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Urostomy
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asking for advice
brief synopsis Cervical cancer 1985 with surgery and radiation treatment
Urostomy
1991 Artificial sphincter 2003
Urostomy
revised and most of small bowel cut out because of adhesions leaving only 1.2m 2006 Colostomy formed 2007 Constant mucus from rectum In 2023 developed high inflammatory markers
brief synopsis Cervical cancer 1985 with surgery and radiation treatment
Urostomy
1991 Artificial sphincter 2003
Urostomy
revised and most of small bowel cut out because of adhesions leaving only 1.2m 2006 Colostomy formed 2007 Constant mucus from rectum In 2023 developed high inflammatory markers
Imakelace
in
Pelvic Pain Support Network
5 months ago
perineal myxoid pseudotumor of fat
They performed the surgery (8.5 hrs) removing the bladder and creating a stoma opening in the abdomen from a bowel resection and created a a little pocket for the ureters to flow into which then flows into the
urostomy
bag outside on the abdomen.
They performed the surgery (8.5 hrs) removing the bladder and creating a stoma opening in the abdomen from a bowel resection and created a a little pocket for the ureters to flow into which then flows into the
urostomy
bag outside on the abdomen.
snoochy
in
Kidney Disease
25 days ago
Long time PRD sufferer.
As a result I've had a
urostomy
bag for best part of 45 years! (This does not bother me at all its part of me š). Since then I've been admitted to hospital for numerous problems. I've had a kidney removed, part of my bowel removed. A testical removedš .
As a result I've had a
urostomy
bag for best part of 45 years! (This does not bother me at all its part of me š). Since then I've been admitted to hospital for numerous problems. I've had a kidney removed, part of my bowel removed. A testical removedš .
Tel76
in
Pelvic Radiation Disease Association
6 months ago
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What's on at Ovacome next week (week commencing 17 April 2023)?
This is a friendly environment for people who have a colostomy, ileostomy or
urostomy
because of ovarian cancer to speak with others in similar circumstances.
This is a friendly environment for people who have a colostomy, ileostomy or
urostomy
because of ovarian cancer to speak with others in similar circumstances.
OvacomeSupport
My Ovacome Team
in
My Ovacome
1 year ago
Urostomy advice
My husband is about to have a
urostomy
surgery. He is scared, of course. He is 68 and needs the
urostomy
because of irreparable damage from post radiation strictures after prostate cancer treatment. Just wondering if anyone has any advice for someone about to go down this road.
My husband is about to have a
urostomy
surgery. He is scared, of course. He is 68 and needs the
urostomy
because of irreparable damage from post radiation strictures after prostate cancer treatment. Just wondering if anyone has any advice for someone about to go down this road.
Stressbaker
in
Living with a Stoma
1 year ago
What's on at Ovacome next week (commencing 14 November 2022)?
This is a friendly environment for people who have a colostomy, ileostomy or
urostomy
because of ovarian cancer to speak with others in similar circumstances.
This is a friendly environment for people who have a colostomy, ileostomy or
urostomy
because of ovarian cancer to speak with others in similar circumstances.
OvacomeSupport
My Ovacome Team
in
My Ovacome
2 years ago
Rochester Mayo
If it hasnāt healed enough Dan will have a
urostomy
. Just wondering if anyone else has been down this road and what their experience was?
If it hasnāt healed enough Dan will have a
urostomy
. Just wondering if anyone else has been down this road and what their experience was?
Stressbaker
in
Advanced Prostate Cancer
2 years ago
Ive found support š
Its never gotten any higher than that and constantly drops sometimes as low as 14.i had a
urostomy
performed about 20 years ago due to bladder disease and the slow degeneration of my kidney function may be as a result of that but no definitive cause has ever been found.
Its never gotten any higher than that and constantly drops sometimes as low as 14.i had a
urostomy
performed about 20 years ago due to bladder disease and the slow degeneration of my kidney function may be as a result of that but no definitive cause has ever been found.
19Willow62
in
Kidney Disease
2 years ago
Fnd and crps
Fnd occured after mesh removal in2019
urostomy
in 2020 diagnosis 2021 what foods have people successfully retained ok please. I live in new zealand im 56
Fnd occured after mesh removal in2019
urostomy
in 2020 diagnosis 2021 what foods have people successfully retained ok please. I live in new zealand im 56
Cherub1992
in
Functional Neurological Disorder - FND Hope
2 years ago
Introducing myself ( in a fashion ) ā¤ļø
I had a Ileostomy a few years bk then 4 months ago had to have my bladder taken away so ended up with a
Urostomy
, for some reason itās caused a complication with my digestive system causing blockages which means I eat for 2 days then haved to have those lovely supplement drinks for 3-4 days !
I had a Ileostomy a few years bk then 4 months ago had to have my bladder taken away so ended up with a
Urostomy
, for some reason itās caused a complication with my digestive system causing blockages which means I eat for 2 days then haved to have those lovely supplement drinks for 3-4 days !
Pink17
in
Anxiety and Depression Support
2 years ago
Scared
I have 2 stomas (colostomy and an
urostomy
). The
urostomy
is fine but the colostomy does what it wants. My colostomy is very slow and there isnāt much poo in my stoma bag. I think it is constipation because with a bowel obstruction I get terrible pain.
