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Has anyone had medication changed from bisoprolol?
My previous posts were related to my mum and her anxiety. Mum has permanent AF. We ended up going private to see a consultant and mum had a monitor for a week to monitor her heart rate. The results did show that her heart rate was high - around 160 was the higher results. The consultant increased bisoprolol
My previous posts were related to my mum and her anxiety. Mum has permanent AF. We ended up going private to see a consultant and mum had a monitor for a week to monitor her heart rate. The results did show that her heart rate was high - around 160 was the higher results. The consultant increased bisoprolol
Nickybhf
in
Atrial Fibrillation Support
3 months ago
Olaparib for Metastatic Castration-Resistant Prostate Cancer With BRCA1 and/or BRCA2 Alterations
I know these results have been known for a while but me being germline and somatic BRCA 2, I thought it would be important to post this for those warriors with this condition. TAKE-HOME MESSAGE The phase III PROfound trial showed that patients with metastatic castration-resistant prostate cancer
I know these results have been known for a while but me being germline and somatic BRCA 2, I thought it would be important to post this for those warriors with this condition. TAKE-HOME MESSAGE The phase III PROfound trial showed that patients with metastatic castration-resistant prostate cancer
Balsam01
in
Advanced Prostate Cancer
7 months ago
Please help my grandfather
Hi all thanks for accepting me into this group, I would love to help my grandfather feel abit more comfortable.Grandad had 2 replacement hips last year has suspected cancer in lung and ureter (both will stay undiagnosed due to fraility.) He has COPD, AF, Osteoarthritis and now got systolic heart diease
Hi all thanks for accepting me into this group, I would love to help my grandfather feel abit more comfortable.Grandad had 2 replacement hips last year has suspected cancer in lung and ureter (both will stay undiagnosed due to fraility.) He has COPD, AF, Osteoarthritis and now got systolic heart diease
Danielle2419
in
Atrial Fibrillation Support
3 months ago
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Mum update (CBD)
Thought I had finally better give you all an update on mum. Mum had a fall back in Feb which resulted in a broken nose and slight skull fracture, still mobile unaided at this point, but with falls risk. Admitted to hospital after 24 hours in A&E, finally getting a bed in a ward. Ward then had changed
Thought I had finally better give you all an update on mum. Mum had a fall back in Feb which resulted in a broken nose and slight skull fracture, still mobile unaided at this point, but with falls risk. Admitted to hospital after 24 hours in A&E, finally getting a bed in a ward. Ward then had changed
Araucana
in
PSP Association
3 months ago
atypical trigeminal neuralgia
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
PurpleDuckie
in
PMRGCAuk
4 months ago
Dizziness
sorry not been on for a while , moved house then had another scare with my cancer in remission. It’s 2 years since my ruptured brain aneurysm, spoke to rehab consultant ( different one ) at last he listened about my dizziness and falls he has now referred me to a ENT consultant to see if he can help
sorry not been on for a while , moved house then had another scare with my cancer in remission. It’s 2 years since my ruptured brain aneurysm, spoke to rehab consultant ( different one ) at last he listened about my dizziness and falls he has now referred me to a ENT consultant to see if he can help
Blu37
in
Brain Aneurysm Support
7 months ago
Raynaud's in dark skinned patients
Hi all! My mum has secondary Raynaud's, like triggered by heart meds that unfortunately, she has to take. Diagnosis came very late as she didn't get the white-blue-red which they were expecting. Straight to white under the nails and fingertips, it then progressed straight from that to black dots which
Hi all! My mum has secondary Raynaud's, like triggered by heart meds that unfortunately, she has to take. Diagnosis came very late as she didn't get the white-blue-red which they were expecting. Straight to white under the nails and fingertips, it then progressed straight from that to black dots which
CarerEdi
in
Scleroderma & Raynaud's UK (SRUK)
3 months ago
Newly Diagnosed
Hello, I’m new to this forum and was only diagnosed with SLE in late December. I’ve also got secondary triple positive antiphospholipid antibodies. I’m 26 and I’ve always lived a very active/outgoing lifestyle and have always tried to be healthy so it I’m finding it all a bit difficult to process.
Hello, I’m new to this forum and was only diagnosed with SLE in late December. I’ve also got secondary triple positive antiphospholipid antibodies. I’m 26 and I’ve always lived a very active/outgoing lifestyle and have always tried to be healthy so it I’m finding it all a bit difficult to process.
ChloeScotland
in
LUPUS UK
4 months ago
Saliva cortisol test: should I talk to GP?
These are the results of my recent online purchased cortisol tests. The midday one was actually just above zero, the evening just below 1 (I think). I took the morning one at 6am, as I wake up stupid early all the time, and im wondering if it was too early. I have hashimotos, and take 150 levo per day
These are the results of my recent online purchased cortisol tests. The midday one was actually just above zero, the evening just below 1 (I think). I took the morning one at 6am, as I wake up stupid early all the time, and im wondering if it was too early. I have hashimotos, and take 150 levo per day
Where_am_I
in
Thyroid UK
7 months ago
Recent blood test results
Hi everyone I am new to the forum and would like your advice on recent blood test results please. My story of under active thyroid and now diagnosed with Graves’ disease. 2010 I was told I had an under active thyroid and was started on levothyroxine 50mcg, I was on levothyroxine in varying amounts
Hi everyone I am new to the forum and would like your advice on recent blood test results please. My story of under active thyroid and now diagnosed with Graves’ disease. 2010 I was told I had an under active thyroid and was started on levothyroxine 50mcg, I was on levothyroxine in varying amounts
Senior1449
in
Thyroid UK
7 months ago
Returning to Warfarin after 4 months on Edoxaban ...... part 2
I posted on here my original comments on this subject. Hopefully, this update, will be of interest. I made the decision to quit Edoxaban on 6 April. I didn't /couldn't be bothered to make contact with my GP, whenever I phone up for a chat I'm asked to make an appointment which usually is about 10 days
I posted on here my original comments on this subject. Hopefully, this update, will be of interest. I made the decision to quit Edoxaban on 6 April. I didn't /couldn't be bothered to make contact with my GP, whenever I phone up for a chat I'm asked to make an appointment which usually is about 10 days
BenHall1
in
Atrial Fibrillation Support
3 months ago
biopsy report, still waiting to see consultant.
