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Bisoprolol
Hi Just wondering about my dosage of Bisoprol. When I read related posts on here, most people seem to be on a maximum of 5mg. I’m on 12.5 which I take at night. At my most recent appointment with my cardiologist in March, I asked if it could be reduced as I get so tired on an afternoon and I often have
Hi Just wondering about my dosage of Bisoprol. When I read related posts on here, most people seem to be on a maximum of 5mg. I’m on 12.5 which I take at night. At my most recent appointment with my cardiologist in March, I asked if it could be reduced as I get so tired on an afternoon and I often have
Jonhel
in
Atrial Fibrillation Support
2 months ago
Pulse rate
Since I had stents in my heart two years ago I still have af and are on Bisoporol and clopidogrel. But I'm still suffering dizzy spells and blurred vision when doing anything too stressful.I have a seven day monitor on at the moment but also have smart watch which shows me end of day briefing. It showed
Since I had stents in my heart two years ago I still have af and are on Bisoporol and clopidogrel. But I'm still suffering dizzy spells and blurred vision when doing anything too stressful.I have a seven day monitor on at the moment but also have smart watch which shows me end of day briefing. It showed
Puffnstuff
in
Atrial Fibrillation Support
2 months ago
IBS and chest pain
I have just come out of hospital having been admitted with severe chest pain and pain radiating down my arm. The symptoms all appeared to be a heart attack but my troponin levels came back negative. Drs now think it was oesophageal spasm following an IBS flare up which traveled up my oesophagus causing
I have just come out of hospital having been admitted with severe chest pain and pain radiating down my arm. The symptoms all appeared to be a heart attack but my troponin levels came back negative. Drs now think it was oesophageal spasm following an IBS flare up which traveled up my oesophagus causing
Oatsforme1
in
IBS Network
3 months ago
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wobbly walking
persistent a fib on lopressor. 50 twice a day increased problems with balance and walking any comments
persistent a fib on lopressor. 50 twice a day increased problems with balance and walking any comments
farewelltoarms
in
Atrial Fibrillation Support
3 months ago
Abnormal ECG
So the arrhythmia team contacted me yesterday to discuss the result of my ECG done at my local surgery . Apparently although the test showed an an abnormal pattern with wide QRS it was a minimal deviation and not any form of AF . It could be an age related change but my sinus rhythm was normal and the
So the arrhythmia team contacted me yesterday to discuss the result of my ECG done at my local surgery . Apparently although the test showed an an abnormal pattern with wide QRS it was a minimal deviation and not any form of AF . It could be an age related change but my sinus rhythm was normal and the
Hammerboy
in
Atrial Fibrillation Support
3 months ago
Taste alteration
Hi, Has anyone experienced loss of taste after transplant? My partner says everything tastes absolutely horrendous. Will this come back?!
Hi, Has anyone experienced loss of taste after transplant? My partner says everything tastes absolutely horrendous. Will this come back?!
Gemmax
in
British Liver Trust
7 months ago
Few issues
Hi, ongoing issues, HF (EF 40%), LVSD, AF.Total heart block, 2 lead Pacemaker dependant due to AV node ablation with no rate response, set at 70bpm (HR doesn't go above) had rate response activated but made AF worse so back to 70bpm. Seen consultant yesterday and looking at upgrading PM to CRT (3 lead
Hi, ongoing issues, HF (EF 40%), LVSD, AF.Total heart block, 2 lead Pacemaker dependant due to AV node ablation with no rate response, set at 70bpm (HR doesn't go above) had rate response activated but made AF worse so back to 70bpm. Seen consultant yesterday and looking at upgrading PM to CRT (3 lead
Nomis21
in
Atrial Fibrillation Support
3 months ago
Creatine and Whey protein
I was diagnosed with Parkinson's in July 2020. In the last year I have lost weight by around 3.5 kg I went to a nutritionist because of the weight loss and, in particular, the loss of muscle mass.In addition to a diet and the recommendation to continue going to the gym twice a week for bodybuilding,
I was diagnosed with Parkinson's in July 2020. In the last year I have lost weight by around 3.5 kg I went to a nutritionist because of the weight loss and, in particular, the loss of muscle mass.In addition to a diet and the recommendation to continue going to the gym twice a week for bodybuilding,
Crepe
in
Cure Parkinson's
7 months ago
Ramipril
Briefly, I was prescribed this by my consultant to help with the pumping function/blood flow through my left ventricle. It has definitely helped as shown by a follow echocardiogram, and my consultant pleased. However, I was warned by my GP that it might give me a cough.. and it most certainly has!
Briefly, I was prescribed this by my consultant to help with the pumping function/blood flow through my left ventricle. It has definitely helped as shown by a follow echocardiogram, and my consultant pleased. However, I was warned by my GP that it might give me a cough.. and it most certainly has!
Wightbaby
in
Atrial Fibrillation Support
3 months ago
Now in Persistent Atrial Fibrillation
I was diagnosed with PAF about 23 years ago, and have managed it with medication, at present on 300mg of Flecainide daily, along with Bisoprolol 2.5mg and Apixaban 10mg, For the last 6 months I've been in AF for weeks and then a couple of day I'm in rhythm. I don't want an ablation. Would I receive
I was diagnosed with PAF about 23 years ago, and have managed it with medication, at present on 300mg of Flecainide daily, along with Bisoprolol 2.5mg and Apixaban 10mg, For the last 6 months I've been in AF for weeks and then a couple of day I'm in rhythm. I don't want an ablation. Would I receive
Bee-Honest
in
Atrial Fibrillation Support
3 months ago
delay..
