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Heavy legs and low energy feeling
My recent thyroid results showed a below range T3, and I have been having trouble with a brand of thyroxine and feeling generally unwell as previously posted with some helpful advice. But, I have a feeling of heavy legs and low energy and wondered whether when the T3 is low it can cause this? I am
My recent thyroid results showed a below range T3, and I have been having trouble with a brand of thyroxine and feeling generally unwell as previously posted with some helpful advice. But, I have a feeling of heavy legs and low energy and wondered whether when the T3 is low it can cause this? I am
Sailing14
in
Thyroid UK
8 months ago
Not PMR
I have been told that I don't have PMR from my rheumatologist but rheumatoid arthritis so must I leave this invaluable site and find one more suitable for my ailment? If so I will be sorry to miss my family of helpers.
I have been told that I don't have PMR from my rheumatologist but rheumatoid arthritis so must I leave this invaluable site and find one more suitable for my ailment? If so I will be sorry to miss my family of helpers.
Petertaffy
in
PMRGCAuk
5 months ago
new members
I know all too well how overwhelming this diagnosis can be to anyone. All of the emotions that can follow are hard to deal with for sure. If any new member doesn't feel comfortable posting anything here initially, please feel free to send me a message via 'chat'. We have all been exactly where you
I know all too well how overwhelming this diagnosis can be to anyone. All of the emotions that can follow are hard to deal with for sure. If any new member doesn't feel comfortable posting anything here initially, please feel free to send me a message via 'chat'. We have all been exactly where you
DonnaBoll
Administrator
in
PBC Foundation
2 months ago
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travelling as Lupus patient
hi everyone, Been long time since I wrote here. please I will like some advice regarding travelling in Africa. I have been here in Europe for over 15 years and I haven’t been to Africa all this years. Was diagnosed with lupus 2018 in Italy. I wanted to ask for any advice on sun cream and any
hi everyone, Been long time since I wrote here. please I will like some advice regarding travelling in Africa. I have been here in Europe for over 15 years and I haven’t been to Africa all this years. Was diagnosed with lupus 2018 in Italy. I wanted to ask for any advice on sun cream and any
Saralife
in
LUPUS UK
5 months ago
Do you live with advanced liver disease? Are you interested in attending an in-person workshop in Bristol or Liverpool this month?
The British Liver Trust are working with UK CLIF, a dynamic new network of clinicians, patients, carers/relatives and researchers coming together over our shared interest to improve research and clinical outcomes for people with chronic liver failure. Cases of liver disease are rising alarmingly and
The British Liver Trust are working with UK CLIF, a dynamic new network of clinicians, patients, carers/relatives and researchers coming together over our shared interest to improve research and clinical outcomes for people with chronic liver failure. Cases of liver disease are rising alarmingly and
BritishLiverTrust1
Partner
in
British Liver Trust
8 months ago
Ectopic atrial Bradycardia
My last ECG before I saw EP said that Ectopic atrial Bradycardia treatment shad replaced Afib . I have an ablation scheduled end of month and he didn’t say anything about this? Does anyone have the same thing? I had a cardio version Sept and small Afib Nov but way overdue now for an Afib and wondering
My last ECG before I saw EP said that Ectopic atrial Bradycardia treatment shad replaced Afib . I have an ablation scheduled end of month and he didn’t say anything about this? Does anyone have the same thing? I had a cardio version Sept and small Afib Nov but way overdue now for an Afib and wondering
Krissy55
in
Atrial Fibrillation Support
5 months ago
PSMA pet scan negative
My PSA was 0.1 on july 17th and 0.3 on Oct 16th. PSMA scan was done on Nov 7th but was negative. Am I safe to assume there must be some prostate cancer cell present that are not showing up on the scan? I am meeting with my MO at Dana Farber next week Any suggestions moving forward? I appreciate the
My PSA was 0.1 on july 17th and 0.3 on Oct 16th. PSMA scan was done on Nov 7th but was negative. Am I safe to assume there must be some prostate cancer cell present that are not showing up on the scan? I am meeting with my MO at Dana Farber next week Any suggestions moving forward? I appreciate the
Rfs1975
in
Advanced Prostate Cancer
8 months ago
Update on AFIB after Doctor visit
