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Wednesday The 14th.
I promised a painting for the 14 and being a heart shape canvas I could not use the easel. I ruined the picture with my sleeve going in paint on palate and it got onto painting - Ruined. I have done one not as good by painting the canvas black, and painted a picture ok for black canvas, Could not
I promised a painting for the 14 and being a heart shape canvas I could not use the easel. I ruined the picture with my sleeve going in paint on palate and it got onto painting - Ruined. I have done one not as good by painting the canvas black, and painted a picture ok for black canvas, Could not
Ern007
in
Lung Conditions Community Forum
3 months ago
Elmiron making nocturia worse?
Hello everyone, I have been prescribed Elmiron for Bladder Pain Syndrome as my cystoscopy showed glomurations and water fall bleeding. I've only been on it for 4 days and I'm now getting up every hour rather than 3 times a night. I'm so tired, I have a lot of other chronic pain conditions and 2 young
Hello everyone, I have been prescribed Elmiron for Bladder Pain Syndrome as my cystoscopy showed glomurations and water fall bleeding. I've only been on it for 4 days and I'm now getting up every hour rather than 3 times a night. I'm so tired, I have a lot of other chronic pain conditions and 2 young
Cat00
in
Bladder Health UK
5 months ago
Oncolytic Virotherapy Platform Designed to Target All Tumor Sites: we will have some news soon, oncolytics are very promising (CLD-201)
– Preclinical models have demonstrated the ability to resist oncolytic virus inactivation by human serum and target diverse tumor types – Novel therapeutic approach allows for ease of administration, increased cost-effectiveness, and the ability to reach a broad patient population Enough for me to
– Preclinical models have demonstrated the ability to resist oncolytic virus inactivation by human serum and target diverse tumor types – Novel therapeutic approach allows for ease of administration, increased cost-effectiveness, and the ability to reach a broad patient population Enough for me to
Maxone73
in
Advanced Prostate Cancer
3 months ago
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Yellowish skin,
Hi,i have yellows.skin for 3 years.now but my liver test come back normal,i had a really high.consume alcohol,i look yellowish but with.normal bilirubin test,i have take.billirubin test seven times now,all normal,albumin normal,inr,normal,alt normal,what can it be?
Hi,i have yellows.skin for 3 years.now but my liver test come back normal,i had a really high.consume alcohol,i look yellowish but with.normal bilirubin test,i have take.billirubin test seven times now,all normal,albumin normal,inr,normal,alt normal,what can it be?
Okki49
in
British Liver Trust
5 months ago
Advice if possible
Hi, Apologies in advance for the long story but I have been so worried about this and am hoping there may be someone on here with similar experience who may be able to reassure me. I am a 65 year old female. I rarely drink alcohol, am only 5 lbs into the overweight bracket, do some form of exercise
Hi, Apologies in advance for the long story but I have been so worried about this and am hoping there may be someone on here with similar experience who may be able to reassure me. I am a 65 year old female. I rarely drink alcohol, am only 5 lbs into the overweight bracket, do some form of exercise
Husband2022
in
British Liver Trust
1 year ago
Prednisolone and Omeprazole
I have had PMR and GCA for 7 Years and was told I had to take 10 mg daily of Omeprazole which I have been on for the 7 Years. I am now on 3mg steroids but have been getting a lot of tummy upsets and wondered if the long term use of Omeprazole is causing it. I have gone Lactose and Gluten free as well
I have had PMR and GCA for 7 Years and was told I had to take 10 mg daily of Omeprazole which I have been on for the 7 Years. I am now on 3mg steroids but have been getting a lot of tummy upsets and wondered if the long term use of Omeprazole is causing it. I have gone Lactose and Gluten free as well
Sorop
in
PMRGCAuk
10 months ago
Positive Cologuard
63 years old, never had colonoscopy and now feel I’m gonna pay the price. No cancer in family (yet), was having no symptoms, went with Cologuard which came back positive in June. Right after that developed extreme stress and anxiety due to mother passing and trouble in family. Then the next week symptoms
63 years old, never had colonoscopy and now feel I’m gonna pay the price. No cancer in family (yet), was having no symptoms, went with Cologuard which came back positive in June. Right after that developed extreme stress and anxiety due to mother passing and trouble in family. Then the next week symptoms
james3389
in
Colon Cancer Connected
10 months ago
New and struggling to cope.
