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Eliquis and Wet AMD
My mom has been getting injections for Wet AMD for 13 years. They have worked well and her vision has been stable. She was diagnosed with Afib in April and put on Eliquis. Since then she has been having more bleeding in her eyes at her eye doctor appointments. It probably didn’t occur to her to mention
My mom has been getting injections for Wet AMD for 13 years. They have worked well and her vision has been stable. She was diagnosed with Afib in April and put on Eliquis. Since then she has been having more bleeding in her eyes at her eye doctor appointments. It probably didn’t occur to her to mention
nyla668
in
Atrial Fibrillation Support
2 months ago
Protein c protein s
Hi I have a question looking back over all my blood tests I've gone back years lol my protein c and s have always been slightly elevated anyone found this?
Hi I have a question looking back over all my blood tests I've gone back years lol my protein c and s have always been slightly elevated anyone found this?
DonnaD123
in
LUPUS UK
2 months ago
new PSA
my PSA rose from .04 in Jan to now .21 so it’s moving up. I assume this is still too low for a scan to determine where pc is at. I was undetected for 2 years after radiation of pelvic area.
my PSA rose from .04 in Jan to now .21 so it’s moving up. I assume this is still too low for a scan to determine where pc is at. I was undetected for 2 years after radiation of pelvic area.
Howard53545
in
Advanced Prostate Cancer
6 months ago
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REMINDER! Northern Ireland Lupus Group and LUPUS UK Virtual Volunteering Event - 26th June 7pm!
Don't forget, if you live in Northern Ireland and are interested in volunteering, there is a great opportunity to learn about how you can get involved! The Northern Ireland Lupus Group and LUPUS UK National Office are hosting an online volunteer information event on Wednesday 26th June, from 7pm until
Don't forget, if you live in Northern Ireland and are interested in volunteering, there is a great opportunity to learn about how you can get involved! The Northern Ireland Lupus Group and LUPUS UK National Office are hosting an online volunteer information event on Wednesday 26th June, from 7pm until
michaellasmith
Administrator
in
LUPUS UK
3 months ago
Healthy liver to Cirrhosis
Hello, approximately two years ago I was submitted to hospital with Jaundice after a binge drinking session. I was given an Ultrasound, and told that my results were “clear” and that my liver was normal sized and regular in outline. I was released the next day and given a prescription of Thymine .
Hello, approximately two years ago I was submitted to hospital with Jaundice after a binge drinking session. I was given an Ultrasound, and told that my results were “clear” and that my liver was normal sized and regular in outline. I was released the next day and given a prescription of Thymine .
DJK78
in
British Liver Trust
6 months ago
PAIN PATH studies
Many people with rheumatoid arthritis suffer from pain every day. NRAS are working with researchers at Keele University to undertake two new studies to improve how pain is treated in people with rheumatoid arthritis and other types of inflammatory arthritis. The first study involves people with inflammatory
Many people with rheumatoid arthritis suffer from pain every day. NRAS are working with researchers at Keele University to undertake two new studies to improve how pain is treated in people with rheumatoid arthritis and other types of inflammatory arthritis. The first study involves people with inflammatory
Aribah-NRAS
NRAS
in
NRAS
3 months ago
General Update - I got lost in the site
Sorry everyone, I managed to get totally confused again, and I think I've posted duplicate replies, then lost other replies and now I can't find all the replies that were left for me so I think I've managed to delete them. Trouble is my hands shake so much these days that I keep pressing wrong buttons
Sorry everyone, I managed to get totally confused again, and I think I've posted duplicate replies, then lost other replies and now I can't find all the replies that were left for me so I think I've managed to delete them. Trouble is my hands shake so much these days that I keep pressing wrong buttons
Blondgrassblowing
in
PMRGCAuk
2 months ago
Bechets
I am still very much at the beginning of my journey. I have suffered from mouth ulsers most of my life with no diagnosis or reason to why. It was when I was pregnant in 2020 that I started suffering with vaginal uslers to be told it was due to my pregnancy, they continued after my son was born to
I am still very much at the beginning of my journey. I have suffered from mouth ulsers most of my life with no diagnosis or reason to why. It was when I was pregnant in 2020 that I started suffering with vaginal uslers to be told it was due to my pregnancy, they continued after my son was born to
Mummyof7
in
Behçet's UK
6 months ago
High dose Ergocalciferol (Vit. D-2) for Osteoporosis?
Since losing my long time primary doctor last year, I am on my second doctor for advice for osteoporosis. I was reluctant to take Prolia recommended by the first D.O. doctor and the second Internist Doctor recommended 50,000 (I think IU) weekly for a couple of months. I haven't picked up the prescription
Since losing my long time primary doctor last year, I am on my second doctor for advice for osteoporosis. I was reluctant to take Prolia recommended by the first D.O. doctor and the second Internist Doctor recommended 50,000 (I think IU) weekly for a couple of months. I haven't picked up the prescription
pegpowell
in
PMRGCAuk
2 months ago
Parkinson's Patients See Hope in Novel Stem Cell Repair Method
In work funded by The Michael J. Fox Foundation for Parkinson's Research (MJFF) and Science Foundation Ireland, published this week in the Journal of Neural Engineering, the team in the College of Medicine, Nursing and Health Sciences at University of Galway have shown that transplanting the immature
In work funded by The Michael J. Fox Foundation for Parkinson's Research (MJFF) and Science Foundation Ireland, published this week in the Journal of Neural Engineering, the team in the College of Medicine, Nursing and Health Sciences at University of Galway have shown that transplanting the immature
Farooqji
in
Cure Parkinson's
6 months ago
Xtandi worked great
After radiation to prostate bed and to one pelvic metastasis, I was on xtandi and Lupton for three years and now have been on "vacation " for a year with PSA of 0.02 and testosterone at 4. No meds at all for last11 months!Had a heart attack in May '23 (which I attribute to covid shots) , doctors told
After radiation to prostate bed and to one pelvic metastasis, I was on xtandi and Lupton for three years and now have been on "vacation " for a year with PSA of 0.02 and testosterone at 4. No meds at all for last11 months!Had a heart attack in May '23 (which I attribute to covid shots) , doctors told
JAK2243
in
Advanced Prostate Cancer
6 months ago
I have a question.