Update from my Electrophylogist Doc. Yesterday. He said since the afib just started and was persistent he wanted to start slowly and start with cardio version. Will be scheduled within next two weeks. Said ekg showed afib with heart rate from 70 to 92 beats per minute. Said afib has no cure but many
Update from my Electrophylogist Doc. Yesterday. He said since the afib just started and was persistent he wanted to start slowly and start with cardio version. Will be scheduled within next two weeks. Said ekg showed afib with heart rate from 70 to 92 beats per minute. Said afib has no cure but many
Stetson
in
AF Association
5 months ago
Xarelto and enoxaprin sodium at the same time
Is there anyone in this community that is taking Xarelto and enoxaprin sodium at the same time. I am looking for an alternative to aspirin and I’m already on enoxaprin sodium. just wanted to know if there’s anyone else in our group who might be taking both
Is there anyone in this community that is taking Xarelto and enoxaprin sodium at the same time. I am looking for an alternative to aspirin and I’m already on enoxaprin sodium. just wanted to know if there’s anyone else in our group who might be taking both
Thick_Blood
in
Hughes Syndrome APS Forum
5 months ago
Behcets + Personal Independence Payment (UK)
I have relatively mild behcets syndrome (frequent mouth ulcers, joint swelling are the main symptoms but there have been periods where i have been unable to walk) Has anyone UK based living with the disease been able to claim
Personal Independence Payment? I'm quite tired of having to pay for my
I have relatively mild behcets syndrome (frequent mouth ulcers, joint swelling are the main symptoms but there have been periods where i have been unable to walk) Has anyone UK based living with the disease been able to claim
Personal Independence Payment? I'm quite tired of having to pay for my
jaquarius
in
Behçet's UK
8 months ago
GCA-Lyme Disease Connection?
Hi all, My wife is a long-time Lyme Disease sufferer, and has recently had a consultation with a biologist/pathologist. This person takes a blood sample and then looks at it under the microscope while the patient is present -- and then comments on what has been seen. My wife had the classic signs
Hi all, My wife is a long-time Lyme Disease sufferer, and has recently had a consultation with a biologist/pathologist. This person takes a blood sample and then looks at it under the microscope while the patient is present -- and then comments on what has been seen. My wife had the classic signs
montebello
in
PMRGCAuk
8 months ago
Nicorandil and AF.
i have periodic AF and on pill in pocket bisoprolol but i take half of a small one daily which keeps the attacks at bay, Blood thinners, Statins lansoprosole. Now as i am getting breathless saw my GP and he is more or less sure he says i have angina too (but not diagnosed by cardio as yet) he has
i have periodic AF and on pill in pocket bisoprolol but i take half of a small one daily which keeps the attacks at bay, Blood thinners, Statins lansoprosole. Now as i am getting breathless saw my GP and he is more or less sure he says i have angina too (but not diagnosed by cardio as yet) he has
Nightmare2
in
AF Association
5 months ago
difference between portal vein thrombosis and portal hypertension?
Good evening. New here. Husband in hospital with liver cirrhosis. Having scope on Monday and we were told today that he has portal vein thrombosis. I understand what that is but I’m confused after doing some research as to the difference between portal vein thrombosis and portal vein hypertension? Or
Good evening. New here. Husband in hospital with liver cirrhosis. Having scope on Monday and we were told today that he has portal vein thrombosis. I understand what that is but I’m confused after doing some research as to the difference between portal vein thrombosis and portal vein hypertension? Or
Lvbv
in
British Liver Trust
5 months ago
CT scan instead of gastroscopy / colonoscopy with all PA tests normal
My Active B12 was just about into the sufficient range. My H Pylorii was negative, as was anti IFAB and coeliac. Homocysteine was fine too. My neurologist’s physical exam was normal ( though the sharp stimulus was a little less sharp on the feet. ) I have been taking sublingual B12 and the tingling
My Active B12 was just about into the sufficient range. My H Pylorii was negative, as was anti IFAB and coeliac. Homocysteine was fine too. My neurologist’s physical exam was normal ( though the sharp stimulus was a little less sharp on the feet. ) I have been taking sublingual B12 and the tingling
Applethorpe
in
Pernicious Anaemia Society
5 months ago
Confused, Don’t know what’s going on!
