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Stopping apixaban before a bladder tumour removal
Hi all, I have afib but this question is for my brother who is really anxious about an upcoming procedure to remove a bladder tumour (Friday 9th Feb).He has had an awful 12 months with 4 mini strokes (caused by undiagnosed afib), early stage Parkinson's and now a bladder tumour. He has severe health
Hi all, I have afib but this question is for my brother who is really anxious about an upcoming procedure to remove a bladder tumour (Friday 9th Feb).He has had an awful 12 months with 4 mini strokes (caused by undiagnosed afib), early stage Parkinson's and now a bladder tumour. He has severe health
Karendeena
in
AF Association
6 months ago
DMARD trial
Some input needed please. I am in Norwich under the care of Max Yates and currently on 3.5/4mg of pred. He thinks that i will stay on 4mg. My inflammation markers are in the normal range. I have a lot of disfunction in my legs but cant decide if that is PMR or collateral knee/muscle damage. My upper
Some input needed please. I am in Norwich under the care of Max Yates and currently on 3.5/4mg of pred. He thinks that i will stay on 4mg. My inflammation markers are in the normal range. I have a lot of disfunction in my legs but cant decide if that is PMR or collateral knee/muscle damage. My upper
marionofnorwich
in
PMRGCAuk
6 months ago
Bronchoscopie advice
Hello everyone I was recently due to have a bronchoscopie but cancelled at the last minute. I was told that I would have a local anesthetic in my nose and that they would be working on my lungs for 15 minutes. The idea of someone playing around in my lungs for 15 minutes whilst I was awake was very
Hello everyone I was recently due to have a bronchoscopie but cancelled at the last minute. I was told that I would have a local anesthetic in my nose and that they would be working on my lungs for 15 minutes. The idea of someone playing around in my lungs for 15 minutes whilst I was awake was very
Wibble28
in
Lung Conditions Community Forum
2 months ago
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PMR and brachial neuritis
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
dmart7
in
PMRGCAuk
6 months ago
Worrying
I suffer with IBS and have done now for more than 20 years it can be constipation or loose no weeks are the same no pattern to it at all but over the last few days the constipation has lasted most of the week I take a daily fibergel sometimes this helps other times it doesn’t my problem today is when
I suffer with IBS and have done now for more than 20 years it can be constipation or loose no weeks are the same no pattern to it at all but over the last few days the constipation has lasted most of the week I take a daily fibergel sometimes this helps other times it doesn’t my problem today is when
Poppyseed8
in
IBS Network
7 months ago
Persistent pelvic pain & next to no support. Does anyone know of any support groups or services, please?
Hi - I was diagnosed with interstitial cystitis last April, and have experienced ongoing pelvic pain since I caught covid in September 2022. Next two paragraphs are just venting, request for resources is in the last paragraph if you want to skip it. I have vaginal pain, bladder pain, and stabbing pain
Hi - I was diagnosed with interstitial cystitis last April, and have experienced ongoing pelvic pain since I caught covid in September 2022. Next two paragraphs are just venting, request for resources is in the last paragraph if you want to skip it. I have vaginal pain, bladder pain, and stabbing pain
purpleheresy
in
Pelvic Pain Support Network
7 months ago
NTG and thin corneas
Hi I was diagnosed with NTG in my left eye over 20 years ago. Since then my pressures have been stable with apparently no cause for concern. Last year I had a severe infection in both eyes which has increased the pressure in my left eye from 11 to 14. I didn't think that was too bad as it had been
Hi I was diagnosed with NTG in my left eye over 20 years ago. Since then my pressures have been stable with apparently no cause for concern. Last year I had a severe infection in both eyes which has increased the pressure in my left eye from 11 to 14. I didn't think that was too bad as it had been
NoraBoneGirl
in
Glaucoma UK
7 months ago
Vital Role of B12 and Folate
https://www.sciencedirect.com/science/article/abs/pii/S0193953X12001001?via%3Dihub This article focuses on the role of b12 and folate in the synthesis of methionine and one of the side effects of improper synthesis is depression and cognitive impairment. However, I want to emphasise that poor synthesis
https://www.sciencedirect.com/science/article/abs/pii/S0193953X12001001?via%3Dihub This article focuses on the role of b12 and folate in the synthesis of methionine and one of the side effects of improper synthesis is depression and cognitive impairment. However, I want to emphasise that poor synthesis
B12life
in
Pernicious Anaemia Society
7 months ago
Simbrinza shortage?
