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Perthes disease pain management
I was diagnosed with perthes disease when I was 2, I'm now 19 and My pain is getting worse and worse nothing helps ibuprofen doesn't and I got prescribed ultram and lortab but neither works I try elevating my leg, heat pads, and ice NOTHING helps! If I can't get the pain under control I'll have to have
I was diagnosed with perthes disease when I was 2, I'm now 19 and My pain is getting worse and worse nothing helps ibuprofen doesn't and I got prescribed ultram and lortab but neither works I try elevating my leg, heat pads, and ice NOTHING helps! If I can't get the pain under control I'll have to have
Snels28
in
NRAS
7 years ago
Does hormones cause ulcerative colitis flares?
I'm curious as to whether anyone has suffered with colitis flares when they have altered either their thyroid meds or contraceptives? I'm still flaring since last August and the changes I made back then was an increase in thyroid meds slightly from 75/100mg to 100mg and the Merina coil fitted to control
I'm curious as to whether anyone has suffered with colitis flares when they have altered either their thyroid meds or contraceptives? I'm still flaring since last August and the changes I made back then was an increase in thyroid meds slightly from 75/100mg to 100mg and the Merina coil fitted to control
jostafford0
in
Crohn's and Colitis Support
7 years ago
Ulcerative colitis
Hi there I have ulcerative colitis for the past 12 years and have been using Asacol. At the moment I'm experiencing the same symptoms being anxiety attack, heart palpitations and just not feeling myself since I've started taking Salazopyrin for the last two weeks. Ive been using Asacol but this has
Hi there I have ulcerative colitis for the past 12 years and have been using Asacol. At the moment I'm experiencing the same symptoms being anxiety attack, heart palpitations and just not feeling myself since I've started taking Salazopyrin for the last two weeks. Ive been using Asacol but this has
Lynnejoy
in
NRAS
7 years ago
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Ulcerative Colitis
Due to rectal bleeding my GP sent me for a colonoscopy which I had today. It turns out I have UC and I never knew. Apparently I'm currently having a flare up hence the bleeding.
Due to rectal bleeding my GP sent me for a colonoscopy which I had today. It turns out I have UC and I never knew. Apparently I'm currently having a flare up hence the bleeding.
Shoeysmum
in
Crohn's and Colitis Support
8 years ago
Apixaban and stomach
Can any apixaban takers tell me if you find you need to take apixaban with some food, or if it's gentle enough on your stomach to have with just water? (I know the guidelines say don't need food but is that your experience?) With taking twice a day, I don't really want to have to eat early & late.
Can any apixaban takers tell me if you find you need to take apixaban with some food, or if it's gentle enough on your stomach to have with just water? (I know the guidelines say don't need food but is that your experience?) With taking twice a day, I don't really want to have to eat early & late.
JaneFinn
in
AF Association
8 years ago
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
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
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
Hypothyroid but possible PBC symptoms :(
My only 'symptom' is tinnitus- constant over the past 7-8 years and an insanely itchy ear -
otitis
media
- and also serious anxiety.....all attributable to Thyroid issues. The cholesterol also is associated with unmanaged Thyroid.
My only 'symptom' is tinnitus- constant over the past 7-8 years and an insanely itchy ear -
otitis
media
- and also serious anxiety.....all attributable to Thyroid issues. The cholesterol also is associated with unmanaged Thyroid.
luley
in
PBC Foundation
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
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