In my previous posts I mentioned that we booked a private appointment with cardiologist. After mum had a heart monitor for a week, the consultant confirmed that mum’s average heart rate was around 86, and the peak was around 160. The consultant has doubled the dose of bisoprolol so now mum is to take
In my previous posts I mentioned that we booked a private appointment with cardiologist. After mum had a heart monitor for a week, the consultant confirmed that mum’s average heart rate was around 86, and the peak was around 160. The consultant has doubled the dose of bisoprolol so now mum is to take
Nickybhf
in
AF Association
5 months ago
Rheumatology consultant with specialist interest in Lupus
Hello, is anyone in the Humberside/ Lincolnshire area under a n NHS Rheumatologist that has a special interest in SLE. ( Lupus) I have moved house and need to find a new rheumatologist. Many thanks
Hello, is anyone in the Humberside/ Lincolnshire area under a n NHS Rheumatologist that has a special interest in SLE. ( Lupus) I have moved house and need to find a new rheumatologist. Many thanks
Jenfy34
in
LUPUS UK
5 months ago
Shortness of breath and chest pains
Two years after afib started I slipped into persistent afib and had an ablation. 60% of the way through the ablation I developed pericardial effusion and the ablation stopped and a drainage tube was placed in my heart. A couple of weeks later I developed chest pain from an autoimmune reaction called
Two years after afib started I slipped into persistent afib and had an ablation. 60% of the way through the ablation I developed pericardial effusion and the ablation stopped and a drainage tube was placed in my heart. A couple of weeks later I developed chest pain from an autoimmune reaction called
loghousegal
in
AF Association
5 months ago
IBS and Coeliac
I have managed my Coeliac disease since 2009 but last year had a colonoscopy which confirmed my new symptoms were IBS D!! I struggle to know what to eat and feel my quality of life has taken a dive. I have never been someone who gets down but this is seriously effecting my mental health. Two weeks ago
I have managed my Coeliac disease since 2009 but last year had a colonoscopy which confirmed my new symptoms were IBS D!! I struggle to know what to eat and feel my quality of life has taken a dive. I have never been someone who gets down but this is seriously effecting my mental health. Two weeks ago
Mollydav
in
IBS Network
5 months ago
Lexiscan Chemical Stress Test
My EP wants me to have a chemical stress test before he puts me on Flecainide. I have so many problems with Afib and PACs that I’m terrified to have them inject me with something that’s going to make my heart take off. I contacted the doctors office to ask them if I can have the treadmill stress test
My EP wants me to have a chemical stress test before he puts me on Flecainide. I have so many problems with Afib and PACs that I’m terrified to have them inject me with something that’s going to make my heart take off. I contacted the doctors office to ask them if I can have the treadmill stress test
Debjimmay
in
Atrial Fibrillation Support
5 months ago
PSA Rising Dx 06/2022 PSA 864.42 to 01/2023 <0.06 now no longer undetectable, I won’t see DR until next month, What will the Dr do?
Diagnosed 07/01/2022 PSA 942.40 Gleason 8 ductal without large cribform gland / Gleason 9 4+5 after Davinci RP w/ LNR cT3b CN0 cM1b Gleason 8/9 Stage 4 Grade 5 : 4+5=9 Low Volume High Grade ypT3a YPT3a 3 lytic lesions resolved to 1 mild avid lesion Biopsy 15 samples 4 adenocarcinoma
Diagnosed 07/01/2022 PSA 942.40 Gleason 8 ductal without large cribform gland / Gleason 9 4+5 after Davinci RP w/ LNR cT3b CN0 cM1b Gleason 8/9 Stage 4 Grade 5 : 4+5=9 Low Volume High Grade ypT3a YPT3a 3 lytic lesions resolved to 1 mild avid lesion Biopsy 15 samples 4 adenocarcinoma
Shorehousejam
in
Advanced Prostate Cancer
8 months ago
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