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Brain metastasis on Ovarian Cancer
Hello everyone, I'm writing this post on behalf of my mother. My mother, aged 48, was diagnosed with OC back in Feb '21. Since then, she has undergone several surgeries and chemotherapy rounds. I know everyone here has either faced these challenges or witnessed a loved one going through them, so you
Hello everyone, I'm writing this post on behalf of my mother. My mother, aged 48, was diagnosed with OC back in Feb '21. Since then, she has undergone several surgeries and chemotherapy rounds. I know everyone here has either faced these challenges or witnessed a loved one going through them, so you
selosh16
in
My Ovacome
8 months ago
Hi, im on lercanidipine and olmesartan, does anyone get bone pain with these? My .
Hi, im on lercanidipine and olmesartan, i was on irbesartan alone with no side effects for years but had to come off them as they were getting discontinued.does anyone get bone pan with these? I can barely put my arms behind my back.
Hi, im on lercanidipine and olmesartan, i was on irbesartan alone with no side effects for years but had to come off them as they were getting discontinued.does anyone get bone pan with these? I can barely put my arms behind my back.
Nannyvee
in
High Blood Pressure Support
8 months ago
CT Angio Test Results
First off, I’m so grateful for this forum and those listen to us and advise and support all of us on this unwanted journey we are on. I got the results of my chest, abdominal, and pelvis CT scan today. Chest: Ascending and descending aorta normal. Everything else normal. Abdominal Aorta: “No significant
First off, I’m so grateful for this forum and those listen to us and advise and support all of us on this unwanted journey we are on. I got the results of my chest, abdominal, and pelvis CT scan today. Chest: Ascending and descending aorta normal. Everything else normal. Abdominal Aorta: “No significant
Lenore58
in
PMRGCAuk
8 months ago
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Two questions concerning RLS
1.For the past few months l have had horrendous bladder pain and l can no longer cope with that and the RLS. I am making an appointment to see my GP who knows nothing about RLS so l need some advice about treatment for the bladder pain which won’t worsen the RL S. l would be very grateful if anyone knows
1.For the past few months l have had horrendous bladder pain and l can no longer cope with that and the RLS. I am making an appointment to see my GP who knows nothing about RLS so l need some advice about treatment for the bladder pain which won’t worsen the RL S. l would be very grateful if anyone knows
bedith6
in
Restless Legs Syndrome
8 months ago
Dizziness
Sorry to ask another question, as you know I've seen ENT Consultant, had CT angiogram Aortic Arch, Carotid arteries and Intracranial, 2 weeks ago. Not heard anything back - my results don't get posted on my NHS account although my Hubs can access all his so I am going to ring tomorrow and try to get
Sorry to ask another question, as you know I've seen ENT Consultant, had CT angiogram Aortic Arch, Carotid arteries and Intracranial, 2 weeks ago. Not heard anything back - my results don't get posted on my NHS account although my Hubs can access all his so I am going to ring tomorrow and try to get
hollyrain
in
Tinnitus UK
8 months ago
Not sure what to do next
Hello. I suddenly developed loud tinnitus in my left ear 3 months ago and went to the doctors. It's a very high pitched ringing and varies between loud and very loud and sometimes has different pitches all at once like an orchestra. It's constant, 24/7. I'd had a very slight ringing for several months
Hello. I suddenly developed loud tinnitus in my left ear 3 months ago and went to the doctors. It's a very high pitched ringing and varies between loud and very loud and sometimes has different pitches all at once like an orchestra. It's constant, 24/7. I'd had a very slight ringing for several months
Sootymouse
in
Acoustic Neuroma Support
8 months ago
Aortitis
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
Dance62
in
PMRGCAuk
6 months ago
Can’t sleep
I was diagnosed in May of this year.. Started with double vision. I also have seizures, mostly controlled. I can’t sleep hardly at all. Tried several meds, nothing. Very frustrating. I get maybe 3, maybe 4 hours if lucky. There have been some nights I haven’t slept at all? Anyone else have
I was diagnosed in May of this year.. Started with double vision. I also have seizures, mostly controlled. I can’t sleep hardly at all. Tried several meds, nothing. Very frustrating. I get maybe 3, maybe 4 hours if lucky. There have been some nights I haven’t slept at all? Anyone else have
Cinjav
in
PSP Association
8 months ago
Laxido and acid reflux
I swear every time I take this stuff I end up with really bad regurgitation and heartburn. Coincidence? I am on other medications.
I swear every time I take this stuff I end up with really bad regurgitation and heartburn. Coincidence? I am on other medications.
Spaceboy_60
in
IBS Network
8 months ago
Colonoscopy
hello everyone😊 I wrote on here about 2 weeks ago for some advice in regards to a colonoscopy, I wanted to update you on my progress so that anyone who may be feeling afraid or anxious about this process can hopefully take something from this Today I had my colonoscopy, terrified and lost count of
hello everyone😊 I wrote on here about 2 weeks ago for some advice in regards to a colonoscopy, I wanted to update you on my progress so that anyone who may be feeling afraid or anxious about this process can hopefully take something from this Today I had my colonoscopy, terrified and lost count of
Purplecake97
in
Colon Cancer Connected
5 hours ago
Famotidine as a substitute for Omeprazole?
Hello friends, Has anyone been prescribed Famotidine to replace Omeprazole? I’ve been experiencing gut issues for several months now and my gp has suggested a change in H2 antagonist to see if the frequency symptoms resolve. The list of potential side effects on the PIL don’t inspire me to make the
Hello friends, Has anyone been prescribed Famotidine to replace Omeprazole? I’ve been experiencing gut issues for several months now and my gp has suggested a change in H2 antagonist to see if the frequency symptoms resolve. The list of potential side effects on the PIL don’t inspire me to make the
Heron82
in
PMRGCAuk
1 day ago
peptic ulcers?
