- Joined
- Sep 5, 2016
- Messages
- 3
Hi there,
I'm new to the forum as I decided to register and reach out to people who know what IBD is and won't call it IBS! Lol Sorry that was a jab at a Senior Nurse who didn't know the difference between IBD and IBS! Lol
Anyway, since a very young child I have had severe gastro problems from top to bottom. Fast forward many years of being fobbed off with IBS and reflux, I started passing large amounts of blood, pus, mucus with the most unimaginable pain when doing so to the point of literally groaning and screaming on the toilet. I've given birth twice (sons are 5 and 10 years old) and I would much rather go through childbirth! The passage of blood etc started at 5am when it woke me up with severe pain in December 2015.
Anyway, since December 2015 and having to deal with constant diarherra, nausea, vomiting, passage of blood, mucus, pus, diarherra, joint swelling and pain, constant daily migraines, and swollen lymph nodes (in addition to a few life traumas) I find myself completely lonely- friends don't care- and incredibly depressed.
I am literally homebound and try and get out as much as I can but my joint problems present a lot of problems.
I finished my fourth therapy of high dose steroids a month ago and I'm still 2 stone over weight (from being skinny with this illness) and with terrible oedema all over my body, noticeably my hands, feet and abdo.
I feel ugly, fat, my family have completely abandoned me since my diagnosis in March 2016 (my mother has UC and a perm colostomy whom I nursed for 10 years), I'm in constant pain and feel empty and a complete shell of myself.
My friends used to take the mick out of me by calling me 'Miss Popular' as I used to talk and know every one. Now I'm just emotionless with pain, loneliness, no support and it makes me feel like life isn't worth living.
My current consultant is useless and doesn't listen to me despite being in and out of hospital with flares, fever, tachycardia and severe pain. So I've put in a transfer to a more specialist hospital.
Since getting this illness, I've lost my family, friends, job, career, money, children (ex is refusing me contact so I'm having to now go through the family courts)- I've lost everything and it makes me think that I'm a bad person that no one wants to be there for me like I have been there unconditionally for everyone else.
Has anyone suffering crippling depression as a result of this illness? Has anyone found themselves so lonely with no support whatsoever?
My only social outings are to see my doctor or Hospital Consultant and I just feel pathetic and lost and more overly, trapped at home due to chronic pain in all my joints, abdo pain, constant toilet trips (my body gives me 5 seconds warning), all body lymph node swelling and pain. I do try and go out for walks but when my knees or hips seize up and I've 10 mins from home, I have no one to help me.
I feel completely abandoned by everyone when I was always there to help and support others- I still am.
I just hope I'm not alone in this.
I'm new to the forum as I decided to register and reach out to people who know what IBD is and won't call it IBS! Lol Sorry that was a jab at a Senior Nurse who didn't know the difference between IBD and IBS! Lol
Anyway, since a very young child I have had severe gastro problems from top to bottom. Fast forward many years of being fobbed off with IBS and reflux, I started passing large amounts of blood, pus, mucus with the most unimaginable pain when doing so to the point of literally groaning and screaming on the toilet. I've given birth twice (sons are 5 and 10 years old) and I would much rather go through childbirth! The passage of blood etc started at 5am when it woke me up with severe pain in December 2015.
Anyway, since December 2015 and having to deal with constant diarherra, nausea, vomiting, passage of blood, mucus, pus, diarherra, joint swelling and pain, constant daily migraines, and swollen lymph nodes (in addition to a few life traumas) I find myself completely lonely- friends don't care- and incredibly depressed.
I am literally homebound and try and get out as much as I can but my joint problems present a lot of problems.
I finished my fourth therapy of high dose steroids a month ago and I'm still 2 stone over weight (from being skinny with this illness) and with terrible oedema all over my body, noticeably my hands, feet and abdo.
I feel ugly, fat, my family have completely abandoned me since my diagnosis in March 2016 (my mother has UC and a perm colostomy whom I nursed for 10 years), I'm in constant pain and feel empty and a complete shell of myself.
My friends used to take the mick out of me by calling me 'Miss Popular' as I used to talk and know every one. Now I'm just emotionless with pain, loneliness, no support and it makes me feel like life isn't worth living.
My current consultant is useless and doesn't listen to me despite being in and out of hospital with flares, fever, tachycardia and severe pain. So I've put in a transfer to a more specialist hospital.
Since getting this illness, I've lost my family, friends, job, career, money, children (ex is refusing me contact so I'm having to now go through the family courts)- I've lost everything and it makes me think that I'm a bad person that no one wants to be there for me like I have been there unconditionally for everyone else.
Has anyone suffering crippling depression as a result of this illness? Has anyone found themselves so lonely with no support whatsoever?
My only social outings are to see my doctor or Hospital Consultant and I just feel pathetic and lost and more overly, trapped at home due to chronic pain in all my joints, abdo pain, constant toilet trips (my body gives me 5 seconds warning), all body lymph node swelling and pain. I do try and go out for walks but when my knees or hips seize up and I've 10 mins from home, I have no one to help me.
I feel completely abandoned by everyone when I was always there to help and support others- I still am.
I just hope I'm not alone in this.