can manage current and future issues and keep a quality of life.
However, years ago, it got bad. I was in the ER 8 times in two weeks and nobody would listen to me. Called me a drug addict even though I refused all pain killers and made it clear I had an opioid allergy. I finally got to the point I let my family know I had a week to live and if nothing changed, I would be CTB. On day 5 of the 7 days, I went to the ER again and they finally listened. I got flown by helicopter and needed 17 hour emergency surgery. Recently, I started thinking about all of this and how I had no plan for Day 7 and what options I would have selected in desperation. If/when the time comes, I don't want to act in desperation and be even worse off, so that's why I'm here. I hope that day never comes and I never need to use all the helpful information everyone shares on SaSu.
Reactions:
outrider567, peacefulexit and divinemistress87
Happy to. I was diagnosed last year with EDS, a connective tissue disorder. My whole life I'd struggled with seemingly random, disconnected medical issues - weekly migraines, joints dislocating in bizarre ways, dizziness, terrible insomnia, stomach pain, chronic joint pain, etc etc. Then I was diagnosed with interstitial cystitis a few years ago. Funny enough, all of the other medical issues bothered me but weren't really a large factor when I was younger, mostly because I thought they'd be able to be fixed. It wasn't until the IC diagnosis which makes it painful to next to impossible to do anything intimate with my husband most days that I started to say, "wow, this is just one more thing..." Then finding out that all my other stuff was connected, and I was going to be in chronic pain for the rest of my life? It's exhausting to even think about having to deal with this until I'm elderly. No thanks.
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Bear1234, outrider567, peacefulexit and 1 other person
Not only because of health problems but it's a big part of it. I have a tumor in my head (not brain, just behind the eye ball) which causes me to lose my vision, pass out, and constantly get migraines among some other stuff. Additionally, I have dysautonomia and mental problems. I try not to let it bother me and just ignore it to try to live with it but it's hard when I can barely go for a few moments without being affected in some way.
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Immensevoid, outrider567, Joker2003 and 1 other person
I think the main reason I'm going to CTB is due to Peyronie's Disease. It causes a bent and unusable penis. Treatments don't sound very promising. I feel absolutely disgusting, and any chance of a relationship is now gone.
I think the main reason I'm going to CTB is due to Peyronie's Disease. It causes a bent and unusable penis. Treatments don't sound very promising. I feel absolutely disgusting, and any chance of a relationship is now gone.
I am diagnosed with 5 psychological disorders (Autism, ADHD, Gender Dysphoria, GAD, MDD), which all make life incredibly difficult.
I also suffer from Raynaud's phenomenon (my hands are always cold and hurt), stomach problems, and an MRI recently indicated that I have multiple brain lesions and demyelination.
I am meeting with a neurologist soon to see if I have Multiple Sclerosis.
Thanks to everybody for replying. This is helping me not to feel so alone in having multiple health problems all at once. I was certain I was the only one and was cursed.
Unfortunately, it bends to the left so that's rather hard to do. Also, it's nearly impossible to get an erection as I feel absolutely disgusted by the look of my penis. And I would be far too embarrassed for a woman to see my penis anyway.
I should have mentioned, on top of all the health problems I've had to deal with over the past six months I've pretty much had 24/7 crippling anxiety for 20 years. I feel like I've tried everything, yet nothing has worked. It feels horrible to know that your own brain is your biggest cause of suffering.
Not only because of health problems but it's a big part of it. I have a tumor in my head (not brain, just behind the eye ball) which causes me to lose my vision, pass out, and constantly get migraines among some other stuff. Additionally, I have dysautonomia and mental problems. I try not to let it bother me and just ignore it to try to live with it but it's hard when I can barely go for a few moments without being affected in some way.
Happy to. I was diagnosed last year with EDS, a connective tissue disorder. My whole life I'd struggled with seemingly random, disconnected medical issues - weekly migraines, joints dislocating in bizarre ways, dizziness, terrible insomnia, stomach pain, chronic joint pain, etc etc. Then I was diagnosed with interstitial cystitis a few years ago. Funny enough, all of the other medical issues bothered me but weren't really a large factor when I was younger, mostly because I thought they'd be able to be fixed. It wasn't until the IC diagnosis which makes it painful to next to impossible to do anything intimate with my husband most days that I started to say, "wow, this is just one more thing..." Then finding out that all my other stuff was connected, and I was going to be in chronic pain for the rest of my life? It's exhausting to even think about having to deal with this until I'm elderly. No thanks.
How do you even get a ic diagnosis? My male uro says oab over and over. I been to so many uro and uro gyns and it's just we don't know and prob not ic. had at least four or five cystoscoppies now and I'm still suffering. Twenty plus years of this. They give me anti cholinergics that I don't want due to dementia risk.
How do you even get a ic diagnosis? My male uro says oab over and over. I been to so many uro and uro gyns and it's just we don't know and prob not ic. had at least four or five cystoscoppies now and I'm still suffering. Twenty plus years of this. They give me anti cholinergics that I don't want due to dementia risk.
God I'm sorry that's atrocious. I was actually sent around to a few uros and obgyns until I basically had a breakdown at my PCP and she agreed there was really nothing else it could be. After that conversation I was prescribed the low dose of Amitriptyline etc.
You might already do this, but a lot of my treatment comes from OTC stuff. I take cystex (easier on me than azo) pretty religiously, I use D. Mannose pretty much every day, and I was really careful to keep records of my symptoms so I could narrow down what was the likely cause of flare ups. For example I can absolutely not drink alcohol, it causes pain no matter what. Acidity can also be tough, so I add baking soda to a lot of things like tomato sauce etc. None of this is perfect but it usually mitigates things enough I can function. Idk if I have unlocked DMs yet but please feel free to message me if you need more help with it. It's awful and I'm sorry you're going through it too.
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