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Otitis externa
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Newcomer!
Hi! I have suffered with stomach problems for a while, I've had loads of tests which have come back as normal to think I have IBS! I struggle more with bloating and excess wind! Especially I the evening! I have tried windeze tablets, buscopan and loads more but nothing seems to help. I have also tried
Hi! I have suffered with stomach problems for a while, I've had loads of tests which have come back as normal to think I have IBS! I struggle more with bloating and excess wind! Especially I the evening! I have tried windeze tablets, buscopan and loads more but nothing seems to help. I have also tried
Dee_500
in
IBS Network
8 years ago
Interpretation of results please
My main symptom is a 'stuffy' head and a blocked ear but I think this is my recurring
otitis
externa
(although I did note on a recent post that one symptom of a dysfunctional thyroid is blocked ears!). Any help would be appreciated.
My main symptom is a 'stuffy' head and a blocked ear but I think this is my recurring
otitis
externa
(although I did note on a recent post that one symptom of a dysfunctional thyroid is blocked ears!). Any help would be appreciated.
n1mble2
in
Thyroid UK
8 years ago
Ulcerative Colitis
Saw my specialist today was given the all clear and now my colitis has settled. So I'm a very happy lady today. Getting good results from the acupuncture and now the colitis. I am really glad to post some good news. I truly wish that some off you all on this site gets some relief or feel a bit better
Saw my specialist today was given the all clear and now my colitis has settled. So I'm a very happy lady today. Getting good results from the acupuncture and now the colitis. I am really glad to post some good news. I truly wish that some off you all on this site gets some relief or feel a bit better
Jan101
in
Fibromyalgia Action UK
8 years ago
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GP Blood Test
Hi all. I was diagnosed with ulcerative colitis after a colonoscopy in September. I had been having symptoms for a couple of years which got worse and worse. Back in March, I had blood tests done for colitis, Crohn's and cealiac but they came back normal. One of the doctors in the GI dept at the hospital
Hi all. I was diagnosed with ulcerative colitis after a colonoscopy in September. I had been having symptoms for a couple of years which got worse and worse. Back in March, I had blood tests done for colitis, Crohn's and cealiac but they came back normal. One of the doctors in the GI dept at the hospital
STC789
in
Crohn's and Colitis Support
8 years ago
Hi, new here!
Hi, my name is T and my 15 year old son is now getting worked up for some type of inflammatory bowel disease. He was diagnosed at 1 with eosinophilic gastroenteritis and now we need another scope. He was negative for celiac at that time but his blood work this time around did suggest it could be celiac
Hi, my name is T and my 15 year old son is now getting worked up for some type of inflammatory bowel disease. He was diagnosed at 1 with eosinophilic gastroenteritis and now we need another scope. He was negative for celiac at that time but his blood work this time around did suggest it could be celiac
bff4ever
in
Gluten Free Guerrillas
8 years ago
Newbie
Hi community this is my first post, I was very recently diagnosed with crohns, I had an appointment with the gastroenterologist yesterday and he has started me on Pentasa 4 a day. Anyone else on this? Has it helped? Thanks
Hi community this is my first post, I was very recently diagnosed with crohns, I had an appointment with the gastroenterologist yesterday and he has started me on Pentasa 4 a day. Anyone else on this? Has it helped? Thanks
Pixielula
in
Crohn's and Colitis Support
8 years ago
Is there a connection endo and colitis?
