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Experiences with
Chronic kidney disease (CKD)
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confused
Hello I have
ckd
b . It has approved over the last year to upwards 3a. I’m being pressured into a colonoscopy because of anemia. I’ve told them and told over and over I have anemia of a chronic disease/ diseases( I even had a stupid hysterectomy because of anemia!!)
Hello I have
ckd
b . It has approved over the last year to upwards 3a. I’m being pressured into a colonoscopy because of anemia. I’ve told them and told over and over I have anemia of a chronic disease/ diseases( I even had a stupid hysterectomy because of anemia!!)
Chimama
in
Kidney Disease
1 year ago
Our CBD Journey With Dad
I would like to start this off with a brief insight to our CBD journey. I know we all have had to go through very similar caring procedures! But, I need to open up my sadness and talk with others about tackling the day to day guilt after losing a huge part of your being.
I would like to start this off with a brief insight to our CBD journey. I know we all have had to go through very similar caring procedures! But, I need to open up my sadness and talk with others about tackling the day to day guilt after losing a huge part of your being.
lilot
in
PSP Association
10 months ago
ckd aahhh
Had rug pulled out from under me Just learnt I have stage 2
ckd
maybe down to Hydroxy ? Anyone else told this ?
Had rug pulled out from under me Just learnt I have stage 2
ckd
maybe down to Hydroxy ? Anyone else told this ?
Hidden
in
MPN Voice
1 year ago
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Bisoprolol and low heart rate
As my heart palpitations were becoming unbearable, I finally agreed to try bisoprolol, just 1,25mg daily. Well, the good news is that the palpitations and the breathlessness have almost gone . The bad news is that my resting heart rate is down to 45 in the afternoon, going up to 58 when I'm active.
As my heart palpitations were becoming unbearable, I finally agreed to try bisoprolol, just 1,25mg daily. Well, the good news is that the palpitations and the breathlessness have almost gone . The bad news is that my resting heart rate is down to 45 in the afternoon, going up to 58 when I'm active.
Norfolk_spaniel
in
AF Association
8 months ago
FYI for all
I am hoping this will post https://link.medtechdive.com/click/32589143.48654/aHR0cHM6Ly93d3cubWVkdGVjaGRpdmUuY29tL25ld3MvZ2UtaGVhbHRoY2FyZS1zb2Z0d2FyZS1hZmliLWF0cmlhbC1maWJyaWxsYXRpb24tZ2VoYy82OTE4Mzkv/648eaad0629034b19a05774eB370d4a06 It took eight months to have an absolute diagnosis for me. As
I am hoping this will post https://link.medtechdive.com/click/32589143.48654/aHR0cHM6Ly93d3cubWVkdGVjaGRpdmUuY29tL25ld3MvZ2UtaGVhbHRoY2FyZS1zb2Z0d2FyZS1hZmliLWF0cmlhbC1maWJyaWxsYXRpb24tZ2VoYy82OTE4Mzkv/648eaad0629034b19a05774eB370d4a06 It took eight months to have an absolute diagnosis for me. As
DawnTX
in
AF Association
8 months ago
When You Can't Do It All–Living with End-Stage Kidney Disease
Living with end-stage
CKD
can be overwhelming. Here are 3 simple tips to help you cope. Learn more at: https://www.kidney.org/newsletter/when-you-can-t-do-it-all-living-end-stage-kidney-disease
Living with end-stage
CKD
can be overwhelming. Here are 3 simple tips to help you cope. Learn more at: https://www.kidney.org/newsletter/when-you-can-t-do-it-all-living-end-stage-kidney-disease
JackieJ_NKF
Partner
in
Kidney Dialysis
1 year ago
When You Can't Do It All–Living with End-Stage Kidney Disease
Living with end-stage
CKD
can be overwhelming. Here are 3 simple tips to help you cope. Learn more at: https://www.kidney.org/newsletter/when-you-can-t-do-it-all-living-end-stage-kidney-disease
Living with end-stage
CKD
can be overwhelming. Here are 3 simple tips to help you cope. Learn more at: https://www.kidney.org/newsletter/when-you-can-t-do-it-all-living-end-stage-kidney-disease
JackieJ_NKF
Partner
in
Kidney Disease
1 year ago
Should I lower flecainide dose to 1X per day instead of twice a day.
