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Covid vax and AFIB
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
Awksom
in
CLL Support
8 months ago
Help on what to expect with this 6 month follow up?
Hi All, My father will be going in for his 6 month follow up on August 2nd. 6 months since he has completed radiation. So my extreme anxiety and worrying has officially returned in full force. In the past gaining knowledge here on this forum has restored some of my sanity so hope it is okay that pry
Hi All, My father will be going in for his 6 month follow up on August 2nd. 6 months since he has completed radiation. So my extreme anxiety and worrying has officially returned in full force. In the past gaining knowledge here on this forum has restored some of my sanity so hope it is okay that pry
FormulaRob
in
Advanced Prostate Cancer
1 year ago
...and now I have a cold!
The last couple of weeks have been so busy with commitments both during the day and the evenings that I've only managed 2 runs in the last 10 days. Today should be Week 5 run 3 but I've woken up with a cold, headache and sore throat. AND it's raining AGAIN! Think I might just stay in bed.
The last couple of weeks have been so busy with commitments both during the day and the evenings that I've only managed 2 runs in the last 10 days. Today should be Week 5 run 3 but I've woken up with a cold, headache and sore throat. AND it's raining AGAIN! Think I might just stay in bed.
Sewandrunmore
in
Couch to 5K
3 months ago
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Anti viral?
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Vqueen
in
Vasculitis UK
8 months ago
Being taking off Pegasys. :( Looking for alternatives
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
JustKeepSw1mming
in
MPN Voice
9 months ago
Flu shot debate, I've noticed a decline
My mom is 94 and a sibling took her for a flu shot without my knowledge. I then visited my mom about 10 days later and noticed her blood pressure was up to 198, even while lying down. I took her to immediate care where they brought it down but it continues to stay higher than usual and the cardiologist
My mom is 94 and a sibling took her for a flu shot without my knowledge. I then visited my mom about 10 days later and noticed her blood pressure was up to 198, even while lying down. I took her to immediate care where they brought it down but it continues to stay higher than usual and the cardiologist
GooseEggs
in
Atrial Fibrillation Support
3 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
6 months ago
Intro
All my life, since first fickle finger test at 16, I have had either an enlarged prostate or a VERY large prostate. Annual PSA for well over 20 years, always good. 18 months ago, 5, which they tell me for my advanced age is "good". Urologist followup due to a kidney stone previous year 3 months after
All my life, since first fickle finger test at 16, I have had either an enlarged prostate or a VERY large prostate. Annual PSA for well over 20 years, always good. 18 months ago, 5, which they tell me for my advanced age is "good". Urologist followup due to a kidney stone previous year 3 months after
Flathead
in
Advanced Prostate Cancer
1 year 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
7 months ago
Need advice about T3 levels
Hi, I have had some tests recently which included thyroid levels and my free T3 levels are 3.1 which appears to me, to be right on the borderline of normal. The free T4 and the TSH are fine by the look of them. Im just wondering if that T3 level is a bit low. I dont have any symptoms I would describe
Hi, I have had some tests recently which included thyroid levels and my free T3 levels are 3.1 which appears to me, to be right on the borderline of normal. The free T4 and the TSH are fine by the look of them. Im just wondering if that T3 level is a bit low. I dont have any symptoms I would describe
soupfiend
in
Thyroid UK
4 months ago
Ambiee
Hi there diagnosed with PMR April 23, after having very bad lower middle back pain, pain in shoulders arms & neck (ha MRI as originally thought it was slipped lower disc, but negative on this, raised blood results confirmed PMRBeen on Prednisolone tapering regime started on 30mg now at 1mg only seen
Hi there diagnosed with PMR April 23, after having very bad lower middle back pain, pain in shoulders arms & neck (ha MRI as originally thought it was slipped lower disc, but negative on this, raised blood results confirmed PMRBeen on Prednisolone tapering regime started on 30mg now at 1mg only seen
Singham1
in
PMRGCAuk
4 months ago
B12 Ampoules
Hello everyone. I hope you are all keeping well 🙏 I am slowly recovering from Covid which I caught 6 weeks ago. I had the booster vaccine- the 4th vaccine-It takes 2 weeks to become effective and I managed to catch Covid before the vaccine kicked in. Just my luck ! 🙄Wish I could be so lucky with
Hello everyone. I hope you are all keeping well 🙏 I am slowly recovering from Covid which I caught 6 weeks ago. I had the booster vaccine- the 4th vaccine-It takes 2 weeks to become effective and I managed to catch Covid before the vaccine kicked in. Just my luck ! 🙄Wish I could be so lucky with
dollcat
in
Pernicious Anaemia Society
8 months ago
Anyone had hand therapy for Chronic repetitive strain injury of the wrists?
