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Update and advice please
Hi everyone So past few months have been a rollercoaster. After my last GP blood tests which indicated overactive thyroid (I did point out could it be a Hashis flare as per my previous results but they confirmed Graves) and I was referred to the endocrinologists at the hospital and managed to get an
Hi everyone So past few months have been a rollercoaster. After my last GP blood tests which indicated overactive thyroid (I did point out could it be a Hashis flare as per my previous results but they confirmed Graves) and I was referred to the endocrinologists at the hospital and managed to get an
Jules99929
in
Thyroid UK
4 years ago
Diagnosed with Primary Sjorgrens Syndrome today
My Rheumy gave me the results this morning I have been diagnosed with Primary sjorgrens Disorder. He has give me Hydroxychloroquine Sulphate 1 x 200mg 2 times per day and Pilocarpine Hydrochloride 3 x 5mg start with 1 per day for a month then 2 per day for following month and so on. I'm feeling very
My Rheumy gave me the results this morning I have been diagnosed with Primary sjorgrens Disorder. He has give me Hydroxychloroquine Sulphate 1 x 200mg 2 times per day and Pilocarpine Hydrochloride 3 x 5mg start with 1 per day for a month then 2 per day for following month and so on. I'm feeling very
Yellow-Petal
in
LUPUS UK
4 years ago
Pneumococcal vaccine in short supply.
Today, Sharon has officially been diagnosed with moderate COPD, about which I have had strong suspicions about, for over a month. The GP has said she needs to have the Pneumococcal vaccine, of course, especially with working in a nursing home. Sharon then asks the receptionist to make an appointment
Today, Sharon has officially been diagnosed with moderate COPD, about which I have had strong suspicions about, for over a month. The GP has said she needs to have the Pneumococcal vaccine, of course, especially with working in a nursing home. Sharon then asks the receptionist to make an appointment
2greys
in
Lung Conditions Community Forum
4 years ago
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Coronavirus concerns
I'm sure we're all worrying about this but as they didn't think I was 'vulnerable' enough for a flu jab as I'm undiagnosed (I have FM and ME) I'm wondering if I'm considered vulnerable for this. I'm 60 and had pleurisy over 25 years ago. I also worry about other family members, one who has MS and also
I'm sure we're all worrying about this but as they didn't think I was 'vulnerable' enough for a flu jab as I'm undiagnosed (I have FM and ME) I'm wondering if I'm considered vulnerable for this. I'm 60 and had pleurisy over 25 years ago. I also worry about other family members, one who has MS and also
FoggyMoggy
in
Myalgic Encephalomyelitis Community
4 years ago
Supplements. Where are we now?
In the first years following my diagnosis in 2016, i picked up a lot of ideas and suggestions for supplementation. There was a lot of promotion of Co-enzyme Q10, NAC, Creatine, Omega 3, Milk Thistle and lots of others as well. Recently and over a period of time, talk about supplements on this forum and
In the first years following my diagnosis in 2016, i picked up a lot of ideas and suggestions for supplementation. There was a lot of promotion of Co-enzyme Q10, NAC, Creatine, Omega 3, Milk Thistle and lots of others as well. Recently and over a period of time, talk about supplements on this forum and
Buckholt
in
Cure Parkinson's
4 years ago
Is a universal flu vaccine on the horizon?
Every fall, millions of people roll up their sleeves for a flu vaccine, hoping to give their immune system a leg up on influenza. But the flu virus has thousands of strains that mutate and evolve across seasons, and the vaccine can’t guard against all of them. Now, two groups of researchers have independently
Every fall, millions of people roll up their sleeves for a flu vaccine, hoping to give their immune system a leg up on influenza. But the flu virus has thousands of strains that mutate and evolve across seasons, and the vaccine can’t guard against all of them. Now, two groups of researchers have independently
2greys
in
Lung Conditions Community Forum
4 years ago
Coronavirus Facts: What You Need to Know If You Have Chronic Illness or Are Immune-Compromised. US Advice.
