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Started simple stretching today.
I'm 67, have a bad hip, first stage hypertension, am overweight (though have lost 10kg !) And am as stiff as a board. I had a complete knee replacement 18 months ago.I've started simple stretching today, with a view to continuing daily. This is a prelude to commencing an exercise routine, probably at
I'm 67, have a bad hip, first stage hypertension, am overweight (though have lost 10kg !) And am as stiff as a board. I had a complete knee replacement 18 months ago.I've started simple stretching today, with a view to continuing daily. This is a prelude to commencing an exercise routine, probably at
Jeffjones297
in
Couch to 5K
3 months ago
Worried
I am now extremely worried about having had a ct scan with contrast. I knew nothing about the contrast as I was just feeling very ill at the time. I am now petrified that this is going to cause me all sorts of problems with my hypothyroidism. I've not been feeling great with various issues going on with
I am now extremely worried about having had a ct scan with contrast. I knew nothing about the contrast as I was just feeling very ill at the time. I am now petrified that this is going to cause me all sorts of problems with my hypothyroidism. I've not been feeling great with various issues going on with
Catlover3
in
Thyroid UK
3 months ago
Have you downloaded the AF Discussion Guide?
If you have recently been diagnosed with atrial fibrillation (AF), or have been living with AF for sometime, or maybe just have a follow up medical appointment with your Dr? To provide a greater understanding of AF or offer guidance on what questions to ask at the appointment, download our AF Discussion
If you have recently been diagnosed with atrial fibrillation (AF), or have been living with AF for sometime, or maybe just have a follow up medical appointment with your Dr? To provide a greater understanding of AF or offer guidance on what questions to ask at the appointment, download our AF Discussion
TracyAdmin
Partner
in
AF Association
3 months ago
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CATCH Up CORNER...WEEK 4... Time to kick off the running shoes, and Slow things down...
Hello.... Welcome to the Corner... It is warm and cosy and hopefully, many of you will have escaped the reaches of the latest storm! It is so good to be here welcoming you all, for another week of running... or if you are unlucky enough to be out if it for a while ,another day or so of. Self care
Hello.... Welcome to the Corner... It is warm and cosy and hopefully, many of you will have escaped the reaches of the latest storm! It is so good to be here welcoming you all, for another week of running... or if you are unlucky enough to be out if it for a while ,another day or so of. Self care
Oldfloss
Administrator
in
Couch to 5K
3 months ago
Update
Well this is a long story,Mick started loosing weight In February. We then went too the GP in March,who did a blood, when I rang up they said it was normal.Mick continued to loose weight so went back to the GP on April 9th,who then said his blood test showed dangerously high blood sugars,this is the
Well this is a long story,Mick started loosing weight In February. We then went too the GP in March,who did a blood, when I rang up they said it was normal.Mick continued to loose weight so went back to the GP on April 9th,who then said his blood test showed dangerously high blood sugars,this is the
very
in
CLL Support
4 months ago
Kardiamobile says sinus rhythm but Galaxy watch says AFib
Just wondering if anyone's had this experience I have both the Kardia mobile and a Samsung smartwatch Samsung says afib but kardiamobile normal. heart rate in the 70s does anyone know one could be trusted more than the other
Just wondering if anyone's had this experience I have both the Kardia mobile and a Samsung smartwatch Samsung says afib but kardiamobile normal. heart rate in the 70s does anyone know one could be trusted more than the other
easygoer13
in
AF Association
3 months ago
Could chronic urticaria be related to underactive thyroid?
I've had under active thyroid for 5/6 years and have been on a dose of 50mcg of Levothyroxine for all of this time. This year I developed chronic urticaria and then a different kind of dermatitis/eczema and I want to rip my skin off it's so itchy. This week I did an Advanced Thyroid Function Blood Test
I've had under active thyroid for 5/6 years and have been on a dose of 50mcg of Levothyroxine for all of this time. This year I developed chronic urticaria and then a different kind of dermatitis/eczema and I want to rip my skin off it's so itchy. This week I did an Advanced Thyroid Function Blood Test
Chestercheese
in
Thyroid UK
4 months ago
LUPUS 100 Answers to the most important questions about lupus, verified by world renowned lupus doctors
LUPUS 100
Answers to the most important questions about lupus, verified by world renowned lupus doctors in Europe.