This is going to be a bit of a muddle to read as I am struggling to concentrate. About 3-4 weeks I started to get a 'clicking' in my left ear but only in response to certain sounds happening around me, running a tap for example would trigger it. As soon as the external noise stopped so did the clicking
This is going to be a bit of a muddle to read as I am struggling to concentrate. About 3-4 weeks I started to get a 'clicking' in my left ear but only in response to certain sounds happening around me, running a tap for example would trigger it. As soon as the external noise stopped so did the clicking
Randy101
in
Tinnitus UK
5 months ago
Pain relief for endo nightmare!
My very first time to ever post anything, anywhere so I hope I do it correctly! I had surgery 10 months ago for stage IV endometriosis (my ovaries were engulfed with big cysts & various sites scattered around pelvis). Unfortunately symptoms are back already and I'm truly suffering 😢 DESPERATE bloating
My very first time to ever post anything, anywhere so I hope I do it correctly! I had surgery 10 months ago for stage IV endometriosis (my ovaries were engulfed with big cysts & various sites scattered around pelvis). Unfortunately symptoms are back already and I'm truly suffering 😢 DESPERATE bloating
Roellen
in
Endometriosis UK
10 months ago
Mixed thyroid drugs🤷♀️
Hi everyone ❤️ As many on here will know I'm lactose intolerant and have colitis, I've been on ROMA for around 21 wks started on 10mg now built up to 25mg (20mg morning, 5mg evening) but I've had to spread this out to 10mg morning, 10 mg afternoon, 5mg evening as the bowle /stomach issues are still affecting
Hi everyone ❤️ As many on here will know I'm lactose intolerant and have colitis, I've been on ROMA for around 21 wks started on 10mg now built up to 25mg (20mg morning, 5mg evening) but I've had to spread this out to 10mg morning, 10 mg afternoon, 5mg evening as the bowle /stomach issues are still affecting
birkie
in
Thyroid UK
10 months ago
Sinemet Plus 25mg/100mg tablets Side effects?
My brother takes Sinemet plus 25mg/100mg tablets - One and a half tablets at 8am, 11am, 2pm, 5pm and 8pm. Half Sinemet CR 25mg/100mg tablets - one taken at bedtime. I have noticed after taking Sinemet plus he is unable to get out of chair or bed for up to an hour, dizziness and sleepiness. His vision
My brother takes Sinemet plus 25mg/100mg tablets - One and a half tablets at 8am, 11am, 2pm, 5pm and 8pm. Half Sinemet CR 25mg/100mg tablets - one taken at bedtime. I have noticed after taking Sinemet plus he is unable to get out of chair or bed for up to an hour, dizziness and sleepiness. His vision
Sarah106
in
Cure Parkinson's
5 months ago
Gina cmb
I have suffered with severe RLS for over 30 years. At first with no sign of treatment I used strong pain meds which I regularly took too much of just trying to calm my legs down enough to sleep, that didn’t work. In 2005 I saw a right up in a Sunday news paper about a treatment called adartrel, this
I have suffered with severe RLS for over 30 years. At first with no sign of treatment I used strong pain meds which I regularly took too much of just trying to calm my legs down enough to sleep, that didn’t work. In 2005 I saw a right up in a Sunday news paper about a treatment called adartrel, this
Geniemb
in
Restless Legs Syndrome
8 months ago
Needing some suggestions to sitting for hours in hospital
I am 26 and on warfarin for a mechanical aortic valve inserted in April 23. I need to be tested very regularly, normally every 2 weeks atleast. It must be a blood test as the pin prick tests proved unreliable in my case. I spend hours and hours waiting at St Barts for a blood test which is where I am
I am 26 and on warfarin for a mechanical aortic valve inserted in April 23. I need to be tested very regularly, normally every 2 weeks atleast. It must be a blood test as the pin prick tests proved unreliable in my case. I spend hours and hours waiting at St Barts for a blood test which is where I am
Pefki
in
Anticoagulation Support
5 months ago
Possible lung metastasis
hi everyone I am 10 years just gone since the start of my journey, usual operation and chemo in 2014. then recurrence in the bowel in 2018 with resection and further chemo. I now have a single lung lesion noticed in March last year. Its now grown from 6mm in October to 9mm now. I have been told that