People with chronic illness that affects the immune system, such as many forms of inflammatory arthritis, are understandably worried — if not downright freaking out — about the spread of this new virus. Here’s what infectious disease experts and rheumatologists want you to know. Being immunocompromised
People with chronic illness that affects the immune system, such as many forms of inflammatory arthritis, are understandably worried — if not downright freaking out — about the spread of this new virus. Here’s what infectious disease experts and rheumatologists want you to know. Being immunocompromised
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
Coronavirus Anxiety: Key Advice for Chronic Illness Patients from Health Psychologists
‘Remind yourself: I’ve been practicing this. This is already how I live so I don’t have to be more frightened.’
Coronavirus Anxiety
If you’re feeling anxious and helpless about the coronavirus right now, join the club. This sentiment is very common among CreakyJoints members, especially those
‘Remind yourself: I’ve been practicing this. This is already how I live so I don’t have to be more frightened.’
Coronavirus Anxiety
If you’re feeling anxious and helpless about the coronavirus right now, join the club. This sentiment is very common among CreakyJoints members, especially those
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
how to test levels of vitamins, etc.
Does anybody know what vitamins, etc., (i.e., folic acid, B vitamins, magnesium, etc.) we need to have our doctor test to see if it is normal or if it is low and we need to supplement by taking it orally? If so, how much or what level should we aim for to help our RLS?
Does anybody know what vitamins, etc., (i.e., folic acid, B vitamins, magnesium, etc.) we need to have our doctor test to see if it is normal or if it is low and we need to supplement by taking it orally? If so, how much or what level should we aim for to help our RLS?
LanaCSR
in
Restless Legs Syndrome
4 years ago
COVID-19---US White House to meet 03/02/2020 in afternoon with Major US Drug Company CEOs re: Vaccine development
Supposedly, the US WH will meet with CEOs of the 8 major US drug companies to explore exactly where they are (as well as the future) in developing a vaccine which would stop the spread of COVID-19 ASAP. My guess is that we are probably 1-2 years away from a truly “novel, unique” vaccine for COVDI
Supposedly, the US WH will meet with CEOs of the 8 major US drug companies to explore exactly where they are (as well as the future) in developing a vaccine which would stop the spread of COVID-19 ASAP. My guess is that we are probably 1-2 years away from a truly “novel, unique” vaccine for COVDI
sharoncrayn
in
Cure Parkinson's
4 years ago
Bowel disease ?
My daughter has had stomach , kidney and left sided pain for five weeks , hospital confirm ct scan clear and she has stretched bowel and impacted feaces , she is on movicol and buscopan at the moment . Today she has woke up with very painful throat neck and mouth sore especially on roof of mouth . Is
My daughter has had stomach , kidney and left sided pain for five weeks , hospital confirm ct scan clear and she has stretched bowel and impacted feaces , she is on movicol and buscopan at the moment . Today she has woke up with very painful throat neck and mouth sore especially on roof of mouth . Is
Kristaapril
in
Crohn's and Colitis Support
4 years ago
Pneumonia
I am 51 year old male, I have had pneumonia 3 times in the last 5 years. Would I be more at risk with this corona virus. Is there anything I can do or take to boost my immune system? Do lungs recover completely from pneumonia or are they always weakened? I have had the NHS pneumonia jab and always have
I am 51 year old male, I have had pneumonia 3 times in the last 5 years. Would I be more at risk with this corona virus. Is there anything I can do or take to boost my immune system? Do lungs recover completely from pneumonia or are they always weakened? I have had the NHS pneumonia jab and always have
Nickent68
in
Lung Conditions Community Forum
4 years ago
Things to try that help my tinnitus
Hi everyone, I developed tinnitus 8 years ago following a head injury.l had a few years of relief but then it started again in December with hissing,whooshing,pitches and electric current sounds. I had a breakdown at Christmas but I am now in more or less in control and the volume has have gone from
Hi everyone, I developed tinnitus 8 years ago following a head injury.l had a few years of relief but then it started again in December with hissing,whooshing,pitches and electric current sounds. I had a breakdown at Christmas but I am now in more or less in control and the volume has have gone from
Hidden
in
British Tinnitus Association
4 years ago
Flu jab - anyone have suspected autoimmune reactions?
