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Collapse then AF
Dad has mixed dementia and is 90 in May. He lives alone with my support. He has a history of collapse dating back to the 1990's but only three in all that time. He had a pacemaker in 2017 due to another collapse and found to have some heart block. A year later he had another and this is when we noticed
Dad has mixed dementia and is 90 in May. He lives alone with my support. He has a history of collapse dating back to the 1990's but only three in all that time. He had a pacemaker in 2017 due to another collapse and found to have some heart block. A year later he had another and this is when we noticed
ian16527
in
AF Association
6 months ago
Is it a choice? Pacemaker v Implanted defibrillator?
Hi, it's #chinkoflight here with an update. Things are moving on. I'm in coronary care, and the evidence for my fainting whilst running story has now shown an arrthymia at the time of the fall, effectively stopping my heart functioning, leading to the drop in blood pressure and the syncope event. It's
Hi, it's #chinkoflight here with an update. Things are moving on. I'm in coronary care, and the evidence for my fainting whilst running story has now shown an arrthymia at the time of the fall, effectively stopping my heart functioning, leading to the drop in blood pressure and the syncope event. It's
Chinkoflight
in
Atrial Fibrillation Support
6 months ago
Starting Abiraterone and predniSONE
Tomorrow morning I take my first dose of Abiraterone (Zytiga) and predniSONE for metastatic castrate resistant prostate cancer. I don't know what kind of side effects I would get. I hope I would tolerate the treatment well. Reaching this stage of my cancer I reflect on my 12 year journey with prostate
Tomorrow morning I take my first dose of Abiraterone (Zytiga) and predniSONE for metastatic castrate resistant prostate cancer. I don't know what kind of side effects I would get. I hope I would tolerate the treatment well. Reaching this stage of my cancer I reflect on my 12 year journey with prostate
dac500
in
Advanced Prostate Cancer
8 months ago
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Legal Advice?
Hi All, Although this post is not MS-related, I wanted to reach out to my MSAA Community for their input. Perhaps someone here can point me in the right direction, as I don't really have the money to hire an attorney. Unfortunately, this situation doesn't lend itself to any "free advice and/or attorneys
Hi All, Although this post is not MS-related, I wanted to reach out to my MSAA Community for their input. Perhaps someone here can point me in the right direction, as I don't really have the money to hire an attorney. Unfortunately, this situation doesn't lend itself to any "free advice and/or attorneys
DM0329
in
My MSAA Community
8 months ago
Research Lounge FREE Online Event: Does knowledge of liver scarring affect drinking behaviour?
Does knowing the effects of alcohol on your liver change your drinking?
Researchers have been looking at how people's drinking behaviours may change when they know that alcohol is damaging their liver. They have some interesting and thought-provoking results to share with you on:
Wednesday
Does knowing the effects of alcohol on your liver change your drinking?
Researchers have been looking at how people's drinking behaviours may change when they know that alcohol is damaging their liver. They have some interesting and thought-provoking results to share with you on:
Wednesday
BritishLiverTrust1
Partner
in
British Liver Trust
8 months ago
Multiple mechanisms to clear a-synuclein with natural substances (in mice).
For informational purposes only Alpha Synuclein 1. INTRODUCTION: There are no effective treatments nor drugs available to modify disease progression
For informational purposes only Alpha Synuclein 1. INTRODUCTION: There are no effective treatments nor drugs available to modify disease progression
House2
in
Cure Parkinson's
8 months ago
Scientists have discovered a new cause of Parkinsons disease
https://scitechdaily.com/scientists-have-discovered-a-new-cause-of-parkinsons-disease/ A major discovery sheds light on the underlying mechanisms of Parkinson’s disease, opening the door for novel therapeutic approaches down the line. Until recently, our understanding of Parkinson’s disease has been
https://scitechdaily.com/scientists-have-discovered-a-new-cause-of-parkinsons-disease/ A major discovery sheds light on the underlying mechanisms of Parkinson’s disease, opening the door for novel therapeutic approaches down the line. Until recently, our understanding of Parkinson’s disease has been
NextStage
in
Cure Parkinson's
8 months ago
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
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
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
Persistent AF
Hi everyone, I have been to see my cardiologist today. Had all the usual tests done he asked me how I was feeling I said I felt really well. He then told me I was no longer in Paroxysmal AF and I was in Persistent AF. How can they tell? I have got to have an echocardiogram done and a machine fitted
Hi everyone, I have been to see my cardiologist today. Had all the usual tests done he asked me how I was feeling I said I felt really well. He then told me I was no longer in Paroxysmal AF and I was in Persistent AF. How can they tell? I have got to have an echocardiogram done and a machine fitted
Gillybean123
in
AF Association
6 months ago
Introduction
Hello everyone, I am new to this site so let me introduce myself I live with my husband on the outskirts of Llandudno on the North Wales coast. I am very fortunate that both my children & grandchildren live locally. We have a 2 year old cavapoo who together with our 2 year old grand-twins provide
Hello everyone, I am new to this site so let me introduce myself I live with my husband on the outskirts of Llandudno on the North Wales coast. I am very fortunate that both my children & grandchildren live locally. We have a 2 year old cavapoo who together with our 2 year old grand-twins provide
Ildivolover
in
Scleroderma & Raynaud's UK (SRUK)
2 months ago
Enter our poster competition for World Lupus Day 2024!
