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hypothyroid pins and needles in feet
I have been Hypo for 20+ years and since last winter I have pins and needle like pain in my feet. This is almost constant but becomes much worse when cold. Toes are cold to the touch and not pink. Dr has diagnosed Reynards but I’m not sure this is correct as it doesn’t appear in bursts. Does anyone
I have been Hypo for 20+ years and since last winter I have pins and needle like pain in my feet. This is almost constant but becomes much worse when cold. Toes are cold to the touch and not pink. Dr has diagnosed Reynards but I’m not sure this is correct as it doesn’t appear in bursts. Does anyone
Ju17
in
Thyroid UK
10 months ago
Pneumonia
Hi. I had my follow up chest x-ray for pneumonia 3 weeks ago and the good news is that it's come back clear. I'm really pleased but I'm still coughing at night and feel a bit breathless in the mornings. I told the doctor when he rang me with the results and he said, the infection has gone but lungs take
Hi. I had my follow up chest x-ray for pneumonia 3 weeks ago and the good news is that it's come back clear. I'm really pleased but I'm still coughing at night and feel a bit breathless in the mornings. I told the doctor when he rang me with the results and he said, the infection has gone but lungs take
Scooby1967
in
Lung Conditions Community Forum
10 months ago
flu and covid booster
I had several texts from the NHS inviting me for both flu and covid shots due to my medical condition. My only condition is AF. I booked in with my local pharmacy today, but he would not give me the booster as I am now on Flecanide and he said under new guidelines it is not recommended. I am very confused
I had several texts from the NHS inviting me for both flu and covid shots due to my medical condition. My only condition is AF. I booked in with my local pharmacy today, but he would not give me the booster as I am now on Flecanide and he said under new guidelines it is not recommended. I am very confused
Deepbreath27
in
Atrial Fibrillation Support
10 months ago
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flu and baby at home
So I think I have awful flu, body aches feeling sick the lot!😭 my baby is really congested and struggling too. I’m going into a flat panic that I have to look after him while barely being able to move😩 I feel like the worst mum and I don’t know what to do, also this flu just doesn’t seem to be shifting
So I think I have awful flu, body aches feeling sick the lot!😭 my baby is really congested and struggling too. I’m going into a flat panic that I have to look after him while barely being able to move😩 I feel like the worst mum and I don’t know what to do, also this flu just doesn’t seem to be shifting
Jayde_96
in
Anxiety Support
10 months ago
Coughing badly after virus ...
Hi allI had a really nasty cold/cough which has left me with a bad cough and a flare up of asthma. Currently on holiday in India and although I am taking Fostair with a a couple of shots of ventolin inbetween, the cough is not dissipating. It's particularly bad at night. The pollution in India is bad
Hi allI had a really nasty cold/cough which has left me with a bad cough and a flare up of asthma. Currently on holiday in India and although I am taking Fostair with a a couple of shots of ventolin inbetween, the cough is not dissipating. It's particularly bad at night. The pollution in India is bad
Padders
in
Asthma Community Forum
10 months ago
Lung nodule
I had a CT scan in hospital while being treated for pneumonia. I understand it could be due to infections or scaring in my lungs. It is also quite common (35%) for people to have these. I going back for an x ray in early January.
I had a CT scan in hospital while being treated for pneumonia. I understand it could be due to infections or scaring in my lungs. It is also quite common (35%) for people to have these. I going back for an x ray in early January.
