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Medical lecture and Q&A - Hosted by Dr. Arvind Kaul (with guest speakers) - 15th June 9.30am
Consultant Rheumatologist Dr Arvind Kaul, the Head of Rheumatology & Lupus Patient Care at St. George's Hospital will be hosting the next South London Lupus Group Medical Patient-Focused Lecture. Our agenda for the morning as follows: 1. 09.30: Registration and Welcome 2. 10.00: Melanie Sloan:
Consultant Rheumatologist Dr Arvind Kaul, the Head of Rheumatology & Lupus Patient Care at St. George's Hospital will be hosting the next South London Lupus Group Medical Patient-Focused Lecture. Our agenda for the morning as follows: 1. 09.30: Registration and Welcome 2. 10.00: Melanie Sloan:
michaellasmith
Administrator
in
LUPUS UK
4 months ago
Anca vasculitis
I have had this illness about seven years now and am not having infusions now though I do have an injection of methotrexate every week. I live a quite busy life but am always tired as vasculitis gives me chronic fatigue and bad pains in joints. Now apparently a lot of the pain is I'm told arthritis
I have had this illness about seven years now and am not having infusions now though I do have an injection of methotrexate every week. I live a quite busy life but am always tired as vasculitis gives me chronic fatigue and bad pains in joints. Now apparently a lot of the pain is I'm told arthritis
Westley
in
Vasculitis UK
3 months ago
overdose
I was diagnosed Feb 1 2024. Is it possible to overdose on Co-Beneldopa 200 MG. I take three doses a day [3 x 200 mg]. I try to take them at 8-hour intervals but often screw up, as my memory is so bad. Any side effects of Co-Beneldopa?
I was diagnosed Feb 1 2024. Is it possible to overdose on Co-Beneldopa 200 MG. I take three doses a day [3 x 200 mg]. I try to take them at 8-hour intervals but often screw up, as my memory is so bad. Any side effects of Co-Beneldopa?
disilusioned
in
PSP Association
7 months ago
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What is folic acid used for?
For other reasons, nothing to do with Pernicious Anaemia, I was checking the Patient Information Leaflet for a UK folic acid product. And I noticed this bit: [i]Ennogen Pharma Limited[/i] [i]
Folic Acid Tablets 5mg
[/i] [i]1. WHAT FOLIC ACID TABLETS ARE AND[/i] [i]WHAT THEY ARE USED FOR[/i]
For other reasons, nothing to do with Pernicious Anaemia, I was checking the Patient Information Leaflet for a UK folic acid product. And I noticed this bit: [i]Ennogen Pharma Limited[/i] [i]
Folic Acid Tablets 5mg
[/i] [i]1. WHAT FOLIC ACID TABLETS ARE AND[/i] [i]WHAT THEY ARE USED FOR[/i]
helvella
in
Pernicious Anaemia Society
4 months ago
Burning pain in thigh
last night I woke with a sharp burning pain in my thigh, it felt like a hot knife. As I went to move my leg it spasms and pain became intense. This lasted for about 20 mins. Even today I still get the odd niggling pain again feeling hot. Does anyone have any ideas ? Thanks
last night I woke with a sharp burning pain in my thigh, it felt like a hot knife. As I went to move my leg it spasms and pain became intense. This lasted for about 20 mins. Even today I still get the odd niggling pain again feeling hot. Does anyone have any ideas ? Thanks
Snookercheese
in
Men's Health Forum
7 months ago
Kardiamobile reading
Hi all , I was feeling a bit wobbly this afternoon and felt like I was having quite a few ectopics so took a reading on my device . The result was ‘ sinus rythm with wide QRS . This is the first time I’ve ever had this result so was wondering if it should concern me . I had my last ablation nearly 2
Hi all , I was feeling a bit wobbly this afternoon and felt like I was having quite a few ectopics so took a reading on my device . The result was ‘ sinus rythm with wide QRS . This is the first time I’ve ever had this result so was wondering if it should concern me . I had my last ablation nearly 2
Hammerboy
in
Atrial Fibrillation Support
3 months ago
Liver disease, mast cells and antihistamine
I’ve just seen a post on X about mast cells and Covid-19 which mentioned a link with autoimmune diseases of the gut and the use of antihistamines as a treatment.. I wondered if anything was known about autoimmune liver diseases, mast cells and antihistamines. I found this 2017 research paper https://
I’ve just seen a post on X about mast cells and Covid-19 which mentioned a link with autoimmune diseases of the gut and the use of antihistamines as a treatment.. I wondered if anything was known about autoimmune liver diseases, mast cells and antihistamines. I found this 2017 research paper https://
Readlots
in
PBC Foundation
6 months ago
Autoimmune disease?