I need to apologize to so many of our newer members. Beginning in this role February 1st, I am still learning. I just found out, being new as the facilitator of this amazing group, how to find the names of the 'new' members..... let me introduce myself to all of you. Hi - and welcome! My name is
I need to apologize to so many of our newer members. Beginning in this role February 1st, I am still learning. I just found out, being new as the facilitator of this amazing group, how to find the names of the 'new' members..... let me introduce myself to all of you. Hi - and welcome! My name is
DonnaBoll
Administrator
in
PBC Foundation
7 months ago
persistent A/F
Hi I have recently been in continuous a/f for 7 weeks with HR of on average 130 but peaking at 200 or so. I have seen a cardiologist who has increased Bisoprolol from 1.25 to 5 daily and introduced flecanide( since Monday).I also take warfarin. I feel dreadful! Very out of breath very tired and my
Hi I have recently been in continuous a/f for 7 weeks with HR of on average 130 but peaking at 200 or so. I have seen a cardiologist who has increased Bisoprolol from 1.25 to 5 daily and introduced flecanide( since Monday).I also take warfarin. I feel dreadful! Very out of breath very tired and my
123Elizabeth
in
Atrial Fibrillation Support
3 months ago
Is Low Dose Naltrexone (LDN) ever used in Sjogren's syndrome?
Is Low Dose Naltrexone (LDN) ever used in Sjogren's syndrome? Answered by Linda Elsegood, LDNRT Founder https://youtu.be/NQXRcsKpdOk
Is Low Dose Naltrexone (LDN) ever used in Sjogren's syndrome? Answered by Linda Elsegood, LDNRT Founder https://youtu.be/NQXRcsKpdOk
Shewulf
Administrator
in
LDN Research Trust
4 months ago
lupus or fibromyalgia
hi has anyone else in a similarly position my GP can’t tell whether I have fibromyalgia or lupus or a combination of the two
hi has anyone else in a similarly position my GP can’t tell whether I have fibromyalgia or lupus or a combination of the two
Pricey110
in
Fibromyalgia Action UK
4 months ago
fibromyalgia or lupus
hi has anyone else been diagnosed with fibromyalgia but you think it’s more likely to be Lupus. I am constantly tired and just don’t have any energy, hate direct sunlight and have constant pain in my joints. How do I get my GP to actually come to a conclusion it’s so frustrating not knowing.
hi has anyone else been diagnosed with fibromyalgia but you think it’s more likely to be Lupus. I am constantly tired and just don’t have any energy, hate direct sunlight and have constant pain in my joints. How do I get my GP to actually come to a conclusion it’s so frustrating not knowing.
Pricey110
in
LUPUS UK
4 months ago
Cholesterol Issues Question
Hi, I recently had a routine physical (first time in a few years) and my cholesterol was through the roof LDL 188 Overall 260 I had a few questions as I am in full panic mode. 1) I had a few beers the night before the test and buffalo chicken pizza (11 hours before test) following a week of hot
Hi, I recently had a routine physical (first time in a few years) and my cholesterol was through the roof LDL 188 Overall 260 I had a few questions as I am in full panic mode. 1) I had a few beers the night before the test and buffalo chicken pizza (11 hours before test) following a week of hot
Bostonj
in
Anxiety Support
3 months ago
Does fear play a role with pernicious anemia?
Hey guys, I hope this message finds you well. It's good to have a place to come that someone has some understanding of what you're going through! I messaged here before about having fear of a lot of things that I didn't have before this PA/B12 deficiency and sometimes I think of myself as a wimp because
Hey guys, I hope this message finds you well. It's good to have a place to come that someone has some understanding of what you're going through! I messaged here before about having fear of a lot of things that I didn't have before this PA/B12 deficiency and sometimes I think of myself as a wimp because
25092
in
Pernicious Anaemia Society
4 months ago
DC Cardioversion
So, had a private consultation with a Cardiologist yesterday to investigate my AF and subsequent shortness of breath. I had previously had 2 separate lung function tests and seen a respiratory consultant twice as well. The net result was that my lungs were normal, and a low key level of emphysema was
So, had a private consultation with a Cardiologist yesterday to investigate my AF and subsequent shortness of breath. I had previously had 2 separate lung function tests and seen a respiratory consultant twice as well. The net result was that my lungs were normal, and a low key level of emphysema was
Dastardly
in
Atrial Fibrillation Support
3 months ago
New Research: multisensory gamma stimulation promotes the influx of cerebrospinal fluid and the efflux of interstitial fluid in mice
New Research: multisensory gamma stimulation promotes the influx of cerebrospinal fluid and the efflux of interstitial fluid in mice:
• How 40Hz sensory gamma rhythm stimulation clears amyloid in Alzheimer's mice 2024 https://medicalxpress.com/news/2024-02-40hz-sensory-gamma-rhythm-amyloid.html
New Research: multisensory gamma stimulation promotes the influx of cerebrospinal fluid and the efflux of interstitial fluid in mice:
• How 40Hz sensory gamma rhythm stimulation clears amyloid in Alzheimer's mice 2024 https://medicalxpress.com/news/2024-02-40hz-sensory-gamma-rhythm-amyloid.html
Bolt_Upright
in
Cure Parkinson's
7 months ago
Increased thyroid stimulating hormone (TSH) as a possible risk factor for atherosclerosis in subclinical hypothyroidism.
Have to admit, it is quite hard to read and I have not managed the entirety yet! But it does appear to read that even subclinical hypothyroidism might be important in itself - due to the increased TSH. [i]
Increased thyroid stimulating hormone (TSH) as a possible risk factor for atherosclerosis
Have to admit, it is quite hard to read and I have not managed the entirety yet! But it does appear to read that even subclinical hypothyroidism might be important in itself - due to the increased TSH. [i]
Increased thyroid stimulating hormone (TSH) as a possible risk factor for atherosclerosis
helvella
Thyroid UK
in
Thyroid UK
3 months ago
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