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Experiences with
Cystitis
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Pain
The surgery also seemed to exacerbate my interstitial
cystitis
. I am allergic to acetaminophen (Tylenol), with aspirin I have breathing problems. My pain doctor has prescribed 10mg Oxycodone IR up to three times per day for severe pain.
The surgery also seemed to exacerbate my interstitial
cystitis
. I am allergic to acetaminophen (Tylenol), with aspirin I have breathing problems. My pain doctor has prescribed 10mg Oxycodone IR up to three times per day for severe pain.
PurpleMinded
in
Kidney Disease
5 years ago
Moon face and continued swelling.
Really want to get down to at least 10 pred but at each step down I get
cystitis
, muscle cramps etc. Any suggestions as to what I can do ?
Really want to get down to at least 10 pred but at each step down I get
cystitis
, muscle cramps etc. Any suggestions as to what I can do ?
ragdollcat4
in
PMRGCAuk
5 years ago
Quinolones
In July 2016, the FDA issued a more comprehensive alert, warning that fluoroquinolones should not be prescribed if other alternatives are available for patients with: Acute sinusitis
Cystitis
Acute bacterial exacerbations of chronic bronchitis The risks with use of this class of medications outweigh
In July 2016, the FDA issued a more comprehensive alert, warning that fluoroquinolones should not be prescribed if other alternatives are available for patients with: Acute sinusitis
Cystitis
Acute bacterial exacerbations of chronic bronchitis The risks with use of this class of medications outweigh
EngMac
in
AF Association
5 years ago
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Little White Bumps on Chest, Shoulders, Back, Arms, Jaw etc with PBC?
Hi Everyone, I was diagnosed not quite a year and a half ago. I have been taking Urso since then and I'm currently waiting for my follow up appointment to see how I am reacting to them. I keep finding little white bumps on my skin, with what seems like tiny, hard white cores. They are not like spots
Hi Everyone, I was diagnosed not quite a year and a half ago. I have been taking Urso since then and I'm currently waiting for my follow up appointment to see how I am reacting to them. I keep finding little white bumps on my skin, with what seems like tiny, hard white cores. They are not like spots
FairyFae
in
PBC Foundation
5 years ago
Medichecks Tiredness & Fatigue test
My conditions are Hashi's, Endometriosis, Ulcerative Colitis & Interstitial
Cystitis
.
My conditions are Hashi's, Endometriosis, Ulcerative Colitis & Interstitial
Cystitis
.
jostafford0
in
Thyroid UK
5 years ago
Can Graves' Disease present with lower urinary tract symptoms?
Hello, I was diagnosed with Graves disease back in May 2017. At the time I had a general feeling of unwell, a rapid heartbeat, nausea and excessive sweating. I was put on Carbimozole - my medication eventually lowered to just 5MG every other day, when I was told a month ago that as my levels were 'normal
Hello, I was diagnosed with Graves disease back in May 2017. At the time I had a general feeling of unwell, a rapid heartbeat, nausea and excessive sweating. I was put on Carbimozole - my medication eventually lowered to just 5MG every other day, when I was told a month ago that as my levels were 'normal
GioFarmani
in
Thyroid UK
5 years ago
A case of Cystitis and bilateral renal parenchymal disease
I was diagnosed of
Cystitis
and bilateral renal parenchymal disease around September 2018 through ultrasound test. But this year around February 2019, I repeated the ultrasound test and did blood creatinine test and also a CT scan. Nothing was found wrong at all.
I was diagnosed of
Cystitis
and bilateral renal parenchymal disease around September 2018 through ultrasound test. But this year around February 2019, I repeated the ultrasound test and did blood creatinine test and also a CT scan. Nothing was found wrong at all.
Bright50
in
Early CKD Support
5 years ago
Endometriosis and Interstitial Cystitis warriors out there?
Hi everyone, I hope you're having as comfortable a day as possible. So I was diagnosed with IC years ago and it went in remission of its own accord (no idea how!). Anyway 5 weeks ago I had a major lap to remove stage 4 endo and I believe the surgeon was quite aggressive in his approach. A week into
Hi everyone, I hope you're having as comfortable a day as possible. So I was diagnosed with IC years ago and it went in remission of its own accord (no idea how!). Anyway 5 weeks ago I had a major lap to remove stage 4 endo and I believe the surgeon was quite aggressive in his approach. A week into
Catness
in
Endometriosis UK
5 years ago
Started Tricor
I am a 64 year old woman and I was diagnosed with PBC in 2012. I had high LFT's and it was confirmed with a liver biopsy. I was put on URSO and my LFT'S came down. About 2 years ago my numbers went way up. I have been very fortunate as I don't experience the itching or extreme fatigue. My gastroenterologist
I am a 64 year old woman and I was diagnosed with PBC in 2012. I had high LFT's and it was confirmed with a liver biopsy. I was put on URSO and my LFT'S came down. About 2 years ago my numbers went way up. I have been very fortunate as I don't experience the itching or extreme fatigue. My gastroenterologist
brjl
in
PBC Foundation
5 years ago
Pundendl nerve hell
I have been suffering 24/7 burning &
cystitis
like pain in bladder & backside. I have had all the tests & investigations for water infection, bowels checked , gynaecologist, MRI , C T , etc all come back normal...!
