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stiffness
Hi I have read that people experience lot of stiffness with PMR , especially in the mornings . However , I never do , maybe slightly for a few mins. GPS say I do have pmr. My inflammation levels were 39 in the spring . I was given 40mg steroids per day , as suspected GCA . Then saw a rheumy who
Hi I have read that people experience lot of stiffness with PMR , especially in the mornings . However , I never do , maybe slightly for a few mins. GPS say I do have pmr. My inflammation levels were 39 in the spring . I was given 40mg steroids per day , as suspected GCA . Then saw a rheumy who
TedTheMaineCoon
in
PMRGCAuk
7 months ago
Post Covid for a Cllier
Came down with Covid 7 days ago - like a horrid bout of flu. Managed to get anti virals sent by the hospital on the second day at 10pm- great service Chelsea and Westminster hospital. Now tested negative yesterday but still got heavy cold and sore throat and feel weak. When will it go away??
Came down with Covid 7 days ago - like a horrid bout of flu. Managed to get anti virals sent by the hospital on the second day at 10pm- great service Chelsea and Westminster hospital. Now tested negative yesterday but still got heavy cold and sore throat and feel weak. When will it go away??
Nucleusman
in
CLL Support
4 months ago
Delay starting hydrea for vaccines?
Unfortunately, this question came to me after I saw the doctor. A month ago, I was referred to a hematologist for abdominal pain, abnormal CBC and splenomegaly. This week, after finding JAK2 and a confirmatory bone marrow analysis, the doctor prescribed 500mg HU per day for PV and scheduled a return
Unfortunately, this question came to me after I saw the doctor. A month ago, I was referred to a hematologist for abdominal pain, abnormal CBC and splenomegaly. This week, after finding JAK2 and a confirmatory bone marrow analysis, the doctor prescribed 500mg HU per day for PV and scheduled a return
Scroop
in
MPN Voice
6 months ago
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Can I transmit Covid19 if I have recovered?
I live at home, and tested positive for Covid 9 days ago, and did not isolate from my parents during this time. I am now testing negative, and have plans with my girlfriend this weekend. However, it turns out my parents have now tested positive and I still have cold symptoms (even with a neg test).
I live at home, and tested positive for Covid 9 days ago, and did not isolate from my parents during this time. I am now testing negative, and have plans with my girlfriend this weekend. However, it turns out my parents have now tested positive and I still have cold symptoms (even with a neg test).
Dannyboy2023
in
Men's Health Forum
6 months ago
The way you access free COVID-19 testing is changing in England and Northern Ireland.
The way you access free COVID-19 testing is changing in England and Northern Ireland. If you are eligible for COVID-19 treatments, you can get free lateral flow tests to test for COVID-19. The way you access these is changing in England and Northern Ireland. You can no longer order them online and you
The way you access free COVID-19 testing is changing in England and Northern Ireland. If you are eligible for COVID-19 treatments, you can get free lateral flow tests to test for COVID-19. The way you access these is changing in England and Northern Ireland. You can no longer order them online and you
Debbie_kinsey
Administrator
in
LUPUS UK
6 months ago
update on knee pain
As most of you will probably know, I injured my knee on holiday at the end of June, when my knee would buckle. Over the months Drs have always been more concerned that my back or pelvis was injured with a fall in the shower, due to the knee buckling. I had CT scans and MRIof the spine and pelvis, but
As most of you will probably know, I injured my knee on holiday at the end of June, when my knee would buckle. Over the months Drs have always been more concerned that my back or pelvis was injured with a fall in the shower, due to the knee buckling. I had CT scans and MRIof the spine and pelvis, but
Runrig01
in
NRAS
7 months ago
Dry achey eyes
I have ET Calr diagnosed 5 years ago on Hydroxycarbamide. Recently I have had problems with my eyes. Very achey, dry, frequent styes. My GP gave me eyedrops for the dry eyes, which have helped but the eye ache is still a problem. Anyone else experienced this?
