J
Jolene40
Specialist
- Oct 6, 2018
- 370
Im sorry this is so long guys. I have nowhere else to go.
Ive been in hospital a long time. Im in for problems with digestion originally. My bowel perforated and ive had sepsis and peritonitis so severe i cant believe im not dead - i wish it had killed me. I am also severely malnourished and have been for some time despite eating. I have an ileostomy as was attacked so badly by chrons / colitis i had to have my colon removed at christmas and now use a bag. It hasnt stopped things though. With this and multiple autoimmune diseases my whole body is degenerating and i cant walk properly or stand. My spine is literally collapsing down and the pain i am in is mind altering. No one seems to have any clue exactly why or can be bothered to look hard enough. I have some sort of disease wasting my muscles and it is now at the stage its virtually killing me. I have gone on about it to every doctor who would listen for the last 4 years. I cant eat anymore so on iv nutrition now.
I dont think anyone realises the extent of my suffering. If i cry it is pure desparation and sadness and fear over the state i am in, the fact i will never be the same again and torturous pain rendering me a complete invalid. The nerve damage is in my neck face and head now and causes pure agony and vertigo dizziness you name it. If doctors see me cry here theyre more concerned with my mental state than the fact i am ravaged by horrific disease and this is a normal human reaction. I have neuropathy from head to toe, blood clots, fluid round my lungs heart, arthritis in all my bones, it goes on and on.
Im desparate to end my suffering yet want my story known - mainly for my little one. No one seems to acknowledge how seriously horiifically ill i am. I want my little one to realise i did not abandon him lightly. I don't want anyone saying i was just weak of mind when im the strongest person i know dealing with pain on a scale that has you screaming to f****g god every day.
I have about 4 documented horrid autoimmune illnesses but they don't explain all of it. My fsther took his own life on return from war. The fact my dad took his life means it will look like im just another mental health job. I am not. I also dont want to undermine anyone suffering mentally ( i am suffering mentally too and know what depression is)
No one sees me crying all the time in agony. I hide it and use all i have and mass amounts of oxycodon to get through a conversation. When the agony is too much i cry. If a doctor sees me cry i get asked about my state of mind. Im crying because i feel like im physically tortured 24 hours a day ffs and have some but not all the answers as to what is actually happening physically!! Im virtually bedridden at the age of 39! My body and mind know im on my way out and it isnt going to be bloody quick but long and torturous as it has been. Of course im distressed.
I dont know how i can make sure everyone who knows me knows how bad this is. I want it out there what i am suffering in full detail before i die ( when i get the courage).
This is long and rambling but i am getting sicker by rhe week and i fear i may try do something snappy and my legacy will be oh she just had chrons and couldnt cope with it. Ive seen physios who i can see think my inability to walk properly is somehow psychologically linked or just sore muscles and my crying is alot to do with my mental state. It 100% is not. My nervous system is being hammered and has done for a long time but the incompetence and lack of knowledge from middle class male doctors often leaves you feeling like a nut job if they dont identify the cause. I spent all my life savings seeing private doctors to get the diagnosees i already have. Before that each moron i saw would suggest it was anxiety! My wasted muscles are obvious to the eye now after years of saying somethings wasting my muscles yet still i get shoulder shrugs.
If the cause of my muscle wasting / collapsing bent spine is not identified it will be ignored and the full horror of my illnesses wont be reflected after i die. My little ones father only knows and accepts so much regarding how ill i am. I honestly think some people think its a state of mind. It is unbelievable but when doctors dont have all the answers even they have suggested anxiety! My perforated bowel which has been killing me was missed for weeks and i was asked about my state of mind and stress levels by one doctor!
I almost want to write a blimmin book with it all in so there is never any doubt as to how much i have endured / am enduring. I hate reading stories about suicide where it is always related to mental health. It absolutely is not. I imagine for many it is because of horrific illness and this gets glossed over or ignored. I absolutely cannot have that.
Ive applied to Dignitas. My family support me 100% now as does a very close friend who comes to see me often. My family still.cant even pronounce the name of some of the health issues ive got so their story alone isnt enough if my little one ever has questions in the future. I absolutely cannot have any questions over this for the future of my little one. I want anyine around him influencing him or even any strangers to know the whole story.
I dont know if that makes any sense. It is too much to document the detail of my illnesses for my little one at this current age so it needs to be out there so to speak in another way. I just dont know how to do that.