Does anyone's rheumatologist order a CRP HS blood test? I heard of CRP, but not this one. Is it solely for heart disease, or something to do with other diseases too like Lupus?? Mine was high.
Does anyone's rheumatologist order a CRP HS blood test? I heard of CRP, but not this one. Is it solely for heart disease, or something to do with other diseases too like Lupus?? Mine was high.
Willow7733
in
LUPUS UK
2 months ago
Diagnosing Arrhythmias
When the heart is beating normally, it is referred to as ‘sinus rhythm’. An extra beat (ectopic beat) can trigger a short circuit, and a fast heartbeat. It can travel down an extra pathway and up the normal conduction system. If this continues, palpitations can result. For more information, please download
When the heart is beating normally, it is referred to as ‘sinus rhythm’. An extra beat (ectopic beat) can trigger a short circuit, and a fast heartbeat. It can travel down an extra pathway and up the normal conduction system. If this continues, palpitations can result. For more information, please download
SamAdmin
Administrator
in
Heart Rhythm Disorders Support
2 months ago
Accept nothing question everything...with the proviso that you are well informed
Everything that I have been complaining about for 8 years has now been seen on MRI. The private MRI that I paid for last week. Some of the best money I have ever spent. Not only do I have 'florid' synovitis in my hands, I have widespread enhanced bone erosions in both hands and feet. I also have
Everything that I have been complaining about for 8 years has now been seen on MRI. The private MRI that I paid for last week. Some of the best money I have ever spent. Not only do I have 'florid' synovitis in my hands, I have widespread enhanced bone erosions in both hands and feet. I also have
Mmrr
in
NRAS
3 months ago
Low red cell count but eat lots of red meat!
Hello again, just wanted to check this out with people as I do get quite tired in the afternoon and need to rest. Is this anaemia and so do I supplement with iron? Is there a good one for people with hashimotos?I have been told I have weak digestion and I feel I don't absorb things like iron very well
Hello again, just wanted to check this out with people as I do get quite tired in the afternoon and need to rest. Is this anaemia and so do I supplement with iron? Is there a good one for people with hashimotos?I have been told I have weak digestion and I feel I don't absorb things like iron very well
Pinkpetite
in
Thyroid UK
3 months ago
Can you have “attacks” when in persistent/constant afib?
If you are in persistent/constant bradycardic (40-60ish bpm) afib can you still have “attacks” of afib? Sort of ad-hoc exasperation of say breathlessness, chest pressure etc. I’m not even sure that question makes any sense… we are still trying to sort out what are “afib symptoms” and what isn’t after
If you are in persistent/constant bradycardic (40-60ish bpm) afib can you still have “attacks” of afib? Sort of ad-hoc exasperation of say breathlessness, chest pressure etc. I’m not even sure that question makes any sense… we are still trying to sort out what are “afib symptoms” and what isn’t after
Efka
in
Atrial Fibrillation Support
2 months ago
The Idea of White Coat Syndrome led to me having many mini strokes.
"White coat syndrome, or white coat hypertension, is the term for when you get a high blood pressure reading in a doctor's office and a normal reading at home. The anxiety of being around doctors in white coats can make your blood pressure rise. Most people don't need treatment if their blood pressure
"White coat syndrome, or white coat hypertension, is the term for when you get a high blood pressure reading in a doctor's office and a normal reading at home. The anxiety of being around doctors in white coats can make your blood pressure rise. Most people don't need treatment if their blood pressure
Tugun
in
Lung Conditions Community Forum
2 months ago
Persistent AF
Hi all,I have recently gone back In to AF and just seen my cardiologist after having an echo and 24 hour monitor. The echo has shown the hearts looks OK with a good EF and moderate dilation of left atrium, the monitor showed my HR anywhere between low 70's and mid 120's with an average of 94! The cardiologist
Hi all,I have recently gone back In to AF and just seen my cardiologist after having an echo and 24 hour monitor. The echo has shown the hearts looks OK with a good EF and moderate dilation of left atrium, the monitor showed my HR anywhere between low 70's and mid 120's with an average of 94! The cardiologist
Bigredhear
in
Atrial Fibrillation Support
2 months ago
people with parents of lupus
hey!! im a teen living with a mum struggling with lupus + bipolar and i would love to learn more about lupus and what it affects so i can easily help my mum better !! if anyone could help and give tips thats so so appreciated :)
hey!! im a teen living with a mum struggling with lupus + bipolar and i would love to learn more about lupus and what it affects so i can easily help my mum better !! if anyone could help and give tips thats so so appreciated :)
b99lover
in
LUPUS UK
3 months ago
Compression socks for travel
Hello, wondering if anyone has a good experience with compression socks for long haul travel? I do experience some feet swelling these days during the day which usually goes away with elevation for a brief period of time. I have flights coming up in the 7 to 14 hour range so am thinking that apart
Hello, wondering if anyone has a good experience with compression socks for long haul travel? I do experience some feet swelling these days during the day which usually goes away with elevation for a brief period of time. I have flights coming up in the 7 to 14 hour range so am thinking that apart
Support_helps
in
Vasculitis UK
2 months ago
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