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can pleural effusion alone come back?
when I was first diagnosed with HGS OC in December 2021, it had spread till the lungs. There were 2 small nodules in the lungs along with pleural effusion in the right lung, which was also tested to be malignant. Have been NED since first line ended in June 22, and been on olaparib since. Day before
when I was first diagnosed with HGS OC in December 2021, it had spread till the lungs. There were 2 small nodules in the lungs along with pleural effusion in the right lung, which was also tested to be malignant. Have been NED since first line ended in June 22, and been on olaparib since. Day before
Goodgirl98
in
My Ovacome
3 months ago
Heart worries
Hi All, I have been having an ache in my chest for a number of weeks. The other night I woke up with chest pain. Ended up in A & E and had all the usual tests - ecg., bloods, chest x-ray. Very conscientious doctor couldn't find a problem although he did say troponin was 'slightly elevated'. Repeated
Hi All, I have been having an ache in my chest for a number of weeks. The other night I woke up with chest pain. Ended up in A & E and had all the usual tests - ecg., bloods, chest x-ray. Very conscientious doctor couldn't find a problem although he did say troponin was 'slightly elevated'. Repeated
Sitosea
in
British Heart Foundation
3 months ago
Exercise intolerance
Hi all. Does anyone have any idea how to tackle this please? Just over four months into PCS. At first I had to build exercise back up but managed to get to walking about five miles a few months ago. Not without symptoms and obviously pretty shattered the next day, but I could do it. Over the last
Hi all. Does anyone have any idea how to tackle this please? Just over four months into PCS. At first I had to build exercise back up but managed to get to walking about five miles a few months ago. Not without symptoms and obviously pretty shattered the next day, but I could do it. Over the last
Ideogram
in
Headway
3 months ago
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Suspected Pernicious Anemia - what next?
Hello, I am very glad to have found this forum as I have been researching B12D and PA a lot recently. I became familiar with the society’s website and found it so helpful. I am 29F in the US and I suspect I have Pernicious Anemia. This is what I know so far (sorry in advance if this post rambles on)
Hello, I am very glad to have found this forum as I have been researching B12D and PA a lot recently. I became familiar with the society’s website and found it so helpful. I am 29F in the US and I suspect I have Pernicious Anemia. This is what I know so far (sorry in advance if this post rambles on)
Marlowekat
in
Pernicious Anaemia Society
4 months ago
Achilles tendonitis and damage due to antibiotic side effect - odd icy sensation?
I have had RA for nearly 10 years, currently on Benepali and Metotrexate injections. Rheumatoid factor 74 and Anti-cpp 600 in 2014 and generally do not score above normal for blood CRP tests (interesting anomaly) even when ultrasound in clinic reviews shows inflammation. As well as small joint hand
I have had RA for nearly 10 years, currently on Benepali and Metotrexate injections. Rheumatoid factor 74 and Anti-cpp 600 in 2014 and generally do not score above normal for blood CRP tests (interesting anomaly) even when ultrasound in clinic reviews shows inflammation. As well as small joint hand
Braecoon
in
NRAS
4 months ago
asthma & respiratory illnesses
Hi - I’m asthmatic and it’s always been mild for the most part (managed by salamol & clenil for my reliever and preventer). Whenever I get any form of respiratory illness it goes straight to my chest and I need steroids and antibiotics and have asthma exacerbations not really attacks. Since catching
Hi - I’m asthmatic and it’s always been mild for the most part (managed by salamol & clenil for my reliever and preventer). Whenever I get any form of respiratory illness it goes straight to my chest and I need steroids and antibiotics and have asthma exacerbations not really attacks. Since catching
ellannabanana99
in
Asthma Community Forum
3 months ago
Pernicious anaemia
Hi the result of my intrinsic factor came back positive and I start loading doses on Monday The results were written a little strangely though Intrinsic Factor antibodies 12.0 U/ml Negative=<7 Equiveocal= 7-10 Positive > 10 Looking on other websites the results are given in different measurements