Hi everyone, I recently posted that I’m due a colonoscopy after having a qfit result of >200 with visible blood on my stool, this symptom comes and goes (months between each time) I have discovered today that Ulcers run in my family, on my mums side my great grandad had a duodenal ulcer, my nan had
Hi everyone, I recently posted that I’m due a colonoscopy after having a qfit result of >200 with visible blood on my stool, this symptom comes and goes (months between each time) I have discovered today that Ulcers run in my family, on my mums side my great grandad had a duodenal ulcer, my nan had
Purplecake97
in
Colon Cancer Connected
1 day ago
Update
Hi everyone, I’m on a steroid taper of 10/5 daily so will be on 5 mg when I start Mycophenolate on 20th of this month, I’m starting on a low dose gradually increasing. Hopefully this will take away the inflammation and remove bilateral pleural effusion’s and pericardial effusion caused by Serositis as
Hi everyone, I’m on a steroid taper of 10/5 daily so will be on 5 mg when I start Mycophenolate on 20th of this month, I’m starting on a low dose gradually increasing. Hopefully this will take away the inflammation and remove bilateral pleural effusion’s and pericardial effusion caused by Serositis as
Numptybrain
in
PMRGCAuk
2 days ago
ongoing chronic constipation.. ‘opioid bowel & interstitial cystitis… test results!
following months of waiting I eventually paid to see a private bowel surgeon. Worth every penny. She organised tests through NHS. Won’t bore with details- but I have a dysfunctional opioid bowel ( due to severe back problems). A large rectocele & possibly a cystocele I’m having a transit study…
following months of waiting I eventually paid to see a private bowel surgeon. Worth every penny. She organised tests through NHS. Won’t bore with details- but I have a dysfunctional opioid bowel ( due to severe back problems). A large rectocele & possibly a cystocele I’m having a transit study…
Beakybird58
in
IBS Network
2 days ago
Diverticular disease
hi all Been having abdominal pains since January. Had the fight of my life with gps to get any thing done first visit gp told me it was ibs and he had seen worse. Any way prescription for mebeverine and off I went. All was well for about 3 days then the pain was back but 1000 times worse couldn’t
hi all Been having abdominal pains since January. Had the fight of my life with gps to get any thing done first visit gp told me it was ibs and he had seen worse. Any way prescription for mebeverine and off I went. All was well for about 3 days then the pain was back but 1000 times worse couldn’t
Mrdd
in
Bowel Disease Support
3 days ago
IBS D
having real problems at the minute bad flare up having to get up through the night multiple times loose just like water bad cramps thought i had appendicitis.Been to Gastro said ibs no weight loss and 3 normal FITS really got a grip this time so fed up taking Alverine 120mg any suggestions would be appreciated
having real problems at the minute bad flare up having to get up through the night multiple times loose just like water bad cramps thought i had appendicitis.Been to Gastro said ibs no weight loss and 3 normal FITS really got a grip this time so fed up taking Alverine 120mg any suggestions would be appreciated
Harold2
in
IBS Network
4 days ago
Ferrocalm
I started taking Ferrocalm about 18 weeks ago and suffered adjustment symptoms from day 1 which still persist. I have had severe intractable iBS-C for 10 years which has not responded to all allopathic treatments including Amitriptyline which didn’t work at 100mg at night! I was fully investigated
I started taking Ferrocalm about 18 weeks ago and suffered adjustment symptoms from day 1 which still persist. I have had severe intractable iBS-C for 10 years which has not responded to all allopathic treatments including Amitriptyline which didn’t work at 100mg at night! I was fully investigated
Pangea56
in
IBS Network
4 days ago
Considering orchiectomy due to chronic constipation from Orgovyx
I've been on Orgovyx for 33 months for metastatic prostate cancer. Constipation is a known issue with Orgovyx and it has affected me to some degree most of the 33 months. Earlier this year it seem to get more chronic and intractable. I'm also currently using a 37.5mg weekly E2 patch, up from 0.025 twice
I've been on Orgovyx for 33 months for metastatic prostate cancer. Constipation is a known issue with Orgovyx and it has affected me to some degree most of the 33 months. Earlier this year it seem to get more chronic and intractable. I'm also currently using a 37.5mg weekly E2 patch, up from 0.025 twice
NewPotatoCaboose
in
Advanced Prostate Cancer
4 days ago
Am I being blasé about stomach protectors whilst on Pred?
I have had PMR for 3 and a half years and generally feel lucky that I am not feeling as bad or fatigued as many on this forum. I am certainly not as fit as I was but age has a part to play. I am 75 and used to be able to do big hikes, Zumba and so on but can still walk 4 to 5 miles and have just moved
I have had PMR for 3 and a half years and generally feel lucky that I am not feeling as bad or fatigued as many on this forum. I am certainly not as fit as I was but age has a part to play. I am 75 and used to be able to do big hikes, Zumba and so on but can still walk 4 to 5 miles and have just moved
Stargiver
in
PMRGCAuk
5 days ago
Could this be IBS-C or slow transit?
I'm 79 and suffered with constipation on and off for more than 10 years and got to the stage where I only have a movement by using bisacodyl, nothing else works for me, I take 3 every 5days, which clears me out I feel well, appetite is good and have not lost any weight. Had FIT and blood tests both
I'm 79 and suffered with constipation on and off for more than 10 years and got to the stage where I only have a movement by using bisacodyl, nothing else works for me, I take 3 every 5days, which clears me out I feel well, appetite is good and have not lost any weight. Had FIT and blood tests both
Bazh
in
IBS Network
8 days ago
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