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peacefulexit
Member
- Dec 17, 2023
- 89
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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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.
Hanging. I'm in Australia where options are very limited. However, this does sound like a relatively straightforward and not overly painful method.same boat, how do u plan to do it.
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.Yes, I also am suicidal over it. It's not my only reason but chronic pain adds fuel to the fire ya know
Appreciate you sharing this. As I've had six months of constant health problems. From cancer to deformities no man would accept.I'd say 80% are here because of disability, mental health etc.
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.Nerve pain, eye problems, depression, ADHD, autism. It all sucks.
Agree. I'm too embarrassed to live like this. I already feel like I deserve to be chucked in the bin.Yeah, it's a big contributing factor for me as well. It's like... why bother, I'll be in pain forever anyway.
Thanks for chiming in. I guess mine is health prooblems which then made me feel extreme anxiety as I feel I'm no longer fit to live.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
Whys your name crossed out isn't that supposed to mean u ctb already?I'd say 80% are here because of disability, mental health etc.
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.If anyone is comfortable sharing their health problems that lead to seeking CTB that would be helpful.
Someone said she went back to work so she probably disabled her accountWhys your name crossed out isn't that supposed to mean u ctb already?
What if you just angle it right couldnt you stil have sex?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.
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.What if you just angle it right couldnt you stil have sex?
Oh, I also get absolutely crippling anxiety. Lately, it's been 24/7. Completely floods my brain and body and makes life pure torture.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.
What will your method be?yes I have a learning disability for, rest of my life and depression, sick of living like this and need to end my life
Same as me! However, it sounds like a very hard to do method from what I've been reading here.hanging
Epilepsy for 20+ years with a cause or cure never found. Now I wish my seizures were fatal, not just frustrating.
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.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.
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.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.