I have both a cardiologist and electrophysiologist since my first episode almost five months ago. I have lost twelve pounds and almost to my BMI weight recommended by the cardiologist. I had the Nuclear Stress test in my Cardiologist office because they had the convenience of taking he Lexiscan sitting
I have both a cardiologist and electrophysiologist since my first episode almost five months ago. I have lost twelve pounds and almost to my BMI weight recommended by the cardiologist. I had the Nuclear Stress test in my Cardiologist office because they had the convenience of taking he Lexiscan sitting
Strawberryfields1
in
AF Association
8 months ago
Care at home Worcestershire/Gloucestershire border
My mum haa cbd and psp. She was taken to hospital 10days ago with extreme pains in her legs. This was managed by increasing her gabapentin from 300mg to 600mg. Unfortunatley the hospital did not increase this gradually so she seems to be experiencing some nasty side effects, including extreme tiredness
My mum haa cbd and psp. She was taken to hospital 10days ago with extreme pains in her legs. This was managed by increasing her gabapentin from 300mg to 600mg. Unfortunatley the hospital did not increase this gradually so she seems to be experiencing some nasty side effects, including extreme tiredness
DaughterCare4
in
PSP Association
10 months ago
Tiredness
Hi. I’ve had a few long runs of af this summer. Cardiologist put me on digoxin, ceased Bisoprolol and kept me on apixaban. I’ve also been referred for ablation. Over the last few weeks I’ve had several bouts of af lasting up to three days. Rate has been under 100 but irregular rhythm made me tired/breathless
Hi. I’ve had a few long runs of af this summer. Cardiologist put me on digoxin, ceased Bisoprolol and kept me on apixaban. I’ve also been referred for ablation. Over the last few weeks I’ve had several bouts of af lasting up to three days. Rate has been under 100 but irregular rhythm made me tired/breathless
jd2004
in
AF Association
8 months ago
Seminar about itchy skin
American Kidney Fund (AKF) is having a seminar for all about
CKD
associated pruritis. It will be Nov. 17 @ 1 PM ET.
American Kidney Fund (AKF) is having a seminar for all about
CKD
associated pruritis. It will be Nov. 17 @ 1 PM ET.
nonna70
in
Kidney Disease
1 year ago
Peaceful nights at last!
I started posting on this forum 2 years ago but it is many months since I last posted so I wanted to tell you what is proving to be a happy ending to my long RLS tale of woe. I've had RLS all my life (inherited from my father) and for many years it was just an occasional thing but when I got old it
I started posting on this forum 2 years ago but it is many months since I last posted so I wanted to tell you what is proving to be a happy ending to my long RLS tale of woe. I've had RLS all my life (inherited from my father) and for many years it was just an occasional thing but when I got old it
Skysgal
in
Restless Legs Syndrome
10 months ago
How do you know if you are still in sinus rhythm
I had my first Cardioversion two days ago. I had three shocks to get my heart back into sinus rythmn. I thought I would feel much better but to be honest I feel just the same. I still have palpitations, still feel like I have run a marathon by the end of the day. I think I might have skipped back
I had my first Cardioversion two days ago. I had three shocks to get my heart back into sinus rythmn. I thought I would feel much better but to be honest I feel just the same. I still have palpitations, still feel like I have run a marathon by the end of the day. I think I might have skipped back
Sarn52
in
AF Association
8 months ago
Why today of all days?
