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Inflammatory arthritis & pulmonary embolisms - an update & a question on possible meds.
Hi all , In my 1st ever post on here 6 days ago regarding a link between inflammatory arthritis & pulmonary embolisms - I received many replies - all of them excellent. Thank you so much you lovely people! Today I saw my Rheumatologist & worded my question to him very, very carefully: "So Doctor
Hi all , In my 1st ever post on here 6 days ago regarding a link between inflammatory arthritis & pulmonary embolisms - I received many replies - all of them excellent. Thank you so much you lovely people! Today I saw my Rheumatologist & worded my question to him very, very carefully: "So Doctor
YorkieBard
in
NRAS
21 days ago
Hi, new to this page/forum, looking for information and advice.
Have been on PAS page and Thyroid UK page for a few years but just thought I'd be greedy and join yourselves too. Have been having increasing levels of pain and discomfort for years but just told lose weight, take brufen. Last few years have been awful , eventually got a referral to Rheumatology. Bloods
Have been on PAS page and Thyroid UK page for a few years but just thought I'd be greedy and join yourselves too. Have been having increasing levels of pain and discomfort for years but just told lose weight, take brufen. Last few years have been awful , eventually got a referral to Rheumatology. Bloods
Polo22
in
NRAS
27 days ago
Steroid injection into Kiloid Scars
I have a dermatology appointment on Saturday (yes an NHS appointment on a Saturday) to review treatment of kiloid scars. I think one of the options suggested may be direct steroid injections into the scars themselves. I have had PMR for 9 years and have at last got stable on 7 mg prednisolone daily
I have a dermatology appointment on Saturday (yes an NHS appointment on a Saturday) to review treatment of kiloid scars. I think one of the options suggested may be direct steroid injections into the scars themselves. I have had PMR for 9 years and have at last got stable on 7 mg prednisolone daily
scrambledegg
in
PMRGCAuk
29 days ago
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Worse after an UTI and Covid
Good afternoon. About five weeks ago I developed an UTI for which I took three separate courses of antibiotics as it wouldn't clear. In the same period I contracted Covid which didn't affect me much. I only found out that I had it because a friend who I'd spent time with had done a Covid test and it
Good afternoon. About five weeks ago I developed an UTI for which I took three separate courses of antibiotics as it wouldn't clear. In the same period I contracted Covid which didn't affect me much. I only found out that I had it because a friend who I'd spent time with had done a Covid test and it
Siena62
in
PMRGCAuk
17 hours ago
COVID-19 and Parkinson’s disease: a single-center study and Mendelian randomization study
More than one-third of patients with PD exhibits exacerbated motor symptoms, with bradykinesia being the most prominent. The findings from this cross-sectional study suggest that COVID-19 infection contributes to the deterioration of motor symptoms in PD patients. https://www.nature.com/articles/s41598
More than one-third of patients with PD exhibits exacerbated motor symptoms, with bradykinesia being the most prominent. The findings from this cross-sectional study suggest that COVID-19 infection contributes to the deterioration of motor symptoms in PD patients. https://www.nature.com/articles/s41598
Farooqji
in
Cure Parkinson's
18 hours ago
Germantara
Hi everyone excuse me rant but as you know I have copd well I did post I've got covid it started Sunday well I've take my trimbow 2 times a day I've got my ventolin and carberstien I always have rescue pack steriod tablets so I started my steriod tablets on Sunday I take 6 once a day I'm still
Hi everyone excuse me rant but as you know I have copd well I did post I've got covid it started Sunday well I've take my trimbow 2 times a day I've got my ventolin and carberstien I always have rescue pack steriod tablets so I started my steriod tablets on Sunday I take 6 once a day I'm still
Germantara
in
Lung Conditions Community Forum
2 days ago
Covid with TCZ
I am on my second bout of Covid. Because I am on TCZ, I have had the antiviral Paxlovid both times. The first time it effected a rapid cure, but not this time. Although I am not particularly ill, I still have a productive cough and have tested strongly positive again this morning. Proper fed up. Have
I am on my second bout of Covid. Because I am on TCZ, I have had the antiviral Paxlovid both times. The first time it effected a rapid cure, but not this time. Although I am not particularly ill, I still have a productive cough and have tested strongly positive again this morning. Proper fed up. Have
Sharitone
in
PMRGCAuk
2 days ago
Covid
I tested positive for covid a few days ago and got the oddest symptom: very, very sore throat keeping me unable to swallow and thus unable to drink my water. Been to ER twice and getting admitted now to jydrste me. Gfr dropped from 30 to 24. Wish me luck.