hello, Looking for advice/reassurance just need somewhere to unload really. It all started off with upper right sided abdominal pain which took me to the doctors back in February. Dull ache burning sensation not unbearable but I’m aware of the pain. Ultrasound scan on upper abdo normal. Bloods showed
hello, Looking for advice/reassurance just need somewhere to unload really. It all started off with upper right sided abdominal pain which took me to the doctors back in February. Dull ache burning sensation not unbearable but I’m aware of the pain. Ultrasound scan on upper abdo normal. Bloods showed
Farfield
in
British Liver Trust
4 months ago
Anyone know about Dr's or consultants prescribing metformin for endometriosis?
I recently got access to ALL my medical records from the consultants I had been referred to over the years and saw that in the past I had been prescribed metformin, altavita and amitryptaline at the same time by an endocrinologist. I presumed at the time it was for my underactive Thyroid and wasn't on
I recently got access to ALL my medical records from the consultants I had been referred to over the years and saw that in the past I had been prescribed metformin, altavita and amitryptaline at the same time by an endocrinologist. I presumed at the time it was for my underactive Thyroid and wasn't on
Escapologygirl
in
Endometriosis UK
4 months ago
Health anxiety
I m having health anxiety since 15 years. I lost my very precious 15 years almost sitting in one corner. It's very difficult to write everything at once. Pls any one here help.I m under medication Daxid 100mg - 2 tablets per day ( sertraline) Clonotril 2mg - 2 tablets per day (Clonazapam) One glucose
I m having health anxiety since 15 years. I lost my very precious 15 years almost sitting in one corner. It's very difficult to write everything at once. Pls any one here help.I m under medication Daxid 100mg - 2 tablets per day ( sertraline) Clonotril 2mg - 2 tablets per day (Clonazapam) One glucose
Blackandwhite1
in
Anxiety Support
3 months ago
New Post, community only please
HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
Dawnm10
in
Hughes Syndrome APS Forum
4 months ago
Shingles Jab
I noted that Lupus sufferers over 50 were supposed to be eligible for the Shingrix jab. However, after requesting one from the Surgery the receptionist said no. I did recently get the over 75s Covid booster without asking, courtesy of my immune system, , which I thought over the top. However, as rashes
I noted that Lupus sufferers over 50 were supposed to be eligible for the Shingrix jab. However, after requesting one from the Surgery the receptionist said no. I did recently get the over 75s Covid booster without asking, courtesy of my immune system, , which I thought over the top. However, as rashes
Stewart64
in
LUPUS UK
4 months ago
Verapamil Allergy/Vasculitis
I am so, so devastated. I have been down a long road of medications for my persistent PACs/Bigeminy. They were able to ablate the SVT but couldn't get the PACs. So at the end of a long road of meds, I finally found Verapamil, which actually stopped the PACs, and I was so, so thankful. I was able to
I am so, so devastated. I have been down a long road of medications for my persistent PACs/Bigeminy. They were able to ablate the SVT but couldn't get the PACs. So at the end of a long road of meds, I finally found Verapamil, which actually stopped the PACs, and I was so, so thankful. I was able to
MeganMN
in
Atrial Fibrillation Support
3 months ago
Bisoprolol and Amiodarone
I have been on Flecainide for over a year , very few Afib episodes and feeling fit and healthyAfter a sudden episode this week , my heart up to 170 beats a minute , and three days in hospital , I find myself on 500mg Bisoprolol Fumarate and 200mg Amiodarone Chlorhydrate Pulse now hovering between 40
I have been on Flecainide for over a year , very few Afib episodes and feeling fit and healthyAfter a sudden episode this week , my heart up to 170 beats a minute , and three days in hospital , I find myself on 500mg Bisoprolol Fumarate and 200mg Amiodarone Chlorhydrate Pulse now hovering between 40
Summerlily
in
Atrial Fibrillation Support
3 months ago
Can B12 injections help with tinnitus symptoms?