elanaoali
in
Asthma Community Forum
10 months ago
feeling cold
got af and am always cold is this a symptom of it . Also pain in left arm when I lay on that side in bed . It usually happens in middle of arm .advice welcome
got af and am always cold is this a symptom of it . Also pain in left arm when I lay on that side in bed . It usually happens in middle of arm .advice welcome
Jarvo977
in
Atrial Fibrillation Support
10 months ago
Switch to Mucuna
Apologies if this has been asked and answered earlier. I am looking for a guide to switch from C/L to Green tea/Mucuna. Is there a method to calculate green tea against equivalent carbidopa doses? Is brewed green tea better or green tea extract capsule? Is there any interaction between green tea and
Apologies if this has been asked and answered earlier. I am looking for a guide to switch from C/L to Green tea/Mucuna. Is there a method to calculate green tea against equivalent carbidopa doses? Is brewed green tea better or green tea extract capsule? Is there any interaction between green tea and
JayPwP
in
Cure Parkinson's
1 year ago
Are We Restoring Thyroid Hormone Signaling in Levothyroxine-Treated Patients With Residual Symptoms of Hypothyroidism?
Not yet even glanced - so no comments! [i]
Are We Restoring Thyroid Hormone Signaling in Levothyroxine-Treated Patients With Residual Symptoms of Hypothyroidism?
[/i] [i]Sabina Casula MD[/i] [i]Department of Endocrinology, Miami Veterans Affairs Healthcare System, Miami, Florida[/i] [i]Matthew
Not yet even glanced - so no comments! [i]
Are We Restoring Thyroid Hormone Signaling in Levothyroxine-Treated Patients With Residual Symptoms of Hypothyroidism?
[/i] [i]Sabina Casula MD[/i] [i]Department of Endocrinology, Miami Veterans Affairs Healthcare System, Miami, Florida[/i] [i]Matthew
helvella
Thyroid UK
in
Thyroid UK
1 year ago
Rise in CA125
I’ve recently have had Pneumonia and Pleurisy. My CA125 was checked yesterday and my CNS has just called me to say that it has risen to 64. She also said that it can rise due to the pneumonia and they will discuss it at next weeks MDT meeting. There is a possibility they may repeat my bloods in 4 weeks
I’ve recently have had Pneumonia and Pleurisy. My CA125 was checked yesterday and my CNS has just called me to say that it has risen to 64. She also said that it can rise due to the pneumonia and they will discuss it at next weeks MDT meeting. There is a possibility they may repeat my bloods in 4 weeks
Hota
in
My Ovacome
10 months ago
Reynaud's Problems
Hi there, I'm wondering if anyone has any help or suggestions for me keeping my fingers warm at my work, I'm a postman and my Reynaud's is causing me big problems when the weather is cold my fingers go so cold and numb, I've tried different kind of gloves but nothing works.
Hi there, I'm wondering if anyone has any help or suggestions for me keeping my fingers warm at my work, I'm a postman and my Reynaud's is causing me big problems when the weather is cold my fingers go so cold and numb, I've tried different kind of gloves but nothing works.
Craig_
in
Scleroderma & Raynaud's UK (SRUK)
10 months ago
eosinophilia and nasty chest cold
everything has been good for a year now. I have been prescribed another bio - Tezzy which has been life savingly wonderful. I have reduced steroids and consultant is hopeful of elimination soon. Energy levels have really improved too. So, in the last two days I have nosedived. I put this down to cold
everything has been good for a year now. I have been prescribed another bio - Tezzy which has been life savingly wonderful. I have reduced steroids and consultant is hopeful of elimination soon. Energy levels have really improved too. So, in the last two days I have nosedived. I put this down to cold
Villager2
in
Asthma Community Forum
10 months ago
succumbed with guilt and what if….
Hello friends I don’t know why I am posting, maybe to get advice from people who understand but my dear father lost his battle 2 weeks ago due to sepsis and pneumonia. I took him A&E 4 days before and they completed tests and discharged him saying he just had a cough infection and provided him with
Hello friends I don’t know why I am posting, maybe to get advice from people who understand but my dear father lost his battle 2 weeks ago due to sepsis and pneumonia. I took him A&E 4 days before and they completed tests and discharged him saying he just had a cough infection and provided him with
Khalissi
in
PSP Association
10 months ago
flu shot
I got the flu shot a month ago and I can barely move my arm it’s so painful
I got the flu shot a month ago and I can barely move my arm it’s so painful
Joanecindy
in
PMRGCAuk
10 months ago
Anyone with ET tried ginseng, ginko bilboa, or pomegranates to lower PC?