I tested positive for covid a few days ago and got the oddest symptom: very, very sore throat keeping me unable to swallow and thus unable to drink my water. Been to ER twice and getting admitted now to jydrste me. Gfr dropped from 30 to 24. Wish me luck.
drmind
in
Kidney Disease
3 days ago
IVF after covid
Hello, I had Covid last month and was due to start another round at the end of this month. However the clinic have recommended that I wait at least 3 months after having Covid to complete my next round. I am 43 and running out of time and would just like to get on with it but worried about a potential
Hello, I had Covid last month and was due to start another round at the end of this month. However the clinic have recommended that I wait at least 3 months after having Covid to complete my next round. I am 43 and running out of time and would just like to get on with it but worried about a potential
Rowan80
in
Fertility Network UK
4 days ago
Has anyone who has had an ablation, caught Covid and it’s brought their AFib back. ?
My Sister in law has just tested positive with Covid and we were at her 70th birthday party last night. When I have an AFib episode, I have been told by the Doctors, to go to A&E, as my heart rate and blood pressure soar and they want to keep an eye on me and try and stop it, so when I had a AFib episode
My Sister in law has just tested positive with Covid and we were at her 70th birthday party last night. When I have an AFib episode, I have been told by the Doctors, to go to A&E, as my heart rate and blood pressure soar and they want to keep an eye on me and try and stop it, so when I had a AFib episode
Sixtychick
in
British Heart Foundation
4 days ago
Atrial Fibrillation and Covid
I had been in normal sinus rhythm for 2 months until just over a week ago when I went into constant AF for 5 days, then it just corrected itself. I didn't do a Covid Test and am sure that I would have tested positive if I had, because a few days before this happened I'd had headaches, feeling tired
I had been in normal sinus rhythm for 2 months until just over a week ago when I went into constant AF for 5 days, then it just corrected itself. I didn't do a Covid Test and am sure that I would have tested positive if I had, because a few days before this happened I'd had headaches, feeling tired
KeepingHealthy
in
British Heart Foundation
5 days ago
COVID VACCINE.?
I had PMR from 2013-2018 when I had the all clear. Posting this new information because i have had all my covid vaccines, but since the last 2 boosters I have had aching shoulders and legs pain. My doctor after blood tests because my cp level is 13 I have PMR again and has put me on pred.again 15mgs
I had PMR from 2013-2018 when I had the all clear. Posting this new information because i have had all my covid vaccines, but since the last 2 boosters I have had aching shoulders and legs pain. My doctor after blood tests because my cp level is 13 I have PMR again and has put me on pred.again 15mgs
Zampalion
in
PMRGCAuk
5 days ago
Any recommended cardiologists in far NW/NE England for specific BP problems
Now on 4+ years Long Covid problems with a mix of high BP when for eg sitting ( systolic into 160s), but very low postural hypotension when standing. Have been on 6 pills to reduce BP, left on 5 for 2 years until last Jan. when a Falls consultant with tilt test table diagnosed the postural hypotension
Now on 4+ years Long Covid problems with a mix of high BP when for eg sitting ( systolic into 160s), but very low postural hypotension when standing. Have been on 6 pills to reduce BP, left on 5 for 2 years until last Jan. when a Falls consultant with tilt test table diagnosed the postural hypotension
Judithdalston
in
British Heart Foundation
8 days ago
Post Covid B12 and Vitamin D crash
Hi,I have had multiple health problems since my first bout of Covid in 2022, and blood panels revealed low B12, D and very low ferritin (11). I started having B12 injections and got my ferritin to 159 and my folate up to 45 from 5. I was feeling healthy and many of my symptoms had stopped. I had been
Hi,I have had multiple health problems since my first bout of Covid in 2022, and blood panels revealed low B12, D and very low ferritin (11). I started having B12 injections and got my ferritin to 159 and my folate up to 45 from 5. I was feeling healthy and many of my symptoms had stopped. I had been
