T
tiredofchronicpain
Member
- Dec 26, 2018
- 51
Yes, I am numb too, and unable to sleep at all.I am just numb, no motivation, no focus. Havent left the house in weeks. Horrible
Yes, I am numb too, and unable to sleep at all.I am just numb, no motivation, no focus. Havent left the house in weeks. Horrible
Everything is in our heads. Pain is difficult to measure, and when you're in pain for a long period (more than 3 months), something happens in your nervous system, and you're at high risk to develop chronic pain syndrome (CPS). This doesn't mean you're imagining pain! I was in an accident, crushed both arms and had to replace one arm. Worse pain I've ever experienced, and even though I'm much better now, 3y later, I still struggle and use painkillers everyday. Doctors/health system here in Norway suck, unless you have money or even better, contacts.
Let me ask this: for all of you with chronic extreme physical pain where you have shooting pains and feelings of wanting to pass out, which is worse: "feeling blue, depressed", or being in physical pain like Trigeminal Neuralgia, Fibromyalgia, facial pain, etc.
I am really curious.
Does anyone else suffer from a chronic illness that is their main reason for wanting to ctb??
Chronic illness has ruined my life and is most definitely the main reason I want to go.
I feel for my loved ones immenselyThanks for replying and nodding a head at my post. Healthcare and palliative treatments have zero quality these days. You are slapped on the arse and made to leave after a "rough" evaluation. I went to the pharmacy once in Australia after a severe bout of shocking pains and emphatically told the front assistant that I urgently need help and pills to help me get through the day. Next time you are in pain, feel free to go ask for help, and report back on the responsiveness and the care from the medical units. I am certain no one really gives a toss about anyone these days. She was so unresponsive, I left almost throwing stuff of the shelves. For anyone screaming "victim mentality" I want to alert them at the intensity chronic pain drives you to, and the society has a myopic respect for individuals representing bad health that this causes symbiotic depression.
Life does have meaning to me. I tear up a lot because I do not want to transmit the feelings of suicide to the people loving me. I am afraid of the pain they will go through with me suiciding. That is all keeping me here and I hope you can also see value in your life. I am sorry about it. But let's get together and sing the blues, we owe it to ourselves :)
Yes, for 40 years I overcame illness invisible to all, untreatable, except to me, who worked with it, had too many responsibilities, and have adult children with problems. I had another operation 6 years ago, and have been so slowly getting worse and worse, I can't stand it anymore. My life, and all that kept me motivated is now impossible; every night I pray to not wake up, and every morning I wake to the height of dysfunction and discomfort, upset to be here still. And, though I think of CBT all the time, I'm so sick now I have no way to get it done. Does being alone in all of this, end in my being alone in doing something desperate.. ON top of that I have 2 adult children who are suffering their own complications in life, and there's nothing anymore I can do to help them. I know so many are suffering their own desperate situations concerning health, miserable, always in threat of homelessness, suffering pain and FORCED to live the last of their lives in increasing misery until they die anyway.Does anyone else suffer from a chronic illness that is their main reason for wanting to ctb??
Chronic illness has ruined my life and is most definitely the main reason I want to go.
wELL, I HAVE read all of the above, and I am wondering if anyone has any idea of what we can do about it. It is law that we are forced to live through torment with no good ending. When should it be a choice for those with misery of illness which leads only to death, to choose their end? There's probably millions of us, what about advocacy, petitions, making the situation known and accepted and aided?yes chronic nausea , and headache , cant eat solid foods, only liquids so been surviving on fresh milk only , nothing else, but its catching up with me now, getting bone pain , blured vision, cant take vitamin tablets as they make me very sick, it never goes away , so fed up , i feel for every one who has a chronic illness , its hell
You're so right, not only about the medical community, but friends and family, for the ones who are not totally alone. They just don't know.Its somehow surprising.... yet not all that surprising to see just how many of us suffer with chronic pain. I myself have multiple diagnoses that started in my teens and progressed over the last 30 years.
Dealing with chronic daily pain like that can only lead one to depression, especially in a world where we are told to just deal with it by people who can't possibly understand what it feels like to live in our skin.
I'm so sorry. The very same here but didn't hit until I was almost 40. It's a horrible experience and feels very....unfair, though I realize there are no guarantees in life. It seems so cruel.Chronic illness is the main reason why I want to cbt as well. It has ruined my life, there is no cure, I will never get better, only worse over time. All I can do to have any quality of life is to take expensive daily medications and go through lots of medical treatments, appointments, tests, etc. Chronic pain, even if I am one of the lucky ones to be able to get monthly supplies of narcotics and other pain relief, is awful and makes me unable to be employed full time or do any of the careers I had dreamed of doing. I have been sick as long as I can remember, but finally started finding out how severe things were when I was about 21 years old, I am 26 now. There are several things preventing me from ctb currently. I am stuck in this limbo until some things in my life are sorted out. As much as I want to go, I don't have the heart to put anyone I leave behind in a huge mess. I hope you eventually find the peace your looking for.
It speaks to a sudden eclipse to the dreams of life, with the intrusions of worsening symptoms, and normal life, in any meaning, falling away leaving one empty and in physical pain and mental anguish..I'm so sorry. The very same here but didn't hit until I was almost 40. It's a horrible experience and feels very....unfair, though I realize there are no guarantees in life. It seems so cruel.
I myself have multiple diagnoses that started in my teens and progressed over the last 30 years.
Dealing with chronic daily pain like that can only lead one to depression, especially in a world where we are told to just deal with it by people who can't possibly understand what it feels like to live in our skin.
I can certainly empathize with you, I've had CHF for 40 years, after my last cardiac operation 6 years ago, the ME set in and never lets up. Thanks to my being a retired nurse, and having been through the same nonsense with doctor after doctor, I researched things to diminish the various system breakdowns that have occurred over the years, just to function, but there is really no cure now. I've never had fibro, and I know from others how the excruciating pain adds to the other dysfunctions time passing brings. I wouldn't be surprised if some of the other issues you mentioned are instigated by the CFS, as many who suffer, don't realize the infections that are running around doing damage. I agree with you, I'm at the end of trying to subdue the increasing symptoms and dysfunctions leaving life empty of any meaning, and I'm ready, to be rid of this rotting flesh.Adding myself to this list. Although we can commiserate together here, seeing the destruction chronic illness wreaks on the lives of so many of us just breaks my heart (please excuse the dramatic tone there).
I hit the jackpot with chronic illnesses, because I've got quite a few (cue over a decade of wasted time and money on medical professionals writing me off as a hypochondriac, only for me to eventually be proved correct all along). CFS/ME and fibromyalgia are the worst, though.The others are unpleasant, and restrict my life to an extent, but they're bearable, and for all intents and purposes I could lead a relatively "normal" life with them. The CFS and fibro are why I have been considering suicide for a while -- they completely dashed my prospects in life before it had properly begun.
The plus side to the fibro, however, is that I'm accustomed to intense pain, so if there has to be a degree of pain in whatever suicide method I choose it doesn't perturb me. Obviously I'd prefer as painless as possible, but some amount would definitely be tolerable.
I really feel with you. It sounds awful. I dislocated both my elbows, and the pain was immense. Sending you lots of love.I suffer from Ehlers Danlos Syndrome which makes me dislocate my bones and live in agony.. this is a huge influence in my choice to CTB