Hello! I wondered if anybody had any experience with tinnitus and b12 deficiency please? I have hashimotos/ underactive thyroid that is now being successfully treated with NDT medication. I have also recently been diagnosed with b12 deficiency and have started b12 injections every other day for 3 weeks
Hello! I wondered if anybody had any experience with tinnitus and b12 deficiency please? I have hashimotos/ underactive thyroid that is now being successfully treated with NDT medication. I have also recently been diagnosed with b12 deficiency and have started b12 injections every other day for 3 weeks
MissMonty
in
Pernicious Anaemia Society
11 days ago
MELD and UKELD score
Hello everyone, I have Autoimmune hepatitis and have progressed to cirrhosis. I have a MELD score of 23 but i’m not sure how to get my UKELD score. I googled a calculator for UKELD score but it took me to a MELD calculator. My hepatologist is seeing me in 3 minths and I just want to find out where I
Hello everyone, I have Autoimmune hepatitis and have progressed to cirrhosis. I have a MELD score of 23 but i’m not sure how to get my UKELD score. I googled a calculator for UKELD score but it took me to a MELD calculator. My hepatologist is seeing me in 3 minths and I just want to find out where I
Trish02
in
British Liver Trust
7 months ago
Sudden Cardiac Arrest (SCA) vs Heart Attack
Sudden Cardiac Arrest (SCA) vs Heart Attack
The difference between a sudden cardiac arrest is an 'electrical' malfunction in the heart - causing it to stop beating. A heart attack is a 'plumbing' problem when one of the coronary arteries becomes blocked preventing oxygen rich blood reaching
Sudden Cardiac Arrest (SCA) vs Heart Attack
The difference between a sudden cardiac arrest is an 'electrical' malfunction in the heart - causing it to stop beating. A heart attack is a 'plumbing' problem when one of the coronary arteries becomes blocked preventing oxygen rich blood reaching
SamAdmin
Administrator
in
Sudden Cardiac Arrest & Heart Attack
3 months ago
The whites of your eyes?
Sorry to bother but these last several days the whites of my eyes are grayish and bloodshot when I wake. Not yellow though. They get better as the day goes on but its curious to me and slightly worrisome. Will be weeks before I can see my liver dr. Has anyone else had this? Is it a common side effect
Sorry to bother but these last several days the whites of my eyes are grayish and bloodshot when I wake. Not yellow though. They get better as the day goes on but its curious to me and slightly worrisome. Will be weeks before I can see my liver dr. Has anyone else had this? Is it a common side effect
CuriousFish
in
British Liver Trust
7 months ago
Anyone used Dr Dani Gordon @The London Resilience Clinic
hi I have a diagnosis of Fibromyalgia, along with underactive thyroid, arthritis, chronic fatigue (long covid) and diverticula desiease (from pain relief meds). Although I have managed to cope and work full time for a number of years, I was hit with COVID and flu together at Christmas and it has
hi I have a diagnosis of Fibromyalgia, along with underactive thyroid, arthritis, chronic fatigue (long covid) and diverticula desiease (from pain relief meds). Although I have managed to cope and work full time for a number of years, I was hit with COVID and flu together at Christmas and it has
Field007
in
Fibromyalgia Action UK
4 months ago
UPDATE on my dad. A story of hope.❤️ #advancedPC
Hi my dad was diagnosed with advanced prostate cancer in Oct 2021. With Mets to spine, lungs, liver. He is 85. His PSA was 5000. (Today 28 months later his PSA is 0.031 and still dropping) He was told at the time he had 2 months to live. He had spinal surgery the morning after being diagnosed because
Hi my dad was diagnosed with advanced prostate cancer in Oct 2021. With Mets to spine, lungs, liver. He is 85. His PSA was 5000. (Today 28 months later his PSA is 0.031 and still dropping) He was told at the time he had 2 months to live. He had spinal surgery the morning after being diagnosed because
YC22
in
Advanced Prostate Cancer
7 months ago
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