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COVID-19 Infection effect on Urinary Incontinence and Mirabegron.
Dear Simon Foundation, I'm an old member of HU as a CLL type Leukaemia patient in the UK, but only just discovered your Simon foundation. Now I've always had poor bladder control and that could be due to bladder sensitivity, BPH, or damaged nerves in my lower back or all three, or more. I've gone through
Dear Simon Foundation, I'm an old member of HU as a CLL type Leukaemia patient in the UK, but only just discovered your Simon foundation. Now I've always had poor bladder control and that could be due to bladder sensitivity, BPH, or damaged nerves in my lower back or all three, or more. I've gone through
Ernest2
in
The Simon Foundation for Continence
11 months ago
Overactive Bladder Syndrome
Bit strange to post this here but bear with me please. It seems that many of the med's for OAB have a side effect of high heart rate. I've been diagnosed with Paroxysmal Tachycardia and am trying Tolterodine for my OAB (which increased my comfort level considerably) but have had to stop as my monthly
Bit strange to post this here but bear with me please. It seems that many of the med's for OAB have a side effect of high heart rate. I've been diagnosed with Paroxysmal Tachycardia and am trying Tolterodine for my OAB (which increased my comfort level considerably) but have had to stop as my monthly
Oggy99
in
AF Association
1 year ago
Shingles vaccination - or not?
Hi all, hope to get some helpful advice on subject of shingles vaccination. Shingrix is available in my country (Norway) so I enquired of my GP about any recommendation in the light of my long-term polymyalgia (7+ years, maintained on 2.5 mg daily pred for about a year but unbelievably resistant to even
Hi all, hope to get some helpful advice on subject of shingles vaccination. Shingrix is available in my country (Norway) so I enquired of my GP about any recommendation in the light of my long-term polymyalgia (7+ years, maintained on 2.5 mg daily pred for about a year but unbelievably resistant to even
11541stella
in
PMRGCAuk
1 year ago
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self funded NHS route vs private clinics: pros & cons ?; quality of treatment, costs & Time
Hi, I'm pretty new to the process and would appreciate all the advice I can get. I reached out to an NHS clinic in my area Dec 23 for a fertility check for my husband and I, first appointment was in Jan and we didn't get results/follow up consultation until march. the consultant mentioned my husband
Hi, I'm pretty new to the process and would appreciate all the advice I can get. I reached out to an NHS clinic in my area Dec 23 for a fertility check for my husband and I, first appointment was in Jan and we didn't get results/follow up consultation until march. the consultant mentioned my husband
Grateful_heart
in
Fertility Network UK
4 months ago
Otomize ear spray
HiI have an outer ear infection in both ears and I've been prescribed Otomize ear spray but it's making me feel really sick when I use it, has anyone else had this experience? I don't know if it's helping my tinnitus as I only started taking it yesterday afternoon. I'm currently using a hot water bottle
HiI have an outer ear infection in both ears and I've been prescribed Otomize ear spray but it's making me feel really sick when I use it, has anyone else had this experience? I don't know if it's helping my tinnitus as I only started taking it yesterday afternoon. I'm currently using a hot water bottle
Coxy00
in
Tinnitus UK
1 year ago
Scared my AFib will come back due to very nasty cough.
i had an Ablation in September and have developed this horrendous cough, that’s causing me to nearly throw up. My AFib started in 2014, when I had a nasty coughing virus, so I’m scared this coughing virus will bring it back. This one seems much worse. Has anyone else had this horrible cough. ? Any tips
i had an Ablation in September and have developed this horrendous cough, that’s causing me to nearly throw up. My AFib started in 2014, when I had a nasty coughing virus, so I’m scared this coughing virus will bring it back. This one seems much worse. Has anyone else had this horrible cough. ? Any tips
Sixtychick
in
Atrial Fibrillation Support
8 months ago
independent fertility advice any suggestions?