Over the years my opthamologist and I have settled on Simbrinza eye drops as the best for my glaucoma. Yesterday my pharmacist tells me he can't find the drops anywhere and he's going to keep looking. We're in SE London area. Any suggestions? Thanks
Over the years my opthamologist and I have settled on Simbrinza eye drops as the best for my glaucoma. Yesterday my pharmacist tells me he can't find the drops anywhere and he's going to keep looking. We're in SE London area. Any suggestions? Thanks
meandpd
in
Glaucoma UK
7 months ago
How long before ablation to start Edoxaban?
Morning all. There seems to have been a flurry of recent posts about anticoagulants. And here’s another question from me. Does anyone know how long before my ablation I need to take the Edoxaban I’ve been prescribed? I know some years ago, when preparing for a cardioversion, they said to take the anticoagulant
Morning all. There seems to have been a flurry of recent posts about anticoagulants. And here’s another question from me. Does anyone know how long before my ablation I need to take the Edoxaban I’ve been prescribed? I know some years ago, when preparing for a cardioversion, they said to take the anticoagulant
Outsidethelines
in
Atrial Fibrillation Support
7 months ago
QoL: Moonrise at a liminal place No. 2
I painted three versions of this mixed media work, being drawn repeatedly to the reference photograph. It is a place called Cwmtudu (pronounced Coom-ti-di to my American and, I imagine, most of my English friends here), and here we are looking down jnto the valley from a rocky outcrop on some clifftops
I painted three versions of this mixed media work, being drawn repeatedly to the reference photograph. It is a place called Cwmtudu (pronounced Coom-ti-di to my American and, I imagine, most of my English friends here), and here we are looking down jnto the valley from a rocky outcrop on some clifftops
BrentW
in
Advanced Prostate Cancer
3 months ago
Any relation between CLL and Atherosclerosis
Hi All, I am in CLL remission for three years and had a stroke in June, 2023. The diagnosis is Atherosclerosis and since June the arteries in my brain have further occluded. Based on my lifestyle and physical condition Atherosclerosis was the furthest thing on my mind. My question is whether others have
Hi All, I am in CLL remission for three years and had a stroke in June, 2023. The diagnosis is Atherosclerosis and since June the arteries in my brain have further occluded. Based on my lifestyle and physical condition Atherosclerosis was the furthest thing on my mind. My question is whether others have
FiddleMD
in
CLL Support
7 months ago
Stopped Methotrexate being screened for Adalimumab
So after being on Methotrexate (injections) for 2 years since diagnosis and feeling dreadful on it (swollen fingers, nausea, constant headaches, depression) I last injected on 18th December 2023. Needless to say my RA is raging in every joint now! Just had a steroid injection and being screened for
So after being on Methotrexate (injections) for 2 years since diagnosis and feeling dreadful on it (swollen fingers, nausea, constant headaches, depression) I last injected on 18th December 2023. Needless to say my RA is raging in every joint now! Just had a steroid injection and being screened for
Amandaazz
in
NRAS
7 months ago
My Tinnitus disappeared from the left side of my head for a few minutes.