Hi the result of my intrinsic factor came back positive and I start loading doses on Monday The results were written a little strangely though Intrinsic Factor antibodies 12.0 U/ml Negative=<7 Equiveocal= 7-10 Positive > 10 Looking on other websites the results are given in different measurements
mully
in
Pernicious Anaemia Society
4 months ago
PVCs experience
Iv posted a few story's of what's been happening recently to me since having palpitations.I havent been diagnosed yet with a heart condition or anxiety by a GP or specialist. I have changed so many things in my life style to try and eliminate where my palpitation came from and where they protionally
Iv posted a few story's of what's been happening recently to me since having palpitations.I havent been diagnosed yet with a heart condition or anxiety by a GP or specialist. I have changed so many things in my life style to try and eliminate where my palpitation came from and where they protionally
AWhittaker
in
British Heart Foundation
3 months ago
Pernicious Anemia treatment
Hi I am writing to share my recent health diagnosis and to seek your advice on a more efficient treatment approach. I am a 37-year-old man who has been battling a series of debilitating symptoms for several years, including extreme fatigue, depression, anxiety, brain fog, decreased mental concentration
Hi I am writing to share my recent health diagnosis and to seek your advice on a more efficient treatment approach. I am a 37-year-old man who has been battling a series of debilitating symptoms for several years, including extreme fatigue, depression, anxiety, brain fog, decreased mental concentration
merfi
in
Pernicious Anaemia Society
4 months ago
⁹Newbie: can anybody help with local support to me? Surrey/Sussex/South London
Hello! I was diagnosed with UCTD 3 years ago after contracting awful covid. However during routine check-up bloods last month, for the first time, my Rheu picked up positive Lupus screen, ANA, rheumatoid factor alongside others i cant remember. (I have always had a negative autoimmune panel, but high
Hello! I was diagnosed with UCTD 3 years ago after contracting awful covid. However during routine check-up bloods last month, for the first time, my Rheu picked up positive Lupus screen, ANA, rheumatoid factor alongside others i cant remember. (I have always had a negative autoimmune panel, but high
Gm131987
in
LUPUS UK
4 months ago
A cause for concern or?
For the past couple of months i started getting notifications via my Samsung 6 watch that my HR was anything from 44 to 52,for more than 10 minutes, numerous times a day or night . I am taking various medications, Bu trans patch, HRT co-codamol 30/500 Pregabalin tramadol & citalopram 40mg. They are
For the past couple of months i started getting notifications via my Samsung 6 watch that my HR was anything from 44 to 52,for more than 10 minutes, numerous times a day or night . I am taking various medications, Bu trans patch, HRT co-codamol 30/500 Pregabalin tramadol & citalopram 40mg. They are
caz1967
in
British Heart Foundation
3 months ago
Should I put my t3 back up.
I,ll try and keep this short...So I went to see my Endo last November, still not feeling great, he said you can always take a bit if extra t3 when not feeling well..Foolishly I did!!!Got the shakes, stop taking it but the shakes carried on.Went to the Docs she sent me straight to A&E.They asked what
I,ll try and keep this short...So I went to see my Endo last November, still not feeling great, he said you can always take a bit if extra t3 when not feeling well..Foolishly I did!!!Got the shakes, stop taking it but the shakes carried on.Went to the Docs she sent me straight to A&E.They asked what
sylus_911
in
Thyroid UK
3 months ago
Help! Have I messed up
I have just had a telephone consultation with a GP hoping for help with the symptoms I have been experiencing. I tried to point him in the direction of the relevant guidelines for treating B12 deficiency, he said that he was familiar with the NICE CKS as he deals with B12 all the time and I m not anaemic
I have just had a telephone consultation with a GP hoping for help with the symptoms I have been experiencing. I tried to point him in the direction of the relevant guidelines for treating B12 deficiency, he said that he was familiar with the NICE CKS as he deals with B12 all the time and I m not anaemic
SpringerMom
in
Pernicious Anaemia Society
4 months ago
help please
Hi I’ve just joined the forum , I’ve been diagnosed with pernicious anaemia it’s in the family ,and low folate , I’d had the basic B12 bloods done they said I was ok ? Bloods for B12 showed 2,000 high I only got diagnosed because I asked for an intrinsic factor antibodies gastric parietal cell blood
