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Heat does it cause problems
Hi allBoth ankles and knees swollen does this often happen with underactive thyroid I am on 75 to 100mg daily which I alternate as recommended by you lovely lot which has helped me become stable and feel better for last year I do have inflammatory arthritis also and am on DMARS for Any advise tips will
Hi allBoth ankles and knees swollen does this often happen with underactive thyroid I am on 75 to 100mg daily which I alternate as recommended by you lovely lot which has helped me become stable and feel better for last year I do have inflammatory arthritis also and am on DMARS for Any advise tips will
Castroll
in
Thyroid UK
3 months ago
so. Is Undifferentiated Connective Tissue Disease latent lupus or lupus?
diagnosed with UCTD in October 2023. Fatigue, weird blood results which sent down rabbit hole for heart, liver. Scans showed all okay… fatigue, dry eyes, dry mouth, ulcers on parotid glands, thyroid, testes, mouth ulcers, Yesterday taken into hospital for suspected brain bleed, aneurism. One protein
diagnosed with UCTD in October 2023. Fatigue, weird blood results which sent down rabbit hole for heart, liver. Scans showed all okay… fatigue, dry eyes, dry mouth, ulcers on parotid glands, thyroid, testes, mouth ulcers, Yesterday taken into hospital for suspected brain bleed, aneurism. One protein
Bigdave79
in
LUPUS UK
3 months ago
Unsure how to proceed after flare continues
I wrote awhile back about having a return of PMR symptoms after successfully (over a year and a half) tapering to 5mg and staying on that dose for two months. The weather had gotten a lot colder here in Seattle and I attributed the flare partly to that. I increased my dose to 10mg for a week and had
I wrote awhile back about having a return of PMR symptoms after successfully (over a year and a half) tapering to 5mg and staying on that dose for two months. The weather had gotten a lot colder here in Seattle and I attributed the flare partly to that. I increased my dose to 10mg for a week and had
Donna5658
in
PMRGCAuk
6 months ago
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Sustaining friendships in the 21st century
When I got Parkinsons, I knew that there'd be a few years before I became housebound (and I'm not there yet). When that point was actually reached, I comforted myself with the knowledge that I had many friends, some of whome have admittedly moved away either to far flung place in the UK, or abroad.
When I got Parkinsons, I knew that there'd be a few years before I became housebound (and I'm not there yet). When that point was actually reached, I comforted myself with the knowledge that I had many friends, some of whome have admittedly moved away either to far flung place in the UK, or abroad.
jeeves19
in
Cure Parkinson's
6 months ago
AASLD organization
www.aasld.org This is the site for the [u][i]
American
[/i][/u] Association for the Study of Liver Diseases. They make the AASLD Guidelines for the Diagnosis and Treatment of PBC. Every one should take the time to read this. Take a copy of it to your doctor as well. They should be familiar
www.aasld.org This is the site for the [u][i]
American
[/i][/u] Association for the Study of Liver Diseases. They make the AASLD Guidelines for the Diagnosis and Treatment of PBC. Every one should take the time to read this. Take a copy of it to your doctor as well. They should be familiar
DonnaBoll
Administrator
in
PBC Foundation
6 months ago
Coping
My story starting in 2020,light headed,weight loss,in and out if the toilet.When i eventually went to the hospital was tokd Cirrhosis,been in and out since,they never explained diet so i have had a couple of burst blood vessels not nice. Now i am aware this us my 1st week of rabbit food!! No booze for
My story starting in 2020,light headed,weight loss,in and out if the toilet.When i eventually went to the hospital was tokd Cirrhosis,been in and out since,they never explained diet so i have had a couple of burst blood vessels not nice. Now i am aware this us my 1st week of rabbit food!! No booze for
Rawai
in
British Liver Trust
6 months ago
Results from blood tests
These is what my blood results came back has. I'm been treated for underactive . But to be told I'm hyperthyroidism instead
These is what my blood results came back has. I'm been treated for underactive . But to be told I'm hyperthyroidism instead
Salsybar73
in
Thyroid UK
3 months ago
Disease remission achieved in SLE with dual-target CAR T-cell therapy
Disease remission achieved in SLE with dual-target CAR T-cell therapy Nearly all patients in small trial see long-term medication-free remission Nearly all people with systemic lupus erythematosus (SLE) treated with iCell Gene Therapeutics’ dual-target CAR T-cell therapy achieved medication-free
Disease remission achieved in SLE with dual-target CAR T-cell therapy Nearly all patients in small trial see long-term medication-free remission Nearly all people with systemic lupus erythematosus (SLE) treated with iCell Gene Therapeutics’ dual-target CAR T-cell therapy achieved medication-free
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
3 months ago
Levodopa effect on AF?