LUPUS CHALLENGES
LUPUS MANIFESTATION
LUPUS MANAGEMENT
LIVING WITH LUPUS
LUPUS EUROPE is the European umbrella organisation that brings together
LUPUS 100
Answers to the most important questions about lupus, verified by world renowned lupus doctors in Europe.
LUPUS CHALLENGES
LUPUS MANIFESTATION
LUPUS MANAGEMENT
LIVING WITH LUPUS
LUPUS EUROPE is the European umbrella organisation that brings together
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 months ago
Car-T cell therapy might cure Systemic Autoimmune Diseases
Hi my dear lupies, I hope you are well. Another promising article about car-T cell therapy ππππ: https://www.medscape.com/viewarticle/car-t-cell-therapy-cure-systemic-autoimmune-diseases-2023a1000usm?src=WNL_conf_ash_231220_MSCPEDIT&uac=342465EY&impID=6175634
Hi my dear lupies, I hope you are well. Another promising article about car-T cell therapy ππππ: https://www.medscape.com/viewarticle/car-t-cell-therapy-cure-systemic-autoimmune-diseases-2023a1000usm?src=WNL_conf_ash_231220_MSCPEDIT&uac=342465EY&impID=6175634
Naladog
in
LUPUS UK
4 months ago
Waiting for ablation
I started in Afib June 2022 after covid, was diagnosed in August and put on Edoxaban and bisoprolol by my GP. In October I was seen by a specialist and put on Amiodarone (I've mentioned the side effects before.. thanks for the responses) and put on the waiting list for a cardioversion. That was done
I started in Afib June 2022 after covid, was diagnosed in August and put on Edoxaban and bisoprolol by my GP. In October I was seen by a specialist and put on Amiodarone (I've mentioned the side effects before.. thanks for the responses) and put on the waiting list for a cardioversion. That was done
JoDogBlue
in
Atrial Fibrillation Support
3 months ago
cirrhosis and rheumatoid arthritis
My partner originally decompensated now compensated has suffered from bad aches and pains since diagnosis with ALD - always told it was a side effect of cirrhosis but as he started to become decompensated they started to entertain the idea it might be something else. Cut to almost 2 years later and
My partner originally decompensated now compensated has suffered from bad aches and pains since diagnosis with ALD - always told it was a side effect of cirrhosis but as he started to become decompensated they started to entertain the idea it might be something else. Cut to almost 2 years later and
Rshc
in
British Liver Trust
6 months ago
PSA SCREEN VS SYMPTOMATIC
My current PSA test is called PROSTATE SPC AG, SCREEN. My previous PSA test from the same lab was called PROSTATE SPC AG, SYMPTOMATIC. Both labs were off the same order from my MO. Whats the difference?
My current PSA test is called PROSTATE SPC AG, SCREEN. My previous PSA test from the same lab was called PROSTATE SPC AG, SYMPTOMATIC. Both labs were off the same order from my MO. Whats the difference?
6357axbz
in
Advanced Prostate Cancer
7 months ago
Some key differences found in lupus symptoms in men vs. women: Study
Men at higher risk of heart attack; women more likely to have arthritis Men with systemic lupus erythematosus (SLE) are more likely to experience kidney failure and heart attacks, while women with SLE are at higher risk of other symptoms, such as skin problems and arthritis, according to a new study
Men at higher risk of heart attack; women more likely to have arthritis Men with systemic lupus erythematosus (SLE) are more likely to experience kidney failure and heart attacks, while women with SLE are at higher risk of other symptoms, such as skin problems and arthritis, according to a new study
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 months ago
Is it possible for me to get back to skateboard with autoimmune disease ever?Or do I need to give it up forever?