hi all, had an email with the below conclusion of my biopsy, I have a very minuscule left lobe which they want to biopsy but were unable to due to the size. So the right lobe was biopsied. Until I see the consultant I don’t really understand the results, I know none of you are specialist or doctors
hi all, had an email with the below conclusion of my biopsy, I have a very minuscule left lobe which they want to biopsy but were unable to due to the size. So the right lobe was biopsied. Until I see the consultant I don’t really understand the results, I know none of you are specialist or doctors
Goneinsixtyseconds
in
British Liver Trust
7 months ago
Lupus Diagnosis
I haven't been online for some times, perhaps years. I don't think I have posted since losing my Mum in August 2021 and then I lost my Dad last year June. My health, not surprisingly, has been all over the place and under the following hospital departments: Lupus Rheumatology, General Rheumatology -
I haven't been online for some times, perhaps years. I don't think I have posted since losing my Mum in August 2021 and then I lost my Dad last year June. My health, not surprisingly, has been all over the place and under the following hospital departments: Lupus Rheumatology, General Rheumatology -
KeepingUpBeat
in
LUPUS UK
4 months ago
Any readers?
Would really appreciate recommendation for books linking autoimmune disease and trauma. Somebody I care about wants to read about it. Thank you. 😊
Would really appreciate recommendation for books linking autoimmune disease and trauma. Somebody I care about wants to read about it. Thank you. 😊
Pawsedagain
in
Thyroid UK
4 months ago
Help and advice for mum
Hey All, My mum has hidden her drinking, liver issues and cirrorsis for 15 years as I’ve been living in a different country. She was taken into hospital last winter, and I was told it was related to her liver, but no real further detail. Attending a consultant appointment with her last week has unearthed
Hey All, My mum has hidden her drinking, liver issues and cirrorsis for 15 years as I’ve been living in a different country. She was taken into hospital last winter, and I was told it was related to her liver, but no real further detail. Attending a consultant appointment with her last week has unearthed
PerpetuallySad
in
British Liver Trust
7 months ago
Compensated liver
I have went from ddcompensatd to compensated liver disease since being diagnosed in August 2023. I keep seeing prognosis is 9 to 12 years. Is this correct or can you live past 12 years. I haven't had any alcohol since diagnosed
I have went from ddcompensatd to compensated liver disease since being diagnosed in August 2023. I keep seeing prognosis is 9 to 12 years. Is this correct or can you live past 12 years. I haven't had any alcohol since diagnosed
Oasisman
in
British Liver Trust
7 months ago
Confused and seeking clarification
Hi folks . . . I have attached a letter from Hepatology which (to me anyway!) appears to contradict itself? In summary . . . a US in September 2021 showed increased parenchymal echogenicity (PE) due to fatty liver. Follow up bloods and a CT in April 2022 revealed nothing further. I then had a telephone
Hi folks . . . I have attached a letter from Hepatology which (to me anyway!) appears to contradict itself? In summary . . . a US in September 2021 showed increased parenchymal echogenicity (PE) due to fatty liver. Follow up bloods and a CT in April 2022 revealed nothing further. I then had a telephone
HouseHead
in
British Liver Trust
7 months ago
Feeling overwhelmed
After a routine lung screening CT scan I was diagnosed with mild emphysema and some calcification of my heart arteries. I was also referred for a further high definition CT Scan to confirm bronchiectasis. My GP prescribed Salamol which did nothing to help the breathlessness and chest tightness I'd been
After a routine lung screening CT scan I was diagnosed with mild emphysema and some calcification of my heart arteries. I was also referred for a further high definition CT Scan to confirm bronchiectasis. My GP prescribed Salamol which did nothing to help the breathlessness and chest tightness I'd been
Roxdale
in
Lung Conditions Community Forum
3 months ago
Cryo ablation 6 days ago..am I back in AF?
I've been for an ECG this afternoon the results of which are being passed to the arrhythmia nurse team at the JR in Oxford, where I had a cryo ablation last Friday. AF symptoms of breathlessness and feeling faint and then some for a couple of days and now a bit more settled but irregular and fast pulse
I've been for an ECG this afternoon the results of which are being passed to the arrhythmia nurse team at the JR in Oxford, where I had a cryo ablation last Friday. AF symptoms of breathlessness and feeling faint and then some for a couple of days and now a bit more settled but irregular and fast pulse
JoDogBlue
in
Atrial Fibrillation Support
3 months ago
Obesity Associated With Faster MS Disease Progression
[i]
Obesity in multiple sclerosis (MS) was tied to faster worsening of disability and an increased risk of physical, psychological, and cognitive decline, a prospective cohort study showed.
[/i] [i]
[/i]
https://www.medpagetoday.com/meetingcoverage/actrims/108992?xid=nl_mpt_DHE_2024-03
[i]
Obesity in multiple sclerosis (MS) was tied to faster worsening of disability and an increased risk of physical, psychological, and cognitive decline, a prospective cohort study showed.
[/i] [i]
[/i]
https://www.medpagetoday.com/meetingcoverage/actrims/108992?xid=nl_mpt_DHE_2024-03
BettysMom
in
My MSAA Community
4 months ago
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