I have been suffering 24/7 burning &
cystitis
like pain in bladder & backside. I have had all the tests & investigations for water infection, bowels checked , gynaecologist, MRI , C T , etc all come back normal...!
Deniseshaw56
in
Pelvic Pain Support Network
5 years ago
Persistent PSA after RARP. Rapid rising in one year from 0,33 to 19,7 and then falling without treatment to 11,4 in 7 month!
Then I got
cystitis
(4/17), I believe from my heavy urethral stricture and 5 bladder stones, diameter about 1 cm, which the doctors found out close to the operation. They looked for cancer, I did a in bore biopsy, three stitches, that's how I wanted it, two made it to G4, the third was a failure.
Then I got
cystitis
(4/17), I believe from my heavy urethral stricture and 5 bladder stones, diameter about 1 cm, which the doctors found out close to the operation. They looked for cancer, I did a in bore biopsy, three stitches, that's how I wanted it, two made it to G4, the third was a failure.
Knallkopf
in
Prostate Cancer Network
5 years ago
Uncomfortable feeling in pelvic floor and penis
Occasionally, I suffer
cystitis
-like symptoms - it burns, stings and hurts when urinating. After urinating, it feels like fireworks are going off in the urethra and perineum - burning, tingling and spasms. But momentarily, there is a sense of relief; a release of pressure.
Occasionally, I suffer
cystitis
-like symptoms - it burns, stings and hurts when urinating. After urinating, it feels like fireworks are going off in the urethra and perineum - burning, tingling and spasms. But momentarily, there is a sense of relief; a release of pressure.
Merc7582
in
Pelvic Pain Support Network
5 years ago
Green and confused
The newly middle aged recruited nurse told me mid-March that for : - the endo: nothing could be done - repetitive
cystitis
: nothing could be done - menopause: not much can be done. This is called medical care. By so called qualified GPs and nurse.
The newly middle aged recruited nurse told me mid-March that for : - the endo: nothing could be done - repetitive
cystitis
: nothing could be done - menopause: not much can be done. This is called medical care. By so called qualified GPs and nurse.
Anastasia17
in
Endometriosis UK
5 years ago
CONSTANT reoccurring UTI'S/IC/Cystitis
I suffer from Interstitial
Cystitis
, Overactive bladder, stress incontinence & frequent UTIS. I currently take amitriptyline, mirabegron & solifenacin for my bladder.
I suffer from Interstitial
Cystitis
, Overactive bladder, stress incontinence & frequent UTIS. I currently take amitriptyline, mirabegron & solifenacin for my bladder.
avelvetcrowbar
in
Bladder Health UK
5 years ago
B12 injections and Bladder Irritation
Normally I am not susceptible to
cystitis
so this is somewhat a mystery. Any thoughts would be appreciated. Many thanks
Normally I am not susceptible to
cystitis
so this is somewhat a mystery. Any thoughts would be appreciated. Many thanks
UnitNitrogen73
in
Pernicious Anaemia Society
5 years ago
Interstitial cystitis
Who suffers with this and what are your Symptoms
Who suffers with this and what are your Symptoms
LISaprag
in
Bladder Health UK
5 years ago
Private biofeedback for anismus in the UK
I wonder if anyone can help me. I was diagnosed with anismus over a year ago and I really want to try biofeedback but have been on a waiting list for six months only to discover I was never on it. Really desperate now so I want to go private. Does anyone know where I can access it in Devon. If not Kent
I wonder if anyone can help me. I was diagnosed with anismus over a year ago and I really want to try biofeedback but have been on a waiting list for six months only to discover I was never on it. Really desperate now so I want to go private. Does anyone know where I can access it in Devon. If not Kent
JeanyB
in
IBS Network
5 years ago
My experience of the Mirena IUD and Mirena Crash - please read if you are considering having the coil, or are about to have it removed
I was pushed into having the Mirena by my consultant around the time I was first getting my diagnosis of stage 4 endometriosis, adenomyosis and interstitial
cystitis
.
I was pushed into having the Mirena by my consultant around the time I was first getting my diagnosis of stage 4 endometriosis, adenomyosis and interstitial
cystitis
.
Catness
in
Endometriosis UK
5 years ago
Proctalgia levator Ani
Hi all my name is Tommy, and I have proctalgia levator ani. In schumer's to get the botox shot, and would like to hear some experiences you've all had with it. Kindly yours, Tommy
Hi all my name is Tommy, and I have proctalgia levator ani. In schumer's to get the botox shot, and would like to hear some experiences you've all had with it. Kindly yours, Tommy
Trueballew
in
Pelvic Pain Support Network
5 years ago
Vulvodynia
Hi everyone, I've been suffering from vulvodynia for about 2.5 years now, which is the same length as my relationship so we've only experienced pain-free sex once. When it started, I thought I was getting a UTI because I hadn't that long ago been stuck in a cycle of UTIs, antibiotics, and thrush. However
Hi everyone, I've been suffering from vulvodynia for about 2.5 years now, which is the same length as my relationship so we've only experienced pain-free sex once. When it started, I thought I was getting a UTI because I hadn't that long ago been stuck in a cycle of UTIs, antibiotics, and thrush. However
Herbs2
in
Pelvic Pain Support Network
5 years ago
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