Diagnosed with Parkinsons last year.....medication (Levodopa) seems to be helping AF...anyone else feel the same?
Diagnosed with Parkinsons last year.....medication (Levodopa) seems to be helping AF...anyone else feel the same?
fleckynyde
in
Atrial Fibrillation Support
6 months ago
Feeling rubbish
Hi been feeling achy, exhausted,can sleep 12 hrs but wake up groggy & tired. Everything hurts. Have plantar fasciatis. Patella deformity in knee, spondylitis in my back giving me sciatica. Herniated discs both sides of neck. Causing numbess & pain. Chronic pain syndrome. Cfs/fybro/me. Arthritis in some
Hi been feeling achy, exhausted,can sleep 12 hrs but wake up groggy & tired. Everything hurts. Have plantar fasciatis. Patella deformity in knee, spondylitis in my back giving me sciatica. Herniated discs both sides of neck. Causing numbess & pain. Chronic pain syndrome. Cfs/fybro/me. Arthritis in some
bellemia
in
Thyroid UK
3 months ago
Atrial Fibrillation (AF) Discussion Guide
Atrial Fibrillation (AF) is detected by an irregular pulse and often accompanied by symptoms such as chest pain, fatigue or shortness of breath. AF occurs when chaotic electrical activity develops in the upper chambers or atria and completely takes over from the sinus node. As a result, the atria no
Atrial Fibrillation (AF) is detected by an irregular pulse and often accompanied by symptoms such as chest pain, fatigue or shortness of breath. AF occurs when chaotic electrical activity develops in the upper chambers or atria and completely takes over from the sinus node. As a result, the atria no
TracyAdmin
Partner
in
Atrial Fibrillation Support
1 month ago
NRAS Live: How Important is Nutrition & Diet when Managing Rheumatoid Arthritis?
Join us for our next NRAS Live which will be taking place on Wednesday 26th June at 7pm. This month, we delve into the important role of nutrition and diet when managing a healthy lifestyle living with rheumatoid arthritis. Ailsa will be sitting down with Elena Nikiphorou, Rheumatologist Consultant and
Join us for our next NRAS Live which will be taking place on Wednesday 26th June at 7pm. This month, we delve into the important role of nutrition and diet when managing a healthy lifestyle living with rheumatoid arthritis. Ailsa will be sitting down with Elena Nikiphorou, Rheumatologist Consultant and
Aribah-NRAS
NRAS
in
NRAS
3 months ago
what is the best blood thinner for afib
I was using Flacinide for treating my a fibs as a pill in the pocket. (10 years) Then I caught diabetes and had something happened that made the Flacinide not work to end afib attacks. Now doctors want me on blood thinners. They chose Metropolol for helping with a fibs but not sure what is choice for
I was using Flacinide for treating my a fibs as a pill in the pocket. (10 years) Then I caught diabetes and had something happened that made the Flacinide not work to end afib attacks. Now doctors want me on blood thinners. They chose Metropolol for helping with a fibs but not sure what is choice for
dpm500
in
Atrial Fibrillation Support
1 month ago
thank you for the help! ❤️
I recently posted asking if anyone had pancreatitis issues with lupus (just been diagnosed with cutaneous lupus) and I got some advise & help & support. I spoke to the hepatobillary clinic who removed my gallbladder & they agree it’s most likely the pancreatitis is being caused by an autoimmune issue
I recently posted asking if anyone had pancreatitis issues with lupus (just been diagnosed with cutaneous lupus) and I got some advise & help & support. I spoke to the hepatobillary clinic who removed my gallbladder & they agree it’s most likely the pancreatitis is being caused by an autoimmune issue
Loobie72
in
LUPUS UK
3 months ago
Strange definition of pernicious anemia
Found this questionable definition of pernicious anemia on a Johns Hopkins web page about gastritis: [i]
Pernicious anemia
