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Acute coronary syndrome
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Myocardial bridge
The last month or so been in A&E nearly once a week, with diagnosis from A&E doctors, POTS , at limit of drugs only bypass now but your not at that stage,
coronary
artery spasms and
Acute
coronary
syndrome
. These doctors have never heard of a bridge .
The last month or so been in A&E nearly once a week, with diagnosis from A&E doctors, POTS , at limit of drugs only bypass now but your not at that stage,
coronary
artery spasms and
Acute
coronary
syndrome
. These doctors have never heard of a bridge .
Tricky88
in
British Heart Foundation
4 months ago
Interesting Article on Vulnerable Plaque
https://www.uscjournal.com/articles/vulnerable-plaque-patients-
acute
-
coronary
-
syndrome
-identification-importance-and
https://www.uscjournal.com/articles/vulnerable-plaque-patients-
acute
-
coronary
-
syndrome
-identification-importance-and
MichaelJH
Heart Star
in
British Heart Foundation
1 year ago
A Role of Thyroid Hormones in Acute Myocardial Infarction: An Update
Acute
coronary
syndrome
can be attributed to a significant hemodynamic insult that leads to atherosclerosis of the epicardial coronary arteries. The main causative risk factors, such as obesity, smoking, and alcohol intake, increase the burden of
acute
coronary
syndrome
.
Acute
coronary
syndrome
can be attributed to a significant hemodynamic insult that leads to atherosclerosis of the epicardial coronary arteries. The main causative risk factors, such as obesity, smoking, and alcohol intake, increase the burden of
acute
coronary
syndrome
.
helvella
Thyroid UK
in
Thyroid UK
1 year ago
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22pagents22
Dear everyone is it just me or the media and government talking about economically inactive people feel they are talking about disabled people in chronic pain etc getting the persecution again with pip renewal awards cut or refused and being told nothing wrong with you go get a job etc ie 2014 change
Dear everyone is it just me or the media and government talking about economically inactive people feel they are talking about disabled people in chronic pain etc getting the persecution again with pip renewal awards cut or refused and being told nothing wrong with you go get a job etc ie 2014 change
22pagets22
in
Fibromyalgia Action UK
15 days ago
Me again
Hi all, Hope everyone is as well as can be 😊 Still not sure if I'm posting in the right place but you guys have always been so helpful 💕 Found out this week that the lip biopsy I had done did not have any sjorgrens syndrome showing which is what they were initially looking for, however the new rheumatologist
Hi all, Hope everyone is as well as can be 😊 Still not sure if I'm posting in the right place but you guys have always been so helpful 💕 Found out this week that the lip biopsy I had done did not have any sjorgrens syndrome showing which is what they were initially looking for, however the new rheumatologist
Haylz2109
in
LUPUS UK
22 days ago
systemic sclerosis
Does anyone suffer from terrible heat in veins and arteries(skin) yet raynaud's at the same time? But can also be shaking with cold inside - if that makes sense! I have Sjogren's and Systemic sclerosis but all the Doctors ignore the intolerable symptom of hot and cold I suffer
Does anyone suffer from terrible heat in veins and arteries(skin) yet raynaud's at the same time? But can also be shaking with cold inside - if that makes sense! I have Sjogren's and Systemic sclerosis but all the Doctors ignore the intolerable symptom of hot and cold I suffer
sessull
in
Scleroderma & Raynaud's UK (SRUK)
27 days ago
Sore tongue
Hi folks, is a sore tongue part of UCTD? I've had sore patches (which grow and change shape, and are smooth in the middle) for some years, more on than off. I've assumed it is geographic tongue but that's supposed to be painless from what I've read. I also have a moderately dry mouth and wondering
Hi folks, is a sore tongue part of UCTD? I've had sore patches (which grow and change shape, and are smooth in the middle) for some years, more on than off. I've assumed it is geographic tongue but that's supposed to be painless from what I've read. I also have a moderately dry mouth and wondering
redmaggie
in
LUPUS UK
1 month ago
females & prednisone
does anybody notice vaginal odor while taking prednisone & methotrexate? I remember when on chemotherapy years ago I had a body odor. your thoughts? My gynecologist suggested probiotics with Lactobacillus acidophilus.
does anybody notice vaginal odor while taking prednisone & methotrexate? I remember when on chemotherapy years ago I had a body odor. your thoughts? My gynecologist suggested probiotics with Lactobacillus acidophilus.
Pass7
in
PMRGCAuk
2 months ago
LOW BETA HCG
Hi, me again!!! Iam really worrying about my HCG being low. 10dpt - 64 (4 weeks 1 day) 12dp5dt - 142 (4 weeks 3 days) Â 14dp5dt - 437 (4 weeks 5 days) They are more than doubling but worried they are still low. Any success stories or anything similar please?
Hi, me again!!! Iam really worrying about my HCG being low. 10dpt - 64 (4 weeks 1 day) 12dp5dt - 142 (4 weeks 3 days) Â 14dp5dt - 437 (4 weeks 5 days) They are more than doubling but worried they are still low. Any success stories or anything similar please?
