Search
Search
About
Log in
Join
Experiences with
Mitral valve disease
Posts
Communities
46,154 public posts
Filter results
Metoprol and arrythmias
Thanks first for all the comments in the past. I have long taken Toprol (now Metoprol in the last few weeks), 16 years, before I was diagnosed with Afib recently. And I noticed, through the years, that, say, ten minutes after taking it, I felt a very brief irregularity that then went away. Do any
Thanks first for all the comments in the past. I have long taken Toprol (now Metoprol in the last few weeks), 16 years, before I was diagnosed with Afib recently. And I noticed, through the years, that, say, ten minutes after taking it, I felt a very brief irregularity that then went away. Do any
Pommerania78
in
AF Association
5 months ago
Please check!
Earlier today I posted the link to the PBC Foundaton's Urso calculator. There are so many posts and questions relating to Urso that I thought it was important for everyone to make sure they are on the right dose. This 'calculator' is also available on the PBC app. Knowing you are taking the right dose
Earlier today I posted the link to the PBC Foundaton's Urso calculator. There are so many posts and questions relating to Urso that I thought it was important for everyone to make sure they are on the right dose. This 'calculator' is also available on the PBC app. Knowing you are taking the right dose
DonnaBoll
Administrator
in
PBC Foundation
3 months ago
liver pain in side. Terrified
I am a heavy drinker who had a scare earlier this year where I was told I had reversible liver damage. I was sober for a month and bloods improved. I foolishly slipped back to my old ways of very heavy daily drinking and now have pain in my right side. I am seeing the doctor tomorrow and can’t see how
I am a heavy drinker who had a scare earlier this year where I was told I had reversible liver damage. I was sober for a month and bloods improved. I foolishly slipped back to my old ways of very heavy daily drinking and now have pain in my right side. I am seeing the doctor tomorrow and can’t see how
LeWabbit
in
British Liver Trust
8 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Is APS hereditary?
I'm just wondering because my dad's keeping getting these nose bleeds and it's just not stopping. He's just had an operation to cut the artery and doc said that will be the end of nose bleeds. Well it's not. He's got what looks like clots coming out of his nose. So I've said maybe mention me with APS
I'm just wondering because my dad's keeping getting these nose bleeds and it's just not stopping. He's just had an operation to cut the artery and doc said that will be the end of nose bleeds. Well it's not. He's got what looks like clots coming out of his nose. So I've said maybe mention me with APS
Charts
in
Hughes Syndrome APS Forum
8 months ago
RITUXIMAB
HI I HAVE PMR AND MY ANTIBODIES ARE THROUGH THE ROOF. IT HAS CAUSED MY KIDNEY READING TO DROP TO 11% FUNCTION. THE KIDNEY CONSULTANT HAS DECIDED THAT MY IMMUNE SYSTEM NEEDS TO BE LOWERED TO AVOID TOTAL KIDNEY FAILURE BECAUSE IT HAS CAUSED VASCULITIS AND I AM TO START RITUXIMAB NEXT WEEK. I HAVE HAD
HI I HAVE PMR AND MY ANTIBODIES ARE THROUGH THE ROOF. IT HAS CAUSED MY KIDNEY READING TO DROP TO 11% FUNCTION. THE KIDNEY CONSULTANT HAS DECIDED THAT MY IMMUNE SYSTEM NEEDS TO BE LOWERED TO AVOID TOTAL KIDNEY FAILURE BECAUSE IT HAS CAUSED VASCULITIS AND I AM TO START RITUXIMAB NEXT WEEK. I HAVE HAD
eyeBRing
in
PMRGCAuk
8 months ago
Enzalutamide (Xtandi): Start at half standard dose to extend efficacy time span?