My son (19y/o) has ET, is JAK2+, and is home from college for the summer. He is currently on a daily aspirin, but I am concerned about his PC continuing to increase over the last month (from 1200 ish to 1400ish). His MPN specialist in NYC is awesome and has said that PC can be finicky. Perhaps finals
My son (19y/o) has ET, is JAK2+, and is home from college for the summer. He is currently on a daily aspirin, but I am concerned about his PC continuing to increase over the last month (from 1200 ish to 1400ish). His MPN specialist in NYC is awesome and has said that PC can be finicky. Perhaps finals
trainerliz
in
MPN Voice
1 year ago
Is it just me !
So I had a viral infection in March and pneumonia that sent me into a really bad flare up of symptoms and I'm currently still in this flare up . Whenever I get any sort of infection it sends me into a flare of symptoms. I also had COVID in September which may be contributing to why my flare up is lasting
So I had a viral infection in March and pneumonia that sent me into a really bad flare up of symptoms and I'm currently still in this flare up . Whenever I get any sort of infection it sends me into a flare of symptoms. I also had COVID in September which may be contributing to why my flare up is lasting
Jillgib
in
Fibromyalgia Action UK
10 months ago
Has prevnar13( pneumonia vaccine ) caused a trigger for people with existing inflammatory conditions?
I’m an autoimmune vasucliits patient . My inflammation in the eye was relatively managed well with immunosuppressants. But since having the Prevnar 13 , my inflammation is back in full swing . Has anyone experienced this ? If so, how have you resolved it ? Please advise .
I’m an autoimmune vasucliits patient . My inflammation in the eye was relatively managed well with immunosuppressants. But since having the Prevnar 13 , my inflammation is back in full swing . Has anyone experienced this ? If so, how have you resolved it ? Please advise .
Udupik
in
PMRGCAuk
10 months ago
ADT relief
I exercise often but still wrestle with muscle and joint aches and pains. On a 1 - 10 scale the aches and pains have been magnified 3 - 6X of what they were pre-Lupron. It seems like my low back aches have been consistent 2x-plus since the Lupron Any suggestions on ache and pain relief from adt? Does
I exercise often but still wrestle with muscle and joint aches and pains. On a 1 - 10 scale the aches and pains have been magnified 3 - 6X of what they were pre-Lupron. It seems like my low back aches have been consistent 2x-plus since the Lupron Any suggestions on ache and pain relief from adt? Does
Cyclingrealtor
in
Advanced Prostate Cancer
2 years ago
Feeling very cold
Can anyone tell me if it's normal to feel very cold with CLL. It seems to be a new symptom, I have been like it for last 2 to 3 weeks. I'm wearing 2 jumpers and trousers and still feeling the cold. So am just wondering if it's normal lol. Donnax
Can anyone tell me if it's normal to feel very cold with CLL. It seems to be a new symptom, I have been like it for last 2 to 3 weeks. I'm wearing 2 jumpers and trousers and still feeling the cold. So am just wondering if it's normal lol. Donnax
PusscatsGoodies
in
CLL Support
10 months ago
Colds and flu…🧐🥹?
”Why don’t lupus patients catch cold? Many, many patients comment on this observation – that during cold and flu epidemics they seem to be the only family member not affected…?”
Professor Graham Hughes, [the London Lupus Centre] 2008
Just wondering about this observation but I personally have
”Why don’t lupus patients catch cold? Many, many patients comment on this observation – that during cold and flu epidemics they seem to be the only family member not affected…?”
Professor Graham Hughes, [the London Lupus Centre] 2008
Just wondering about this observation but I personally have
Suvi8901
in
LUPUS UK
10 months ago
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