Search
Search
About
Log in
Join
Experiences with
Colitis
Posts
Communities
1,587 public posts
Filter results
RP, Salvage Radiation with Ulcerative Colitis
After three years of having an undetectable PSA, I am now detectable at 0.1. Is there anyone in the group that has had a RP, salvage radiation, and also has ulcerative coilotis? I am in that place now, and the radiation oncologist does not want to perform salvage radiation because they can’t install
After three years of having an undetectable PSA, I am now detectable at 0.1. Is there anyone in the group that has had a RP, salvage radiation, and also has ulcerative coilotis? I am in that place now, and the radiation oncologist does not want to perform salvage radiation because they can’t install
Fortysstyle
in
Advanced Prostate Cancer
24 days ago
907863
when I have a GCA flare 3 months later my hair comes out and grows back really dry and I cannt do anything with it . I went to a dermatologist who recommended , I take viviscal hair tablets ( not cheap) biotin tablets and then on prescription extrovex shsmpoo. Plus every other night I go to bed with
when I have a GCA flare 3 months later my hair comes out and grows back really dry and I cannt do anything with it . I went to a dermatologist who recommended , I take viviscal hair tablets ( not cheap) biotin tablets and then on prescription extrovex shsmpoo. Plus every other night I go to bed with
9077863
in
PMRGCAuk
1 month ago
introducing myself
hi I’m Leanne I have ulcerative
colitis
was diagnosed in 2009
hi I’m Leanne I have ulcerative
colitis
was diagnosed in 2009
ltyrrell
in
Crohn's and Colitis Support
8 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
colitis symptoms
hello everyone, Any remedies to help alleviate diarrhea from UC? Any over the counter? pepto bismol sometimes works for me but not all the time. thank you
hello everyone, Any remedies to help alleviate diarrhea from UC? Any over the counter? pepto bismol sometimes works for me but not all the time. thank you
alfreddy7
in
Crohn's and Colitis Support
9 months ago
probiotics
I was really hoping they would work because my gut health is not great and I have
colitis
. I’m 4 years post transplant and my doctors said it was safe to take them .
I was really hoping they would work because my gut health is not great and I have
colitis
. I’m 4 years post transplant and my doctors said it was safe to take them .
Winner76
in
Kidney Transplant
5 months ago
Ulcerative proctitis
I have a severe proctitis. The Dr. prescribed me with a Prednisolone suppositories 5mg twice daily plus started oral Mesalazine as Octasa 2.4g/day. I’m on my 3rd week of the medication. But is not working properly. I’m taking Octasa in the morning before breakfast (I tried to take it before dinner
I have a severe proctitis. The Dr. prescribed me with a Prednisolone suppositories 5mg twice daily plus started oral Mesalazine as Octasa 2.4g/day. I’m on my 3rd week of the medication. But is not working properly. I’m taking Octasa in the morning before breakfast (I tried to take it before dinner
MK3L4S
in
Crohn's and Colitis Support
3 months ago
End of the road for PBS-available treaments for me.
Starting in 2019 I've had FCR, Nov 2022 splenomegaly and other leukemia symptoms so January 2023 I started on Ibrutinib, giving partial remission but with
colitis
side effects. Sept 2023 Zanbrutinib but with even worse
colitis
(diarrhrea). I chose to go back to Ibrutinib.
Starting in 2019 I've had FCR, Nov 2022 splenomegaly and other leukemia symptoms so January 2023 I started on Ibrutinib, giving partial remission but with
colitis
side effects. Sept 2023 Zanbrutinib but with even worse
colitis
(diarrhrea). I chose to go back to Ibrutinib.
Jotame
in
CLL Support
2 months ago
Adalimumab
Hi everyone. This is the first time asking a question on here so forgive me if I ramble a bit. I had my first injection of adalimumab for my R.A on Tuesday and it has really knocked me. I feel so tired and queasy and slept most of yesterday and all last night till 10 this morning. Still not feeling
Hi everyone. This is the first time asking a question on here so forgive me if I ramble a bit. I had my first injection of adalimumab for my R.A on Tuesday and it has really knocked me. I feel so tired and queasy and slept most of yesterday and all last night till 10 this morning. Still not feeling
QuacketyQuack
in
NRAS
3 months ago
Had Davinci RP w/ LNR 8 Reoccurrence in Bed, PSA Rising 0.77 CANNOT Do Radiation active Crohn Disease / Colitis, What about Cryotherapy?
Partially imaged proximal sigmoid colon wall thickening, possibly
colitis
. What can I Do, Other than Radiation to Prostate Bed Fossa. I’m fuming listen to first MO and waited, I didn’t follow my gut instinct before chronic disease /
colitis
started and Now I can’t radiate
Partially imaged proximal sigmoid colon wall thickening, possibly
colitis
. What can I Do, Other than Radiation to Prostate Bed Fossa. I’m fuming listen to first MO and waited, I didn’t follow my gut instinct before chronic disease /
colitis
started and Now I can’t radiate
Shorehousejam
in
Advanced Prostate Cancer
6 months ago
5th year of ulcerative colitis.
This is my 5th year of ulcerative
colitis
and I’ve no idea if anyone has what its surgical implications or effects are. Need a little enlightenment!
This is my 5th year of ulcerative
colitis
and I’ve no idea if anyone has what its surgical implications or effects are. Need a little enlightenment!