Hi there, I am new to this forum. Was diagnosed with endo at age 27, was in horrible pain, not knowing the cause was worse though. Under my gyno's suggestion first underwent hormone treatment to stop monthly cycle to try and shrink a mass in my left ovary which later turned out to be endo. Had endo
Hi there, I am new to this forum. Was diagnosed with endo at age 27, was in horrible pain, not knowing the cause was worse though. Under my gyno's suggestion first underwent hormone treatment to stop monthly cycle to try and shrink a mass in my left ovary which later turned out to be endo. Had endo
Laubhealth
in
Endometriosis UK
8 years ago
Simponi
Hi folks, well it's been 2 years since the RoActemra MTX taper trial started but now the inflammation markers are rising again necessitating 6 monthly preds. So I've had advice that Rituximab is the way to go. I didn't like the look of it and after much consultation we agreed the 2nd best option was
Hi folks, well it's been 2 years since the RoActemra MTX taper trial started but now the inflammation markers are rising again necessitating 6 monthly preds. So I've had advice that Rituximab is the way to go. I didn't like the look of it and after much consultation we agreed the 2nd best option was
harryhunt43
in
NRAS
8 years ago
Sclerosing Cholangitis
I have a very complex & extensive surgical history of the liver. Being severely symptomatic the last few years & surgical intervention has not been an option, I have now been diagnosed with SECONDARY Sclerosing Cholangitis. I am writing to you with the hope of some sort of guidance as I feel I have not
I have a very complex & extensive surgical history of the liver. Being severely symptomatic the last few years & surgical intervention has not been an option, I have now been diagnosed with SECONDARY Sclerosing Cholangitis. I am writing to you with the hope of some sort of guidance as I feel I have not
SaffaMum
in
British Liver Trust
8 years ago
Bad Ulcerative Colitis flare and bladder irritation/urgency! Someone help!
I am currently going through a BAD UC flare. Taking 40mg of Prednisone and my daily Lialda pills. My bladder feels like it's under tremendous pressure, which makes me take several trips to the bathroom for a disappointing amount of urine to come out. Has anyone ever had this issue with a UC flare? I
I am currently going through a BAD UC flare. Taking 40mg of Prednisone and my daily Lialda pills. My bladder feels like it's under tremendous pressure, which makes me take several trips to the bathroom for a disappointing amount of urine to come out. Has anyone ever had this issue with a UC flare? I
Wonderer
in
Pelvic Pain Support Network
8 years ago
Bowel routine
Just wondering if anyone can relate to my "bowel routine" and offer any advice. I was diagnosed with Ulcerative Colitis (Proctitis) quite some time ago and I think this is under control. I also think I have IBS though and my own bowel routine is being on and off the loo for 4-5 hours every 2-3 days.
Just wondering if anyone can relate to my "bowel routine" and offer any advice. I was diagnosed with Ulcerative Colitis (Proctitis) quite some time ago and I think this is under control. I also think I have IBS though and my own bowel routine is being on and off the loo for 4-5 hours every 2-3 days.
Jimmy_The_Doo
in
IBS Network
8 years ago
Colitis
I was diagnosed with ulcerative colitis 18 months ago and have been on several different medications, none of which seems to be working for me so it has been suggested by my Consultant that I go on a drug called Simponi (gulimumab). Has anybody experienced this as it is a self injecting drug which sounds
I was diagnosed with ulcerative colitis 18 months ago and have been on several different medications, none of which seems to be working for me so it has been suggested by my Consultant that I go on a drug called Simponi (gulimumab). Has anybody experienced this as it is a self injecting drug which sounds
Caskey
in
Crohn's and Colitis Support
8 years ago
Vaping
I'm new here just today ,I took ulcerative colitis in 1991 within 3 months of stoping smoking ,it just kept getting worse and worse no matter what I did or didn't do . Trying to live life was a nightmare even phyichologicaly the fear of going out (although) I did ) people didn't understand that fear
I'm new here just today ,I took ulcerative colitis in 1991 within 3 months of stoping smoking ,it just kept getting worse and worse no matter what I did or didn't do . Trying to live life was a nightmare even phyichologicaly the fear of going out (although) I did ) people didn't understand that fear
emccarty
in
Crohn's and Colitis Support
8 years ago
New here, please be gentle
I was diagnosed last year and put on Asacol. Was fine (ish) until Nov when they changed meds to salofalk crystals. Turned me into a zombie! Couldn't eat, drink, sleep and had no idea where I was. Changed back to Asacol and to cut a long story short, ended up in hospital to discover it was the med's that
I was diagnosed last year and put on Asacol. Was fine (ish) until Nov when they changed meds to salofalk crystals. Turned me into a zombie! Couldn't eat, drink, sleep and had no idea where I was. Changed back to Asacol and to cut a long story short, ended up in hospital to discover it was the med's that
Kathian19
in
Crohn's and Colitis Support
8 years ago
Scleroderma and colostomy
I have had problems with my bowels for 10 years now and my consultant and GP both suggest I consider a colostomy, which they say transforms the lives of their scleroderma patients. Has anyone experience, (bad or good) they are willing to share about living with scleroderma, Raynauds and a colostomy.