Jess11111
in
Fertility Network UK
2 months ago
Sjogrens
Hi All Does anyone have Sjogrens as well as RA? I have many of the symptoms of Sjogrens but I can’t see my rheumy for a while so I am self diagnosing but I’m pretty sure that’s what it is. I wondered whether anyone has found any otc remedies that help? The worst symptom at the moment is that my
Hi All Does anyone have Sjogrens as well as RA? I have many of the symptoms of Sjogrens but I can’t see my rheumy for a while so I am self diagnosing but I’m pretty sure that’s what it is. I wondered whether anyone has found any otc remedies that help? The worst symptom at the moment is that my
Bizzie
in
NRAS
2 months ago
Rasagiline – Second-Generation MAO-B Inhibitor for the Treatment of Parkinson’s Disease
According to the below article, it slows down the disease progression https://www.clinicaltrialsarena.com/projects/rasagiline-parkinsons-disease/
According to the below article, it slows down the disease progression https://www.clinicaltrialsarena.com/projects/rasagiline-parkinsons-disease/
Farooqji
in
Cure Parkinson's
2 months ago
First IVF consult advice: Very high AMH, ovarian hyperstimulation syndrome
Hi everyoneI'm looking for a bit of advice - I've got my first appointment with our IVF consultant on the 6th April. I just had my results back from my AMH test and the information package for my protocol. My AMH was 80.2 pmol/L and they're pretty sure I'll get ovarian hyperstimulation - I had horrendous
Hi everyoneI'm looking for a bit of advice - I've got my first appointment with our IVF consultant on the 6th April. I just had my results back from my AMH test and the information package for my protocol. My AMH was 80.2 pmol/L and they're pretty sure I'll get ovarian hyperstimulation - I had horrendous
Chubbstep
in
Fertility Network UK
2 months ago
Coping strategies
I have recently had a relative that has been placed in ICU . I am finding it very stressful and worrying with all the ups and downs. Are there any tips of how to cope with the situation ?
I have recently had a relative that has been placed in ICU . I am finding it very stressful and worrying with all the ups and downs. Are there any tips of how to cope with the situation ?
Ashfilm
in
ICUsteps
3 months ago
Advice pls- FET or endometrial testing
Hi ladies, Would appreciate your advice on my situation. Had an MMC at 7 wks in Oct 22 (4th transfer and first time I’ve ever had a positive pregnancy test). It took nearly 2 months for me to naturally have a period after. I had some miscarriage/ implantation testing with a university research clinic
Hi ladies, Would appreciate your advice on my situation. Had an MMC at 7 wks in Oct 22 (4th transfer and first time I’ve ever had a positive pregnancy test). It took nearly 2 months for me to naturally have a period after. I had some miscarriage/ implantation testing with a university research clinic
Elmo13
in
Fertility Network UK
3 months ago
Left atrial enlargement
Hello!I was wondering if anyone has experience of this. What can be done about it, is it reversible with optimal levo? For context, I have Hashi's, I'm 51 and currently experiencing another bout of terrible anxiety ( last time was 5 years ago). Tests have discovered the enlarged LA. I don't have any
Hello!I was wondering if anyone has experience of this. What can be done about it, is it reversible with optimal levo? For context, I have Hashi's, I'm 51 and currently experiencing another bout of terrible anxiety ( last time was 5 years ago). Tests have discovered the enlarged LA. I don't have any
MPG1972
in
Thyroid UK
3 months ago
6 weeks baby implanted on the low side of the womb
hi , I am 6 weeks pregnant, went through so much so far , started with no meds enough ( ivf abroad) , bleeding, …. I still have spotting, my doctor told me to start progynova ( estradiol) 2 times a day. I repeated hcg ( 9000 ) and done a scan . I was told I have a Subchorionic hematoma (SCH) next to
hi , I am 6 weeks pregnant, went through so much so far , started with no meds enough ( ivf abroad) , bleeding, …. I still have spotting, my doctor told me to start progynova ( estradiol) 2 times a day. I repeated hcg ( 9000 ) and done a scan . I was told I have a Subchorionic hematoma (SCH) next to
MariannaB
in
Fertility Network UK
4 months ago
length of time for biopsy results
Hi, had a partial lung lobectomy and lymph node removal, was told biopsy results would be back in 7-10 days. It’s now been 41 days and I’ve heard nothing. When I contact various people I’m just being told this length of timeframe is not uncommon.. this does not sound right to me… Anyone else had to wait
Hi, had a partial lung lobectomy and lymph node removal, was told biopsy results would be back in 7-10 days. It’s now been 41 days and I’ve heard nothing. When I contact various people I’m just being told this length of timeframe is not uncommon.. this does not sound right to me… Anyone else had to wait
Hidden
in
Lung Conditions Community Forum
4 months ago
Surgery
I have had parkinsons for 5 years and need a hip replacement, I fear how the anesthesia will affect my symptons. I have an appointment with a new neurologist, but it's not until the end of March. My surgeon can only tell me that it's my decision,
I have had parkinsons for 5 years and need a hip replacement, I fear how the anesthesia will affect my symptons. I have an appointment with a new neurologist, but it's not until the end of March. My surgeon can only tell me that it's my decision,
davissw
in
Cure Parkinson's
4 months ago
Catastrophic APS
Please help!! My APS has turned catastrophi catastrophic. It has shut down my adrenal gland & now my kidneys. I started dialysis last week. They have tried plasma exchange, high dose steriods to no avail. Im still on Warfarin. Has anybody found a way to get it back under control?
Please help!! My APS has turned catastrophi catastrophic. It has shut down my adrenal gland & now my kidneys. I started dialysis last week. They have tried plasma exchange, high dose steriods to no avail. Im still on Warfarin. Has anybody found a way to get it back under control?
Lind8
in
Hughes Syndrome APS Forum
4 months ago
any experience with vitex / agnus castus / herbs? Help!
I’m in a real panic. I took the Holland and Barrett vitex/Agnus castus supplement for about a week in December (at a high dose). I immediately experienced sore boobs and my period came dramatically a week early. The two cycles after this i have not ovulated but had a period. As I’m TTC this is the
I’m in a real panic. I took the Holland and Barrett vitex/Agnus castus supplement for about a week in December (at a high dose). I immediately experienced sore boobs and my period came dramatically a week early. The two cycles after this i have not ovulated but had a period. As I’m TTC this is the
CarlottaD27
in
Fertility Network UK
4 months ago
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