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Covid booster vaccination : Graves Disease
Any thoughts pl re having the covid booster vaccination when diagnosed with Graves Disease. I have at age 65 Graves Disease - diagnosed June 2023 - latest bloods - TSH/ T3/T4 in range - so improved, weight increasing ( I became under weight by far!) , and other aspects improving / energy a
Any thoughts pl re having the covid booster vaccination when diagnosed with Graves Disease. I have at age 65 Graves Disease - diagnosed June 2023 - latest bloods - TSH/ T3/T4 in range - so improved, weight increasing ( I became under weight by far!) , and other aspects improving / energy a
Littlefoot1thyroiduk
in
Thyroid UK
8 months ago
Stage 5 renal failure plus dialysis and cirrhosis of the liver
Wondering if anyone else in the world is dealing with these two together. My husband is, and we're scared. We're hopeful, but doctors don't know how this happened other than being diabetic for decades. Never a drop of alcohol, but a heavy meat eater. Diabetes is in control, A1C too, but hemodialysis
Wondering if anyone else in the world is dealing with these two together. My husband is, and we're scared. We're hopeful, but doctors don't know how this happened other than being diabetic for decades. Never a drop of alcohol, but a heavy meat eater. Diabetes is in control, A1C too, but hemodialysis
Cinderella60
in
British Liver Trust
8 months ago
Atrial fibrillation
Had an ablation procedure 6 yrs ago and this halted my first experience of atrial fibrillation. Now has started back up again. Leaves you feeling dreadful,short of breath and scared. Obviously went to A n E ,13 hrs to be discharged with app at GP for ECG 8 days later. Still waiting for that. Over the
Had an ablation procedure 6 yrs ago and this halted my first experience of atrial fibrillation. Now has started back up again. Leaves you feeling dreadful,short of breath and scared. Obviously went to A n E ,13 hrs to be discharged with app at GP for ECG 8 days later. Still waiting for that. Over the
chux
in
Anxiety Support
6 months ago
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Low Oxygen linked to Afib?
My Apple Series 8 watch has been showing drops of oxygen. It has shown 71-83% but then can go up to 100%. Sometimes during day I have a very hard time breathing but night even sleeping elevated I am short of breath. Even side sleeping . Back is the worst. I am not on any meds, not overweight. 55,
My Apple Series 8 watch has been showing drops of oxygen. It has shown 71-83% but then can go up to 100%. Sometimes during day I have a very hard time breathing but night even sleeping elevated I am short of breath. Even side sleeping . Back is the worst. I am not on any meds, not overweight. 55,
Krissy55
in
Atrial Fibrillation Support
6 months ago
New To Group
Hello! My name is AR57 & I became a "Pensioner" this September just gone!! :) I have had Rheumatoid Arthritis since 2001 & I had been stable with it for a good few years until quite recently, but it has now started to give a few wobbles again!! :( It will be good to talk with others who may have similar
Hello! My name is AR57 & I became a "Pensioner" this September just gone!! :) I have had Rheumatoid Arthritis since 2001 & I had been stable with it for a good few years until quite recently, but it has now started to give a few wobbles again!! :( It will be good to talk with others who may have similar
Ghost87
in
NRAS
6 months ago
I have a partner in crime now
It turns out my husband has just been diagnosed with NAFLD. Not that he was not supporting me but he can now properly join me me on my journey get both my liver back to normal 😊 I have NASH Fibrosis 1 and my husband has NAFLD. Apparently he was told a year ago but completely forgot about it and our
It turns out my husband has just been diagnosed with NAFLD. Not that he was not supporting me but he can now properly join me me on my journey get both my liver back to normal 😊 I have NASH Fibrosis 1 and my husband has NAFLD. Apparently he was told a year ago but completely forgot about it and our
Redgreenblue
in
British Liver Trust
8 months ago
Heart Bypass Soon
Hi all I’ve got my pre op on Thursday at Wythenshawe Hospital Manchester for valve replacement and heart bypass. I’m female 56 years old and obese was a smoker but stopped 3 weeks ago. I’m so scared so much that i keep thinking what if I don’t survive the procedure I’ve written letters to my mum husband
Hi all I’ve got my pre op on Thursday at Wythenshawe Hospital Manchester for valve replacement and heart bypass. I’m female 56 years old and obese was a smoker but stopped 3 weeks ago. I’m so scared so much that i keep thinking what if I don’t survive the procedure I’ve written letters to my mum husband