This year we're launching a poster competition for our 2024 World Lupus Day campaign. The theme of the poster will be centred around those who have been newly diagnosed with lupus to coincide with the launch of our new information video on World Lupus Day! For more information on what the poster needs
This year we're launching a poster competition for our 2024 World Lupus Day campaign. The theme of the poster will be centred around those who have been newly diagnosed with lupus to coincide with the launch of our new information video on World Lupus Day! For more information on what the poster needs
Debbie_kinsey
Administrator
in
LUPUS UK
6 months ago
Have you visited the Arrhythmia Alliance website?
If you are new to the Forum, or would like updated information relating to a new medication, a scheduled procedure? an information booklet? Make a donation? Register for our monthly patient e-newsletter or simply just find out more about the charity and how we can help you. Our website contains a
If you are new to the Forum, or would like updated information relating to a new medication, a scheduled procedure? an information booklet? Make a donation? Register for our monthly patient e-newsletter or simply just find out more about the charity and how we can help you. Our website contains a
TracyAdmin
Partner
in
Sudden Cardiac Arrest & Heart Attack
6 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
Reminder 'Off Topic'
Good morning everyone, Just a gentle reminder if your topic does not relate directly to Rheumatoid Arthritis please can I ask you to make your post 'Off Topic'. Thank you for your support on the matter. Kind Regards Tim - Head of Services NRAS
Good morning everyone, Just a gentle reminder if your topic does not relate directly to Rheumatoid Arthritis please can I ask you to make your post 'Off Topic'. Thank you for your support on the matter. Kind Regards Tim - Head of Services NRAS
Hidden
in
NRAS
6 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
Abalation Fears
Hi All Today I went and seen my Electrophysiology specialist and have booked in for an ablation in 2 weeks time. I am quite anxious about this whole procedure. He advised me it would be a 70% success rate and mentioned he does not like quoting over this rate. 70% is based on having no more AF episodes
Hi All Today I went and seen my Electrophysiology specialist and have booked in for an ablation in 2 weeks time. I am quite anxious about this whole procedure. He advised me it would be a 70% success rate and mentioned he does not like quoting over this rate. 70% is based on having no more AF episodes
Murphy10
in
Atrial Fibrillation Support
6 months ago
AF and MAD
anyone else have AF and MAD (mitral annular disjunction) . It was picked up during cardiac MRI. The displacement is 5mm, mild mitral valve prolapse and regurgitation. Neither my cardiologist or EP have said anything about it apart from put me on another very long waiting list to see a more specialist
anyone else have AF and MAD (mitral annular disjunction) . It was picked up during cardiac MRI. The displacement is 5mm, mild mitral valve prolapse and regurgitation. Neither my cardiologist or EP have said anything about it apart from put me on another very long waiting list to see a more specialist
LoveRowing
in
Atrial Fibrillation Support
2 months ago
Recommendation for gloves and socks?
Hi Guys, Further to my Post on the Lupus forum (link below) can I ask for recommendations for suitable super warm gloves and socks please? I spent a fortune on some silver lined socks and gloves and found them to be absolutely useless. My M&S bought socks are better than the extortionate silver lined
Hi Guys, Further to my Post on the Lupus forum (link below) can I ask for recommendations for suitable super warm gloves and socks please? I spent a fortune on some silver lined socks and gloves and found them to be absolutely useless. My M&S bought socks are better than the extortionate silver lined
SurferGuy
in
Scleroderma & Raynaud's UK (SRUK)
6 months ago
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