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Excessive Nasal Mucous
I have been treated for underactive thyroid for around 30 years. The past decade I keep experiencing what is like very severe cold symptoms on a regular basis. My body produces excess amounts of thick green slimy sticky mucous, my sinuses get blocked, I have endless nasal drip/cough and it makes me really
I have been treated for underactive thyroid for around 30 years. The past decade I keep experiencing what is like very severe cold symptoms on a regular basis. My body produces excess amounts of thick green slimy sticky mucous, my sinuses get blocked, I have endless nasal drip/cough and it makes me really
OzMan
in
Thyroid UK
5 months ago
‘Normal’ results but feeling terrible
Hi, I have an underactive thyroid (35f) and was diagnosed 5 years ago. I think my Dad (60m) does too, in April 2021 I persuaded him to get a medichecks test done. I have attached a screenshot of those results. I have persuaded him to get another medichecks done to see if his results are different. He
Hi, I have an underactive thyroid (35f) and was diagnosed 5 years ago. I think my Dad (60m) does too, in April 2021 I persuaded him to get a medichecks test done. I have attached a screenshot of those results. I have persuaded him to get another medichecks done to see if his results are different. He
ZDA23
in
Thyroid UK
5 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
4 months ago
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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
4 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
AF Association
4 months ago
Latest re -Lupus and Covid?
Hello All - I hope you all had a very happy Christmas. Does anyone know the latest position regarding Lupus patients testing positive for Covid please. My wife has had cold symptoms for the past couple of days and we decided to test for Covid this morning and we were both positive. My wife (who has
Hello All - I hope you all had a very happy Christmas. Does anyone know the latest position regarding Lupus patients testing positive for Covid please. My wife has had cold symptoms for the past couple of days and we decided to test for Covid this morning and we were both positive. My wife (who has
BeeManShrop
in
LUPUS UK
5 months ago
New therapy (I hope I am not repeating myself)
https://www.urologytimes.com/view/antibody-drug-conjugate-plus-docetaxel-shows-promise-in-metastatic-prostate-cancer The novel antibody-drug conjugate PDS0301 (M9241) in combination with docetaxel demonstrated promising safety and immune response signals in patients with metastatic castration-sensitive
https://www.urologytimes.com/view/antibody-drug-conjugate-plus-docetaxel-shows-promise-in-metastatic-prostate-cancer The novel antibody-drug conjugate PDS0301 (M9241) in combination with docetaxel demonstrated promising safety and immune response signals in patients with metastatic castration-sensitive
Maxone73
in
Advanced Prostate Cancer
7 months ago
PSA Test
Hello everybody Where can I find good information about the readings on PSA tests. As I have posted earlier, my husband had the prostate removed, developed a rezidiv after 5 years, was treated with Proton (based on Hydrogen) radiation in Heidelberg January this year. PSA went down from 0,8 to 0,3.
Hello everybody Where can I find good information about the readings on PSA tests. As I have posted earlier, my husband had the prostate removed, developed a rezidiv after 5 years, was treated with Proton (based on Hydrogen) radiation in Heidelberg January this year. PSA went down from 0,8 to 0,3.
Grommi
in
Advanced Prostate Cancer
7 months ago
cortisol blood test
I’m due a GP blood test at 8:35am today. Can I have a decaf coffee before??? It’s a waste of time test I think as my saliva test showed the only normal one was the morning but that private test wasn’t good enough! Also my DHEA of less than 10 was completely sidetracked by GP. Very little hope this
I’m due a GP blood test at 8:35am today. Can I have a decaf coffee before??? It’s a waste of time test I think as my saliva test showed the only normal one was the morning but that private test wasn’t good enough! Also my DHEA of less than 10 was completely sidetracked by GP. Very little hope this
Joant24
in
Thyroid UK
7 months ago
PSA 9 , age 66 , is there an alternative to biopsy ?
My friend’s PSA went from 5 to 9 in 8 months . He asked me if there is an alternative to biopsy . I told him that there may be something new since I last had a biopsy in 2009.
My friend’s PSA went from 5 to 9 in 8 months . He asked me if there is an alternative to biopsy . I told him that there may be something new since I last had a biopsy in 2009.
PBnative
in
Advanced Prostate Cancer
7 months ago
any tests for Familial hypocholesterolemia?