I have had problems with my bowels for 10 years now and my consultant and GP both suggest I consider a colostomy, which they say transforms the lives of their scleroderma patients. Has anyone experience, (bad or good) they are willing to share about living with scleroderma, Raynauds and a colostomy.
Lyndabickley
in
Scleroderma & Raynaud's UK (SRUK)
8 years ago
I have had this for 3 years and its getting me down.
Today i have received my official diagnosis of ulcerative colitis .i have been on prednisolone suppositories for two years on and off.I am allergic to Mesalazine so that was of no use.am am now on prednisolone tablets 6 a day 30mg for two weeks then reducing 5mg every two weeks. they are looking at a
Today i have received my official diagnosis of ulcerative colitis .i have been on prednisolone suppositories for two years on and off.I am allergic to Mesalazine so that was of no use.am am now on prednisolone tablets 6 a day 30mg for two weeks then reducing 5mg every two weeks. they are looking at a
CONSTANTGUTACHE
in
Crohn's and Colitis Support
8 years ago
Running and Inflammatory Bowel Disease
Since graduating from the c25k programme I have been diagnosed with colitis and have had to stop running whilst I have treatment . I am missing running hugely, especially as it took such effort for me to make the end of the programme. Does anyone have any experience of running with IBD they can share
Since graduating from the c25k programme I have been diagnosed with colitis and have had to stop running whilst I have treatment . I am missing running hugely, especially as it took such effort for me to make the end of the programme. Does anyone have any experience of running with IBD they can share
adadoom-adadoom
in
Couch to 5K
8 years ago
IBS AND COLITIS
I've suffered from IBS C for years. Just been diagnosed with Colitis. Has anyone heard of GREG Williams who offer a program to heal your ulcerative colitis. What was the outcome? Thank you
I've suffered from IBS C for years. Just been diagnosed with Colitis. Has anyone heard of GREG Williams who offer a program to heal your ulcerative colitis. What was the outcome? Thank you
Idalmis
in
IBS Network
8 years ago
Ibrutinib/Imbruvica brings hope to stem cell transplant patients with chronic graft-versus-host-disease
[i]'FDA granted a fourth Breakthrough Therapy Designation (BTD) for ibrutinib (IMBRUVICA®) as a potential treatment of chronic graft-versus-host-disease (cGVHD) after failure of one or more lines of systemic therapy. The FDA also granted the therapy Orphan Drug Designation for the condition. cGVHD is
[i]'FDA granted a fourth Breakthrough Therapy Designation (BTD) for ibrutinib (IMBRUVICA®) as a potential treatment of chronic graft-versus-host-disease (cGVHD) after failure of one or more lines of systemic therapy. The FDA also granted the therapy Orphan Drug Designation for the condition. cGVHD is
AussieNeil
Partner
in
CLL Support
8 years ago
microscopic Lymphocytic
although I suffer with this and all the symptoms I am not sure I am suppose to be on this support group . this is just for crohns and ulcerative colitis?
although I suffer with this and all the symptoms I am not sure I am suppose to be on this support group . this is just for crohns and ulcerative colitis?
sandybeach12066
in
Crohn's and Colitis Support
8 years ago
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