Hi all, Does anyone here believe they have had/know they have had a an episode of autoimmune thyroid disease precipitated by the flu jab? Does anyone know if it is a known thing, that flu jabs can kick off an autoimmune reaction in thyroid patients? I am looking into any events which may have possibly
Hi all, Does anyone here believe they have had/know they have had a an episode of autoimmune thyroid disease precipitated by the flu jab? Does anyone know if it is a known thing, that flu jabs can kick off an autoimmune reaction in thyroid patients? I am looking into any events which may have possibly
BigBrownBear
in
Thyroid UK
4 years ago
Coronavirus - are we at increased risk?
I'm sure we're all worrying about this but as they didn't think I was 'vulnerable' enough for a flu jab as I'm undiagnosed (I have FM and ME) I'm wondering if I'm considered vulnerable for this. I'm 60 and had pleurisy over 25 years ago. I also worry about other family members, one who has MS and also
I'm sure we're all worrying about this but as they didn't think I was 'vulnerable' enough for a flu jab as I'm undiagnosed (I have FM and ME) I'm wondering if I'm considered vulnerable for this. I'm 60 and had pleurisy over 25 years ago. I also worry about other family members, one who has MS and also
FoggyMoggy
in
LUPUS UK
4 years ago
Unable to have Cystoscopy and BCG treatment
I’m due for a Cystoscopy and BCG Treatment for my Bladder Cancer but I received a phone call from the Hospital who told me “Sorry Phil, type 2 operations due to the Coronavirus are unable to be done at the moment and may not be for 6mths. Doesn’t worry me as the Virus is more important. I’ve been through
I’m due for a Cystoscopy and BCG Treatment for my Bladder Cancer but I received a phone call from the Hospital who told me “Sorry Phil, type 2 operations due to the Coronavirus are unable to be done at the moment and may not be for 6mths. Doesn’t worry me as the Virus is more important. I’ve been through
phil3
in
Fight Bladder Cancer
4 years ago
Coronavirus - how much of a risk?
I'm sure we're all worrying about this but as they didn't think I was 'vulnerable' enough for a flu jab, I'm wondering if I'm considered vulnerable for this. I'm 60 and had pleurisy over 25 years ago. I also worry about other family members, one who has MS and also my mother who is elderly but very
I'm sure we're all worrying about this but as they didn't think I was 'vulnerable' enough for a flu jab, I'm wondering if I'm considered vulnerable for this. I'm 60 and had pleurisy over 25 years ago. I also worry about other family members, one who has MS and also my mother who is elderly but very
FoggyMoggy
in
Fibromyalgia Action UK
4 years ago
Pneumonia
Hello. Just a thought,had flu jab but never been asked to have Pneumonia jab. I thought it only applied if you were over 80. I think I might ask my GP about this. Any info please. Stay well everybody.
Hello. Just a thought,had flu jab but never been asked to have Pneumonia jab. I thought it only applied if you were over 80. I think I might ask my GP about this. Any info please. Stay well everybody.
orange33
in
NRAS
4 years ago
Liver cirrhosis
Hi I have my liver scan which says my liver has coarse and patchyechoc
Hi I have my liver scan which says my liver has coarse and patchyechoc
bottleofdog199
in
British Liver Trust
4 years ago
Starting Journey with T3 - need advice :)
Hi all, I have moved my story to my profile I have just started taking T3 and have questions about dosage. I research different brands of T3 and manged to find a brand sold in turkey that is a good price. I bought 1 box and started taking them last week. From doing research I realised I need to start
Hi all, I have moved my story to my profile I have just started taking T3 and have questions about dosage. I research different brands of T3 and manged to find a brand sold in turkey that is a good price. I bought 1 box and started taking them last week. From doing research I realised I need to start
lizziee1234
in
Thyroid UK
4 years ago
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