Roi12
in
Crohn's and Colitis Support
8 months ago
Colonoscopy
Just have a question. I was put on a 5 Day taper of 16mg of prednisolone. I took my first dose today along with a one time dose of diflucan. Will I be ok to have my colonoscopy tomorrow?
Just have a question. I was put on a 5 Day taper of 16mg of prednisolone. I took my first dose today along with a one time dose of diflucan. Will I be ok to have my colonoscopy tomorrow?
Babciboys
in
PMRGCAuk
3 months ago
colitis and Psoriasis
Hello, I’ve recently been diagnosed with
colitis
and also experienced some Psoriasis. Some people seem to think this all leads back to the liver. I just wondered if anyone had a similar experience and if there are tests available to see what I can possibly do?
Hello, I’ve recently been diagnosed with
colitis
and also experienced some Psoriasis. Some people seem to think this all leads back to the liver. I just wondered if anyone had a similar experience and if there are tests available to see what I can possibly do?
Nick1954
in
British Liver Trust
8 months ago
Questran for Bile Acid Malabsorption
Does anyone know an alternative medication for Questran as there is now unavailability due to supply problems? I am having a bad attack of Bile Acid Malabsorption at the moment and am virtually housebound by it! Any help would be much appreciated 🙏
Does anyone know an alternative medication for Questran as there is now unavailability due to supply problems? I am having a bad attack of Bile Acid Malabsorption at the moment and am virtually housebound by it! Any help would be much appreciated 🙏
laurajn087
in
IBS Network
4 months ago
Interesting research
Just saw this interesting research on DNA cause of inflammatory bowel disease, but they say it might also apply to autoimmune liver diseases. https://amp.theguardian.com/society/article/2024/jun/05/bowel-disease-hope-researchers-find-biological-pathway They hope treatments will be in use within 5
Just saw this interesting research on DNA cause of inflammatory bowel disease, but they say it might also apply to autoimmune liver diseases. https://amp.theguardian.com/society/article/2024/jun/05/bowel-disease-hope-researchers-find-biological-pathway They hope treatments will be in use within 5
Readlots
in
British Liver Trust
4 months ago
Tenesmus - Urgency
Anyone out there struggling with tenesmus? Been experiencing urgency for 3 months virtually nonstop. Only a couple of days relief here and there. Also it gets worse whenever I walk or stand, if I sit all day I am usually fine. Also seems to get worse after a shower or after bm. Tried everything from
Anyone out there struggling with tenesmus? Been experiencing urgency for 3 months virtually nonstop. Only a couple of days relief here and there. Also it gets worse whenever I walk or stand, if I sit all day I am usually fine. Also seems to get worse after a shower or after bm. Tried everything from
yakodik
in
IBS Network
4 months ago
the down there
This week diagnosed with
colitis
. What is it and why is it so painful ? Is it part of MS ?
This week diagnosed with
colitis
. What is it and why is it so painful ? Is it part of MS ?
309Ygi
in
My MSAA Community
8 months ago
Screening for Colorectal Cancer
.🤔👍 You may need to be tested [u]
earlier than 45, or more often than other people
[/u], if you have: * Inflammatory bowel disease such as Crohn's disease or ulcerative
colitis
. * A personal or family history of colorectal cancer or colorectal polyps.
.🤔👍 You may need to be tested [u]
earlier than 45, or more often than other people
[/u], if you have: * Inflammatory bowel disease such as Crohn's disease or ulcerative
colitis
. * A personal or family history of colorectal cancer or colorectal polyps.
GCCA-Survivor
Administrator
in
Colon Cancer Connected
19 days ago
colonoscopy in 2 weeks - anxious as hospitalised last time with chest pain
Hi, I have a colonoscopy in 2 weeks as I suffer with ulcerative
colitis
and was born with anal altreasia. Soon after my last colonscopy, I had severe chest pains and was admitted to swindon hospital. I don’t know what may have caused this heart pain (gas / air / drugs)??
Hi, I have a colonoscopy in 2 weeks as I suffer with ulcerative
colitis
and was born with anal altreasia. Soon after my last colonscopy, I had severe chest pains and was admitted to swindon hospital. I don’t know what may have caused this heart pain (gas / air / drugs)??
Bucket13
in
Crohn's and Colitis Support
25 days ago
I need help
They keep saying I have
colitis
about prescribing me antibiotics and has just recently prescribed me some steriods but I'm still in so much pain. I had an upper and lower Colonoscopy but I just won't stop bleeding. Please some one help me. How can I stop the pain and the blood??
They keep saying I have
colitis
about prescribing me antibiotics and has just recently prescribed me some steriods but I'm still in so much pain. I had an upper and lower Colonoscopy but I just won't stop bleeding. Please some one help me. How can I stop the pain and the blood??
Sosadme
in
Crohn's and Colitis Support
6 months ago
Raynauds and Hypermobility
I've also got
colitis
, irritable bladder, some joint hypermobility so I'm wondering if there's a connection to all that. Thank you
I've also got
colitis
, irritable bladder, some joint hypermobility so I'm wondering if there's a connection to all that. Thank you
Boudica78
in
Scleroderma & Raynaud's UK (SRUK)
7 months ago
1
2
3
...
80
Next page
10
20
30
40
50
60
70
80
Filter results
Clear filters
Posted in
All communities
Crohn's and Colitis Support
325 results
IBS Network
165 results
Thyroid UK
146 results
View top 10 communities
Sort by
Most Relevant
Newest