Good Morning AllI was disgnosed 6 years ago with oligometastic prostate cancer Gleeson 8, PSA 22. Since January 2018 I have been on ADT, had docetaxel chemo in April 2018, radiotherapy to the prostate, seminal vessel and pelvis in November 2018 when PSA dropped to <0.1. PSMA PET CT scan in March 2019
Good Morning AllI was disgnosed 6 years ago with oligometastic prostate cancer Gleeson 8, PSA 22. Since January 2018 I have been on ADT, had docetaxel chemo in April 2018, radiotherapy to the prostate, seminal vessel and pelvis in November 2018 when PSA dropped to <0.1. PSMA PET CT scan in March 2019
KGU1
in
Advanced Prostate Cancer
8 months ago
Zoloft and parkinson's
I take Zoloft (Sertraline) 100mgs daily. I have been on this medication for many years before the parkinson's diagnosis. My hand tremors are not stopping after starting 6 weeks ago C/L 25/100 (generic Sinemet) 1 pill, three times a day? My family Doc said that maybe the Zoloft is the reason for the continuity
I take Zoloft (Sertraline) 100mgs daily. I have been on this medication for many years before the parkinson's diagnosis. My hand tremors are not stopping after starting 6 weeks ago C/L 25/100 (generic Sinemet) 1 pill, three times a day? My family Doc said that maybe the Zoloft is the reason for the continuity
Patitou
in
Cure Parkinson's
8 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
1 year ago
longest bout of AF , am I doing the right thing?
Hi everybody, Before I begin , I wish everybody a merry Xmas and a happy healthy new year!! My Xmas present has come early this year with my longest bout of AF ever! 40 hours and still going . I have an ablation booked for 18th January at St Bart’s , it will be my 3rd. A brief outline is I have had
Hi everybody, Before I begin , I wish everybody a merry Xmas and a happy healthy new year!! My Xmas present has come early this year with my longest bout of AF ever! 40 hours and still going . I have an ablation booked for 18th January at St Bart’s , it will be my 3rd. A brief outline is I have had
Kjsp
in
Atrial Fibrillation Support
5 months ago
Unsure what to do?
Yesterday [Friday 22nd Sept] I recieved a call from the Hospital treating my Cirrhosis to inform me they have had a request from my Heptoligy Doctor for a Biopsy due to them not being able to determine the cause of continued elevating blood results, they have had a cancellation for Monday [25th]. This
Yesterday [Friday 22nd Sept] I recieved a call from the Hospital treating my Cirrhosis to inform me they have had a request from my Heptoligy Doctor for a Biopsy due to them not being able to determine the cause of continued elevating blood results, they have had a cancellation for Monday [25th]. This
tipovtong
in
British Liver Trust
8 months ago
Low heart rate while resting
Hey guys. I'm kinda worried about my resting heart rate. If I'm sitting or laying it can go as low as 48bpm, even in sitting. My range is mostly between 48 and 56/57. As soon as I get up my heart rate also jumps quickly and sometimes I get a bit dizzy for few seconds like you would normally get when
Hey guys. I'm kinda worried about my resting heart rate. If I'm sitting or laying it can go as low as 48bpm, even in sitting. My range is mostly between 48 and 56/57. As soon as I get up my heart rate also jumps quickly and sometimes I get a bit dizzy for few seconds like you would normally get when
NewOne2023
in
Atrial Fibrillation Support
5 months ago
Post cardioversion
1 week post cardioversion and am in NSR, and no palpitations any more. However I am still feeling exhausted and steps and hills are a real problem ........anyone else had the same experience ?
1 week post cardioversion and am in NSR, and no palpitations any more. However I am still feeling exhausted and steps and hills are a real problem ........anyone else had the same experience ?
OldTown
in
AF Association
5 months ago
Next Oxfordshire Lupus Group meeting - 6th December 2pm!
