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COVID diagnosis
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Guinness4822
in
CLL Support
2 months ago
COVID, FND, and Cymbalta Ruined My Life
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
LoverOfAllThings
in
Functional Neurological Disorder - FND Hope
2 months ago
Increase in Synthroid Dose Worse Before Feeling Better?
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Clarabethk
in
Thyroid UK
2 months ago
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Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse
Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse
Trish_PBG
in
FND Action
2 months ago
Hello again
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Trish_PBG
in
Functional Neurological Disorder - FND Hope
2 months ago
covid booster (Maderna)
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
Mybirthday1975
in
NRAS
2 months ago
Omicron variant
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
swimmer
in
Lung Conditions Community Forum
2 months ago
Scared and lost
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Foi24
in
British Liver Trust
2 months ago
Covid and extending NHS funded time
I am due to start long protocol in exactly a week, with a prostrap injection. My husband has tested positive for Covid today and although I am testing negative I think I’m bound to get it. Our clinic will delay by 7-10 weeks depending if we both test positive for Covid. I’m devastated as we are only
I am due to start long protocol in exactly a week, with a prostrap injection. My husband has tested positive for Covid today and although I am testing negative I think I’m bound to get it. Our clinic will delay by 7-10 weeks depending if we both test positive for Covid. I’m devastated as we are only
Rachiebabe
in
Fertility Network UK
2 months ago
Covid Booster Eligibility
I am 65 with compensated cirrhosis. I have portal hypertension and grade 1/2 oesophagal varices with bloods mostly in range. I do have anaemia and low platelets but thankfully no ascites or HE (fingers crossed). Following a post on here a few days ago about cirrhosis and eligibility for a spring Covid
I am 65 with compensated cirrhosis. I have portal hypertension and grade 1/2 oesophagal varices with bloods mostly in range. I do have anaemia and low platelets but thankfully no ascites or HE (fingers crossed). Following a post on here a few days ago about cirrhosis and eligibility for a spring Covid
AnxiousPete
in
British Liver Trust
2 months ago
shall CLL patient do Covid vaccination?
shall CLL patients do covid 19 vaccine?
shall CLL patients do covid 19 vaccine?
al444
in
CLL Support
2 months ago
Covid booster UK
Does anyone know if we can get spring boosters for Covid? I got the autumn one because of epilepsy, but it looks as though neurological conditions aren’t on the spring list.
Does anyone know if we can get spring boosters for Covid? I got the autumn one because of epilepsy, but it looks as though neurological conditions aren’t on the spring list.
GillyA
in
Epilepsy Action
2 months ago
No Cominarty Vaccine!!
I've had the call for my Spring covid booster, but unfortunately I can't have Spikevax (Moderna) as last time I was given it I spent the next 6mths sorting out a heart arrhythmia that seemed to have been triggered by it. My cardiologist said he'd seen a really significant number of new patients, all
I've had the call for my Spring covid booster, but unfortunately I can't have Spikevax (Moderna) as last time I was given it I spent the next 6mths sorting out a heart arrhythmia that seemed to have been triggered by it. My cardiologist said he'd seen a really significant number of new patients, all
Kendrew
in
PMRGCAuk
3 months ago
reaction to Spikevax XBB 1.5Moderna
Just want to share that I had the above covid booster on Thursday (2nd May) and it appears to have triggered a lupus flare (in my case, rash, aching joints, splitting headache, extreme fatigue). I normally take prednisolone when I have a flare but feel it would be counter productive to what the vaccination
Just want to share that I had the above covid booster on Thursday (2nd May) and it appears to have triggered a lupus flare (in my case, rash, aching joints, splitting headache, extreme fatigue). I normally take prednisolone when I have a flare but feel it would be counter productive to what the vaccination
Larks0ng
in
LUPUS UK
3 months ago
Do I need an ablation?
i’ve been on the waiting list for an ablation and the appointment has finally come up however I am really having second thoughts about having this procedure as I’ve finally been feeling very well lately after three years of highly symptomatic long Covid. Also I’ve only had one episode of AF in the last
i’ve been on the waiting list for an ablation and the appointment has finally come up however I am really having second thoughts about having this procedure as I’ve finally been feeling very well lately after three years of highly symptomatic long Covid. Also I’ve only had one episode of AF in the last
Midnight2022
in
Atrial Fibrillation Support
3 months ago
Headaches / update, also Spring Covid Vaccine update.
I was grateful for everyone’s’ replies to my recent post and I telephoned my Haematologist who advised a blood test and to see a doctor as soon as possible If I couldn’t see my GP the Haematologist said they’d fit me in at the hospital clinic. However, I had a full blood test that day at my G.P’s and
I was grateful for everyone’s’ replies to my recent post and I telephoned my Haematologist who advised a blood test and to see a doctor as soon as possible If I couldn’t see my GP the Haematologist said they’d fit me in at the hospital clinic. However, I had a full blood test that day at my G.P’s and
azaelea
in
MPN Voice
3 months ago
Covid booster
I had my Covid booster jab yesterday,my ibs was settling down ,but has got worse since I had it.Has anybody else experienced this ?
I had my Covid booster jab yesterday,my ibs was settling down ,but has got worse since I had it.Has anybody else experienced this ?
mousey1
in
IBS Network
3 months ago
First time COVID
I got really poorly on the 7th September last year, I phoned the doctors and they wouldn't see me at all, don't really blame them, they are under so much strain.I phoned 111 and when I told them me my illnesses, they wanted to send an ambulance, three different people I talked to all wanted to send an
I got really poorly on the 7th September last year, I phoned the doctors and they wouldn't see me at all, don't really blame them, they are under so much strain.I phoned 111 and when I told them me my illnesses, they wanted to send an ambulance, three different people I talked to all wanted to send an
Itsmeok
in
Lung Conditions Community Forum
3 months ago
Reactions to COVID boosters
Hi, I've been getting the COVID boosters in the UK on a regular basis, but my reaction each time has gotten worse. With the one six months ago and the one last week, I was wiped out for 24 hours afterward, which hadn't happened with the previous boosters. The pharmacist last week was surprised at my
Hi, I've been getting the COVID boosters in the UK on a regular basis, but my reaction each time has gotten worse. With the one six months ago and the one last week, I was wiped out for 24 hours afterward, which hadn't happened with the previous boosters. The pharmacist last week was surprised at my
SAT_poet
in
CLL Support
3 months ago
Upcoming hospital appointment
I was diagnosed with a 25mm AN last October. It totally came out of the blue. I'd been suffering from Long Covid for over a year and I started to have dizziness and body veer to the left when walking. I was also struggling with being in a room where multiple conversations were happening, as I couldn't
I was diagnosed with a 25mm AN last October. It totally came out of the blue. I'd been suffering from Long Covid for over a year and I started to have dizziness and body veer to the left when walking. I was also struggling with being in a room where multiple conversations were happening, as I couldn't
EssEmBee
in
Acoustic Neuroma Support
3 months ago
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