I have 2 stomas (colostomy and an
urostomy
). The
urostomy
is fine but the colostomy does what it wants. My colostomy is very slow and there isnāt much poo in my stoma bag. I think it is constipation because with a bowel obstruction I get terrible pain.
CrochetDancer
in
Pelvic Radiation Disease Association
3 years ago
Radiation Enteritis - I feel very alone
I also have two stomas (colostomy and an
urostomy
). I was told in April that I would need an ileostomy, so I would have 3 stomas and this was reiterated over the weekend. I am home now but I get a lot of pain with wind.
I also have two stomas (colostomy and an
urostomy
). I was told in April that I would need an ileostomy, so I would have 3 stomas and this was reiterated over the weekend. I am home now but I get a lot of pain with wind.
CrochetDancer
in
Pelvic Radiation Disease Association
3 years ago
Worried
I have a colostomy and an
urostomy
. I have a fistula which constantly leaks, PTSD and I have recently been diagnosed with radiation enteritis. The fistula leaks all sorts including a.bit of blood.
I have a colostomy and an
urostomy
. I have a fistula which constantly leaks, PTSD and I have recently been diagnosed with radiation enteritis. The fistula leaks all sorts including a.bit of blood.
CrochetDancer
in
Pelvic Radiation Disease Association
3 years ago
Disabled living aids.
Irrigation & Faecal Collectors Catheters Changing Mats Disposable Pads Drainage Bags Female Devices Home Delivery & Prescription Services Male Devices ā Including Penile Sheaths & Bodyworn Urinals Odour Control Pelvic floor Equipment Probiotics Skin Care Stoma Care & Accessories ā Colostomy, Ileostomy,
Urostomy
Irrigation & Faecal Collectors Catheters Changing Mats Disposable Pads Drainage Bags Female Devices Home Delivery & Prescription Services Male Devices ā Including Penile Sheaths & Bodyworn Urinals Odour Control Pelvic floor Equipment Probiotics Skin Care Stoma Care & Accessories ā Colostomy, Ileostomy,
Urostomy
wobblybee
in
Ataxia UK
4 years ago
In focus: stomas - travel
You can get this, as well as information and advice, from your stoma nurse, the Ileostomy and Internal Pouch Association, The Colostomy Association and The
Urostomy
Association, including certificates in different languages. The links to their information are at the bottom of this post.
You can get this, as well as information and advice, from your stoma nurse, the Ileostomy and Internal Pouch Association, The Colostomy Association and The
Urostomy
Association, including certificates in different languages. The links to their information are at the bottom of this post.
OvacomeSupport
Administrator
in
My Ovacome
4 years ago
In focus: stomas - introduction
Information and support for people with urostomies is available from the
Urostomy
Association at https://urostomyassociation.org.uk/ . A stoma can be permanent or temporary.
Information and support for people with urostomies is available from the
Urostomy
Association at https://urostomyassociation.org.uk/ . A stoma can be permanent or temporary.
OvacomeSupport
Administrator
in
My Ovacome
4 years ago
In focus: travel - practicalities of travel
You can get this, as well as information and advice, from your stoma nurse, the Ileostomy and Internal Pouch Association (https://iasupport.org/about/publications/factsheets/travel-tips/), The Colostomy Association (http://www.colostomyuk.org/information/travel-advice/) and The
Urostomy
Association (
You can get this, as well as information and advice, from your stoma nurse, the Ileostomy and Internal Pouch Association (https://iasupport.org/about/publications/factsheets/travel-tips/), The Colostomy Association (http://www.colostomyuk.org/information/travel-advice/) and The
Urostomy
Association (
OvacomeSupport
Administrator
in
My Ovacome
5 years ago
New to new way of life
very keen to read peoples experiences and just see how much courage people really have .I have been in the care sector for over 30yrs and have always been the one who looked after people now people are looking after me as I am a lady who is 5wks after having bladder removal due to cancer and having a
urostomy
very keen to read peoples experiences and just see how much courage people really have .I have been in the care sector for over 30yrs and have always been the one who looked after people now people are looking after me as I am a lady who is 5wks after having bladder removal due to cancer and having a
urostomy
munkieone
in
Fight Bladder Cancer
5 years ago
Doing well with Bladder Cancer
Those organs were removed, they created a
urostomy
and it was hoped that I might be "cured". My next scans showed that my cancer had metastasized to my lungs. At this point, my doctors thought I had a year or two to live.
Those organs were removed, they created a
urostomy
and it was hoped that I might be "cured". My next scans showed that my cancer had metastasized to my lungs. At this point, my doctors thought I had a year or two to live.
Jim47
in
Fight Bladder Cancer
6 years ago
Newly diagnosed with Essential Thrombocythemia
I get a lot of urinary tract infections as I have ongoing problems with my
urostomy
. Has anyone been to the patient forums that mpnvoice organise. I'm sure this will be the first of many posts as I get my head around this latest medical challenge Cheers
I get a lot of urinary tract infections as I have ongoing problems with my
urostomy
. Has anyone been to the patient forums that mpnvoice organise. I'm sure this will be the first of many posts as I get my head around this latest medical challenge Cheers
alastair70
in
Fight MPN
7 years ago
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