Skater21
in
Pernicious Anaemia Society
8 days ago
Belated COVID
Three years free but got unlucky last month with horrible covid. Husband also. I hadn’t had latest booster, he did. Same outcome. I’m feeling back to square one (almost). Any hints about picking up post virus please? Im supplementing igennus B and 3,000 D plus K2 spray. Is it worth testing in a few
Three years free but got unlucky last month with horrible covid. Husband also. I hadn’t had latest booster, he did. Same outcome. I’m feeling back to square one (almost). Any hints about picking up post virus please? Im supplementing igennus B and 3,000 D plus K2 spray. Is it worth testing in a few
Calceolaria
in
Thyroid UK
9 days ago
UTI experience with Imbruvica
hello, when I was on Imbruvica I had many UTI. This is side effects of Imbruvica. I asked my doctor to switch me for another medication and now they m on Venclecta. This is even worse. I do not have UTI anymore , but I’m already sick for Ramsay Hunt this is like Bels Pasley. All these pills for CLL have
hello, when I was on Imbruvica I had many UTI. This is side effects of Imbruvica. I asked my doctor to switch me for another medication and now they m on Venclecta. This is even worse. I do not have UTI anymore , but I’m already sick for Ramsay Hunt this is like Bels Pasley. All these pills for CLL have
farber
in
CLL Support
9 days ago
catching Covid worries
Hi Lupus people! I’m still petrified of catching Covid. I clean all my shopping when it arrives, I wash my hands a lot, I hardly have friends over and go out to restaurants seldom with a friend. I’m a bag of anxiety. What does your life look like? Do you clean a lot? Has the worry of Covid stolen your
Hi Lupus people! I’m still petrified of catching Covid. I clean all my shopping when it arrives, I wash my hands a lot, I hardly have friends over and go out to restaurants seldom with a friend. I’m a bag of anxiety. What does your life look like? Do you clean a lot? Has the worry of Covid stolen your
LilyMistri2
in
LUPUS UK
9 days ago
How do you know it’s b12 deficiency and not ms?
Ok maybe I am going down a bad rabbit hole here and you can save me. But,… All my symptoms of b12 deficiency overlap completely with MS. urinary issues and pain, Blurred vision in one eye Fatigue Depression Anxiety Tingling and buzzing Etc How do I know it’s not one or the other as no tests
Ok maybe I am going down a bad rabbit hole here and you can save me. But,… All my symptoms of b12 deficiency overlap completely with MS. urinary issues and pain, Blurred vision in one eye Fatigue Depression Anxiety Tingling and buzzing Etc How do I know it’s not one or the other as no tests
Gobbozoid
in
Pernicious Anaemia Society
10 days ago
Crash after Covid?
I’m really struggling to balance my body back out after having Covid and so so puzzled. Not sure why this has happened or where to go with it next. Has anyone had a really bad crash after Covid? I’m diagnosed pernicious anaemia and hypothyroid Hashimotos. I had been in the same routine with supplements
I’m really struggling to balance my body back out after having Covid and so so puzzled. Not sure why this has happened or where to go with it next. Has anyone had a really bad crash after Covid? I’m diagnosed pernicious anaemia and hypothyroid Hashimotos. I had been in the same routine with supplements
Littledancingtiger
in
Pernicious Anaemia Society
10 days ago
IBS and Covid
Had Covid for the third time around 2 weeks ago and my IBS is pretty bad over the last few days. This strain gave me different symptoms , got the sore throat and stomach issues . Anyone else found the same after a bout of Covid recently ? Probably doesn’t help I’ve been taking lots of antibiotics
Had Covid for the third time around 2 weeks ago and my IBS is pretty bad over the last few days. This strain gave me different symptoms , got the sore throat and stomach issues . Anyone else found the same after a bout of Covid recently ? Probably doesn’t help I’ve been taking lots of antibiotics
BabblingBrooks
in
IBS Network
11 days ago
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