Shanty123
in
British Heart Foundation
1 year ago
Swollen ankles
Hi,not been on for a while had cardioversion which only lasted a week then back into AF felt so rough afterwards not been right since still on list for an ablation anyway recently my ankles and sometimes my calves have been swelling up mainly my right one can this be normal with AF never had it before
Hi,not been on for a while had cardioversion which only lasted a week then back into AF felt so rough afterwards not been right since still on list for an ablation anyway recently my ankles and sometimes my calves have been swelling up mainly my right one can this be normal with AF never had it before
bobify
in
AF Association
6 months ago
Apixaban
Hi, I've just been prescribed apixaban and bisoprolol due to AF, I'm a bit worried to take apixaban due to the change of lifestyle you need to take, am I getting overly concerned or is there precautions I need to take, also we like to have many continental holidays yearly and I've read some travel insurance
Hi, I've just been prescribed apixaban and bisoprolol due to AF, I'm a bit worried to take apixaban due to the change of lifestyle you need to take, am I getting overly concerned or is there precautions I need to take, also we like to have many continental holidays yearly and I've read some travel insurance
Fones
in
Anticoagulation Support
6 months ago
Back in sinus rhythm
I posted last week about return of AF following a lung cancer operation. The GP (in UK) increased Bisoprolol from 5 mg to 7.5 mg and after a week I am back with a steady heart rate and rhythm.
I posted last week about return of AF following a lung cancer operation. The GP (in UK) increased Bisoprolol from 5 mg to 7.5 mg and after a week I am back with a steady heart rate and rhythm.
Gincalpe
in
AF Association
6 months ago
Musselburgh Coffee and Chat meeting - 2nd December!
Join the Musselburgh Lupus Group for our next Coffee and Chat meeting on Saturday 2nd December, from 10am until 12pm. Meeting at Brunton Hall Bistro, Brunton Hall, Ladywell Way, Musselburgh, EH21 6AF. This is a great way to connect with others affected by lupus, learn more about lupus and share your
Join the Musselburgh Lupus Group for our next Coffee and Chat meeting on Saturday 2nd December, from 10am until 12pm. Meeting at Brunton Hall Bistro, Brunton Hall, Ladywell Way, Musselburgh, EH21 6AF. This is a great way to connect with others affected by lupus, learn more about lupus and share your
michaellasmith
Administrator
in
LUPUS UK
7 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
9 months ago
Zanubrutinib and ACE inhibitors
I am approaching the start of treatment for the first time. I have for many years been taking an ACE inhibitor (perindropril) for high blood pressure, which is now well controlled. I have CLL, my lymphocyte count is doubling quickly (~2 months) and my haematologist is considering options for treatment
I am approaching the start of treatment for the first time. I have for many years been taking an ACE inhibitor (perindropril) for high blood pressure, which is now well controlled. I have CLL, my lymphocyte count is doubling quickly (~2 months) and my haematologist is considering options for treatment
Fogey
in
CLL Support
7 months ago
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
9 months ago
Gabapentin for lupus pain
Hi, does anyone take gabapentin for lupus pain? Wanting some advice on how or if this has helped you, thank you.
Hi, does anyone take gabapentin for lupus pain? Wanting some advice on how or if this has helped you, thank you.
BonnyB
in
LUPUS UK
7 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
9 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
9 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
9 months ago
Help understanding my blood test results.
Hi M54 Have been diagnosed with underactive thyroid for about 4 years now. Symptoms were fatigue, insomnia, depression,feeling cold all the time.However lately have been experiencing memory and concentration problems. Have an appointment with an Endo on the 30th of this month what should I raise with
Hi M54 Have been diagnosed with underactive thyroid for about 4 years now. Symptoms were fatigue, insomnia, depression,feeling cold all the time.However lately have been experiencing memory and concentration problems. Have an appointment with an Endo on the 30th of this month what should I raise with
gerrycrilley1
in
Thyroid UK
7 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
9 months ago
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