. This is a form of anemia that happens when your stomach can't digest vitamin B-12.[/i] Even the best seem to get it wrong. https://www.hopkinsmedicine.org/health/conditions-and-diseases
Found this questionable definition of pernicious anemia on a Johns Hopkins web page about gastritis: [i]
Pernicious anemia
. This is a form of anemia that happens when your stomach can't digest vitamin B-12.[/i] Even the best seem to get it wrong. https://www.hopkinsmedicine.org/health/conditions-and-diseases
palmier
in
Pernicious Anaemia Society
3 months ago
Heart attack
Hi. Not really sure what to put. I had a heart attack on the 31st of July. And a stent fitted. I was discharged on the 8th of August. My life style was not great as I'm in recovery and use to abuse steroids. Am trying not to beat my self up to much as I'm scared and very anxious. I.never thought when
Hi. Not really sure what to put. I had a heart attack on the 31st of July. And a stent fitted. I was discharged on the 8th of August. My life style was not great as I'm in recovery and use to abuse steroids. Am trying not to beat my self up to much as I'm scared and very anxious. I.never thought when
Bramall87
in
Sudden Cardiac Arrest & Heart Attack
1 month ago
Afib stressed out :(
Hi, Hello all i wondered if any could help settle my mind about afib. I am a 48 yo guy and have suffered many years with palpitations and such i was in and out the doctors all the time and always got told its stress, depression, i have had quite a few 24hr ecg recorders and a few 7 day ones and was never
Hi, Hello all i wondered if any could help settle my mind about afib. I am a 48 yo guy and have suffered many years with palpitations and such i was in and out the doctors all the time and always got told its stress, depression, i have had quite a few 24hr ecg recorders and a few 7 day ones and was never
Pepsicoke
in
Atrial Fibrillation Support
1 month ago
Once I start supplementing B12, will my B12 blood tests still be accurate?
I would like to know if blood tests will still be a useful measure of my B12 levels, once I have started supplementing B12. I would be testing active B12. The reason I ask is that I have read pernicious anemia people saying that once they start injections (and supplements too maybe), that the B12 blood
I would like to know if blood tests will still be a useful measure of my B12 levels, once I have started supplementing B12. I would be testing active B12. The reason I ask is that I have read pernicious anemia people saying that once they start injections (and supplements too maybe), that the B12 blood
Carrie234
in
Thyroid UK
3 months ago
Telephone Consultation
I have a telephone consultation with the Cardio team this Thursday, my first one. I have had a 24 hour heart monitor, an ECG and a chest x-ray all of which have come back as normal, yet the palpitations have become much worse in the last month that when I'm having one, I can barely speak and it feels
I have a telephone consultation with the Cardio team this Thursday, my first one. I have had a 24 hour heart monitor, an ECG and a chest x-ray all of which have come back as normal, yet the palpitations have become much worse in the last month that when I'm having one, I can barely speak and it feels
CavendishCool
in
LUPUS UK
1 month ago
Ablate and pace
I started with left sided atrial flutter which responded well to cardioversion and kept me symptom free for nearly two years. I have stage one heart block so when I started to get occasional further episodes I had a pacemaker fitted so my dose of Bisoprolol could be increased from 1.25mg to 5mg daily
I started with left sided atrial flutter which responded well to cardioversion and kept me symptom free for nearly two years. I have stage one heart block so when I started to get occasional further episodes I had a pacemaker fitted so my dose of Bisoprolol could be increased from 1.25mg to 5mg daily
Borderterriorist
in
Atrial Fibrillation Support
1 month ago
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