hi there, Asking for hubby 54 who runs twice a week, plays table tennis, walks 40 mins a day, healthy diet (although we are looking at sugars, fats and the various debates), has done dry January due to a dodgy bilirubin result which corrected in 4 weeks not drinking. Cholesterol blood tests from
hi there, Asking for hubby 54 who runs twice a week, plays table tennis, walks 40 mins a day, healthy diet (although we are looking at sugars, fats and the various debates), has done dry January due to a dodgy bilirubin result which corrected in 4 weeks not drinking. Cholesterol blood tests from
Regenallotment
in
Cholesterol Support
4 months ago
Pain below right ribcage
I have had multiple CT scans and MRIs and none of them show cirrhosis, but they show fatty liver. I've had a burning pain below my right rib cage for over a month...it hurts bad! My last liver enzyme tests were within range. I have been on a diet since this started and I've lost 18lbs, but still have
I have had multiple CT scans and MRIs and none of them show cirrhosis, but they show fatty liver. I've had a burning pain below my right rib cage for over a month...it hurts bad! My last liver enzyme tests were within range. I have been on a diet since this started and I've lost 18lbs, but still have
Csbass828
in
British Liver Trust
7 months ago
shortness of breath subsequent to zoledronic acid infusion
Because of GI problems, bisphosphonate tablets are not an option for me, so I have gone down the infusion path. I had my first infusion on December 28th, and experienced about three days of bad muscle pain, which then resolved itself. It was a couple of weeks later that I noticed that my ankles were
Because of GI problems, bisphosphonate tablets are not an option for me, so I have gone down the infusion path. I had my first infusion on December 28th, and experienced about three days of bad muscle pain, which then resolved itself. It was a couple of weeks later that I noticed that my ankles were
Angel_doll
in
PMRGCAuk
4 months ago
Monitor for Afib
Hi all,Having gone into permanent Afib after a covid infection with no previous history I've had a cardioversion whist on amiodarone. As far as I'm aware I'm still in sinus rhythm and now off amiodarone (thank goodness). I'm on the waiting list for an ablation. My question is it worth getting some kind
Hi all,Having gone into permanent Afib after a covid infection with no previous history I've had a cardioversion whist on amiodarone. As far as I'm aware I'm still in sinus rhythm and now off amiodarone (thank goodness). I'm on the waiting list for an ablation. My question is it worth getting some kind
JoDogBlue
in
Atrial Fibrillation Support
4 months ago
Folic acid and b12
Hi all, I’m new here. I have low B12 (390 -180-900), but have been tested for pernicious anaemia and the test came back clear. I have low folic acid (3.4 -3.00-17.00) and was perscribed folic acid 5mg. I just read that taking folic acid when low in b12 can cause neurological symptoms. I was tested
Hi all, I’m new here. I have low B12 (390 -180-900), but have been tested for pernicious anaemia and the test came back clear. I have low folic acid (3.4 -3.00-17.00) and was perscribed folic acid 5mg. I just read that taking folic acid when low in b12 can cause neurological symptoms. I was tested
Angie10116
in
Pernicious Anaemia Society
5 months ago
Coming home
So after 4.5 years in Nigeria and an APS diagnosis in summer 2020 I’m coming back to the U.K. In many ways I’m looking forward to it and I know my consultants - all 3 of them - will be much more comfortable with me being near better medical care (APS, warfarin and epilepsy are not a good combination
So after 4.5 years in Nigeria and an APS diagnosis in summer 2020 I’m coming back to the U.K. In many ways I’m looking forward to it and I know my consultants - all 3 of them - will be much more comfortable with me being near better medical care (APS, warfarin and epilepsy are not a good combination
GillyA
in
Hughes Syndrome APS Forum
6 months ago
afib and chest infection
hi. My afib has been steady for around 3 months (ie no episodes). My HR runs around 52-60. I’ve started with a chest infection yesterday (can remember feeling like this for a long time) I checked my afib via Apple Watch and although it says I’m in sinus rhythm my HR is low to mid 90’s. Could this
hi. My afib has been steady for around 3 months (ie no episodes). My HR runs around 52-60. I’ve started with a chest infection yesterday (can remember feeling like this for a long time) I checked my afib via Apple Watch and although it says I’m in sinus rhythm my HR is low to mid 90’s. Could this
macymoo007
in
AF Association
4 months ago
Delayed Lynparza (Olaparib)Reaction
I started Lynparza (Olaparib) on 5/19 (PSA 172). By 7/5 (+7 weeks ) my PSA was 222 and it was decided to discontinue the drug, get a port, and prepare for chemo. At the first chemo appt on 8/10 (+12 weeks), the blood test showed that my PSA had fallen to 194. The general literature says you evaluate
I started Lynparza (Olaparib) on 5/19 (PSA 172). By 7/5 (+7 weeks ) my PSA was 222 and it was decided to discontinue the drug, get a port, and prepare for chemo. At the first chemo appt on 8/10 (+12 weeks), the blood test showed that my PSA had fallen to 194. The general literature says you evaluate
OhioGuy2
in
Advanced Prostate Cancer
7 months ago
Are you ready to kick neurotoxins to the curb?
You can start by not eating them and clean up your diet. The next step is to remove neurotoxins from your personal care and cleaning products. Edit: Would you be more motivated to change your lifestyle if you understood how Roundup is used and why it's poison? Roundup kills any actively growing plant
You can start by not eating them and clean up your diet. The next step is to remove neurotoxins from your personal care and cleaning products. Edit: Would you be more motivated to change your lifestyle if you understood how Roundup is used and why it's poison? Roundup kills any actively growing plant
SilentEchoes
in
Cure Parkinson's
7 months ago
Dont panic.All I could think of was Corporal Jones.
Hi everyone. Earlier today I had to go to the Post Office to renew my driving licence. Couldn't do it online as passport had expired. They take your old licence, payment and then take your photo. Made a proper spectacle of myself as I was literally gasping for air. The Post Office counter lady was
Hi everyone. Earlier today I had to go to the Post Office to renew my driving licence. Couldn't do it online as passport had expired. They take your old licence, payment and then take your photo. Made a proper spectacle of myself as I was literally gasping for air. The Post Office counter lady was
DaveLister
in
Lung Conditions Community Forum
4 months ago
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