Hi everyone I have an autoimmune disease they say it might be lupus and myosis and Systemic Sclerosis. I don't even now which one it is or if it's all of them combined. I got diagnosed in 2022 and at this point all exercise and sports declined to none. I used to skate board, do boxing and play basketball
Hi everyone I have an autoimmune disease they say it might be lupus and myosis and Systemic Sclerosis. I don't even now which one it is or if it's all of them combined. I got diagnosed in 2022 and at this point all exercise and sports declined to none. I used to skate board, do boxing and play basketball
Crow9
in
LUPUS UK
4 months ago
My turn to go to A&E
Well what a day i had yesterday, at about 4am i woke up in a right state as couldn't breathe. It took quite a while for me t get back to sleep. When i woke up i didn't feel well at all. It was as much as i wanted to do just to get up and go to the loo before coming downstairs to get myself a cup of tea
Well what a day i had yesterday, at about 4am i woke up in a right state as couldn't breathe. It took quite a while for me t get back to sleep. When i woke up i didn't feel well at all. It was as much as i wanted to do just to get up and go to the loo before coming downstairs to get myself a cup of tea
sylvi
in
NRAS
3 months ago
Parkinson's medications and T3 interactions?
I've been hypothyroid for decades, in recent years self-dosing T3 (split dose - 50 mcg AM, 50 mcg afternoon, 12.5 mcg evening). Recently, I was formally diagnosed with Parkinson's disease (informally undiagnosed for years), and now my doctor put me on gradually increasing doses of a Levodopa/Carbidopa
I've been hypothyroid for decades, in recent years self-dosing T3 (split dose - 50 mcg AM, 50 mcg afternoon, 12.5 mcg evening). Recently, I was formally diagnosed with Parkinson's disease (informally undiagnosed for years), and now my doctor put me on gradually increasing doses of a Levodopa/Carbidopa
chrysalis56
in
Thyroid UK
7 months ago
Sticky blood! A thing or not?
Many years ago my blood tests often had to be repeated at the pathology lab because the first and second samples had set solid in transit before testing. I was told it was because I had sticky blood. Last week I saw a cardiologist who initially wanted me to take blood thinners, but as I only scored 1
Many years ago my blood tests often had to be repeated at the pathology lab because the first and second samples had set solid in transit before testing. I was told it was because I had sticky blood. Last week I saw a cardiologist who initially wanted me to take blood thinners, but as I only scored 1
jointpain
in
Arrhythmia Alliance
7 months ago
B1 Question ( nothing comes easy )
question at the bottom I have been reading everything I could get my hands on that was about vitamin B1 over the last couple years and I tried one B1 100 mg per day for one week about a year ago. It did not help and actually it seemed to make shaking worse. Finally I purchased Daphne Bryan's
question at the bottom I have been reading everything I could get my hands on that was about vitamin B1 over the last couple years and I tried one B1 100 mg per day for one week about a year ago. It did not help and actually it seemed to make shaking worse. Finally I purchased Daphne Bryan's
Gymsack
in
Cure Parkinson's
7 months ago
Post-Covid lung issues - what to expect?
Hi all, I had Covid in mid November and have been sick ever since, particularly (and perhaps only) breathlessness and fatigue. I was first diagnosed with asthma, but the meds only seemed to stave off a worse episode of breathlessness. So I went back to the docs and insisted on being seen, as I was
Hi all, I had Covid in mid November and have been sick ever since, particularly (and perhaps only) breathlessness and fatigue. I was first diagnosed with asthma, but the meds only seemed to stave off a worse episode of breathlessness. So I went back to the docs and insisted on being seen, as I was
Treetop33
in
Lung Conditions Community Forum
3 months ago
Cardio and thyroidism
5and a half years ago I suffered a heart attack. I had a stent implanted and went to cardio rehab. I have noticed over the last year I get tired quickly and have shortage of breath. I was shocked to be told by my new doctor that I have an underactive thyroid. My question is this! Is my heart contributing
5and a half years ago I suffered a heart attack. I had a stent implanted and went to cardio rehab. I have noticed over the last year I get tired quickly and have shortage of breath. I was shocked to be told by my new doctor that I have an underactive thyroid. My question is this! Is my heart contributing
gunnerred67
in
Thyroid UK
5 months ago
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