Hi I’ve just joined the forum , I’ve been diagnosed with pernicious anaemia it’s in the family ,and low folate , I’d had the basic B12 bloods done they said I was ok ? Bloods for B12 showed 2,000 high I only got diagnosed because I asked for an intrinsic factor antibodies gastric parietal cell blood
Windyway
in
Pernicious Anaemia Society
5 months ago
Pneumonia and collapsed lung after catching the ‘100 day cough’
For all you folks who have Lupus, please be careful of this ‘100’ day cough that is going around at the moment, as this is what caused me to end up in hospital. I was diagnosed with Lupus in February 2022. I’ve had a rough ride for the past few years, ending up in hospital every year for one thing
For all you folks who have Lupus, please be careful of this ‘100’ day cough that is going around at the moment, as this is what caused me to end up in hospital. I was diagnosed with Lupus in February 2022. I’ve had a rough ride for the past few years, ending up in hospital every year for one thing
Loopy1971
in
LUPUS UK
3 months ago
Fear brought on by test result” my chart”
I have gone into total melt down. Living alone and having multiple co morbidities is terrifying ! I was moved from my trusted GP to 2 part time gps, I used to have a cardiology check then f to f every year , not been seen now for three years. Also have various Rheumatoid arthritis diseases , biologics
I have gone into total melt down. Living alone and having multiple co morbidities is terrifying ! I was moved from my trusted GP to 2 part time gps, I used to have a cardiology check then f to f every year , not been seen now for three years. Also have various Rheumatoid arthritis diseases , biologics
Luludean
in
Atrial Fibrillation Support
3 months ago
Raised MMA result
Hi everyone Have written before about my low active B12 results(medichecks). Latest one had been 36.7 (37.5~188). My previous 3 were slowly dropping from 60s to 50s to 40s. Advised to do MMA by medichecks. Eventually afforded one last week which came back high 38.5 (<32). They are now suggesting
Hi everyone Have written before about my low active B12 results(medichecks). Latest one had been 36.7 (37.5~188). My previous 3 were slowly dropping from 60s to 50s to 40s. Advised to do MMA by medichecks. Eventually afforded one last week which came back high 38.5 (<32). They are now suggesting
Pomart
in
Pernicious Anaemia Society
5 months ago
More Challenges to Overcome!
Some of you may recall that for some years, I've frequently experienced ectopic beats. They've been calmed down with a lowish dose of a beta blocker (Propranolol) and don't usually give me too much cause for concern......until about a week ago when they re-emerged, but with a different manifestation
Some of you may recall that for some years, I've frequently experienced ectopic beats. They've been calmed down with a lowish dose of a beta blocker (Propranolol) and don't usually give me too much cause for concern......until about a week ago when they re-emerged, but with a different manifestation
Kendrew
in
PMRGCAuk
3 months ago
Persistant cough
hi everyone I haven’t posted for a while it was about my persistant cough. I now have had this cough for over a year now it has gradually got worse over the past few months. Coughing day and night. People come up to me in the street becauthey think I’m choking. My GP has treated me with antibiotics and
hi everyone I haven’t posted for a while it was about my persistant cough. I now have had this cough for over a year now it has gradually got worse over the past few months. Coughing day and night. People come up to me in the street becauthey think I’m choking. My GP has treated me with antibiotics and
Mudmaker
in
MPN Voice
3 months ago
Ramipril
I thought I would share with you my experience of a cough due to ramipril in case it helps someone else as I didn’t believe it would cause such an awful cough. I was prescribed ramipril after having a HA in July last years. No side effects at all. I got an awful cold in November which also came with
I thought I would share with you my experience of a cough due to ramipril in case it helps someone else as I didn’t believe it would cause such an awful cough. I was prescribed ramipril after having a HA in July last years. No side effects at all. I got an awful cold in November which also came with
trafar
in
British Heart Foundation
4 months ago
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