Following a successful first meeting for the Oxfordshire Lupus Group, we are thrilled to announced our next virtual meeting, which will be the 6th December at 2pm. This is a fantastic opportunity to meet others with lupus and associated conditions, friends and family also welcome to join! If you would
Following a successful first meeting for the Oxfordshire Lupus Group, we are thrilled to announced our next virtual meeting, which will be the 6th December at 2pm. This is a fantastic opportunity to meet others with lupus and associated conditions, friends and family also welcome to join! If you would
michaellasmith
Administrator
in
LUPUS UK
6 months ago
Help Develop a Sexual Quality of Life Questionnaire for Men-Who-Have-Sex-with-Men with Prostate Cancer
Please consider being part of the COMPASS Study here: https://malecare.org/compass-study/ "Development and Validation of Sexual Quality of Life Questionnaire for Men-Who-Have-Sex-with-Men with Prostate Cancer" This study aims to develop a sexual function survey specific for men who have sex with men
Please consider being part of the COMPASS Study here: https://malecare.org/compass-study/ "Development and Validation of Sexual Quality of Life Questionnaire for Men-Who-Have-Sex-with-Men with Prostate Cancer" This study aims to develop a sexual function survey specific for men who have sex with men
Darryl
Partner
in
Advanced Prostate Cancer
8 months ago
Updates to the EULAR guidelines on managing lupus
The European Alliance of Associations for Rheumatology (EULAR) have updated their guidelines on how doctors should manage lupus. You can find out about how these guidelines are used in the UK, and how they've been updated, on our website here: https://lupusuk.org.uk/updates-to-the-eular-guidelines-on-managing-lupus
The European Alliance of Associations for Rheumatology (EULAR) have updated their guidelines on how doctors should manage lupus. You can find out about how these guidelines are used in the UK, and how they've been updated, on our website here: https://lupusuk.org.uk/updates-to-the-eular-guidelines-on-managing-lupus
Debbie_kinsey
Administrator
in
LUPUS UK
6 months ago
In a sexual relstionship with someone who has Lupus type SLE.
How do i maintain a healthy sexual relationship with someone who has Lupus. At times frustrated how do i treat person. Feel like have to be careful delicate with him. I cannot be in control and neither can he. Treating him very delicately intimacy problems sometimes communication barrier. Anyone advice
How do i maintain a healthy sexual relationship with someone who has Lupus. At times frustrated how do i treat person. Feel like have to be careful delicate with him. I cannot be in control and neither can he. Treating him very delicately intimacy problems sometimes communication barrier. Anyone advice
Tameeka723
in
LUPUS UK
6 months ago
No treatment offered for A F
I rang a friend last night who has had permanent AF for about 6 years. She's now 83 and lives in the Black Mountains in Wales. The only treatment she's ever had is warfarin , bisopralol and something else she couldn't remember the name of. She's never been offered cardioversion, ablation or anything
I rang a friend last night who has had permanent AF for about 6 years. She's now 83 and lives in the Black Mountains in Wales. The only treatment she's ever had is warfarin , bisopralol and something else she couldn't remember the name of. She's never been offered cardioversion, ablation or anything
Qualipop
in
AF Association
5 months ago
Blip but back on track
As some of your are aware, I’ve been a bit unwell,unfortunately I contracted Pneumonia, instead of resting I decided I knew best and continued with my plans granted more slowly but continued none the less. By Saturday I was feeling much better, then wham irregular heart beat, got home about 3 hrs later
As some of your are aware, I’ve been a bit unwell,unfortunately I contracted Pneumonia, instead of resting I decided I knew best and continued with my plans granted more slowly but continued none the less. By Saturday I was feeling much better, then wham irregular heart beat, got home about 3 hrs later
4chickens
in
AF Association
5 months ago
Not good news on my heart........
Well it wasn't good news yesterday. I found out it i had arterial stenosis and my valve was blocked. So i am a lot worse than i thought, mind you i really didn't know how ill i really was. The consultant showed Bob and i my MRI scan that i had and he explained what had happened to me. He also explained
Well it wasn't good news yesterday. I found out it i had arterial stenosis and my valve was blocked. So i am a lot worse than i thought, mind you i really didn't know how ill i really was. The consultant showed Bob and i my MRI scan that i had and he explained what had happened to me. He also explained
sylvi
in
NRAS
5 months ago
Thoughts and Help
Hello all! I am new here. I know this is a lupus / autoimmune group, but before joining I noticed some helpful posts for other conditions, so I am hoping I can find some advice here. I have been dealing with declining health for a few years now, but have not received any diagnoses. I do have a positive
Hello all! I am new here. I know this is a lupus / autoimmune group, but before joining I noticed some helpful posts for other conditions, so I am hoping I can find some advice here. I have been dealing with declining health for a few years now, but have not received any diagnoses. I do have a positive
Hidden
in
LUPUS UK
6 months ago
1
...
88
89
90
...
100
Next page
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
7027 results
British Liver Trust
4435 results
Advanced Prostate Cancer
4320 results
View top 10 communities
Sort by
Most Relevant
Newest