My question is has anyone ever had hand therapy for chronic tendonitis or like a chronic repetitive strain injury in your wrist? And if so did it help with the pain? This is the only thing that I've not tried besides obviously I've not tried surgery and I asked my orthopedic hand dr about it and he doesn't
My question is has anyone ever had hand therapy for chronic tendonitis or like a chronic repetitive strain injury in your wrist? And if so did it help with the pain? This is the only thing that I've not tried besides obviously I've not tried surgery and I asked my orthopedic hand dr about it and he doesn't
Hidden
in
Pain Concern
8 months ago
anti NMDA encephalitis
Hi! My husband had HSV1 encephalitis in March-April 2023, then anti NMDA encephalitis May-August 2023. He had the steroids, the plasma exchange but it was the Rituximab that finally got it sorted. I’m just looking to connect with anyone that has suffered with it or their families?! We don’t have
Hi! My husband had HSV1 encephalitis in March-April 2023, then anti NMDA encephalitis May-August 2023. He had the steroids, the plasma exchange but it was the Rituximab that finally got it sorted. I’m just looking to connect with anyone that has suffered with it or their families?! We don’t have
AntiNMDAWarriorWife
in
Headway
4 months ago
Pneumonia vaccine
Hi all I have Lupus SLE, and numerous other thing, just wondering how often do we need the pneumonia vaccine TIA
Hi all I have Lupus SLE, and numerous other thing, just wondering how often do we need the pneumonia vaccine TIA
MrGrey1234
in
LUPUS UK
9 months ago
enlarged lymp node
I had a ct scan yesterday and got the results today. I have enlarged left axillary lymph nodes, largest measuring 19x14 mm, previously subcentimeter and measured 10x8.5. Enlarged left subpectoral lymph nodes are identified. Nothing on the right side. I had a covid vacine about 2-3 weeks ago. The
I had a ct scan yesterday and got the results today. I have enlarged left axillary lymph nodes, largest measuring 19x14 mm, previously subcentimeter and measured 10x8.5. Enlarged left subpectoral lymph nodes are identified. Nothing on the right side. I had a covid vacine about 2-3 weeks ago. The
DianeSH
in
CLL Support
8 months ago
Covid
Hello, everyone I have severe emphysema and I did a test yesterday and I got covid 😱 I am scared it gonna attack my lungs, my chest feeling tighter.Anyone else had covid with emphysema, how did you take care of yourself to stop it going to the lungs.
Hello, everyone I have severe emphysema and I did a test yesterday and I got covid 😱 I am scared it gonna attack my lungs, my chest feeling tighter.Anyone else had covid with emphysema, how did you take care of yourself to stop it going to the lungs.
Madonna1
in
COPD Friends
8 months ago
Pituitary gland not producing TSH
Oct 14, 2022 I had a 3rd Covid Booster shot. The next day I had the "normal" flu symptoms. Oct 20, six days later, I felt I had been hit by a bus, hurting literally from head to toe with different kinds of pain along with heartburn and leg swelling. I figured this was just a reaction that would subside
Oct 14, 2022 I had a 3rd Covid Booster shot. The next day I had the "normal" flu symptoms. Oct 20, six days later, I felt I had been hit by a bus, hurting literally from head to toe with different kinds of pain along with heartburn and leg swelling. I figured this was just a reaction that would subside
Cricket-mas
in
Thyroid UK
8 months ago
Newbie - Should have wrapped up warm! Any tips? 😊
Hi all. I am new here so I thought I would say hi 👋. I started the C25K programme (again!) in Sept 23 and everything was going really well until I picked up a flu bug. I had to stop for a few weeks and I started the programme up again, only to the catch COVID 😭. I tried to start again after Christmas
Hi all. I am new here so I thought I would say hi 👋. I started the C25K programme (again!) in Sept 23 and everything was going really well until I picked up a flu bug. I had to stop for a few weeks and I started the programme up again, only to the catch COVID 😭. I tried to start again after Christmas
N3vrGiv3up
in
Couch to 5K
4 months ago
Exercise and PMR
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
Indigo2417
in
PMRGCAuk
8 months ago
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