I have ET Calr diagnosed 5 years ago on Hydroxycarbamide. Recently I have had problems with my eyes. Very achey, dry, frequent styes. My GP gave me eyedrops for the dry eyes, which have helped but the eye ache is still a problem. Anyone else experienced this?
Pippapot
in
MPN Voice
8 months ago
T since Covid
My T started just after I had Covid . It is up and down in volume but every day. Have any others on here had T since Covid and still have it. Andy
My T started just after I had Covid . It is up and down in volume but every day. Have any others on here had T since Covid and still have it. Andy
Andy4713
in
Tinnitus UK
6 months ago
UTI/bladder issues/pain
This article is an interesting read… https://www.medicalnewstoday.com/articles/overactive-bladder-thyroid Especially as of a lately iv been struggling with my bladder, and a UTI, the UTI cleared up with antibiotics (which nearly killed me off!) but now certain foods/drinks trigger bladder pain!? I
This article is an interesting read… https://www.medicalnewstoday.com/articles/overactive-bladder-thyroid Especially as of a lately iv been struggling with my bladder, and a UTI, the UTI cleared up with antibiotics (which nearly killed me off!) but now certain foods/drinks trigger bladder pain!? I
ThyroidObsessed
in
Thyroid UK
6 months ago
Postnasal Drip
Help everybody again! Doctor being really unhelpful. I still have this horrendous post nasal drip that finally I have discovered by going private to an ENT chap is silent reflux. I am having an Ensoscopy on Friday to determine it is my Hyitas Hernia playing up. In the meantime my post nasal drip has
Help everybody again! Doctor being really unhelpful. I still have this horrendous post nasal drip that finally I have discovered by going private to an ENT chap is silent reflux. I am having an Ensoscopy on Friday to determine it is my Hyitas Hernia playing up. In the meantime my post nasal drip has
Bronchiectasislady69
in
Lung Conditions Community Forum
6 months ago
Ear infection
Hi everyone I post about my ear infection before you know. Still I have infection fluid in my ear. 2 weeks ago ENT community service did micro-suction in my ear I feel bit okay but again fluid coming and feel really uncomfortable . I went Gp last monday they put me again antibiotics co amoxiclav
Hi everyone I post about my ear infection before you know. Still I have infection fluid in my ear. 2 weeks ago ENT community service did micro-suction in my ear I feel bit okay but again fluid coming and feel really uncomfortable . I went Gp last monday they put me again antibiotics co amoxiclav
sun_1234
in
Tinnitus UK
8 months ago
Am I at risk of shingles
Hello - i'm about to go and spend a weekend with my in laws and they have just announced they have shingles. Am I at risk of this having ET?
Hello - i'm about to go and spend a weekend with my in laws and they have just announced they have shingles. Am I at risk of this having ET?