I was sitting down watching the T V last week when I felt dizzy and light headed, although it worried me. I noticed my Tinnitus disappeared from the left side of my head. I only had the noise in the right side of my head. After a few moments my balance came back and so did the tinnitus across my head
I was sitting down watching the T V last week when I felt dizzy and light headed, although it worried me. I noticed my Tinnitus disappeared from the left side of my head. I only had the noise in the right side of my head. After a few moments my balance came back and so did the tinnitus across my head
benchmove
in
Tinnitus UK
7 months ago
What should I do - follow-ups not feeling thorough
Hi everyone, before I start my question I want to send out love to everyone on here and I really wish being well for everyone. I wish there wasn’t a load of experts on here because it means we are all in this. I was diagnosed in 2022 - they thought they would find ovarian but they were surprised to
Hi everyone, before I start my question I want to send out love to everyone on here and I really wish being well for everyone. I wish there wasn’t a load of experts on here because it means we are all in this. I was diagnosed in 2022 - they thought they would find ovarian but they were surprised to
OrdinarySoul
in
My Ovacome
7 months ago
Suddenly, my tinnitus became overbearingly loud in one ear!
Good evening I have had tinnitus for a decade. It has mostly been like a whistling in both ears. Last autumn, I had a severe bout of vertigo and my tinnitus changed around that time. I started to get a popping seeds sound, this went on for a few weeks, then on New Year's Day, I got a loud tuning fork
Good evening I have had tinnitus for a decade. It has mostly been like a whistling in both ears. Last autumn, I had a severe bout of vertigo and my tinnitus changed around that time. I started to get a popping seeds sound, this went on for a few weeks, then on New Year's Day, I got a loud tuning fork
TinyTin
in
Tinnitus UK
7 months ago
Anyone successful at reducing cholesterol levels without statins?
I’ve been offered statins as a few weeks ago my cholesterol was up to that magic number plus age 70 where they get recommended. I suggested to cardio team and GP that this may be due to a bit of over indulgence over Christmas period so it’s agreed I’ll re-test in a few months. I have eaten mainly plant
I’ve been offered statins as a few weeks ago my cholesterol was up to that magic number plus age 70 where they get recommended. I suggested to cardio team and GP that this may be due to a bit of over indulgence over Christmas period so it’s agreed I’ll re-test in a few months. I have eaten mainly plant
Rainfern
in
AF Association
7 months ago
I can’t live with permanent tinnitus and the regret
what's the title for this? I am guilty of constantly using cotton buds and bobby pins to scratch my ears, which caused an ear infection that led to permanent tinnitus. Now I hear this ringing all the time. I just want to hear silence, and I am sad that I can’t hear silence anymore. I also have anxiety
what's the title for this? I am guilty of constantly using cotton buds and bobby pins to scratch my ears, which caused an ear infection that led to permanent tinnitus. Now I hear this ringing all the time. I just want to hear silence, and I am sad that I can’t hear silence anymore. I also have anxiety
Kiitty
in
Tinnitus UK
7 months ago
Are there any contraindications when taking LDN and Ativan?
Are there any contraindications when taking LDN and Ativan? Answered by Pharmacist Stephen Dickson, LDN Specialist Check out www.ldnrtevents.com for LDN Webinars, The LDN Book 3, eBooks, Medical Membership, etc. Please visit our website https://www.ldnresearchtrust.org which is packed with information
Are there any contraindications when taking LDN and Ativan? Answered by Pharmacist Stephen Dickson, LDN Specialist Check out www.ldnrtevents.com for LDN Webinars, The LDN Book 3, eBooks, Medical Membership, etc. Please visit our website https://www.ldnresearchtrust.org which is packed with information
Shewulf
Administrator
in
LDN Research Trust
7 months ago
short term memory
hello everyone!!! Hope everyone is well Has anyone here experienced some memory issues while on ibruvica and venetoclax treatments Unfortunately my mother can only handle 100mg of venetoclax a day for a couple months now and I see she’s forgetting more easily or she seems a little off I had taken
hello everyone!!! Hope everyone is well Has anyone here experienced some memory issues while on ibruvica and venetoclax treatments Unfortunately my mother can only handle 100mg of venetoclax a day for a couple months now and I see she’s forgetting more easily or she seems a little off I had taken
Eirinik
in
CLL Support
7 months ago
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