Today was meant to be the first day of my holiday. A much needed holiday after having had a cardioversion 2 weeks ago. However yesterday I came down with a fever! Two negative covid test (yesterday and today) but heart rate has increased from a resting rate of around 65bpm to 99bpm and I’m getting
Today was meant to be the first day of my holiday. A much needed holiday after having had a cardioversion 2 weeks ago. However yesterday I came down with a fever! Two negative covid test (yesterday and today) but heart rate has increased from a resting rate of around 65bpm to 99bpm and I’m getting
Peakoverload
in
AF Association
8 months ago
The saga of faints and Afib
Many thanks to all those who gave advice. Yesterdays 'attack' of faints and afib was pretty dire. So I called 111 and the clinician I spoke to advised I go,by appointmnet...yes, that is what I said, to A. and E. Mine is the John Radcliffe Oxford. I was recieved and put immediately into an area where
Many thanks to all those who gave advice. Yesterdays 'attack' of faints and afib was pretty dire. So I called 111 and the clinician I spoke to advised I go,by appointmnet...yes, that is what I said, to A. and E. Mine is the John Radcliffe Oxford. I was recieved and put immediately into an area where
10gingercats
in
AF Association
8 months ago
’Endo’ appointment ??
finally had a telephone appointment yesterday with endocrinology……. However, my suspicions were raised when he started discussing my statins ?? ….. I’m not on statins as I don’t have raised cholesterol 🙄 I asked him if I was speaking to endocrinology and he confirmed I was after he apologised for looking
finally had a telephone appointment yesterday with endocrinology……. However, my suspicions were raised when he started discussing my statins ?? ….. I’m not on statins as I don’t have raised cholesterol 🙄 I asked him if I was speaking to endocrinology and he confirmed I was after he apologised for looking
Gbunny
in
Thyroid UK
8 months ago
Palpitations
I have heart palpitations quite often. Lately even two panic attacks. Driving in the car, I feel my heart beating fast. Sitting in the waiting room of doctors also. Or even writing this post. Doesn't take much to set me off. The panic attacks are much worse. My heart feels like it's pounding out of my
I have heart palpitations quite often. Lately even two panic attacks. Driving in the car, I feel my heart beating fast. Sitting in the waiting room of doctors also. Or even writing this post. Doesn't take much to set me off. The panic attacks are much worse. My heart feels like it's pounding out of my
rubyred777
in
Anxiety Support
8 months ago
Curious about Hyper-magnesium and hypothyroidism
Has anyone experienced hyper magnesium with hypothyroidism? Im curious because my mag levels (although not reliable) is on the higher side and Im just wondering about this. Link below that I was reading. https://www.merckmanuals.com/professional/endocrine-and-metabolic-disorders/electrolyte-disorders
Has anyone experienced hyper magnesium with hypothyroidism? Im curious because my mag levels (although not reliable) is on the higher side and Im just wondering about this. Link below that I was reading. https://www.merckmanuals.com/professional/endocrine-and-metabolic-disorders/electrolyte-disorders
Batty1
in
Thyroid UK
8 months ago
Arrhythmia anxieties pre-cardioversion
Hi everyone, just looking for others' experiences and reassurance. Since having open heart surgery 12 weeks ago to correct a hole in my heart (diagnosed out of the blue at Christmas), I have been in arrhythmia for about 6 weeks. I had 48 hours on a holter monitor and this showed atrial flutter. I was
Hi everyone, just looking for others' experiences and reassurance. Since having open heart surgery 12 weeks ago to correct a hole in my heart (diagnosed out of the blue at Christmas), I have been in arrhythmia for about 6 weeks. I had 48 hours on a holter monitor and this showed atrial flutter. I was
LadyZ13
in
AF Association
8 months ago
Protect-V trial
I have vasculitis GPA and have regular infusions of rituximab which is an immunosuppressant. On a recent trip to Addenbrookes (Cambridge Hospital) to see my consultant they signed me up to take part in the Protect-V clinical trial. An anti covid vaccine. Anyone else here involved in that trial or any
I have vasculitis GPA and have regular infusions of rituximab which is an immunosuppressant. On a recent trip to Addenbrookes (Cambridge Hospital) to see my consultant they signed me up to take part in the Protect-V clinical trial. An anti covid vaccine. Anyone else here involved in that trial or any
Gurberly
in
Vasculitis UK
8 months ago
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