Fjdjdjdjd
in
MPN Voice
6 months ago
Pneumonia in CBD
Hi I’ve just found out my mum is in hospital with pneumonia and I’m on holiday in Australia - I’m looking for flights and trying to get home asap. Has anyone had experience of getting this when you already have CBD or has anyone had a loved one who has had pneumonia before? I know it’s not a great thing
Hi I’ve just found out my mum is in hospital with pneumonia and I’m on holiday in Australia - I’m looking for flights and trying to get home asap. Has anyone had experience of getting this when you already have CBD or has anyone had a loved one who has had pneumonia before? I know it’s not a great thing
Chelle1981uk
in
PSP Association
1 year ago
Hypo with CKD & Bradycardia
Him A little about me, 55, female, psoriatic arthritis from a child, treated with biological Cosentxy and Methotrexate. Fatigue/weight gain led to a diagnosis of Fibromyalgia in 2018 after gallbladder removal. I was treated with high dose steroid injections. Over the next 18 months I suffered 12
Him A little about me, 55, female, psoriatic arthritis from a child, treated with biological Cosentxy and Methotrexate. Fatigue/weight gain led to a diagnosis of Fibromyalgia in 2018 after gallbladder removal. I was treated with high dose steroid injections. Over the next 18 months I suffered 12
SimbaT
in
Thyroid UK
7 months ago
COVID Vaccination and Chest pain
Is anyone out there concerned that there might be a link between COVID booster vaccinations and chest pain. I've posted before about my condition but here's a recap - In December 21, about 10 days after a Pfizer booster, I started to develop chest pain at rest and a burning sensation down my left arm
Is anyone out there concerned that there might be a link between COVID booster vaccinations and chest pain. I've posted before about my condition but here's a recap - In December 21, about 10 days after a Pfizer booster, I started to develop chest pain at rest and a burning sensation down my left arm
Acapella
in
British Heart Foundation
6 months ago
Covid exposure at 8 weeks 3 days pregnant
I'm looking for some reassurance or support. I was in contact with my 9 year old nephew yesterday. He had no symptoms but we spent a good length of time in same room together watching TV with minimal ventilation. Last night he got up with a fever and tested positive for covid on an LFT this morning.
I'm looking for some reassurance or support. I was in contact with my 9 year old nephew yesterday. He had no symptoms but we spent a good length of time in same room together watching TV with minimal ventilation. Last night he got up with a fever and tested positive for covid on an LFT this morning.
SMBCnewbie
in
Fertility Network UK - Pregnancy Support
6 months ago
Covid vaccines and Lupus Flare - up
Everytime I get a Covid shot I get a painful Lupus Flare- up for 4 to 5 months . In the 30 years of having Lupus I have never been so sick as since I have been taking Covid shots . I am thinking I will wait at least 1 year , if not longer for another one .
Everytime I get a Covid shot I get a painful Lupus Flare- up for 4 to 5 months . In the 30 years of having Lupus I have never been so sick as since I have been taking Covid shots . I am thinking I will wait at least 1 year , if not longer for another one .
seabreezegirl
in
LUpus Patients Understanding and Support
6 months ago
Vaccines – at what point do they become a disbenefit?
I need to state out front that I’m not anti vaccination, I believe in the benefits having had several as a kid and now 6 anti COVID doses. But I’m now being bombarded with NHS offers of several different vaccines, COVID, Flu and shingles among them, and it has made me think of possible issues before
I need to state out front that I’m not anti vaccination, I believe in the benefits having had several as a kid and now 6 anti COVID doses. But I’m now being bombarded with NHS offers of several different vaccines, COVID, Flu and shingles among them, and it has made me think of possible issues before
IWVC
in
CLL Support
7 months ago
Reactions to Antibiotics and unable to treat UTI/Prostatitis
Hello all, I'll try to keep this as short as possible! Background: Vegan since 2012, vegetarian from 2007. I stopped multivitamin that contained 160 mcg of B12 in July 2021 until late July 2022. Dietary intake 1 mcg b12 /day for a year (swapped out soy milk for another version and it wasn't fortified
Hello all, I'll try to keep this as short as possible! Background: Vegan since 2012, vegetarian from 2007. I stopped multivitamin that contained 160 mcg of B12 in July 2021 until late July 2022. Dietary intake 1 mcg b12 /day for a year (swapped out soy milk for another version and it wasn't fortified
Whoa182
in
Pernicious Anaemia Society
1 year ago
Mouth thrush
Does anyone else suffer from thrush in the mouth, due to taking antibiotics. I think l may have it as my tongue is coated in white and l have lost a lot of my sense of taste. I have just started taking colomycin in Nebuliser for pseudomonas infection.
Does anyone else suffer from thrush in the mouth, due to taking antibiotics. I think l may have it as my tongue is coated in white and l have lost a lot of my sense of taste. I have just started taking colomycin in Nebuliser for pseudomonas infection.
falcon68
in
Lung Conditions Community Forum
8 months ago
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