Ive been in hospital a long time. Im in for problems with digestion originally. My bowel perforated and ive had sepsis and peritonitis so severe i cant believe im not dead - i wish it had killed me. I am also severely malnourished and have been for some time despite eating. I have an ileostomy as was attacked so badly by chrons / colitis i had to have my colon removed at christmas and now use a bag. It hasnt stopped things though. With this and multiple autoimmune diseases my whole body is degenerating and i cant walk properly or stand. My spine is literally collapsing down and the pain i am in is mind altering. No one seems to have any clue exactly why or can be bothered to look hard enough. I have some sort of disease wasting my muscles and it is now at the stage its virtually killing me. I have gone on about it to every doctor who would listen for the last 4 years. I cant eat anymore so on iv nutrition now.
I dont think anyone realises the extent of my suffering. If i cry it is pure desparation and sadness and fear over the state i am in, the fact i will never be the same again and torturous pain rendering me a complete invalid. The nerve damage is in my neck face and head now and causes pure agony and vertigo dizziness you name it. If doctors see me cry here theyre more concerned with my mental state than the fact i am ravaged by horrific disease and this is a normal human reaction. I have neuropathy from head to toe, blood clots, fluid round my lungs heart, arthritis in all my bones, it goes on and on.
Im desparate to end my suffering yet want my story known - mainly for my little one. No one seems to acknowledge how seriously horiifically ill i am. I want my little one to realise i did not abandon him lightly. I don't want anyone saying i was just weak of mind when im the strongest person i know dealing with pain on a scale that has you screaming to f****g god every day.
I have about 4 documented horrid autoimmune illnesses but they don't explain all of it. My fsther took his own life on return from war. The fact my dad took his life means it will look like im just another mental health job. I am not. I also dont want to undermine anyone suffering mentally ( i am suffering mentally too and know what depression is)
No one sees me crying all the time in agony. I hide it and use all i have and mass amounts of oxycodon to get through a conversation. When the agony is too much i cry. If a doctor sees me cry i get asked about my state of mind. Im crying because i feel like im physically tortured 24 hours a day ffs and have some but not all the answers as to what is actually happening physically!! Im virtually bedridden at the age of 39! My body and mind know im on my way out and it isnt going to be bloody quick but long and torturous as it has been. Of course im distressed.
I dont know how i can make sure everyone who knows me knows how bad this is. I want it out there what i am suffering in full detail before i die ( when i get the courage).
This is long and rambling but i am getting sicker by rhe week and i fear i may try do something snappy and my legacy will be oh she just had chrons and couldnt cope with it. Ive seen physios who i can see think my inability to walk properly is somehow psychologically linked or just sore muscles and my crying is alot to do with my mental state. It 100% is not. My nervous system is being hammered and has done for a long time but the incompetence and lack of knowledge from middle class male doctors often leaves you feeling like a nut job if they dont identify the cause. I spent all my life savings seeing private doctors to get the diagnosees i already have. Before that each moron i saw would suggest it was anxiety! My wasted muscles are obvious to the eye now after years of saying somethings wasting my muscles yet still i get shoulder shrugs.
If the cause of my muscle wasting / collapsing bent spine is not identified it will be ignored and the full horror of my illnesses wont be reflected after i die. My little ones father only knows and accepts so much regarding how ill i am. I honestly think some people think its a state of mind. It is unbelievable but when doctors dont have all the answers even they have suggested anxiety! My perforated bowel which has been killing me was missed for weeks and i was asked about my state of mind and stress levels by one doctor!
I almost want to write a blimmin book with it all in so there is never any doubt as to how much i have endured / am enduring. I hate reading stories about suicide where it is always related to mental health. It absolutely is not. I imagine for many it is because of horrific illness and this gets glossed over or ignored. I absolutely cannot have that.
Ive applied to Dignitas. My family support me 100% now as does a very close friend who comes to see me often. My family still.cant even pronounce the name of some of the health issues ive got so their story alone isnt enough if my little one ever has questions in the future. I absolutely cannot have any questions over this for the future of my little one. I want anyine around him influencing him or even any strangers to know the whole story.
I dont know if that makes any sense. It is too much to document the detail of my illnesses for my little one at this current age so it needs to be out there so to speak in another way. I just dont know how to do that.
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