hi everyone I am 10 years just gone since the start of my journey, usual operation and chemo in 2014. then recurrence in the bowel in 2018 with resection and further chemo. I now have a single lung lesion noticed in March last year. Its now grown from 6mm in October to 9mm now. I have been told that
Bettyxxx
in
My Ovacome
3 months ago
Haemorrhagic colitis
Has anyone else been diagnosed with Haemorrhagic colitis, or heard about haemorrhagic colitis. This was diagnosed following a colonoscopy where they found 3 sites x 3cms and treated it with argon cautherisation under general anaesthetic (although they keep telling me it was not ga). I also have endometriosis
Has anyone else been diagnosed with Haemorrhagic colitis, or heard about haemorrhagic colitis. This was diagnosed following a colonoscopy where they found 3 sites x 3cms and treated it with argon cautherisation under general anaesthetic (although they keep telling me it was not ga). I also have endometriosis
Anastasia17
in
Crohn's and Colitis Support
10 months ago
Boron, an interesting article about supplement for T3 increase
Found this article which I found interesting as a possible supplement to assist with T3 may consider after next blood test if no improvement. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712861/?fbclid=IwAR3dMJ-9rLLZ47g1qBU4LbMViJROk8gIbRNhijGMMW3giwHjVbsY06Huppk
Found this article which I found interesting as a possible supplement to assist with T3 may consider after next blood test if no improvement. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712861/?fbclid=IwAR3dMJ-9rLLZ47g1qBU4LbMViJROk8gIbRNhijGMMW3giwHjVbsY06Huppk
Humphre
in
Thyroid UK
5 months ago
Trying to make the most of being chronically ill and unemployed 💕
✨ Just some ideas on how to make the most of something that sucks and can be very isolating and lonely ✨ *depending on what you can do that day x • Quality time with loved ones • Getting a new pet or spending more quality time with yours. • Developing a self care routine • Free adult learning courses
✨ Just some ideas on how to make the most of something that sucks and can be very isolating and lonely ✨ *depending on what you can do that day x • Quality time with loved ones • Getting a new pet or spending more quality time with yours. • Developing a self care routine • Free adult learning courses
x_emily_x
in
Endometriosis UK
5 months ago
being redundant
I have an amazing ability to pick relevant podcasts while driving. Just had my blood work done in preparation of starting Pluvicto and not being able to choose wisely while driving I picked this podcast which i have heard before and have even advocated on this forum before. Dr Chetty is so brilliant
I have an amazing ability to pick relevant podcasts while driving. Just had my blood work done in preparation of starting Pluvicto and not being able to choose wisely while driving I picked this podcast which i have heard before and have even advocated on this forum before. Dr Chetty is so brilliant
spencoid2
in
Advanced Prostate Cancer
5 months ago
Recommendations for a rheumatologist in Merseyside area please.
I was 65 in August, about six to eight weeks ago I started having really painful hips, fatigued, night sweats, eye and temple pains. I have mild lupus (remission) so was discharged by my rheumatologist in January 21 My GP recently did some bloods. ESR 10 He told me to contact rheumatology department
I was 65 in August, about six to eight weeks ago I started having really painful hips, fatigued, night sweats, eye and temple pains. I have mild lupus (remission) so was discharged by my rheumatologist in January 21 My GP recently did some bloods. ESR 10 He told me to contact rheumatology department
Pennypip
in
PMRGCAuk
5 months ago
I'm back....!
Bricking it now....thoracoscopy due on Thursday morning and I'm terrified....has anyone here had it done? I just hate pain of any sort even though I know I'll have sedation - Fentanyl and Midazolam -I'm still really, really panicking....😒🙄
Bricking it now....thoracoscopy due on Thursday morning and I'm terrified....has anyone here had it done? I just hate pain of any sort even though I know I'll have sedation - Fentanyl and Midazolam -I'm still really, really panicking....😒🙄
sue32
in
Lung Conditions Community Forum
5 months ago
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