Hi everyone, Hope you’re all ok. We have just completed our second round of IVF ICSI which was unsuccessful. Our clinic is advising that we just do the same again. I don’t think that’s the best option as we’ve done the same protocol twice and hasn’t been successful. I want to speak to a specialist who
Hi everyone, Hope you’re all ok. We have just completed our second round of IVF ICSI which was unsuccessful. Our clinic is advising that we just do the same again. I don’t think that’s the best option as we’ve done the same protocol twice and hasn’t been successful. I want to speak to a specialist who
Seapark100
in
Infertility Support
4 months ago
Covid vax and AFIB
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
Awksom
in
CLL Support
11 months ago
Pregnant with untested embryo/blastocyst, gives me a lot of anxiety
Hi ladies, It is me again... Long story short, I am 9 week pregnant after multiple failed IVFs and years of trying to conceive (I am turning 40 years old next month). I find this journey extremely nerve wrecking and stressful, it never gets easy, every milestone a new worry comes up. So new concern
Hi ladies, It is me again... Long story short, I am 9 week pregnant after multiple failed IVFs and years of trying to conceive (I am turning 40 years old next month). I find this journey extremely nerve wrecking and stressful, it never gets easy, every milestone a new worry comes up. So new concern
Casperjourney
in
Fertility Network UK
4 months ago
Recurrent implantation failure - please give me hope
Hello my lovely support team. I'll try and keep this rotten history of mine very very brief.......43 years old, all embryos created between 40-42. Trying since I was 36. Just one natural chemical at 41yo. So far, 5 failed transfers of 6 good-decent embryos. All bfn, no chemicals or anything else. 4 collections
Hello my lovely support team. I'll try and keep this rotten history of mine very very brief.......43 years old, all embryos created between 40-42. Trying since I was 36. Just one natural chemical at 41yo. So far, 5 failed transfers of 6 good-decent embryos. All bfn, no chemicals or anything else. 4 collections
Joeysjourney
in
Fertility Network UK
4 months ago
Hanging on
Remarkably mum is still hanging on through sheer grit we think.She's very weak and frail, had another couple of falls. Been in hospital with pneumonia before xmas and had pneumonia again 2 weeks ago. The care home are great but the frustration is the loss of speech for over 2 years now, no way to communicate
Remarkably mum is still hanging on through sheer grit we think.She's very weak and frail, had another couple of falls. Been in hospital with pneumonia before xmas and had pneumonia again 2 weeks ago. The care home are great but the frustration is the loss of speech for over 2 years now, no way to communicate
MRSYafffle
in
PSP Association
8 months ago
Preparing for 2nd cycle
We have just had our first cycle of IVF/ICSI. Unfortunately this failed with a chemical pregnancy and did not get any frosties. We will have our review appointment with the consultant in due course. The nurse has said it will be 6 months before we can try again. Is this a standardised time scale or clinic
We have just had our first cycle of IVF/ICSI. Unfortunately this failed with a chemical pregnancy and did not get any frosties. We will have our review appointment with the consultant in due course. The nurse has said it will be 6 months before we can try again. Is this a standardised time scale or clinic
LittlePea23
in
Fertility Network UK
4 months ago
update on rls treatment
Gp has put me on 20mg Norspan patches and I am having acupunture and reflexology as well. Shumbah has suggested applying the sesame oil on troublesome leg....I have started that and will keep you informed....I have only been doing it for a week, but I think it is having some effect. The tugging, pulling
Gp has put me on 20mg Norspan patches and I am having acupunture and reflexology as well. Shumbah has suggested applying the sesame oil on troublesome leg....I have started that and will keep you informed....I have only been doing it for a week, but I think it is having some effect. The tugging, pulling
Hidden
in
Restless Legs Syndrome
1 year ago
Anti viral?
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Vqueen
in
Vasculitis UK
11 months ago
My story
Hi, it all started by going into hospital for day surgery for Hemorrhoids. Within 36 hours my wife had taken me back to A & E with a high heart rate and low blood pressure. I was also in a lot of pain, which I put down to the surgery for Hemorrhoids. I was soon in majors and within a few hours I was
Hi, it all started by going into hospital for day surgery for Hemorrhoids. Within 36 hours my wife had taken me back to A & E with a high heart rate and low blood pressure. I was also in a lot of pain, which I put down to the surgery for Hemorrhoids. I was soon in majors and within a few hours I was
Hikingman
in
ICUsteps
1 year ago
Greater use of Benlysta, Saphnelo seen in US, EU to treat lupus
Goal to reduce long-term glucocorticoids use to prevent side effects
In both the U.S. and Europe, clinicians want to limit treatment with glucocorticoids — steroid hormones whose long-term use for autoimmune diseases is tied to serious side effects — among people with moderate to severe lupus
Goal to reduce long-term glucocorticoids use to prevent side effects
In both the U.S. and Europe, clinicians want to limit treatment with glucocorticoids — steroid hormones whose long-term use for autoimmune diseases is tied to serious side effects — among people with moderate to severe lupus
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 year ago
Thoughts on Lignosus
Hello, I have just been in hospital for a week with a bad case of pneumonia, which came out of nowhere. I am only 44 and have no history of respiratory problems. The CT scan also showed mild bronchiectasis, which I am now finding out lots more about thanks to forums like this.I am now being bombarded
Hello, I have just been in hospital for a week with a bad case of pneumonia, which came out of nowhere. I am only 44 and have no history of respiratory problems. The CT scan also showed mild bronchiectasis, which I am now finding out lots more about thanks to forums like this.I am now being bombarded
PuzzlePuff
in
Lung Conditions Community Forum
8 months ago
Home now
Hi I would like to share what I've encountered the last 6 months and would love some feedback from anyone I fell ill back in late June 23 It seemed like a cold or flu coming on which turned into pneumonia in both lungs followed by a anti resistant bacterial infection baumanni that led to ards sepsis
Hi I would like to share what I've encountered the last 6 months and would love some feedback from anyone I fell ill back in late June 23 It seemed like a cold or flu coming on which turned into pneumonia in both lungs followed by a anti resistant bacterial infection baumanni that led to ards sepsis
Gl76
in
ICUsteps
8 months ago
mixing meds
if my husband and i have a cold--virus temperature we take lemsips xxx
if my husband and i have a cold--virus temperature we take lemsips xxx
Tut7iFru7i
in
AF Association
8 months ago
Sharing my experience of having the flu with Parkinson's...
Hi everyone. I just wanted to share my experience of combining a severe flu with my Parkinson's symptoms. I've had Parkinson's for six years and I'm generally doing relatively well. But recently, I caught a severe flu while traveling in Italy with my wife and it made my symptoms much worse, with massive
Hi everyone. I just wanted to share my experience of combining a severe flu with my Parkinson's symptoms. I've had Parkinson's for six years and I'm generally doing relatively well. But recently, I caught a severe flu while traveling in Italy with my wife and it made my symptoms much worse, with massive
Michel0220
in
Cure Parkinson's
8 months ago
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